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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; 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. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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In the case of the former, Raman excitation profiles (REPs) for the various vibrational modes have also been computed. It is observed that the calculated absorption spectrum and the REPs compare very well with the experimental results. A comparison of these results with those of the often semiclassical approach reveals that the TDQM method can be used to study polyatomic systems with as much ease as the semiclassical wavepacket method.",{"EN":952},"Resonance raman intensity analysis of polyatomic molecules",{"VOID":954},"Abramowitz M and Stegun I A 1968Handbook of mathematical functions (New York: Dover) p. 886\nAlbrecht A C 1961J. Chem. Phys. 34 1476\nBiswas N and Umapathy S 1995Chem. Phys. Lett. 236 24\nDirac P A M 1927Proc. R. Soc. (London) 114 710\nFeit M D, Fleck J A Jr, and Steiger A 1982J. Comput. Phys. 47 412\nHeller E J 1975J. Chem. Phys. 62 1544\nHeller E J 1978J. Chem. Phys. 68 2066\nHeller E J 1981Acc. Chem. Res. 14 368\nHeller E J, Sundberg R L and Tannor D J 1982J. Phys. Chem. 86 1822\nKalyanaraman C and Sathyamurthy N 1993Chem. Phys. Lett. 209 52\nKalyanaraman C and Sathyamurthy N 1994Chem Phys. 187 219\nKosloff D and Kosloff R 1983aJ. Comput. Phys. 52 35\nKosloff R and Kosloff D 1983bJ. Chem. Phys. 79 1823\nKosloff R 1988J. Phys. Chem. 92 2087\nKramers H A and Heisenberg W 1925Z. Phys. 31 681\nKulander K C and Heller E J 1978J. Chem. Phys. 69 2439\nLee S Y and Heller E J 1979J. Chem. Phys. 71 4777\nLorriaux J L, Merlin J C, Dupaix A and Thomas E W 1979J. Raman Spectrosc. 8 81\nManneback C 1951Physica 17 1001\nManthe U and Köppel H 1990aJ. Chem. Phys. 93 345\nManthe U and Köppel H 1990bJ. Chem. Phys. 93 1658\nMohan V and Sathyamurthy N 1988Comput. Phys. Rep. 7 215\nMyers A B 1990J. Opt. Soc. Am. B,7 1665\nMyers A B and Mathies R A 1984J. Chem. Phys. 81 1552\nMyers A B and Mathies R A 1987Biological applications of Raman spectroscopy (ed.) T G Spiro (New York: John Wiley and Sons) vol 2, p. 1\nMyers A B, Mathies R A, Tannor D J and Heller E J 1982J. Chem. Phys. 77 3857\nMyers A B, Harris R A and Mathies R A 1983J. Chem. Phys. 79 603\nOkamoto H, Hamaguchi H and Tasumi M 1986Chem. Phys. Lett. 130 185\nRamakrishna M V and Coalson R D 1988Chem. Phys. 120 327\nRau H 1984J. Photochem. 26 221\nRau H 1990Photochromism: molecules and systems (eds) H Durr and H Bouas-Lauren (Amsterdam: Elsevier) chap. 4, p. 165\nSiebrand W and Zgierski M Z 1979Chem. Phys. Lett. 62 3\nTang J and Albrecht A C 1970Raman Spectroscopy (ed) H A Szymanski (Plenum: New York) vol. 2, p. 33\nTannor D J and Heller E J 1982J. Chem. Phys. 77 202\nWarshel A 1975J. Chem. Phys. 62 214\nWilliams S O and Imre D G 1988aJ. Phys. Chem. 92 3363\nWilliams S O and Imre D G 1988bJ. Phys. 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this study the preparation and characterization of a zinc MOF which gives blue luminescence and photocatalytic activity have been described The reaction of 2cyanopyridine, Zn(NO3)2⋅4H2O and NaN3 yielded a new 3D Zn(II) coordination polymer {(2PTZ)2Zn}n (1), where 2PTZ =5(2pyridyl)tetrazolate via in situ [2 + 3] cycloaddition reaction of the nitrile and the azide. Compound 1 was characterized by elemental analyses, IR spectroscopy, X-ray powder diffraction (XRPD), scanning electron microscopy (SEM) and single-crystal X-ray crystallography. Crystal structure of the compound belongs to monoclinic space group C2\u002Fc with Z =  2 In 1 the crosslinkage of the PTZ ligands and Zn(II) atoms forms an infinite 1D chain network. Further the one–dimensional chains are assembled into threedimensional network by hydrogen bonding. Thermal photoluminescence and photocatalytic properties of 1 were also been investigated. \n                \n                  \n                    \n                    \n                  \n                  \n                    \n                  \n                \n              ",{"EN":1080},"Synthesis crystal structure, photoluminescence and photocatalytic property of a new three dimensional Zinc(II) tetrazole framework",{"VOID":1082},"Liu W T, Li J Y, Ni Z P, Bao X, Leng J D, Liu J L and Tong M L 2012 Cryst. Growth Des. 12 1482\nCui P, Chen Z, Gao D, Zhao B, Shi W and Cheng P 2010 Cryst. Growth Des. 10 4370\nNasani R, Saha M, Mobin S M and Mukhopadhyay S 2013 Polyhedron 55 24\nSingh S, Gupta D K, Noeth H and Pandey A 2013 J. Chem. Crystallogr. 