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other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. 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Rev.: J. Chem., 6, 18",{"doi":830},{"id":26,"text":835,"url":836,"identifiers":837},"Wang, 2018, Design, synthesis and biological evaluation of chrysin benzimidazole derivatives as potential anticancer agents, Nat. Prod. Res., 32, 2900, 10.1080\u002F14786419.2017.1389940","https:\u002F\u002Fdoi.org\u002F10.1080\u002F14786419.2017.1389940",{"mag":838,"openalex":839,"pm":840,"doi":841},"2767090426","W2767090426","29063798","10.1080\u002F14786419.2017.1389940",{"id":26,"text":843,"url":844,"identifiers":845},"Morais, 2017, Synthesis and biological evaluation of novel 2-aryl benzimidazoles as chemotherapeutic agents, J. Heterocyclic Chem., 54, 255, 10.1002\u002Fjhet.2575","https:\u002F\u002Fdoi.org\u002F10.1002\u002Fjhet.2575",{"mag":846,"openalex":847,"doi":848},"2304812795","W2304812795","10.1002\u002Fjhet.2575",{"id":26,"text":850,"url":851,"identifiers":852},"Shaker, 2015, Synthesis, in vitro and in vivo antitumor and antiviral activity of novel 1-substituted benzimidazole derivatives, J. Enzyme Inhib. Med. Chem., 30, 826, 10.3109\u002F14756366.2014.979344","https:\u002F\u002Fdoi.org\u002F10.3109\u002F14756366.2014.979344",{"mag":853,"openalex":854,"pm":855,"doi":856},"1965654842","W1965654842","25567722","10.3109\u002F14756366.2014.979344",{"id":826,"text":858,"url":828,"identifiers":859},"Onnis, 2016, Design, synthesis and evaluation of antiproliferative activity of new benzimidazolehydrazones, J. Balzarin Mol., 21, 579",{"doi":830},{"id":26,"text":861,"url":862,"identifiers":863},"Acar Çevik, 2018, Antiproliferative cytotoxic, and apoptotic effects of new benzimidazole derivatives bearing hydrazone moiety, J. Heterocyclic Chem., 55, 138, 10.1002\u002Fjhet.3016","https:\u002F\u002Fdoi.org\u002F10.1002\u002Fjhet.3016",{"mag":864,"openalex":865,"doi":866},"2766795847","W2766795847","10.1002\u002Fjhet.3016",{"id":26,"text":868,"url":26,"identifiers":869},"Alanazi, 2017, Design, molecular docking studies, in silico drug likeliness prediction and synthesis of some benzimidazole derivatives as antihypertensive agents, Md. Imranl. Indo American J. of Pharmaceutical Sci., 4, 926",{},{"id":26,"text":871,"url":26,"identifiers":872},"Kankate, 2016, Synthesis and biological evaluation of benzimidazolyl biphenyl derivatives as antihypertensive agents, Int. J. Chem. Concepts, 2, 111",{},{"id":26,"text":874,"url":875,"identifiers":876},"Sharma, 2017, Synthesis of methanesulphonamido-benzimidazole derivatives as gastro-sparing antiinflammatory agents with antioxidant effect, Bioorg. Med. Chem. Lett., 27, 3007, 10.1016\u002Fj.bmcl.2017.05.017","https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.bmcl.2017.05.017",{"mag":877,"openalex":878,"pm":879,"doi":880},"2611222889","W2611222889","28512025","10.1016\u002Fj.bmcl.2017.05.017",{"id":882,"text":883,"url":884,"identifiers":885},"e95c034f-1d5f-4fdd-95bb-9cc8a60abe8c","Sethi, 2017, Synthesis and PASS-assisted evaluation of coumarin–benzimidazole derivatives as potential anti-inflammatory and anthelmintic agents, Med. Chem. Res., 27, 61, 10.1007\u002Fs00044-017-2036-1","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00044-017-2036-1",{"doi":886},"10.1007\u002Fs00044-017-2036-1",{"id":26,"text":888,"url":889,"identifiers":890},"Gaba, 2015, Design, synthesis and biological evaluation of novel 1, 2, 5-substituted benzimidazole derivatives as gastroprotective anti-inflammatory and analgesic agents, Med. Chem., 5, 58, 10.4172\u002F2161-0444.1000243","https:\u002F\u002Fdoi.org\u002F10.4172\u002F2161-0444.1000243",{"mag":891,"openalex":892,"doi":893},"2106936809","W2106936809","10.4172\u002F2161-0444.1000243",{"id":895,"text":896,"url":897,"identifiers":898},"1ce803b7-fd00-445b-b9ef-3aa172d42bb0","Gohary, 2017, Synthesis and biological evaluation of a new series of benzimidazole derivatives as antimicrobial, antiquorum-sensing and antitumor agents, Eur. J. Med. Chem., 131, 255, 10.1016\u002Fj.ejmech.2017.03.018","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0223523417301757",{"doi":899},"10.1016\u002Fj.ejmech.2017.03.018",{"id":26,"text":901,"url":902,"identifiers":903},"Singh, 2017, Coumarin–benzimidazole hybrids as a potent antimicrobial agent: synthesis and biological elevation, J. Antibiotics, 70, 954, 10.1038\u002Fja.2017.70","https:\u002F\u002Fdoi.org\u002F10.1038\u002Fja.2017.70",{"mag":904,"openalex":905,"pm":906,"doi":907},"2661507908","W2661507908","28634338","10.1038\u002Fja.2017.70",{"id":26,"text":909,"url":910,"identifiers":911},"Ajani, 2016, Facile synthesis, characterization and antimicrobial activity of 2-alkanamino benzimidazole derivatives, Oriental J. Chem., 32, 109, 10.13005\u002Fojc\u002F320111","https:\u002F\u002Fdoi.org\u002F10.13005\u002Fojc\u002F320111",{"mag":912,"openalex":913,"doi":914},"2288410116","W2288410116","10.13005\u002Fojc\u002F320111",{"id":26,"text":916,"url":26,"identifiers":917},"Kapoor, 2016, Synthesis and evaluation of 2-aryl substituted benzimidazole derivatives bearing 1,3,4-oxadiazole nucleus for antimicrobial activity, Der. Pharmacia Lett., 8, 97",{},{"id":26,"text":919,"url":26,"identifiers":920},"Shinde, 2016, Design, synthesis and biological evaluation of novel ureidobezimadazole hybrid as potent TNF-α and IL-6 inhibitor, and antimicrobial agents, J. Chem. Pharm. Res., 8, 395",{},{"id":826,"text":922,"url":828,"identifiers":923},"Garrepalli, 2016, Synthesis, characterization and evaluation of new benzimidazole derivatives, World J. Pharm. Sci., 4910, 39",{"doi":830},{"id":26,"text":925,"url":26,"identifiers":926},"Turkey, 2016, Synthesis, characterization and antibacterial activity of new 5-ethoxy-2-mercaptobenzimidazole derivatives, J. Pharm. Res., 10, 814",{},{"id":26,"text":928,"url":26,"identifiers":929},"Archie, 2017, Synthesis and antioxidant activity of 2-substituted-5-nitro benzimidazole derivatives, Int. J. Pharm. Pharm. Sci., 9, 308, 10.22159\u002Fijpps.2017v9i1.14972",{"doi":930},"10.22159\u002Fijpps.2017v9i1.14972",{"id":826,"text":932,"url":828,"identifiers":933},"Abd, 2015, Synthesis, some reactions, cytotoxic evaluation and antioxidant study of novel benzimidazole derivatives, Der Pharma Chemica, 7, 71",{"doi":830},{"id":935,"text":936,"url":937,"identifiers":938},"9c8ab62a-b483-468e-8b22-ef639584b445","Bellam, 2017, Synthesis and antioxidant activity of some new N-alkylated pyrazole-containing benzimidazoles, Chem. Heterocycl. 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Soc., 13, 1155, 10.1007\u002Fs13738-016-0830-1","https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs13738-016-0830-1",{"mag":949,"openalex":950,"doi":951},"2297260439","W2297260439","10.1007\u002Fs13738-016-0830-1",{"id":26,"text":953,"url":26,"identifiers":954},"Nair, 2016, Insilico design, synthesis and in vitro antidiabetic and anti-inflammatory activities of 1,3,4-thiadiazole substituted 2-methylbenzimidazole derivatives, J. Pharm. Res. Clin. Pract., 6, 27",{},{"id":956,"text":957,"url":958,"identifiers":959},"7be77401-50b3-4541-be7e-f3c90bfb0e11","Singalapur, 2010, Derivatives of benzimidazole pharmacophore: synthesis, anticonvulsant, antidiabetic and DNA cleavage studies, Eur. J. Med. 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Tech., 4, 31",{"doi":830},{"id":826,"text":968,"url":828,"identifiers":969},"Lingala, 2011, Synthesis, antimicrobial and anthelmintic activity of some novel benzimidazole derivatives, Der Pharma Chemica, 3, 344",{"doi":830},{"id":971,"text":972,"url":973,"identifiers":974},"d6d5a4d1-c5df-4ded-83f2-21e5205b49ee","Vandeputte, 2021, Synthesis, chemical characterization, and μ-opioid receptor activity assessment of the emerging group of “Nitazene” 2-benzylbenzimidazole synthetic opioids, ACS Chem. Neurosci., 12, 1241, 10.1021\u002Facschemneuro.1c00064","https:\u002F\u002Fpubs.acs.org\u002Fdoi\u002F10.1021\u002Facschemneuro.1c00064",{"doi":975},"10.1021\u002Facschemneuro.1c00064",{"id":826,"text":977,"url":828,"identifiers":978},"Srivastava, 2013, Synthesis and analgesic activity of novel derivatives of 1,2-substituted benzimidazoles, J. 