43 82\nGupta D K, Singh S, Mayer P and Pandey A 2011 Inorg. Chem. Com. 14 1485\nSuh M P, Park H J, Prasad T K and Lim D W 2012 Chem. Rev. 112 (2) 782\nHe Y B, Zhou W, Yildirim T and Chen B L 2013 Energy Environ Sci. 6 2735\nKreno L E, Leong K, Farha K, Allendorf M, Duyne V and Hupp T 2012 Chem. Rev. 112 1105\nLin J B, Xue W, Zhang J P and Chen X M 2011 Chem. Commun. 47 926\nMcKinlay A C, Morris R E, Horcajada P, Ferey G, Gref R, Couvreur P and Serre C 2010 Angew. Chem. Int. Ed. 49 6260\nWanderley M M, Wang C, Wu C D and Lin W B 2012 J. Am. Chem. Soc. 134 (22) 9050\nWang G Y, Yang L L, Li Y, Song H, Ruan W J, Chang Z and Bu X H 2013 Dalton Trans. 42 12865\nZhang T and Lin W 2014 Chem. Soc. Rev. 43 5982\nHantzsch A and Vagt A 1901 Ueber das sogenannte Diazoguanidin. Liebig’s Ann 314 339\nDemko Z P and Sharpless K B 2001 J. Org. Chem. 66 7945\nDemko Z P and Sharpless K B 2002 Angew. Chem. 114 2214; 2002 Angew. Chem. Int. Ed. 41 2110\nHimo F, Demko Z P, Noodleman L and Sharpless K B 2003 J. Am. Chem. Soc. 125 9983\nWang L Z, Qu Z R, Zhao H, Wang X S, Xiong R G and Xue Z L 2003 Inorg. Chem. 42 3969\nSingh S, Mayer P and Pandey A 2010 Indian J. Chem. 49A 1345\nWu J Y, Huang S M, Huang Y C and Lu K L 2012 Cryst. Eng. Comm. 14 1189\nRobson R, Abrahams B F, Batten S R, Gable R W, Hoskins B F and Liu J 1992 ACS Symp. Ser. T Bein (Ed.) (ACS: Washington, DC) 499 256\nHaasnoot G J 2000 Coord. Chem. Rev. 200 131\nSu C Y, Cai Y P, Chen C L, Smith M D, Kaim W and Loye H C 2003 J. Am. Chem. Soc. 125 8595\nBauer A, Timofeeva V, Settersten B, Patterson D, Liu H, Simmons A and Allendorf D 2007 J. Am. Chem. Soc. 129 7136\nMishra A, Nayak P K and Periasamy N 2004 Tetrahedron Lett. 45 6265\nNayak P K, Agarwal N, Ali F, Patankar M P, Narasimhan K L and Periasamy N J. Chem. Sci. 122 847\nFordham S, Wang X, Bosch M and Zhou H 2015 “Lanthanide Metal-Organic Frameworks” In Structure and Bonding P Cheng (Ed.) (Berlin: Heidelberg) 163 p. 1\nMahata P, Madras G and Natarajan S 2006 J. Phys. Chem. B 110 13759\nWang C C, Li J R, Lv X L, Zhang Y Q and Guo G 2014 Energy Environ. Sci. 7 2831\nAltomare A, Burla M C, Camalli M, Cascarano G L, Giacovazzo C, Guagliardi A, Moliterni A G G, Polidori G and Spagna R 1999 J. Appl. Cryst. 32 115\nSheldrick G M 1997 SHELXL-97: Program for refining crystal structure refinement (University of Goettingen: Goettingen)\nZhu H B, Yang W N and Hu J 2013 J. Coord. Chem. 16 2775\nMa H, Xu Y, Meng Q, Zhang L, Wang R and Sun D 2014 Z. Anorg. Allg. Chem. 640 1219\nBernstein J, Davis R E, Shimoni L and Chang N -L 1995 Angew. Chem. Int. Ed. Engl. 34 1555\nEtter M C, MacDonald J C and Bernstein J 1990 Acta Cryst. B 46 256\nXue X, Wang X S, Wang L Z, Xiong R G, Abrahams B F, You X Z, Xue Z L and Che C M 2002 Inorg. Chem. 41 6544",{"VOID":1084},"10.1007\u002Fs12039-015-0925-8","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12039-015-0925-8",[1087,1102,1115],{"id":1088,"sortIndex":32,"researcher":28,"roles":1089,"affiliations":1090,"properties":1099,"displayName":1101,"givenName":28,"familyName":28},"e04fea61-de48-4374-b8ef-5613ec136ea6",[964],[1091],{"id":1092,"sortIndex":32,"affiliation":1093,"properties":28},"8915cf97-f436-4863-9f36-47bb0fa306df",{"id":1092,"createTime":28,"updateTime":28,"relativeEntities":1094,"slug":28,"properties":1095,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1098,"statistic":28},[],{"title":1096},{"VI":1097},"Department of Chemistry, Motilal Nehru National Institute of Technology, Allahabad, India",[],{"title":1100},{"VI":1101},"ARTI 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of 1-octadecyl-1H-benzimidazole (OBI) have been formed on copper surface by self-assembly method. Optimum conditions viz. the solvent, concentration of OBI, immersion period and temperature for the formation of a protective film on copper have been established using impedance studies. The OBI film has been characterized by X-ray photoelectron spectroscopy, reflection absorption Fourier transform infrared (FTIR) spectroscopy, contact angle measurements and atomic force microscopy. Efficiency of the OBI film to protect copper from corrosion has been investigated in aq. HCl solution using electrochemical impedance spectroscopy, potentiodynamic polarization method, cyclic voltammetry, scanning electron microscopy and gravimetry. Results of these studies inferred that the OBI film has an inhibition efficiency in the range of 97–99% under different conditions. Polarization studies inferred that the OBI film functions as a cathodic inhibitor. Cyclic voltammetric studies showed that the film is stable even after 15 cycles, when the copper electrode is polarized to an anodic potential of 0.35 V vs. Ag\u002FAgCl electrode. \n                \n                  \n                    \n                    \n                  \n                  \n                    \n                  \n                \n              ",{"EN":1190},"Self-assembled 1-octadecyl-1H-benzimidazole film on copper surface for corrosion protection",{"VOID":1192},"Ho H M, Lam W, Stoukatch S, Ratchev P, Vath III CJ and Beyne E 2003 Microelectron. Reliab. 43 913\nGracias D H, Method to increase electromigration resistance of copper using self-assembled organic thiolate monolayers. 2005 U.S. Patent 6858527\nAppa Rao B V, Yakub Iqbal Md and Sreedhar B 2009 Corros. Sci. 51 1441\nAppa Rao B V, Yakub Iqbal Md and Sreedhar B 2010 Electrochim. Acta 55 620\nLaibinis P E and Whitesides G M 1992 J. Am. Chem. Soc. 114 9022\nQuan Z, Wu X, Chen S, Zhao S and Ma H 2001 Corrosion 57 195\nChen H, Ren H Y, Zong Y W, Qun J X and Guo D Z 2008 Corros. Sci. 50 3527\nStupnisek-Lisac E, Gazivoda A and Madzarac M 2002 Electrochim. Acta 47 4189\nOtmacic H and Stupnisek L E 2003 Electrochim. Acta 48 985\nNezhada A K, Zareb A, Parhami A, Soltani Rod M N and Nejabat J R 2007 J. Iran. Chem. Soc. 4 271\nFreeman R A and Silverman, D C 1992 Corrosion 48 463\nTan Y S, Srinivasan M P, Pehkonen S O and Simonchooi Y M 2006 Corros. Sci. 48 840\nWang C T, Chen S H, Ma H Y, Hua L and Wang N X 2002 J. Serb. Chem. Soc. 67 685\nCicileo G P, Rosales B M, Varela F E and Vilche J R 1999 Corros. Sci. 41 1359\nYe X R, Xin X Q, Zhu J J and Xue Z L 1998 Appl. Surf. Sci. 135 307\nPetkova G, Sokolova E, Raicheva S and Ivanov P 1998 J. Appl. Electrochem. 28 1067\nKamdem D P, Zhang J and Adnot A 2001 Holzforschung 55 16\nTaneichi D, Haneda R and Aramaki K 2001 Corros. Sci. 43 1589\nHutt D A and Liu C 2005 Appl. Surf. Sci. 252 400\nBeccaria A M and Bertolotto C 1997 Electrochim. Acta 42 1361\nMekhalif Z, Fonder G, Laffineur F and Delhalle J 2008 J. Electroanal. Chem. 621 245\nYoshida S and Ishida H 1995 Appl. Surf. Sci. 89 39\nBaba H, Kodama T, Mori K and Hirahara H 1997 Corros. Sci. 39 555\nKleber C, Hilfrich U and Schreiner M 2007 Appl. Surf. Sci. 253 3712\nMa H, Chen S, Niu L, Zhao S, Li S and Li D 2002 J. Appl. Electrochem. 32 65\nFonsati M, Zucchi F and Trabanelli G 1998 Electrochim. Acta 44 311\nMarconato J C, Bulhoes L O and Temperini M L 1998 Electrochim. Acta. 43 771\nYan C W, Lin H C and Cao C N 2000 Electrochim. Acta 45 2815\nCrundwell F K 1992 Electrochim. Acta 37 2707",{"VOID":1194},"10.1007\u002Fs12039-013-0518-3","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12039-013-0518-3",[1197,1212],{"id":1198,"sortIndex":32,"researcher":28,"roles":1199,"affiliations":1200,"properties":1209,"displayName":1211,"givenName":28,"familyName":28},"023ac42e-9bbb-47e0-b809-570dc3186038",[964],[1201],{"id":1202,"sortIndex":32,"affiliation":1203,"properties":28},"0934bbd4-ea27-4da9-9761-4831abf59501",{"id":1202,"createTime":28,"updateTime":28,"relativeEntities":1204,"slug":28,"properties":1205,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1208,"statistic":28},[],{"title":1206},{"VI":1207},"Department of Chemistry, National Institute of Technology Warangal, Warangal, India",[],{"title":1210},{"VI":1211},"B V APPA RAO",{"id":1213,"sortIndex":40,"researcher":28,"roles":1214,"affiliations":1215,"properties":1222,"displayName":1224,"givenName":28,"familyName":28},"2ce34c4c-32c4-4b09-a7d7-38e5500acadd",[964],[1216],{"id":1202,"sortIndex":32,"affiliation":1217,"properties":28},{"id":1202,"createTime":28,"updateTime":28,"relativeEntities":1218,"slug":28,"properties":1219,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1221,"statistic":28},[],{"title":1220},{"VI":1207},[],{"title":1223},{"VI":1224},"M NARSIHMA REDDY",{"url":1195,"publisher":1226,"properties":1267},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1227,"slug":872,"properties":1228,"entityType":25,"verifyStatus":882,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1232,"manageAffiliations":1236,"indexDatabases":1247,"url":28,"thumbnailPath":28,"statistic":1262,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1229,"title":1230,"eissn":1231},{"VOID":877},{"EN":879},{"VOID":875},[1233],{"id":885,"createTime":28,"updateTime":28,"relativeEntities":1234,"label":1235,"description":28,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":888},[1237,1242],{"id":891,"createTime":28,"updateTime":28,"relativeEntities":1238,"slug":28,"properties":1239,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1241,"statistic":28},[],{"title":1240},{"EN":895},[],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