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Photovolt: Res. Appl., 21, 827, 10.1002\u002Fpip.2404",{"doi":1137},"10.1002\u002Fpip.2404",{"id":26,"text":1139,"url":26,"identifiers":1140},"Mao, 2012, New 2,6-modified BODIPY sensitizers for dye-sensitized solar cells, Dyes Pigments, 94, 224, 10.1016\u002Fj.dyepig.2012.01.011",{"doi":1141},"10.1016\u002Fj.dyepig.2012.01.011",{"id":26,"text":1143,"url":26,"identifiers":1144},"Mehmood, 2014, Recent advances in dye sensitized solar cells, Advances in Materials Science and Engineering, Volume, 2014, 974782",{},{"id":26,"text":1146,"url":26,"identifiers":1147},"Shindy, 2017, Fundamentals in the chemistry of cyanine dyes: a review, Dyes and Pigments, 145",{},{"id":26,"text":1149,"url":26,"identifiers":1150},"Qin, 2016, Simple synthesis regarding novel bianchored metal free organic dyes based on indole for dye sensitized solar cells, J. Mater. Sci. Mater. Electron., 27, 3974, 10.1007\u002Fs10854-015-4251-1",{"doi":1151},"10.1007\u002Fs10854-015-4251-1",{"id":26,"text":1153,"url":26,"identifiers":1154},"Sayama, 1998, Photosensitization of porous TiO2 semiconductor electrode with xanthene dyes, Chem. Lett., 753-754",{},{"id":26,"text":1156,"url":26,"identifiers":1157},"Kakiage, 2015, Highly-efcient dye-sensitized solar cells with collaborative sensitization by silyl-anchor and carboxy-anchor dyes, Chem. Commun., 51, 15894, 10.1039\u002FC5CC06759F",{"doi":1158},"10.1039\u002FC5CC06759F",{"id":26,"text":1160,"url":26,"identifiers":1161},"Dualeh, 2011, Infuence of donor groups of organic D–π–a dyes on open-circuit voltage in solid-state dye-sensitized solar cells, J. Phys. Chem. C, 116, 1572, 10.1021\u002Fjp209691e",{"doi":1162},"10.1021\u002Fjp209691e",{"id":26,"text":1164,"url":26,"identifiers":1165},"Mba, M., D'Acunzo, M., Salice, P., Carofglio, T., Maggini, M., Caramori, S., Campana, A., Aliprandi, A., Argazzi, R., Carli, S., Bignozzi, C.A.: Sensitization of Nanocrystalline TiO2 With Multibranched Organic Dyes and Co (III)\u002F(II) Mediators: Strategies to Improve Charge.",{},{"id":26,"text":1167,"url":26,"identifiers":1168},"Lin, 2011, Efficient organic DSSC sensitisers bearing an electron-deficient pyrimidine as an effective p-spacer, J. Mater. Chem., 21, 5950, 10.1039\u002Fc1jm10201j",{"doi":1169},"10.1039\u002Fc1jm10201j",{"id":26,"text":1171,"url":26,"identifiers":1172},"Zhang, 2009, Employ a bisthienothiophene linker to construct an organic chromophore for efficient and stable dye-sensitized solar cells, Energy Environ. Sci., 2, 92, 10.1039\u002FB817990E",{"doi":1173},"10.1039\u002FB817990E",{"id":26,"text":1167,"url":26,"identifiers":1175},{"doi":1169},{"id":26,"text":1177,"url":26,"identifiers":1178},"Lee, 2011, Organic dyes incorporating low-band-gap chromophores based on p-extended benzothiadiazole for dye-sensitized solar cells, Dyes Pigments, 91, 192, 10.1016\u002Fj.dyepig.2011.03.015",{"doi":1179},"10.1016\u002Fj.dyepig.2011.03.015",{"id":26,"text":1181,"url":26,"identifiers":1182},"Thomas, 2011, Electro-optical properties of new anthracene based organic dyes for dye-sensitised solar cells, Dyes Pigments, 91, 33, 10.1016\u002Fj.dyepig.2011.02.006",{"doi":1183},"10.1016\u002Fj.dyepig.2011.02.006",{"id":26,"text":1185,"url":26,"identifiers":1186},"Albert, 1997, Large molecular hyperpolarizabilities. quantitative analysis of aromaticity and auxiliary donor−acceptor effects, J. Am. Chem. Soc., 119, 6575, 10.1021\u002Fja962968u",{"doi":1187},"10.1021\u002Fja962968u",{"id":26,"text":1189,"url":26,"identifiers":1190},"Ma, 2002, A time-dependent DFT study on band gaps and effective conjugation lengths of polyacetylene, polyphenylene, polypentafulvene, polycyclopentadiene, polypyrrole, polyfuran, polysilole, polyphosphole, and polythiophene, Macromolecules, 35, 1109, 10.1021\u002Fma011279m",{"doi":1191},"10.1021\u002Fma011279m",{"id":26,"text":1193,"url":26,"identifiers":1194},"Hissler, 2005, Conjugated systems: can phosphole offer more than pyrrole?, Pure Appl. Chem., 77, 2099, 10.1351\u002Fpac200577122099",{"doi":1195},"10.1351\u002Fpac200577122099",{"id":26,"text":1197,"url":26,"identifiers":1198},"Becke, 1993, Density-functional thermochemistry: the role of exact exchange, J. Chem. Phys., 98, 5648, 10.1063\u002F1.464913",{"doi":1199},"10.1063\u002F1.464913",{"id":26,"text":1201,"url":26,"identifiers":1202},"Arunkumar, 2020, Computational analysis on D–π–A based perylene organic efficient sensitizer in dye-sensitized solar cells, Optical and Quantum Electronics, 52, 164, 10.1007\u002Fs11082-020-02273-0",{"doi":1203},"10.1007\u002Fs11082-020-02273-0",{"id":26,"text":1205,"url":26,"identifiers":1206},"Dreuw, 2005, Single-reference ab initio methods for the calculation of excited states of large molecules, Chem. Rev., 105, 4009, 10.1021\u002Fcr0505627",{"doi":1207},"10.1021\u002Fcr0505627",{"id":26,"text":1209,"url":26,"identifiers":1210},"Naumov, 2005, Russ. J. Gen. Chem., 75, 1956, 10.1007\u002Fs11176-006-0021-3",{"doi":1211},"10.1007\u002Fs11176-006-0021-3",{"id":26,"text":1213,"url":26,"identifiers":1214},"Fan, 2002, Acene-modified triphenylamine dyes for dye-sensitized solar cells: a computational study, ChemPhysChem, 13, 2051, 10.1002\u002Fcphc.201200064",{"doi":1215},"10.1002\u002Fcphc.201200064",{"id":26,"text":1217,"url":26,"identifiers":1218},"Banjo, 2016, Design of (2 Z) -2-cyano-2-[2-[(E)-2-[5-[(E)-2-(4-dimethylaminophenyl) vinyl]-2-thienyl] vinyl] pyran-4-ylidene] acetic acid derivatives as D-π-A dye-sensitisers in molecular photovoltaic. A density functional theory approach, Res Chem Intermed, 42, 4605, 10.1007\u002Fs11164-015-2303-z",{"doi":1219},"10.1007\u002Fs11164-015-2303-z",{"id":26,"text":1221,"url":26,"identifiers":1222},"Umer, 2015, Density functional theory study on the electronic structures of oxadiazole based dyes as photosensitiser for dye sensitised solar cells, Advance in Material Science and Engineering., 34, 345",{},{"id":26,"text":1224,"url":26,"identifiers":1225},"Gao, 2011, Structures and spectroscopic properties of ruthenium phenanthroline solar-cell sensitisers: A computational study, Chem. Phys. Letter, 506, 146, 10.1016\u002Fj.cplett.2011.03.016",{"doi":1226},"10.1016\u002Fj.cplett.2011.03.016",{"id":26,"text":1228,"url":26,"identifiers":1229},"Besler, 1990, Atomic charges derived from semiempirical methods, J. computational chemistry, 11, 112, 10.1002\u002Fjcc.540110404",{"doi":1230},"10.1002\u002Fjcc.540110404",{"id":26,"text":1232,"url":26,"identifiers":1233},"Preat, 2009, Enhanced efficiency of organic dye-sensitised solar cells: triphenylamine derivatives, J. Phys. Chem. C, 113, 16821, 10.1021\u002Fjp904946a",{"doi":1234},"10.1021\u002Fjp904946a",{"id":26,"text":1236,"url":26,"identifiers":1237},"Siddiqui, 2019, In silico investigation of the coumarin-based organic semiconductors for the possible use in organic electronic devices, Jurnal of physical organic chemistry, 32",{},{"id":26,"text":1239,"url":26,"identifiers":1240},"Izquierdo, 2019, Theoretical study of the charge transfer exciton binding energy in semiconductor materials for polymer:fullerene-based bulk heterojunction solar cells, J. Phys. Chem. A, 123, 1233, 10.1021\u002Facs.jpca.8b12292",{"doi":1241},"10.1021\u002Facs.jpca.8b12292",{"id":26,"text":1243,"url":26,"identifiers":1244},"Kim, 2012, Organic dye design tools for efficient photocurrent generation in dye sensitized solar cells: exciton binding energy and electron acceptors, Adv. Funct. Mater., 22, 1606, 10.1002\u002Fadfm.201101961",{"doi":1245},"10.1002\u002Fadfm.201101961",{"id":26,"text":1247,"url":26,"identifiers":1248},"Gregg, 2003, Excitonic solar cells, J. Phys. Chem. B, 107, 4688, 10.1021\u002Fjp022507x",{"doi":1249},"10.1021\u002Fjp022507x",{"id":26,"text":1251,"url":26,"identifiers":1252},"Obi-Egbedi, 2011, Computational simulation and statistical analysis on the relationship between corrosion inhibition efficiency and molecular structure of some phenanthroline derivatives on mild steel surface, Int J Electro Chem Sci., 6, 5649, 10.1016\u002FS1452-3981(23)18435-5",{"doi":1253},"10.1016\u002FS1452-3981(23)18435-5",{"id":26,"text":1255,"url":26,"identifiers":1256},"Liu, 2005, Dynamic behavior of chemical reactivity indices in density functional theory: a Bohn-Oppenheimer quantum molecular dynamics study, J. Chem. Sci., 117, 477, 10.1007\u002FBF02708352",{"doi":1257},"10.1007\u002FBF02708352",{"id":1259,"createTime":1260,"updateTime":1261,"relativeEntities":1262,"slug":1263,"properties":1264,"entityType":753,"verifyStatus":25,"verifyTime":1273,"verifyNote":755,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"primaryUrl":1274,"fullTextUrl":26,"authors":1275,"publicationType":791,"publisherRelationship":1307,"citationCount":36,"citationInfo":1334,"publishDate":823,"publishYear":821,"citationAnalyzeStatus":1336,"lastCitationAnalyze":1337,"indexDatabases":26,"openAccess":26,"references":26,"isForceReanalyzing":995},"d693df89-1873-4b6b-80c3-cc3436dcda7c","2024-01-28T17:06:11.579+00:00","2026-05-16T16:47:49.745+00:00",[],"Biosynthesis-and-characterization-of-nickel-oxide-nanoparticles-by-using-aqueous-grape-extract-and-evaluation-of-their-biological-applications",{"references":1265,"title":1267,"doi":1269,"gsPaper":1271},{"VOID":1266},"Abbasi, 2020, Environmentally friendly green approach for the fabrication of silver oxide nanoparticles: characterization and diverse biomedical applications, Microsc. Res. Tech., 83, 1308, 10.1002\u002Fjemt.23522\nKrishnan, 2016, Green synthesis of silver nanoparticles using Piper nigrum concoction and its anticancer activity against MCF-7 and Hep-2 cell lines, J. Antimicro, 2, 2472\nThorley, 2013, New perspectives in nanomedicine, Pharmacol. Ther., 140, 176, 10.1016\u002Fj.pharmthera.2013.06.008\nIqbal, 2018, Nano-medicines for developing cancer nano therapeutics: From bench top to bedside and beyond, Appl. Microbiol. Biotechnol., 102, 9449, 10.1007\u002Fs00253-018-9352-3\nIqbal, 2019, Plant-extract mediated green approach for the synthesis of ZnONPs: Characterization and evaluation of cytotoxic, antimicrobial and antioxidant potentials, J. Mol. Struct., 1189, 315, 10.1016\u002Fj.molstruc.2019.04.060\nThovhogi, 2015, Nanoparticles green synthesis by Hibiscus sabdariffa flower extract: Main physical properties, J. Alloy. Compd., 647, 392, 10.1016\u002Fj.jallcom.2015.06.076\nThema, 2016, Single phase Bunsenite NiO nanoparticles green synthesis by Agathosma betulina natural extract, J. Alloy. Compd., 657, 655, 10.1016\u002Fj.jallcom.2015.09.227\nIsmail, 2016, RuO2 nanoparticles by a novel green process via Aspalathus linearis natural extract & their water splitting response, J. Alloy. Compd., 662, 283, 10.1016\u002Fj.jallcom.2015.11.234\nSudha, 2017, Green synthesis of silver nanoparticles using Lippia nodiflora aerial extract and evaluation of their antioxidant, antibacterial and cytotoxic effects, Resour.-Effic. Technol., 3, 506\nAbbasi, 2021, Phytofabrication of cobalt oxide nanoparticles from Rhamnus virgata leaves extract and investigation of different bioactivities, Microsc. Res. Tech., 84, 192, 10.1002\u002Fjemt.23577\nUddin, 2021, Green synthesis of nickel oxide nanoparticles from berberis balochistanica stem for investigating bioactivities, Molecules, 26, 1548, 10.3390\u002Fmolecules26061548\nIqbal, 2017, Plant-derived anticancer agents: A green anticancer approach, Asian Pacific J Tropical Biomed., 7, 1129, 10.1016\u002Fj.apjtb.2017.10.016\nIqbal, 2018, Potential phytocompounds for developing breast cancer therapeutics: nature’s healing touch, Eur. J. Pharmacol., 827, 125, 10.1016\u002Fj.ejphar.2018.03.007\nKar, 2014, Synthesis of nano-spherical nickel by templating hibiscus flower petals, J. Nanosci. Nanotechnol., 2, 17\nSrihasam, 2020, Phytogenic generation of NiO nanoparticles using Stevia leaf extract and evaluation of their in-vitro antioxidant and antimicrobial properties, Biomolecules, 10, 89, 10.3390\u002Fbiom10010089\nDiallo, 2018, Structural, optical and photocatalytic applications of biosynthesized NiO nanocrystals, Green Chem. Lett. Rev., 11, 166, 10.1080\u002F17518253.2018.1447604\nAbbasi, 2019, Plant-mediated synthesis of nickel oxide nanoparticles (NiO) via Geranium wallichianum: characterization and different biological applications, Mater. Res. Express, 6, 0850a7, 10.1088\u002F2053-1591\u002Fab23e1\nAkter, 2021, Non-thermal biocompatible plasma jet induction of apoptosis in brain cancer cells, Cells, 10, 236, 10.3390\u002Fcells10020236\nFeil, 2020, Cancer-selective treatment of cancerous and non-cancerous human cervical cell models by a non-thermally operated electrosurgical argon plasma device, Cancers, 12, 1037, 10.3390\u002Fcancers12041037\nHsu, 2021, Nanotechnology and nano-carrier based drug delivery as the potential therapeutic strategy for glioblastoma multiforme: an update, Cancers, 13, 195, 10.3390\u002Fcancers13020195\nIbrahim, 2010, Effect of salvia trilobite LF extracts on neoplastic cell lines, Jordan J Biol Sci, 147, 1\nFeng, 2018, Breast cancer development and progression: risk factors, cancer stem cells, signaling pathways, genomics, and molecular pathogenesis, Genes & Dis, 5, 77, 10.1016\u002Fj.gendis.2018.05.001\nSweeney, 2014\nComşa, 2015, The story of MCF-7 breast cancer cell line: 40 years of experience in research, Anticancer Res., 35, 3147\nMartin, 2018, Colonization, infection, and the accessory genome of Klebsiella pneumonia, Front. Cell. Infect. Microbiol., 8, 4, 10.3389\u002Ffcimb.2018.00004\nBonasoni, 2021, Klebsiella pneumoniae chorioamnionitis: an underrecognized cause of preterm premature rupture of membranes in the second trimester, Microorganisms, 9, 96, 10.3390\u002Fmicroorganisms9010096\nRağbetli, 2016, Evaluation of antimicrobial resistance in Staphylococcus aureus isolates by years, Interdiscip. Perspect Infectious. Dis., 10.1155\u002F2016\u002F9171395\nHarris, 2006, Staphylococci and implant surfaces: a review, Injury, 37, S3, 10.1016\u002Fj.injury.2006.04.003\nKurlenda, 2012, Alternative therapies in Staphylococcus aureus diseases, Acta Biochim. Pol., 59, 10.18388\u002Fabp.2012_2136\nGeorgiev, 2014, Recent advances and uses of grape flavonoids as nutraceuticals, Nutrients, 6, 391, 10.3390\u002Fnu6010391\nKhosravi-Darani, 2019, Green synthesis of metallic nanoparticles using algae and microalgae, Lett. Appl. NanoBio Sci., 8, 666, 10.33263\u002FLIANBS83.666670\nUpadhyay, 2015, Grape extract assisted green synthesis of reduced graphene oxide for water treatment application, Mater. Lett., 160, 355, 10.1016\u002Fj.matlet.2015.07.144\nMakarov, 2014, “Green” nanotechnologies: synthesis of metal nanoparticles using plants, Acta Nat., 6\nMayedwa, 2018, Green synthesis of nickel oxide, palladium and palladium oxide synthesized via Aspalathus linearis natural extracts: physical properties & mechanism of formation, Appl. Surf. Sci., 446, 266, 10.1016\u002Fj.apsusc.2017.12.116\nDin, 2016, Recent advances in the synthesis and stabilization of nickel and nickel oxide nanoparticles: a green adeptness, Int. J. Anal. Chem.\nKhashan, 2020, Synthesis, characterization and evaluation of anti-bacterial, anti-parasitic and anti-cancer activities of Aluminum-Doped zinc oxide nanoparticles, J. Inorg. Organomet. Polym Mater., 1–17\nJabir, 2020, Linalool-loaded glutathione-modified Gold nanoparticles conjugated with CALNN peptide as apoptosis inducer and NF-KB translocation inhibitor in SKOV-3 cell line, Int. J. Nanomed., 15, 9025, 10.2147\u002FIJN.S276714\nAl-Salman, 2020, 2-Benzhydrylsulfinyl-N-hydroxyacetamide-Na extracted from fig as a novel cytotoxic and apoptosis inducer in SKOV-3 and AMJ-13 cell lines via P53 and caspase-8 pathway, Eur. Food Res. Technol., 246, 1591, 10.1007\u002Fs00217-020-03515-x\nJabir, 2019, Super magnetic Fe3O4-PEG nanoparticles combined with NIR laser and alternating magnetic field as potent anti-cancer agent against human ovarian cancer cell, Mater. Res. Express, 6, 115412, 10.1088\u002F2053-1591\u002Fab50a0\nAl-Ziaydi, 2020, Newcastle disease virus suppress glycolysis pathway and induce breast cancer cells death, Virus Disease, 31, 341, 10.1007\u002Fs13337-020-00612-z\nKhashan, 2019, Carbon nanoparticles prepared by laser ablation in liquid environment, Surf. Rev. Lett., 26, 1950078, 10.1142\u002FS0218625X19500781\nKareem, 2020, Poly vinyl pyrrolidone loaded-MnZnFe2O4 magnetic nanocomposites induce apoptosis in cancer cells through mitochondrial damage and P 53 pathway, J. Inorg. Organomet. Polym Mater., 30, 5009, 10.1007\u002Fs10904-020-01651-1\nJabir, 2021, Green synthesis of silver nanoparticles from Eriobotrya japonica extract: a promising approach against cancer cells proliferation, inflammation, allergic disorders and phagocytosis induction, Artif. Cells Nanomed. Biotechnol., 49, 48, 10.1080\u002F21691401.2020.1867152\nWaheeb, 2020, Effect of hesperidin conjugated with golden nanoparticles on phagocytic activity: In vitro study, AIP Conf. Proc., 2213, 020217, 10.1063\u002F5.0000159\nAl-Shammari, 2020, Galangin enhances gold nanoparticles as anti-tumor agents against ovarian cancer cells, AIP Conf. Proc., 2213, 020206, 10.1063\u002F5.0000162\nKhashan, 2020, Anticancer activity and toxicity of carbon nanoparticles produced by pulsed laser ablation of graphite in water, Adv. Nat. Sci.: Nanosci. Nanotechnol., 11, 035010\nSameen, 2020, Therapeutic combination of gold nanoparticles and LPS as cytotoxic and apoptosis inducer in breast cancer cells, AIP Conf. Proc., 2213, 020215, 10.1063\u002F5.0000161\nKadhim, 2019, Polyethylene glycol-functionalized magnetic (Fe3O4) nanoparticles: A good method for a successful antibacterial therapeutic agent via damage DNA molecule, Surf. Rev. Lett., 26, 1950079, 10.1142\u002FS0218625X19500793\nJabir, 2019, Polyethylene glycol-functionalized magnetic (Fe3O4) nanoparticles: a novel DNA-mediated antibacterial agent, Nano Biomed. Eng., 11, 18, 10.5101\u002Fnbe.v11i1.p18-27\nJabir, 2018, Porous silicon nanoparticles prepared via an improved method: a developing strategy for a successful antimicrobial agent against Escherichia coli and