1243,"slug":28,"properties":1244,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1246,"statistic":28},[],{"title":1245},{"EN":902},[904],[1248,1255],{"id":907,"indexDatabase":1249,"url":913,"indexYears":914,"academicFieldIds":1254,"indexDatabaseRanking":917},{"id":786,"createTime":28,"updateTime":28,"relativeEntities":1250,"label":1251,"description":1252,"key":792,"publicationTags":1253,"standard":28},[],{"EN":789,"VI":789},{"EN":789,"VI":791},[794],[916],{"id":919,"indexDatabase":1256,"url":931,"indexYears":28,"academicFieldIds":1261,"indexDatabaseRanking":28},{"id":921,"createTime":28,"updateTime":28,"relativeEntities":1257,"label":1258,"description":1259,"key":928,"publicationTags":1260,"standard":28},[],{"EN":924,"VI":924},{"EN":926,"VI":927},[930,813],[816],{"impactFactor":32,"impactFactorByYear":1263,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":48,"totalPublicationByYear":1264,"totalCitation":32,"totalCitationByYear":1265,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1266,"hindexLast5Year":32,"hindex":32},{},{"1979":40,"1985":40,"1986":42,"1989":40},{},{},{"pages":1268,"volume":1270},{"VOID":1269},"1325-1338",{"VOID":1271},"125","2013-12-24",2013,[917,930],{"id":1276,"createTime":1277,"updateTime":1278,"relativeEntities":1279,"slug":1280,"properties":1281,"entityType":957,"verifyStatus":26,"verifyTime":1278,"verifyNote":958,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1292,"fullTextUrl":28,"authors":1293,"publicationType":1018,"publisherRelationship":1348,"citationCount":28,"citationInfo":28,"publishDate":1390,"publishYear":1391,"citationAnalyzeStatus":882,"lastCitationAnalyze":28,"indexDatabases":1392,"openAccess":28,"references":28,"isForceReanalyzing":1069},"00429d12-9be0-4c0d-8efc-b4b29b4f96f9","2024-04-05T16:55:50.094+00:00","2024-12-25T02:57:38.617+00:00",[],"Adsorption-of-naphthols-in-the-presence-of-different-electrolytes-and-peptising-agents-and-at-different-temperatures",{"abstract":1282,"title":1284,"keywords":1286,"references":1288,"doi":1290},{"EN":1283},"Adsorption of some dyestuffs of the Naphthol AS series by cotton fibre has been studied in the presence of alcohol, sodium hydroxide, sodium chloride, sodium sulphate, sodium phosphate, soap, gum tragacanth and agar-agar and at different temperatures to understand the mechanism of the process of dyeing. It is observed that adsorption of the dyestuffs decreases with increasing amount of alcohol, gum tragacanth and agar-agar, while it first increases, reaches a maximum and then decreases on adding increasing amounts of sodium hydroxide, sodium chloride, sodium sulphate, sodium phosphate and soap solutions. Regarding the effect of temperature on adsorption, it is found that (1) the rate of adsorption is greater at higher than at lower temperatures, (2) the equilibrium adsorption increases with the rise of temperature, and (3) the amount of increase of adsorption for a particular range of temperature is greater at lower than at higher temperatures. The results obtained become easily intelligible if it is assumed that the dye particles exist in colloidal condition and the process of dyeing is interpreted from that point of view.",{"EN":1285},"Adsorption of naphthols in the presence of different electrolytes and peptising agents and at different temperatures",{"EN":1287},"",{"VOID":1289},"RathJ. Soc. D. C., 1928,44, 10.\nJungmichl and KimovecMelliand Textilber, 1937,18, 7.\nAcharya, Patel and DesaiProc. Ind. Acad. Sci., 1936,4, 503.\nValko’Trans. Faraday Soc., 1935,31, 230, 245, 262.\nDesai and BarveTrans. Nat. Inst. Sci. (India), 1939,2, 39–68.\nMcBain and othersTrans. Faraday Soc., 1935,31, 149–216.\nMortonIbid., 1935,31, 275.\nKhanolkar, Barve andProc. Ind. Acad. Sci., 1936,4, 468.",{"VOID":1291},"10.1007\u002FBF03172524","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF03172524",[1294,1309,1322,1335],{"id":1295,"sortIndex":32,"researcher":28,"roles":1296,"affiliations":1297,"properties":1306,"displayName":1308,"givenName":28,"familyName":28},"18bad8fe-e904-4119-be52-b1422147f327",[964],[1298],{"id":1299,"sortIndex":32,"affiliation":1300,"properties":28},"271b3dae-94b5-460a-8d7c-6c642300e3d2",{"id":1299,"createTime":28,"updateTime":28,"relativeEntities":1301,"slug":28,"properties":1302,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1305,"statistic":28},[],{"title":1303},{"VI":1304},"Physical Chemistry Laboratory, Wilson College, Bombay 7",[],{"title":1307},{"VI":1308},"J. A. 