Staphylococcus aureus, IOP Conf. Series: Mater. Sci. Eng., 454, 012077, 10.1088\u002F1757-899X\u002F454\u002F1\u002F012077\nMohammed, 2020, Functionalization, characterization, and antibacterial activity of single wall and multi wall carbon nanotubes, IOP Conf. Series: Mater. Sci. Eng., 757, 012028, 10.1088\u002F1757-899X\u002F757\u002F1\u002F012028\nKhalil, 2018, Sageretia thea (Osbeck.) modulated biosynthesis of NiO nanoparticles and their in vitro pharmacognostic, antioxidant and cytotoxic potential, Artif. Cells Nanomed. Biotechnol., 46, 838, 10.1080\u002F21691401.2017.1345928\nAbbasi, 2019, Biofabrication of iron oxide nanoparticles by leaf extract of Rhamnus virgata: characterization and evaluation of cytotoxic, antimicrobial and antioxidant potentials, Appl. Organomet. Chem., 33, 10.1002\u002Faoc.4947\nKarthikeyan, 2016, Wet chemical synthesis of diameter tuned NiO microrods: microstructural, optical and optical power limiting applications, CrystEngComm, 18, 601, 10.1039\u002FC5CE02232K\nIqbal, 2020, Phytogenic synthesis of nickel oxide nanoparticles (NiO) using fresh leaves extract of Rhamnus triquetra (wall.) and investigation of its multiple in vitro biological potentials, Biomedicines, 8, 117, 10.3390\u002Fbiomedicines8050117\nDavar, 2009, Nanoparticles Ni and NiO: Synthesis, characterization and magnetic properties, J. Alloy. Compd., 476, 797, 10.1016\u002Fj.jallcom.2008.09.121\nAnandan, 2012, Structural, optical and magnetic properties of well-dispersed NiO nanoparticles synthesized by CTAB assisted solvothermal process, Nanosci. Nanotechnol. Int. J., 2, 24\nAlagiri, 2012, Synthesis and characterization of NiO nanoparticles by sol-gel method, J. Mater. Sci.: Mater. Electron., 23, 728\nKrishnakanth, 2016, Structural and magnetic properties of NiO and Fe-doped NiO nanoparticles synthesized by chemical co-precipitation method, Mater. Today:. Proc., 3, 1370\nIsmail, 2018, Mesoporous WO3-graphene photocatalyst for photocatalytic degradation of Methylene Blue dye under visible light illumination, J. Environ. Sci., 66, 328, 10.1016\u002Fj.jes.2017.05.001\nKhatri, 2019, Visible light photocatalysis of methylene blue using cobalt substituted cubic NiO nanoparticles, Bull. Mater. Sci., 42, 1, 10.1007\u002Fs12034-019-1835-z\nKhan, 2019, Preparation, characterizations and in vitro cytotoxic activity of nickel oxide nanoparticles on HT-29 and SW620 colon cancer cell lines, J. Trace Elem. Med Biol., 52, 12, 10.1016\u002Fj.jtemb.2018.11.003\nRizzello, 2013, Nanotechnology tools for antibacterial materials, Nanomedicine, 8, 807, 10.2217\u002Fnnm.13.63\nShanaj, 2016, Effect of calcination time on structural, optical and antimicrobial properties of nickel oxide nanoparticles, J. Theor. Comput. Sci, 3, 149\nTang, 2014, MgO nanoparticles as antibacterial agent: preparation and activity, Braz. J. Chem. Eng., 31, 591, 10.1590\u002F0104-6632.20140313s00002813\nAgale, 2017, Nanosized synthesis of nickel oxide by electrochemical reduction method and their antifungal screening, J. Cluster Sci., 28, 2097, 10.1007\u002Fs10876-017-1203-3\nEkambaram, 2005, Combustion synthesis and luminescent properties of Eu3+-activated cheap red phosphors, J. Alloy. Compd., 395, 132, 10.1016\u002Fj.jallcom.2004.09.075\nKaviyarasu, 2019, ZnO doped single wall carbon nanotube as an active medium for gas sensor and solar absorber, J. Mater. Sci.: Mater. Electron., 30, 147\nSone, 2016, Single-phase α-Cr2O3 nanoparticles’ green synthesis using Callistemon viminalis’ red flower extract, Green Chem. Lett. 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Chem., 41, 16, 10.1039\u002FC6NJ03181A\nKarrouchi, 2018, Synthesis and pharmacological activities of pyrazole derivatives: a review, Molecules., 23, 134, 10.3390\u002Fmolecules23010134\nFustero, 2011, From 2000 to mid-2010: a fruitful decade for the synthesis of pyrazoles, Chem. Rev., 111, 6984, 10.1021\u002Fcr2000459\nGökhan-Kelekçi, 2007, A new therapeutic approach in Alzheimer disease: Some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics, Bioorganic Med. Chem., 15, 5775, 10.1016\u002Fj.bmc.2007.06.004\nBehr, 1967\nRosiere, 1951, An analog of histamine that stimulates gastric acid secretion without other actions of histamine, Science, 113, 10.1126\u002Fscience.113.2945.651.a\nBailey, 1985, 3,4-Diphenyl-1H-pyrazole-1-propanamine antidepressants, J. Med. Chem., 28, 10.1021\u002Fjm00380a020\nLeenen, 1988, Topical minoxidil: cardiac effects in bald man, Br. J. Clin. Pharmacol., 26, 481, 10.1111\u002Fj.1365-2125.1988.tb03410.x\nMahajan, 1991, Synthesis and biological activity of heterocycles derived from 3-methoxy-1-phenyl-1H-pyrazole-5-carboxylate, J. Indian Chem. Soc., 68, 245\nLin, 2007, Design, synthesis, and evaluation of 3,4-disubstituted pyrazole analogues as anti-tumor CDK inhibitors, Bioorganic Med. Chem. Lett., 17, 4557, 10.1016\u002Fj.bmcl.2007.05.092\nBarcelo, 2007, Synthesis and binding affinity of new pyrazole and isoxazole derivatives as potential atypical antipsychotics, Bioorg. Med. Chem. Lett., 17, 4873, 10.1016\u002Fj.bmcl.2007.06.045\nFarag, 2008, Synthesis of new N-phenylpyrazole derivatives with potent antimicrobial activity, Bioorg. Med. Chem., 16, 4569, 10.1016\u002Fj.bmc.2008.02.043\nLarsen, 1999, Synthesis of triazenopyrazole derivativesas potential inhibitors of HIV-1, Monatsh. Chem., 130, 1167\nChauhan, 1993, Antifilarial profile of substituted pyrazoles: a new class of antifilarial agents, Indian J. Chem. B, 32, 858\nGenin, 2000, Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant: lead identification and SAR of 3- and 4-substituted derivatives, J. Med. Chem., 43, 1034, 10.1021\u002Fjm990383f\nSasmal, 2011, Novel pyrazole-3-carboxamide derivatives as cannabinoid-1 (CB1) antagonists: Journey from non-polar to polar amides, Bioorg. Med. Chem. Lett., 21, 562, 10.1016\u002Fj.bmcl.2010.10.055\nRavinet Trillou, 2004, CB1 cannabinoid receptor knockout in mice leads to leanness, resistance to diet-induced obesity and enhanced leptin sensitivity, Int. J. Obes., 28, 640, 10.1038\u002Fsj.ijo.0802583\nMunro, 1993, Molecular characterization of a peripheral receptor for cannabinoids, Nature, 365, 61, 10.1038\u002F365061a0\nHerkenham, 1990, Characterization and localization of cannabinoid receptors in rat brain: a quantitative in vitro autoradiographic study, Proc. Natl. Acad. Sci. U.S.A., 87, 1932, 10.1073\u002Fpnas.87.5.1932\nHowlet, 1998, Cannabinoid receptors and signal transduction neurobiol, Dis., 5, 405\nAsproni, 2021, Tricyclic pyrazole-based compounds as useful scaffolds for cannabinoid CB1\u002FCB2 receptor interaction, Molecules, 26, 2126, 10.3390\u002Fmolecules26082126\nVasilevsky, 2005, Unexpected results in the heterocyclization of 5-acetylenylpyrazole-4-carboxylic acid hydrazides under the influence of CuCl: formation of a diazepinone and dehydrodimerization into the corresponding bis(pyrazolo[4,3-d][1,2]diazepinone), Tetrahedron Lett., 46, 4457, 10.1016\u002Fj.tetlet.2005.04.127\nZhang, 2006, Coupling of N-heterocycle-fused enyne aldehydes with γ, δ-unsaturated fischer carbene complexes, Organometallics, 25, 1279, 10.1021\u002Fom051008q\nHeller, 2007, Rapid Access to Pyrazolo[3,4-c]pyridines via alkyne annulation: limitations of steric control in nickel-catalyzed alkyne insertions, Org. Lett., 9, 4947, 10.1021\u002Fol701784w\nF. Lepage, B. Hubiot, Derives heterocycliques doues d'activite anticonvulsivante, procede de preparation et composition pharmaceutique. Eur. Pat. Appl. EP, 459, 887; Chem. Abstr. 1992; 116: 128914.