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Các dẫn xuất aminosulphonamide của naphthalene và diphenyl cũng được mô tả.","With the object of studying the antibacterial effect of sulphanilamide derivatives with cyclic substituents at the sulphonamide radical, typical N1-sulphanilamido derivatives of diphenylether, phenanthrene, chrysene, dibenzofuran, carbazole, coumarin, acridine, tetrahydroquinoline and phenanthridine have been synthesised and are reported. Aminosulphonamide derivatives of naphthalene and diphenyl are also described.",{"EN":1475,"VI":1476},"Chemotherapy of bacterial infections","Hóa trị điều trị nhiễm trùng do vi khuẩn",{"VI":1478},"kháng khuẩn, dẫn xuất sulphanilamide, sulphonamide, N1-sulphanilamido",{"VOID":1480},"Ganapathi, K.Curr. Sci., 1940,9, 417.Proc. Ind. Acad. Sci., 1941,13A, 386.\nHaessermann and TeichmannBer., 1896,29, 1447.\nNoller and AdamsJour. Amer. Chem. Soc., 1924,46, 1892.\nBrown —, 1936,58, 1808.\nKraemer and WeissgerberBer., 1901,34, 1662.\nBischler and Napieralsky —, 1893,26, 1903.\nNaegeli, Kundig and BradenburgerHel. Chem. Acta., 1938,21, 1746; 1939,22, 912.\nKahlbaumBrit.,502, 558.\nMeter, Bianculli and LowyJour. Amer. Chem. Soc., 1940,62, 3146.\nNovelli and Somoglins —, 1941,63, 854.\nDonnell, Dietz and Cladwell —, 1941,63, 1161.\nGoldyrev and PostovskiiJ. Applied Chem. (U.S.S.R.), 1938,11, 316.\nTrefouel, Trefouel, Nitti and BovetAnnales List. Pasteur, 1937,58, 30.\nButtleLancet, 1936,1, 1289.\nWalker,J. Jour. Chem. Soc, 1940, 686.\nFildes, P.Lancet, 1940,1, 955.\nWoods, D. D.Brit. Jour. Exp. Pathol., 1940,21, 74.\nNovelli, A.Ciencia, 1940,1, 260;C.A., 1940,34, 7903.\n.—C.A., 1940,34, 6621.",{"VOID":1482},"10.1007\u002FBF03051831","2025-01-23T14:28:51.133+00:00",[30],"https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF03051831",[1487,1502],{"id":1488,"sortIndex":32,"researcher":28,"roles":1489,"affiliations":1490,"properties":1499,"displayName":1501,"givenName":28,"familyName":28},"c8df792a-f681-43b9-830e-1160b7335945",[964],[1491],{"id":1492,"sortIndex":32,"affiliation":1493,"properties":28},"800ec512-e3ce-4f11-93d1-5f8f263d8879",{"id":1492,"createTime":28,"updateTime":28,"relativeEntities":1494,"slug":28,"properties":1495,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1498,"statistic":28},[],{"title":1496},{"VI":1497},"Haffkine Institute, Parel, Bombay",[],{"title":1500},{"VI":1501},"S. 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By the condensation of (I) with the sodium salt and anhydride of trimethylgallic acid, 7-hydroxy-3∶5∶8∶3′∶4′∶5′-hexamethoxyflavone (II) is obtained. Methylation of (II) yields a heptamethyl ether (III) identical with heptamethyl hibiscetin. Demethylation of (II) gives rise to a heptahydroxy flavone (IV) which is found to be identical with hibiscetin in all its properties and reactions. The constitution of hibiscetin is therefore confirmed by synthesis as 3∶5∶7∶8∶3′∶4′∶5′-heptahydroxy flavone.",{"EN":1575},"Synthesis of Hibiscetin",{"VOID":1577},"Rao and SeshadriProc. Ind. Acad. Sci., A, 1942,16, 323.\n—Ibid., 1942,15, 148.\nBaker, Nodzu and RobinsonJ. C. S., 1929, 74.\nRaoCurrent Science, 1942,11, 360.",{"VOID":1579},"10.1007\u002FBF03174821","2025-01-06T19:04:08.969+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF03174821",[1583,1598,1611],{"id":1584,"sortIndex":32,"researcher":28,"roles":1585,"affiliations":1586,"properties":1595,"displayName":1597,"givenName":28,"familyName":28},"6fadcea3-c345-43ee-aa4b-04b2e2fd6534",[964],[1587],{"id":1588,"sortIndex":32,"affiliation":1589,"properties":28},"b0877245-501b-4867-850f-dce8a3b8d537",{"id":1588,"createTime":28,"updateTime":28,"relativeEntities":1590,"slug":28,"properties":1591,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1594,"statistic":28},[],{"title":1592},{"VI":1593},"Department of Chemistry, Andhra University, Waltair",[],{"title":1596},{"VI":1597},"P. Ramachandra Rao",{"id":1599,"sortIndex":40,"researcher":28,"roles":1600,"affiliations":1601,"properties":1608,"displayName":1610,"givenName":28,"familyName":28},"7cc9944c-61a4-4da0-b1ce-72f5f66ccbd4",[964],[1602],{"id":1588,"sortIndex":32,"affiliation":1603,"properties":28},{"id":1588,"createTime":28,"updateTime":28,"relativeEntities":1604,"slug":28,"properties":1605,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1607,"statistic":28},[],{"title":1606},{"VI":1593},[],{"title":1609},{"VI":1610},"P. 