\nLamberth, 2007, Pyrazole chemistry in crop protection, Heterocycles, 71, 1467, 10.3987\u002FREV-07-613\nSasabe, 2011, Multifunctional materials in high-performance OLEDs: challenges for solid-state lighting, Chem. Mater., 23, 621, 10.1021\u002Fcm1024052\nOjwach, 2010, Pyrazole and (pyrazol-1-yl)metal complexes as carbon–carbon coupling catalysts, Inorg. Chim. Acta., 363, 1947, 10.1016\u002Fj.ica.2010.02.014\nAggarwal, 2003, A novel one-pot Method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ, J. Org. Chem., 68, 5381, 10.1021\u002Fjo0268409\nBhat, 2005, Synthesis of 3,5-diphenyl-1H-pyrazoles, Synth. Commun., 35, 1135, 10.1081\u002FSCC-200054225\nEmtiazi, 2015, Nano-silica sulfuric acid as an efficient catalyst for the synthesis of substituted pyrazoles, Arabian J. Chem., 8, 793, 10.1016\u002Fj.arabjc.2013.06.008\nFustero, 2008, Improved regioselectivity in pyrazole formation through the use of fluorinated alcohols as solvents: synthesis and biological activity of fluorinated tebufenpyrad analogs, J. Org. Chem., 73, 3523, 10.1021\u002Fjo800251g\nWang, 2004, Solventless syntheses of pyrazole derivatives, Green Chem., 6, 90, 10.1039\u002Fb312833d\nPolshettiwar, 2008, Greener and rapid access to bio-active heterocycles: room temperature synthesis of pyrazoles and diazepines in aqueous medium, Tetrahedron Lett., 49, 397, 10.1016\u002Fj.tetlet.2007.11.017\nCurini, 2005, Layered zirconium sulfophenyl phosphonate as heterogeneous catalyst in the synthesis of pyrazoles and 4,5,6,7-tetrahydro-1(2)H-indazoles, Synlett, 19, 2927, 10.1055\u002Fs-2005-921904\nXiong, 2009, A general and efficient synthesis of pyrazoles catalyzed by Sc(OTf)3 under solvent-free conditions, J. Braz. Chem. Soc., 20, 367, 10.1590\u002FS0103-50532009000200023\nSreekumar, 1998, Simple, Efficient and convenient synthesis of pyrroles and pyrazoles using zeolites, Synth. Commun., 28, 1661, 10.1080\u002F00397919808006870\nMirjalili, 2010, Mg(CIO4)2: an efficient catalyst for the synthesis of 1,3,5-trisubstituted pyrazoles, Digest J. Nanomat. Biostruct., 5, 897\nBamoniri, 2012, Synthesis of 1,3,5-tri-substituted pyrazoles promoted by P2O5.SiO2, Iranian J. Catal., 2, 75\nNelson, 1998\nBamoniri, 2014, Nano silica phosphoric acid as an efficient catalyst for one-pot synthesis of 2,4,5-trisubstituted imidazoles under solvent free condition, Bulg. Chem. Commun., 46, 79\nMirjalili, 2013, One-pot synthesis of 2,4,5-tri-substituted-1H-imidazoles promoted by trichloromelamine, j.ccl, 2, 35, 10.5267\u002Fj.ccl.2012.12.001\nZarei, 2009, Rapid and efficient diazotization and diazo coupling reactions on silica sulfuric acid under solvent-free conditions, Dyes Pigm., 81, 240, 10.1016\u002Fj.dyepig.2008.10.011\nBamoniri, 2015, Nano-Fe3O4 encapsulated-silica supported boron trifluoride as a novel heterogeneous solid acid for solvent-free synthesis of arylazo-1-naphthol derivatives, RSC Adv., 5, 16911, 10.1039\u002FC4RA12604A\nSafaei-ghomi, 2015, Rapid microwave-assisted synthesis of N-benzyl fulleropyrrolidines under solvent free conditions, RSC Adv., 5, 15591, 10.1039\u002FC4RA16020G\nBamoniri, 2015, Recent developments in the nanomaterial-catalyzed green synthesis of structurally diverse 1,4-dihydropyridines, RSC Adv., 5, 78483, 10.1039\u002FC5RA12734C\nShaabani, 2002, Selective oxidation of alkylarenes in dry media with potassium permanganate supported on Montmorillonite K10, Tetrahedron Lett., 43, 5165, 10.1016\u002FS0040-4039(02)00976-0\nDeer, 1992\nWilson, 2013\nMurray, 2005, Engineered clay products for the paper industry, Appl. Clay Sci., 29, 199, 10.1016\u002Fj.clay.2004.12.005\nMurray, 2000, Traditional and new applications for kaolin, smectite, and palygorskite: a general overview, Appl. Clay Sci., 17, 207, 10.1016\u002FS0169-1317(00)00016-8\nCravero, 1997, Geology, mineralogy, origin and possible applications of some Argentinian kaolins in the Neuquen basin, Appl. Clay Sci., 12, 27, 10.1016\u002FS0169-1317(96)00035-X\nPrasad, 1991, Kaolin: processing, properties and applications, Appl. Clay Sci., 6, 87, 10.1016\u002F0169-1317(91)90001-P\nMurray, 1991, Overview — clay mineral applications, Appl. Clay Sci., 5, 379, 10.1016\u002F0169-1317(91)90014-Z\nBurst, 1991, The application of clay minerals in ceramics, Appl. Clay Sci., 5, 421, 10.1016\u002F0169-1317(91)90016-3\nUgheoke, 2006, Property optimization of kaolin-rice husk in- sulating fire-bricks, Leonardo. El. J. Pract. Technol., 9, 167\nRodríguez Largo, 2009, Novel use of kaolin wastes in blended cements, J. Am. Ceram. Soc., 92, 2443, 10.1111\u002Fj.1551-2916.2009.03231.x\nKumari, 2016, Graphene oxide–TiO2 composite: an efficient heterogeneous catalyst for the green synthesis of pyrazoles and pyridines, New J. Chem., 40, 5053, 10.1039\u002FC5NJ03380B\nMaleki, 2014, Nano α-Al2O3 supported ammonium dihydrogen phosphate (NH4H2PO4\u002FAl2O3): preparation, characterization and its application as a novel and heterogeneous catalyst for the one-pot synthesis of tetrahydrobenzo[b]pyran and pyrano[2,3-c]pyrazole derivatives, RSC Adv., 4, 42873, 10.1039\u002FC4RA07813F\nAzarifar, 2018, γ-Fe2O3@Cu3Al-LDH-TUD as a new Amphoteric, Highly Efficient and Recyclable Heterogeneous Catalyst for the Solvent-free Synthesis of Dihydropyrano[3,2-c]pyrazoles and dihydropyrano[3,2-c]chromens, Appl. Org. Chem., 32, 4293, 10.1002\u002Faoc.4293\nMohammadi Ziarani, 2021, Magnetically recoverable catalysts for the preparation of pyridine derivatives: an overview, RSC Adv., 11, 17456, 10.1039\u002FD1RA02418C\nTayde, 2021, Synthesis of 2, 4 disubstituted 1, 5 benzodiazepines promoted by efficient silica-alumina catalyst, J. Chem. Lett., 2, 25\nMirjalili, 2012, Mg(HSO4)2: an efficient and eco-friendly catalyst for the synthesis of pyrazoles, chemija, 23, 250\nDiko, 2016, Fourier transform infrared spectroscopy and thermal analyses of kaolinitic clays from South Africa and Cameroon, Acta Geodyn. Geomater., 13, 149\nSaikia, 2010, Fourier transform infrared spectroscopic characterization of kaolinite from Assam and Meghalaya, Northeastern India, JMP, 01, 206, 10.4236\u002Fjmp.2010.14031\nRíos, 2007, Synthesis of zeolites and zeotypes by hydrothermal transformation of kaolinite and metakaolinite, BISTUA, 5, 15",{"EN":1348},"Kaolin sulfonic acid nanoparticles: An efficient and reusable heterogeneous catalyst for the synthesis of highly substituted pyrazoles via a green 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Soc., Dalton Trans., 1, 55, 10.1039\u002Fa602311h","https:\u002F\u002Fdoi.org\u002F10.1039\u002Fa602311h",{"mag":1744,"openalex":1745,"doi":1746},"2117723097","W2117723097","10.1039\u002Fa602311h",{"id":26,"text":1748,"url":1749,"identifiers":1750},"Beeby, A.; M. Clarkson, I.; S. Dickins, R.; Faulkner, S.; Parker, D.; Royle, L.; S. de Sousa, A.; A. Gareth Williams, J.; Woods, M. Non-Radiative Deactivation of the Excited States of Europium, Terbium and Ytterbium Complexes by Proximate Energy-Matched OH, NH and CH Oscillators: An Improved Luminescence Method for Establishing Solution Hydration States. J. Chem. Soc., Perkin Trans. 2 1999, No. 3, 493–504. https:\u002F\u002Fdoi.org\u002F10.1039\u002FA808692C.","https:\u002F\u002Fdoi.org\u002F10.1039\u002Fa808692c",{"mag":1751,"openalex":1752,"doi":1753},"1969137131","W1969137131","10.1039\u002Fa808692c",{"id":26,"text":1755,"url":26,"identifiers":1756},"Peppas, 2006, Hydrogels in biology and medicine: from molecular principles to bionanotechnology, Adv. Mater., 18, 1345, 10.1002\u002Fadma.200501612",{"doi":1757},"10.1002\u002Fadma.200501612",{"id":1759,"text":1760,"url":1761,"identifiers":1762},"1dba538b-12b9-4805-97b3-aae4794883ae","Jonassen, 2012, Effects of ionic strength on the size and compactness of chitosan nanoparticles, Colloid Polym. Sci., 290, 919, 10.1007\u002Fs00396-012-2604-3","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs00396-012-2604-3",{"doi":1763},"10.1007\u002Fs00396-012-2604-3",{"id":26,"text":1765,"url":1766,"identifiers":1767},"Callewaert, 2014, Tuning the composition of biocompatible Gd nanohydrogels to achieve hypersensitive dual T1\u002FT2 MRI contrast agents, J. Mater. Chem. B, 2, 6397, 10.1039\u002FC4TB00783B","http:\u002F\u002Fdx.doi.org\u002F10.1039\u002Fc4tb00783b",{"doi":1768},"10.1039\u002Fc4tb00783b",{"id":26,"text":1770,"url":1771,"identifiers":1772},"Dong, 2015, Supramolecular hydrogels: synthesis, properties and their biomedical applications, Biomater. 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Chem., 59, 6648, 10.1021\u002Facs.inorgchem.0c00510","https:\u002F\u002Fdoi.org\u002F10.1021\u002Facs.inorgchem.0c00510",{"mag":1781,"pmc":1782,"openalex":1783,"pm":1784,"doi":1785},"3022600674","8047401","W3022600674","32367714","10.1021\u002Facs.inorgchem.0c00510",{"id":1787,"createTime":1788,"updateTime":1789,"relativeEntities":1790,"slug":1791,"properties":1792,"entityType":753,"verifyStatus":25,"verifyTime":1801,"verifyNote":755,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"primaryUrl":1802,"fullTextUrl":26,"authors":1803,"publicationType":791,"publisherRelationship":1936,"citationCount":36,"citationInfo":1964,"publishDate":1966,"publishYear":1967,"citationAnalyzeStatus":1417,"lastCitationAnalyze":1968,"indexDatabases":26,"openAccess":26,"references":26,"isForceReanalyzing":995},"0cfdd4ad-b289-4df6-80e0-06d16345931e","2024-02-14T13:15:53.943+00:00","2026-06-05T05:41:02.203+00:00",[],"Combined-experimental-and-computational-approach-toward-biological-physicochemical-and-quantum-chemical-aspects-of-substituted-1-5-phenyl-3-2-trifluoromethyl-phenyl-4-5-dihydro-pyrazol-1-yl-ethanone",{"references":1793,"title":1795,"doi":1797,"gsPaper":1799},{"VOID":1794},"Qin, 2015, Molecular docking studies and biological evaluation of chalcone based pyrazolines as tyrosinase inhibitors and potential anticancer agents, RSC Advances, 5, 46330, 10.1039\u002FC5RA02995C\nFarooq, 2022, In vitro Cytotoxic Activities, Molecular Docking and Density Functional Theory (DFT) Evaluation of Chalcone Derived