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Seshadri",{"url":1581,"publisher":1625,"properties":1666},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1626,"slug":872,"properties":1627,"entityType":25,"verifyStatus":882,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1631,"manageAffiliations":1635,"indexDatabases":1646,"url":28,"thumbnailPath":28,"statistic":1661,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1628,"title":1629,"eissn":1630},{"VOID":877},{"EN":879},{"VOID":875},[1632],{"id":885,"createTime":28,"updateTime":28,"relativeEntities":1633,"label":1634,"description":28,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":888},[1636,1641],{"id":891,"createTime":28,"updateTime":28,"relativeEntities":1637,"slug":28,"properties":1638,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1640,"statistic":28},[],{"title":1639},{"EN":895},[],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1642,"slug":28,"properties":1643,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1645,"statistic":28},[],{"title":1644},{"EN":902},[904],[1647,1654],{"id":907,"indexDatabase":1648,"url":913,"indexYears":914,"academicFieldIds":1653,"indexDatabaseRanking":917},{"id":786,"createTime":28,"updateTime":28,"relativeEntities":1649,"label":1650,"description":1651,"key":792,"publicationTags":1652,"standard":28},[],{"EN":789,"VI":789},{"EN":789,"VI":791},[794],[916],{"id":919,"indexDatabase":1655,"url":931,"indexYears":28,"academicFieldIds":1660,"indexDatabaseRanking":28},{"id":921,"createTime":28,"updateTime":28,"relativeEntities":1656,"label":1657,"description":1658,"key":928,"publicationTags":1659,"standard":28},[],{"EN":924,"VI":924},{"EN":926,"VI":927},[930,813],[816],{"impactFactor":32,"impactFactorByYear":1662,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":48,"totalPublicationByYear":1663,"totalCitation":32,"totalCitationByYear":1664,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1665,"hindexLast5Year":32,"hindex":32},{},{"1979":40,"1985":40,"1986":42,"1989":40},{},{},{"pages":1667,"volume":1669},{"VOID":1668},"88-92",{"VOID":1670},"19","1944-01-01",1944,[930],{"id":1675,"createTime":1676,"updateTime":1677,"relativeEntities":1678,"slug":1679,"properties":1680,"entityType":957,"verifyStatus":26,"verifyTime":1677,"verifyNote":958,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1689,"fullTextUrl":28,"authors":1690,"publicationType":1018,"publisherRelationship":1736,"citationCount":28,"citationInfo":28,"publishDate":1783,"publishYear":1784,"citationAnalyzeStatus":882,"lastCitationAnalyze":28,"indexDatabases":1785,"openAccess":28,"references":28,"isForceReanalyzing":1069},"00944ce1-12ce-4680-8deb-a039780ef8d9","2024-01-09T17:35:14.683+00:00","2024-12-23T10:09:01.339+00:00",[],"An-efficient-asymmetric-synthesis-of-wodeshiol",{"abstract":1681,"title":1683,"references":1685,"doi":1687},{"EN":1682},"An efficient synthesis of (–)-wodeshiol 1 is described. The key reactions include highly stereoselective aldol condensation of piperonal with the dianion of chiral oxazolidinone, subsequent intramolecular ring cyclization of the aldol product 8 and a diastereocontrolled oxygenation of dilactone 7 in good yield.",{"EN":1684},"An efficient asymmetric synthesis of (–)-wodeshiol",{"VOID":1686},"Ward R S 1982 Chem. Soc. Rev. 11 75\nTeles H L, Hemerly J P, Paulettit P M, Pandolfi J R C, Araujot A R, Valentini S R, Young M C M, Bolzani V S, Silva D H S 2005 Nat. Prod. Res. 19 319\nDe Leon E J, Olmedo D A, Solis P N, Gupta M P, Terencio M C 2002 Planta Med. 68 1128\nHoang V D, Tan G T, Zhang H J, Tamez P A, Nguyen M C, Soejrto D D, Fong H H S, Pezzuto J M 2002 Phytochemistry 59 325\nMacRae W D, Towers G H N 1984 Phytochemistry 23 1207\nBrown R C, Bataille C J, Bruton G, Hinks J D, Swain N A 2001 J. Org. Chem. 66 6791\nIwakami S, Ebizuka Y, Sankawa U 1990 Heterocycles 30 795\nIchikawa K, Kinoshita T, Nishibe S, Sankawa U 1986 Chem. Pharm. Bull. 34 3514\nNikaido T, Ohmoto T, Kinoshita T, Sankawa U, Nishibe S, Hisada S 1981 Chem. Pharm. Bull. 29 3586\nPlante G E, Prevost C, Chainey A, Braquet P, Sirois P 1987 Am. J. Physiol. 253 R375\nBernard C B, Arnason J T, Philogene B J R, Lam J, Waddell T 1989 Phytochemistry 28 1373\nNajera C, Yus M 2003 Curr. Org. Chem. 7 867\nTakahashi K, Nakagawa T 1966 Chem. Pharm. Bull. 14 641\nTsukamoto H, Hisada S, Nishibe S 1984 Chem. Pharm. Bull. 32 2730\nTsukamoto H, Hisada S, Nishibe S 1985 Chem. Pharm. Bull. 33 1232\nXiaojun H, Corey E 1999 J. Org. Lett. 11 1871\nAnjaneyulu A S R, Ramaiah P A, Row L R, Pelter A, Ward R S 1975 Tetrahedron Lett. 34 2961\nInoue K, Inoue H, Chen C C 1981 Phytochemstry 20 2271\nJung J C, Kim J C, Moon H I, Park O S 2006 Tetrahedron Lett. 47 6433\nKim J C, Kim K H, Jung J C, Park O S 2006 Tetrahedron: Asymmetry 17 3 Selected data; 7: mp. 124–126°C [α]\\(^{20}_{\\,\\,D}\\) (c 1.0, MeOH); IR (neat, NaCl) 1772, 1498, 1247, 1038 cm − 1; 1H NMR (300 MHz, CDCl3) δ 6.81 (s, 4H), 6.75 (s, 2H), 5.99 (s, 4H), 5.82 (s, 2H), 