Pyrazolines, Chemistry Africa, 1\nInsuasty, 2010, Synthesis of novel pyrazolic analogues of chalcones and their 3-aryl-4-(3-aryl-4, 5-dihydro-1H-pyrazol-5-yl)-1-phenyl-1H-pyrazole derivatives as potential antitumor agents, Bioorganic & medicinal chemistry, 18, 4965, 10.1016\u002Fj.bmc.2010.06.013\nSivakumar, 2010, Novel chalcones and 1, 3, 5-triphenyl-2-pyrazoline derivatives as antibacterial agents, Chemical biology & drug design, 76, 407, 10.1111\u002Fj.1747-0285.2010.01020.x\nBukhari, 2015, Synthesis, molecular modeling, and biological evaluation of novel 1, 3-diphenyl-2-propen-1-one based pyrazolines as anti-inflammatory agents, Chemical biology & drug design, 85, 729, 10.1111\u002Fcbdd.12457\nChovatia, 2006, Synthesis and selective antitubercular and antimicrobial inhibitory activity of 1-acetyl-3, 5-diphenyl-4, 5-dihydro-(1H)-pyrazole derivatives, Journal of the Serbian Chemical Society, 71, 713, 10.2298\u002FJSC0607713C\nBadavath, 2021, MAO Inhibitory Activity Of 4, 5-Dihydro-1 H-Pyrazole Derivatives: A Platform To Design Novel Antidepressants, Frontiers in Drug Design & Discovery:, 10, 47, 10.2174\u002F9789811421563121100005\nBeyhan, 2017, Synthesis and anticonvulsant activity of some 2-pyrazolines derived from chalcones, Arabian Journal of Chemistry, 10, S2073, 10.1016\u002Fj.arabjc.2013.07.037\nAbu-Melha, 2020, Clean grinding technique: A facile synthesis and in silico antiviral activity of hydrazones, pyrazoles, and pyrazines bearing thiazole moiety against SARS-CoV-2 main protease (Mpro), Molecules, 25, 4565, 10.3390\u002Fmolecules25194565\nTaj, 2011, One-pot synthesis of pyrazoline derivatised carbazoles as antitubercular, anticancer agents, their DNA cleavage and antioxidant activities, European journal of medicinal chemistry, 46, 4366, 10.1016\u002Fj.ejmech.2011.07.007\nSarkar, 2011, Antimicrobial activity of some novel pyrazoline derivatives, Journal of Advanced Pharmacy Education & Research, 1, 243\nHitge, 2020, Evaluation of nitrocatechol chalcone and pyrazoline derivatives as inhibitors of catechol-O-methyltransferase and monoamine oxidase, Bioorganic & Medicinal Chemistry Letters, 30, 10.1016\u002Fj.bmcl.2020.127188\nKumar, 2018, Pyrazole-pyrazoline as promising novel antimalarial agents: a mechanistic study, European journal of medicinal chemistry, 149, 139, 10.1016\u002Fj.ejmech.2018.01.082\nJin, 2004, Synthesis and properties of photoluminescence and electroluminescence of pyrazoline derivatives, Synthetic metals, 140, 37, 10.1016\u002FS0379-6779(02)01320-6\nAl Sabahi, 2019, Synthesis, photophysical and theoretical studies of substituted ethyl 4-(3-(naphthalen-1-yl)-1-phenyl-4, 5-dihydro-1H-pyrazol-5-yl) benzoate, Journal of Luminescence, 205, 572, 10.1016\u002Fj.jlumin.2018.10.013\nWagner, 1966, Aryl-Δ2-pyrazolines as optical brighteners, Angewandte Chemie International Edition in English, 5, 699, 10.1002\u002Fanie.196606991\nRawat, 2016, Assessment of Antimicrobial Activity, Reactivity and Non-Linear Optical Properties of New Pyrazoline Derivatives having Pyrrole moiety, ChemistrySelect, 1, 4008, 10.1002\u002Fslct.201600826\nNayak, 2021, Synthesis, Crystal Structure, Biological Evaluation, DFT Calculations and Third Order Nonlinear Optical Studies of Pyrazolines, Journal of Molecular Structure, 1243, 10.1016\u002Fj.molstruc.2021.130780\nAsad, 2020, Cyclization of chalcones into N-propionyl pyrazolines for their single crystal X-ray, computational and antibacterial studies, Journal of Molecular Structure, 1201, 10.1016\u002Fj.molstruc.2019.127186\nRasool, 2021, Facile synthesis, DNA binding, Urease inhibition, anti-oxidant, molecular docking and DFT studies of 3-(3-Bromo-phenyl)-1-(2-trifluoromethyl-phenyl)-propenone and 3-(3-Bromo-5 chloro-phenyl)-1-(2-trifluoromethyl-phenyl)-propenone, Journal of Molecular Liquids, 336, 10.1016\u002Fj.molliq.2021.116302\nRasool, F., Hussain, A., Ayub, K., Tariq, M., Mahmood, K., Yousuf, S., Yar, Muhammad., Khalid, M., Samreen, H, S., Lateef, M., & Malik, A. (2022). Experimental and Theoretical investigations on (E)-3-(4-ethoxyphenyl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one and (E)-3-(naphthalen-2-yl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one: DNA binding, Urease inhibition and Promising NLO response.Journal of Molecular Structure,1253, 132194.\nPages, 2015, Metal complex interactions with DNA, Dalton transactions, 44, 3505, 10.1039\u002FC4DT02700K\nSirajuddin, 2013, Drug–DNA interactions and their study by UV–Visible, fluorescence spectroscopies and cyclic voltametry, Journal of Photochemistry and Photobiology B: Biology, 124, 1, 10.1016\u002Fj.jphotobiol.2013.03.013\nRaziq, 2017, A new glycosidic antioxidant from Ranunculus muricatus L. (Ranunculaceae) exhibited lipoxygenasae and xanthine oxidase inhibition properties, Nat Prod Res., 31, 1251, 10.1080\u002F14786419.2016.1236098\nWeatherburn, 1967, Phenol-hypochlorite reaction for determination of ammonia, Analytical chemistry, 39, 971, 10.1021\u002Fac60252a045\nLee, 1988, Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density, Physical review B, 37, 785, 10.1103\u002FPhysRevB.37.785\nChemcraft-Citation.” [Online]. Available: https:\u002F\u002Fwww.chemcraftprog.com\u002Fcitation.html. [Accessed: 31-Mar-2019].\nHanwell, 2012, Avogadro: an advanced semantic chemical editor, visualization, and analysis platform, Journal of cheminformatics, 4, 17, 10.1186\u002F1758-2946-4-17\nO’Boyle, 2008, cclib: a library for package-independent computational chemistry algorithms, J. Comput. Chem., 29, 839, 10.1002\u002Fjcc.20823\nGaussView Version 5 Dennington R Keith T Millam J Semichem Inc Shawnee.” [Online]. Available: https:\u002F\u002Fwww.coursehero.com\u002Ffile\u002Fp6dg8n\u002F2-GaussView-Version-5-Dennington-R-Keith-T-Millam-J-Semichem-Inc-Shawnee\u002F. [Accessed: 07-Apr-2019].\nTruhlar, 1981\nBasri, 2022, Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies, Scientific reports, 12, 1, 10.1038\u002Fs41598-022-08860-3\nLiu, 2005, Study on the prediction of visible absorption maxima of azobenzene compounds, J. Zhejiang Univ. Sci. B, 6, 584, 10.1631\u002Fjzus.2005.B0584\nAdeel, 2017, Synthesis, X-ray crystallographic, spectroscopic and computational studies of aminothiazole derivatives, Journal of Molecular Structure, 1131, 136, 10.1016\u002Fj.molstruc.2016.11.046\nAli, 2020, Efficient synthesis, SC-XRD, and theoretical studies of O-Benzenesulfonylated pyrimidines: Role of noncovalent interaction influence in their supramolecular network, ACS omega, 5, 15115, 10.1021\u002Facsomega.0c00975\nRasool, 2022, Experimental and Theoretical investigations on (E)-3-(4-ethoxyphenyl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one and (E)-3-(naphthalen-2-yl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one: DNA binding, Urease inhibition and Promising NLO response, Journal of Molecular Structure, 1253, 10.1016\u002Fj.molstruc.2021.132194\nSlonimskaya, 1986, Interpretation of the IR spectra of celadonites and glauconites in the region of OH-stretching frequencies, Clay Minerals, 21, 377, 10.1180\u002Fclaymin.1986.021.3.09\nAlaşalvar, 2014, Crystal structure and DFT calculations of 5-(4-Chlorophenyl)-1-(6-methoxypyridazin-3-yl)-1H-pyrazole-3-carboxylic acid, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 132, 555, 10.1016\u002Fj.saa.2014.05.014\nPowell, 1972, Infrared and Raman spectra and the vC=C stretching frequencies of some silver-olefin and platinum-olefin complexes, Spectrochimica Acta Part A: Molecular Spectroscopy, 28, 327, 10.1016\u002F0584-8539(72)80256-3\nKovacic, 1967, The C=N stretching frequency in the infrared spectra of Schiff's base complexes—I. 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K, Liu Y, Lu L. Hydrogen-bonding recognition-induced color change of gold nanoparticles for visual detection of melamine in raw milk and infant formula J. Am. Chem. Soc., 2009, 131(27): 9496-7.\nY.T.K.H.L. Joohee Choi, Rapid quantification of melamine in milk using competitive 1,1′-oxalyldiimidazole chemiluminescent enzyme immunoassay, Analyst, 2010, 135(9): 2445-50.\nLiu, 2010, An enzyme linked immunosorbent assay for the determination of cyromazine and melamine residues in animal muscle tissues, Food Control, 21, 1482, 10.1016\u002Fj.foodcont.2010.04.018\nBeilstein, 1981, Determination of seventeen s-triazine herbicides and derivatives by high-pressure liquid chromatography, J. Agric. Food. Chem., 29, 1132, 10.1021\u002Fjf00108a008\nBloom Ca Mp, 1987, Cyromazine Resistance in the House Fly (Diptera: Muscidae), J. Econ. Entomol., 2, 352, 10.1093\u002Fjee\u002F80.2.352\nHui, 2008, Research advance in biotoxicology and environmental behavior of cyromazine, Trans. Chin. Soci. Agricult. Eng.