3.54 (s, 2H); 13C NMR (75 MHz, CDCl3) δ 175.3, 149.2, 149.0, 132.4, 119.2, 109.4, 105.9, 102.3, 82.5, 48.9; MS(ESI) (m\u002Fz) 383 [M+H] + , 307, 154 (base peak); HRMS calcd for C20H14O8: 383.0767 [M+H] + , found: 383.0695. (–)-Wodeshiol 1: mp. 153–154°C (lit.16 152–153°C; lit.12 150–151°C); [α]\\(^{20}_{\\,\\,D}\\) = −11.2 (c 0.7, CHCl3), (lit.16 [α]\\(^{23}_{\\,\\,D}\\) = −11.7 in CHCl3; lit.12 [α]\\(^{24}_{\\,\\,D}\\) = −34.6 in CHCl3); IR (neat, NaCl) 3432, 1602, 1256, 1032 cm − 1; 1H NMR (400 MHz, CDCl3) δ 6.8–6.6 (m, 6H), 6.05 (s, 4H), 5.13 (s, 2H), 4.0–2.8 (m, 4H); 13C NMR (100 MHz, CDCl3) δ 149.0, 147.9, 128.3, 120.4, 108.8, 101.4, 87.3, 85.7, 76.3; HRMS calcd for C20H19O8: 387.1080 [M+H] + , found: 387.1091. General procedure for the preparation of dihydroxy dilactone 6: To a stirred solution of diisopropylamine (0.25 mL, 1.87 mmol), n-BuLi (1.1 mL, 1.87 mmol) in THF (3 mL) at −78°C and dilactone 7 (300 mg, 0.83 mmol) was added to the reaction mixture at −78°C and the mixture was stirred at same the temperature for 1 h. The reaction mixture was treated with MoOPH (1.08 g, 2.49 mmol) at −78°C. As soon as the sparingly soluble reagent has resolved, the reaction was quenched with aqueous sodium sulfite and extracted with ether (3 × 10 mL). The organic phase was washed with 5% HCl and brine. The combined organic phase was dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give dihydroxy dilactone 6, which were purified by flash column chromatography (silica gel, 25% ethyl acetate in hexanes) to afford pure dihydroxy dilactone 6 (199 mg, 58%) as a clean solution. IR (neat, NaCl) 3329, 1780, 1488, 1042 cm − 1; 1H NMR (300 MHz, CDCl3) δ 6.8 (m, 6H), 6.3 (s, 2H), 6.0 (s, 4H); 13C NMR (75 MHz, CDCl3) δ 175.3, 148.3, 147.3, 135.2, 120.9, 108.6, 101.4, 97.8, 83.7. HRMS calcd for C20H15O10: 415.0665 [M+H] + , found: 415.0652.\nEvans D A, Bartoli J, ShiH T L 1981 J. Am. Chem. Soc. 103 2127\nVan Horn D E, Masamune S 1979 Tetrahedron Lett. 24 2229\nVedejs E 1974 J. Am. Chem. 4 5944\nAnjaneyulu A S R, Ramaiah P A, Row R, Venkateswarlu R, Pelter A, Ward R S 1981 Tetrahedron 37 3641",{"VOID":1688},"10.1007\u002Fs12039-011-0078-3","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12039-011-0078-3",[1691,1706,1721],{"id":1692,"sortIndex":32,"researcher":28,"roles":1693,"affiliations":1694,"properties":1703,"displayName":1705,"givenName":28,"familyName":28},"bfb1bfc7-4823-4fe8-81c6-011f9c2a8176",[964],[1695],{"id":1696,"sortIndex":32,"affiliation":1697,"properties":28},"c3dd7735-1ad5-416f-a48a-fec66346e970",{"id":1696,"createTime":28,"updateTime":28,"relativeEntities":1698,"slug":28,"properties":1699,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1702,"statistic":28},[],{"title":1700},{"VI":1701},"Department of Chemistry, Institute for Basic Sciences, College of Natural Sciences, Chungbuk National University, Cheongju, Korea",[],{"title":1704},{"VI":1705},"SOON HO LEE",{"id":1707,"sortIndex":40,"researcher":28,"roles":1708,"affiliations":1709,"properties":1718,"displayName":1720,"givenName":28,"familyName":28},"e23a4786-60f6-4b96-b19d-b35da3338320",[964],[1710],{"id":1711,"sortIndex":32,"affiliation":1712,"properties":28},"3f4b9acf-125b-4fb2-9079-f02f72214092",{"id":1711,"createTime":28,"updateTime":28,"relativeEntities":1713,"slug":28,"properties":1714,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1717,"statistic":28},[],{"title":1715},{"VI":1716},"Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Woman’s University, Seoul, Korea",[],{"title":1719},{"VI":1720},"JAE-CHUL JUNG",{"id":1722,"sortIndex":123,"researcher":28,"roles":1723,"affiliations":1724,"properties":1733,"displayName":1735,"givenName":28,"familyName":28},"b25fdff7-bac8-497e-be78-7a1963eced34",[964],[1725],{"id":1726,"sortIndex":32,"affiliation":1727,"properties":28},"efd8193e-e970-4bbb-8eaa-4e704d8416fa",{"id":1726,"createTime":28,"updateTime":28,"relativeEntities":1728,"slug":28,"properties":1729,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1732,"statistic":28},[],{"title":1730},{"VI":1731},"Department of Herb Industry\u002FHerb Resources Jungwon University, Goesan-gun, Korea",[],{"title":1734},{"VI":1735},"OEE SOOK