\nLim, 1990, Disposition of cyromazine in plants under environmental conditions, J. Agric. Food. Chem., 38, 860, 10.1021\u002Fjf00093a057\nZhu, 2009, Determination of residues of cyromazine and its metabolite, melamine, in animal-derived food by gas chromatography-mass spectrometry with derivatization, J. Agric. Food. Chem., 57, 11075, 10.1021\u002Fjf902771q\nLi, 2019, Perovskite nanocrystals fluorescence nanosensor for ultrasensitive detection of trace melamine in dairy products by the manipulation of inner filter effect of gold nanoparticles, Talanta, 211\nGrout, 2008, Introduction to Digital Logic Design, Digital Systems Design with FPGAs and CPLDs, 217, 10.1016\u002FB978-0-7506-8397-5.00005-2\nBi, 2010, Colorimetric Logic Gates Based on Supramolecular DNAzyme Structures, Angew. Chem. Int. Ed., 49, 4438, 10.1002\u002Fanie.201000840\nSkarsdóttir, 2019, Towards a decision support framework for technologies used in cold supply chain traceability, J. Food Eng., 240, 153, 10.1016\u002Fj.jfoodeng.2018.07.013\nMunir, 2018, An evaluation of hyperspectral imaging for characterising milk powders, J. Food Eng., 221, 1, 10.1016\u002Fj.jfoodeng.2017.10.001\nSingh, 2017, Thermally buffered corrugated packaging for preserving the postharvest freshness of mushrooms (Agaricus bispours), J. Food Eng., 216, 11, 10.1016\u002Fj.jfoodeng.2017.07.013\nWen-Zhi, Lin, Yi-Hsiang, et al. A competitive immunoassay for biotin detection using magnetic beads and gold nanoparticle probes. Food Chem., 2019, 271, 440-444.\nYang, 2014, Comparison between surface-enhanced Raman scattering and the national standard method for the detection of melamine in milk, J. Food Safety Quality\nChen, 2015, A novel dispersive micro solid phase extraction using PCX as the sorbent for the determination of melamine and cyromazine in milk and milk powder by UHPLC-HRMS\u002FMS, Talanta, 134, 144, 10.1016\u002Fj.talanta.2014.10.036\nLiu, 2009, Functional nucleic acid sensors, Chem. Rev., 109, 1948, 10.1021\u002Fcr030183i\nJia, 2020, High affinity truncated aptamers for ultra-sensitive colorimetric detection of bisphenol A with label-free aptasensor, Food Chem., 317\nShellaiah, 2019, Review on Nanomaterial-Based Melamine Detection, Chemosensors, 7, 10.3390\u002Fchemosensors7010009\nRitota, 2017, Melamine Detection in Milk and Dairy Products: Traditional Analytical Methods and Recent Developments, Food Anal. Methods\nSharma V, Som N N, Pillai S B, et al. Utilization of doped GQDs for ultrasensitive detection of catastrophic melamine: A new SERS platform. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 224: 117352.\nXing, 2013, Sensitive colorimetric detection of melamine in milk with an aptamer-modified nanogold probe, RSC Adv., 3, 17424, 10.1039\u002Fc3ra42138d\nXing, 2018, A simple fluorescent assay for cyromazine detection in raw milk by using CYR-stabilized G-quadruplex formation, RSC Adv., 8, 2418, 10.1039\u002FC7RA12970J\nGe, 2021, Aptamer\u002Fderivatization-based surface-enhanced Raman scattering membrane assembly for selective analysis of melamine and formaldehyde in migration of melamine kitchenware, Talanta, 7\nViehrig, 2020, Quantitative SERS Assay on a Single Chip Enabled by Electrochemically Assisted Regeneration: A Method for Detection of Melamine in Milk, Anal. Chem., 92, 4317, 10.1021\u002Facs.analchem.9b05060\nLiu, 2020, Simultaneous colorimetric and surface-enhanced Raman scattering detection of melamine from milk, Spectrochim. Acta Part A Mol. Biomol. 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Method, 8, 5869, 10.1039\u002FC6AY01845A\nDu, 2013, A colorimetric logic gate based on free gold nanoparticles and the coordination strategy between melamine and mercury ions, Chem Comm, 49, 4196, 10.1039\u002FC2CC36955A",{"EN":1979},"Sensitive SERS detection of melamine and cyromazine in raw milk using aptamer-based in situ silver nanoparticles 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1967, Chem. Ber., 100, 2494, 10.1002\u002Fcber.19671000806\nHuisgen, 1963, Angew. Chem., Int. Ed., 2, 565, 10.1002\u002Fanie.196305651\nRostovtsev, 2002, Angew. Chem., Int. Ed., 41, 2596, 10.1002\u002F1521-3773(20020715)41:14\u003C2596::AID-ANIE2596>3.0.CO;2-4\nWu, 2005, Synthesis, 1314, 10.1055\u002Fs-2005-861860\nBodine, 2004, J. Am. Chem. Soc., 126, 1638, 10.1021\u002Fja039374t\nWang, 2003, J. Am. Chem. Soc., 125, 3192, 10.1021\u002Fja021381e\nSivakumar, 2004, Org. Lett., 6, 4603, 10.1021\u002Fol047955x\nLink, 2004, Am. Chem. Soc., 126, 10598, 10.1021\u002Fja047629c\nDharma Rao, 2017, Chem. Biol. Drug Des., 90, 397, 10.1111\u002Fcbdd.12957\nBonandi, 2017, Drug Discov. Today, 22, 1572, 10.1016\u002Fj.drudis.2017.05.014\nDheer, 2017, Bioorg. Chem., 71, 30, 10.1016\u002Fj.bioorg.2017.01.010\nGaur, 2017, ACS Omega, 2, 8227, 10.1021\u002Facsomega.7b00880\nHuo, 2017, ACS Omega, 2, 5557, 10.1021\u002Facsomega.7b00196\nSinopoli, 2017, Dalton Trans., 46, 1520, 10.1039\u002FC6DT02905A\nM.V. Gil, M.J. Arevalo, O. Lopez, 11 (2007) 1589–1620.\nMoses, 2007, Chem. Soc. Rev., 36, 1249, 10.1039\u002FB613014N\nBock, 2006, Eur. J. Org. Chem., 51, 10.1002\u002Fejoc.200500483\nNieuwdorp, 2008, Appl. Physiol., 104, 845, 10.1152\u002Fjapplphysiol.00440.2007\nVarki, 1993, Glycobiology, 3, 97, 10.1093\u002Fglycob\u002F3.2.97\nBernardi, 2013, Chem. Soc. Rev., 42, 4709, 10.1039\u002FC2CS35408J\nHart, 2010, Cell, 143, 672, 10.1016\u002Fj.cell.2010.11.008\nAnna, 2012, Chem. Soc. Rev., 42, 4709\nKrise, 1996, Adv. Drug Deliv. Rev., 19, 287, 10.1016\u002F0169-409X(95)00111-J\nArtyushin, 2008, Heteroatom Chem., 19, 293, 10.1002\u002Fhc.20420\nInestrosa, 1997, 501\nDharma Rao, 2018, J. Heterocyc. Chem., 55, 2556, 10.1002\u002Fjhet.3309\nDharma Rao, 2013, Tetrahedron Lett., 54, 48, 10.1016\u002Fj.tetlet.2013.09.130\nAcharya, 2015, Med. Chem. Res., 24, 1763, 10.1007\u002Fs00044-014-1253-0\nDharma Rao, 2014, Tetrahedron Lett., 55, 19, 10.1016\u002Fj.tetlet.2013.09.023\nVenugopala, 2016, Dev. Ther., 10, 2681, 10.2147\u002FDDDT.S109760\nEllman, 1961, Biochem. Pharmacol., 7, 88, 10.1016\u002F0006-2952(61)90145-9\nKim, 2001, Synth. Commun., 31, 3315, 10.1081\u002FSCC-100106042\nMirjana, 2013, Curr. 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Ther., 16, R150, 10.1186\u002Far4612\nKuiper, 1996, Cloning of a novel receptor expressed in rat prostate and ovary, Proc. Natl. Acad. Sci. USA, 93, 5925, 10.1073\u002Fpnas.93.12.5925\nNg, 2014, Versatility or promiscuity: the estrogen receptors, control of ligand selectivity and an update on subtype selective ligands, Int. J. Environ. Res. Public Health, 11, 8709, 10.3390\u002Fijerph110908709\nAscenzi, 2006, Structure–function relationship of estrogen receptor α and β: impact on human health, Mol. Aspects Med., 27, 299, 10.1016\u002Fj.mam.2006.07.001\nHolst, 2007, Estrogen receptor alpha (ESR1) gene amplification is frequent in breast cancer, Nat. Genet., 39, 655, 10.1038\u002Fng2006\nCole, 1971, A new anti-oestrogenic agent in late breast cancer: an early clinical appraisal of ICI46474, Br. J. Cancer, 25, 270, 10.1038\u002Fbjc.1971.33\nSharma, 2018, Estrogen alpha receptor antagonists for the treatment of breast cancer: a review, Chem. Cent. J., 18, 107, 10.1186\u002Fs13065-018-0472-8\nJordan, 2006, Tamoxifen (ICI46,474) as a targeted therapy to treat and prevent breast cancer, Br. J. Pharmacol., 147, 269, 10.1038\u002Fsj.bjp.0706399\nCoates, 2015, Panel Members. Tailoring therapies–improving the management of early breast cancer: St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2015, Ann. Oncol., 26, 1533, 10.1093\u002Fannonc\u002Fmdv221\nHakamata, 2008, (2S,2’R)-Analogue of LG190178 is a major active isomer, Bioorg. Med. Chem. Lett., 18, 120, 10.1016\u002Fj.bmcl.2007.11.007\nDemizu, 2011, Facile synthesis of stereoisomers of the non-secosteroidal ligand LG190178 and their evaluation using the mutant vitamin D receptor, Lett. Org. Chem., 8, 43, 10.2174\u002F157017811794557804\nKurihara, 2004, Design and synthesis of cyclic urea compounds: a pharmacological study for retinoidal activity, Bioorg. Med. Chem. Lett., 14, 4131, 10.1016\u002Fj.bmcl.2004.06.038\nMaruyama, 2013, Structure-activity relationships of bisphenol A analogs at estrogen receptors (ERs): discovery of an ERα-selective antagonist, Bioorg. Med. Chem. Lett., 23, 4031, 10.1016\u002Fj.bmcl.2013.05.067\nMisawa, 2017, Efficient synthesis of a multi-substituted diphenylmethane skelton as a steroid mimetic, Bioorg. Med. Chem. Lett., 27, 2590, 10.1016\u002Fj.bmcl.2017.03.066\nMisawa, 2017, Design and synthesis of novel selective estrogen receptor degradation inducers based on the diphenylheptane skeleton, Medchemcomm, 8, 239, 10.1039\u002FC6MD00553E\nEto, 2018, Design and synthesis of estrogen receptor ligands with a 4-heterocycle4-phenylheptane skeleton, Bioorg. Med. Chem., 26, 1638, 10.1016\u002Fj.bmc.2018.02.010\nWutts, 2014, 388\nDaignault, 1973, 2-Cyclohexyloxyethanol, Org. Synth., 5, 303\nFrost, 1994, Enantiomerically pure acetals as ligands for asymmetric catalysis, Synletters, 1994, 551, 10.1055\u002Fs-1994-22925\nFirouzabadi, 1999, Zirconium tetrachloride (ZrCl4) catalyzed highly chemoselective and efficient acetalization of carbonyl compounds, Synletters, 1999, 321, 10.1055\u002Fs-1999-2605\nMOLSIS Inc. https:\u002F\u002Fwww.molsis.co.jp\u002F.\nDelfosse, 2012, Structural and mechanistic insights into bisphenols action provide guidelines for risk assessment and discovery of bisphenol A substitutes, PNAS, 109, 14930, 10.1073\u002Fpnas.1203574109\nLuo, 2017, Design, synthesis, biological evaluation and molecular docking studies of novel 3-aryl-4-anilino-2H-chromen-2-one derivatives targeting ERα as anti-breast cancer agents, Bioorg. Med. Chem. Lett., 27, 2668, 10.1016\u002Fj.bmcl.2017.04.029\nPuranik, 2019, Determination and analysis of agonist and antagonist potential of naturally occurring flavonoids for estrogen receptor (ERα) by various parameters and molecular modelling approach, Sci. Rep., 9, 7450, 10.1038\u002Fs41598-019-43768-5\nMokale, 2015, Synthesis, in-vitro screening, and docking analysis of novel pyrrolidine and piperidine-substituted ethoxy chalcone as anticancer agents, Med. Chem. Res., 24, 1842, 10.1007\u002Fs00044-014-1266-8\nYugandhar, 2017, Isolation, characterization and in silico docking studies of synergistic estrogen receptor α anticancer polyphenols from Syzygium alternifolium (Wt.) Walp, J. Intercult. Ethnopharmacol., 6, 296, 10.5455\u002Fjice.20170709031835\nToray Industries, Inc.,D. Izuhara, Polymers from sulfonic acid group-​containing aromatic compound and use as polymer electrolytes for fuel cells. Japan Patent JP 2011-204253 (2011.09.20).\nNoyori, 1987, Trimethysilyl triflate in organic synthesis, Tetrahedron, 37, 3899, 10.1016\u002FS0040-4020(01)93263-6\nFor reference, Table 2 shows the IC50 value of potent ERα antagonists presented in Figure 1. 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2015, A review on versatile applications of transition metal complexes incorporating Schiff bases, Beni-Suef Univ J. Basic Appl. Sci., 4, 119\nAl Zoubi, 2017, Schiff base complexes and their versatile applications as catalysts in oxidation of organic compounds: part I, Appl. Organomet. Chem., 31, e3574, 10.1002\u002Faoc.3574\nBania, 2012, Enhanced Catalytic Activity of Zeolite Encapsulated Fe(III)-Schiff-Base Complexes for Oxidative Coupling of 2-Napthol, Inorg. Chem., 51, 1657, 10.1021\u002Fic201959g\nGupta, 2008, Catalytic activities of Schiff base transition metal complexes, Coord. Chem. Rev., 252, 1420, 10.1016\u002Fj.ccr.2007.09.005\nKoy, 2021, N-Heterocyclic carbenes as tunable ligands for catalytic metal surfaces, Nat. Catal., 4, 352, 10.1038\u002Fs41929-021-00607-z\nKatsuki, 2004, Unique asymmetric catalysis of cis-β metal complexes of salen and its related Schiff-base ligands, Chem. Soc. Rev., 33, 437, 10.1039\u002Fb304133f\nLeung, 2018, Catalysis in flow: nickel-catalyzed synthesis of primary amines from alcohols and NH 3, ACS Sustain Chem. Eng., 6, 5479, 10.1021\u002Facssuschemeng.8b00338\nLiu, 2018, Multidentate unsymmetrically-substituted Schiff bases and their metal complexes: synthesis, functional materials properties, and applications to catalysis, Coord. Chem. Rev., 357, 144, 10.1016\u002Fj.ccr.2017.11.030\nAl Zoubi, 2016, Organometallic complexes of Schiff bases: Recent progress in oxidation catalysis, J. Organomet. Chem., 822, 173, 10.1016\u002Fj.jorganchem.2016.08.023\nKim, 2003, Preparation of Silica-Supported Bis(imino)pyridyl Iron(II) and Cobalt(II) Catalysts for Ethylene Polymerization, Macromolecules, 36, 6689, 10.1021\u002Fma0347060\nUkoha, 2015, Kinetics and Mechanism of Electron Transfer Reaction of an Adipato Bridged Iron(III)-Salen Complex with Dithionite Ion in Perchloric Acid Medium, Croat. Chem. Acta., 88, 259, 10.5562\u002Fcca2584\nLiotta, 2009, Heterogeneous catalytic degradation of phenolic substrates: Catalysts activity, J. Hazard. Mater., 162, 588, 10.1016\u002Fj.jhazmat.2008.05.115\nKesraoui-Ouki, 1994, Natural zeolite utilisation in pollution control: A review of applications to metals’ effluents, J. Chem. Technol. Biotechnol., 59, 121, 10.1002\u002Fjctb.280590202\nKoopmans, 1933, Ordering of wave functions and eigenenergies to the individual electrons of an atom, Physica, 1, 104, 10.1016\u002FS0031-8914(34)90011-2\nParr, 1983, Absolute hardness: companion parameter to absolute electronegativity, J. Am. Chem. Soc., 105, 7512, 10.1021\u002Fja00364a005\nYan, 2022, The coordination structure and optical property of iron ions in the traditional lead glazes, J. Mol. Struct., 1257, 10.1016\u002Fj.molstruc.2022.132593\nWu, 2022, Dimensional design and core-shell engineering of nanomaterials for electromagnetic wave absorption, Adv. Mater., 34, 2107538, 10.1002\u002Fadma.202107538\nBürgin, 2022, Shedding light on the oxidizing properties of spin-flip excited states in a Cr III polypyridine complex and their use in photoredox catalysis, J. Am. Chem. Soc., 144, 14181, 10.1021\u002Fjacs.2c04465\nKargar, 2022, Synthesis, spectral characterization, crystal structures, biological activities, theoretical calculations and substitution effect of salicylidene ligand on the nature of mono and dinuclear Zn(II) Schiff base complexes, Polyhedron, 213, 10.1016\u002Fj.poly.2021.115636\nHamil, 2009, Synthesis, spectroscopic investigation and antiactivity activity of schiff base complexes of cobalt (II) and copper (II) ions, Rasayan J. Chem., 2, 261\nPalanimurugan, 2019, Electrochemical behavior, structural, morphological Calf Thymus-DNA interaction and in-vitro antimicrobial studies of synthesized Schiff base transition metal complexes, Heliyon, 5, e02039, 10.1016\u002Fj.heliyon.2019.e02039\nYadav, 2005, Organic Spectroscopy, Springer, Netherlands, Dordrecht\nFantacci, 2011, A computational approach to the electronic and optical properties of Ru(II) and Ir(III) polypyridyl complexes: Applications to DSC, OLED and NLO, Coord. Chem. Rev., 255, 2704, 10.1016\u002Fj.ccr.2011.03.008\nP.G. Wadher, S.J., Karande, N.A., Sonawane, S.D. and Yeole, Synthesis and biological evaluation of schiff base and 4-thiazolidinones of amino salicylic acid and their derivatives as an antimicrobial agent, Int. J. ChemTech Res. 1 (2009) 1303–1307.\nAnnapoorani, 2011, Studies on some trinuclear Schiff base complexes, Int. J. ChemTech Res., 3, 1962\nChohan, 2000, Synthesis, characterization and biological properties of tridentate NNO, NNS and NNN donor thiazole-derived furanyl, thiophenyl and pyrrolyl Schiff bases and their Co(II), Cu(II), Ni(II) and Zn(II) metal chelates, Met. Based. Drugs., 7, 10.1155\u002FMBD.2000.17\nJørgensen, 1962, Absorption Spectra and Chemical Bonding in Complexes, Elsevier\nAhmed, 2015, Synthesis, Characterisation, and Biological Evaluation of Zn(II) Complex with Tridentate (NNO Donor) Schiff Base Ligand, Int. J. Inorg. Chem., 2015, 1, 10.1155\u002F2015\u002F607178\nAbirami, 2014, Synthesis and in vitro evaluation of Ni (II) complexes of salicylaldimine, Int. J. Pharma Bio Sci., 5\nMahmoud, 2020, Synthesis and spectral analysis of some metal complexes with mixed Schiff base ligands 1-[2-(2-hydroxybenzylideneamino)ethyl]pyrrolidine-2,5-dione (HL1) and (2-hydroxybenzalidine)glycine (HL2), J. Phys. Conf. Ser., 1660, 012027, 10.1088\u002F1742-6596\u002F1660\u002F1\u002F012027\nAl-Zaidi, 2019, New complexes of chelating Schiffbase: Synthesis, spectral investigation, antimicrobial, and thermal behavior studies, J. Appl. Pharm. Sci., 9, 45, 10.7324\u002FJAPS.2019.90406\nShaker, 2010, Preparation, physico-chemical and spectroscopic investigation of thiacetazone and quinalizarin complexes with Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Pb(II), Aust. J. Basic Appl. Sci., 4\nKudin, 2000, Linear-scaling density-functional theory with Gaussian orbitals and periodic boundary conditions: Efficient evaluation of energy and forces via the fast multipole method, Phys. Rev. B - Condens. Matter Mater. Phys., 61, 16440, 10.1103\u002FPhysRevB.61.16440\nParr, 1991, Principle of maximum hardness, J. Am. Chem. Soc., 113, 1854, 10.1021\u002Fja00005a072\nChattaraj, 1995, The maximum hardness principle in the Gyftopoulos-Hatsopoulos three-level model for an atomic or molecular species and its positive and negative ions, Chem. Phys. Lett., 237, 171, 10.1016\u002F0009-2614(95)00280-H\nHailu, 2019, Computational studies on heterogenization of homogeneous catalyst of iron(III), nickel(II) and copper(II) N, N′-disalicylidene-1,2-phenylenediamine complex, Bull. Chem. Soc. 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