PARK",{"url":1689,"publisher":1737,"properties":1778},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1738,"slug":872,"properties":1739,"entityType":25,"verifyStatus":882,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1743,"manageAffiliations":1747,"indexDatabases":1758,"url":28,"thumbnailPath":28,"statistic":1773,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1740,"title":1741,"eissn":1742},{"VOID":877},{"EN":879},{"VOID":875},[1744],{"id":885,"createTime":28,"updateTime":28,"relativeEntities":1745,"label":1746,"description":28,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":888},[1748,1753],{"id":891,"createTime":28,"updateTime":28,"relativeEntities":1749,"slug":28,"properties":1750,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1752,"statistic":28},[],{"title":1751},{"EN":895},[],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1754,"slug":28,"properties":1755,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1757,"statistic":28},[],{"title":1756},{"EN":902},[904],[1759,1766],{"id":907,"indexDatabase":1760,"url":913,"indexYears":914,"academicFieldIds":1765,"indexDatabaseRanking":917},{"id":786,"createTime":28,"updateTime":28,"relativeEntities":1761,"label":1762,"description":1763,"key":792,"publicationTags":1764,"standard":28},[],{"EN":789,"VI":789},{"EN":789,"VI":791},[794],[916],{"id":919,"indexDatabase":1767,"url":931,"indexYears":28,"academicFieldIds":1772,"indexDatabaseRanking":28},{"id":921,"createTime":28,"updateTime":28,"relativeEntities":1768,"label":1769,"description":1770,"key":928,"publicationTags":1771,"standard":28},[],{"EN":924,"VI":924},{"EN":926,"VI":927},[930,813],[816],{"impactFactor":32,"impactFactorByYear":1774,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":48,"totalPublicationByYear":1775,"totalCitation":32,"totalCitationByYear":1776,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1777,"hindexLast5Year":32,"hindex":32},{},{"1979":40,"1985":40,"1986":42,"1989":40},{},{},{"pages":1779,"volume":1781},{"VOID":1780},"327-330",{"VOID":1782},"123","2011-06-23",2011,[917,930],{"id":1787,"createTime":1788,"updateTime":1789,"relativeEntities":1790,"slug":1791,"properties":1792,"entityType":957,"verifyStatus":26,"verifyTime":1805,"verifyNote":958,"languages":28,"translateLanguages":1806,"viewCount":32,"primaryUrl":1807,"fullTextUrl":28,"authors":1808,"publicationType":1018,"publisherRelationship":1837,"citationCount":28,"citationInfo":28,"publishDate":1884,"publishYear":1885,"citationAnalyzeStatus":882,"lastCitationAnalyze":28,"indexDatabases":1886,"openAccess":28,"references":28,"isForceReanalyzing":1069},"00a0253a-2d02-4471-a0a8-6c9574afc897","2024-02-10T08:57:57.149+00:00","2025-02-02T15:20:56.841+00:00",[],"Crystal-structure-of-benzocaine-A-local-anaesthetic",{"abstract":1793,"title":1796,"keywords":1799,"references":1801,"doi":1803},{"VI":1794,"EN":1795},"Cấu trúc của thuốc gây tê tại chỗ benzocaine đã được xác định bằng phương pháp trực tiếp và được tinh chỉnh đến một hệ số R là 0,12 cho 531 phản xạ quan sát được. Sự đóng gói của phân tử được ổn định bởi các liên kết hydro N−H … O (2–97 Â). Chuỗi alkyl gắn liền với vòng benzen ở trạng thái đồng phân trans-cis. Phân tử benzoate thể hiện tính chất quinonoid như đã tìm thấy ở một số loại thuốc gây tê tại chỗ khác.","The structure of the local anaesthetic benzocaine was solved by direct methods and refined to anR of 0·12 for 531 observed reflections. The packing of the molecule is stabilised by N−H … O hydrogen-bonds (2–97 Â). The alkyl chain attached to the benzene ring is intrans-trans conformation. The benzoic moiety shows a quinonoid character as found in some other local anaesthetics.",{"EN":1797,"VI":1798},"Crystal structure of benzocaine—A local anaesthetic","Cấu trúc tinh thể của benzocaine - Một loại thuốc gây tê tại chỗ",{"VI":1800},"benzocaine, cấu trúc tinh thể, thuốc gây tê tại chỗ, liên kết hydro, đồng phân",{"VOID":1802},"Beall R, Herdklotz J and Sass R L 1970Biochem. Biophys. Res. Commun. 39 324\nBrown G M and Marsh R E 1963Acta Cryst. B16 191\nCesur A F and Richards J P G 1965Z. Kristallogr. 122 283\nDomenicano A, Vaciago A and Coulson C A 1975Acta Cryst. B31 221\nGantzel P K, Sparks R A and Trueblood K N 1961 Program LALS, University of California, USA\nHughes E W 1941J. Am. Chem. Soc. 65 1737\nInternational Tables for X-ray Crystallography 1962 (Birmingham: Kynoch Press) Vol. 3\nKarle J 1968Acta Cryst. B24 182\nKahino S, Ishida M and Haisa M 1982Acta Cryst. B38 1868\nMain P, Fiske S J, Hull S E, Lessinger L, Germain G, Declercq J P and Woolfson M M 1980 A system of computer programs for the automatic solution of crystal structures from X-ray diffraction data, University of York, UK\nPletcher J, Sax M and Yoo C S 1972Acta Cryst. B28 378\nSax M, Pletcher J and Gustaffson B 1970Acta Cryst. B26 114\nSax M, Pletcher J, Yoo C and Stewart J M 1971Acta Cryst. B27 1635\nShiono R 1968 Block diagonal least squares program for the IBM 1130 Department of Crystallography, University of Pittsburgh, USA\nSinha B K, Subramanian E, Vasantha Pattabhi and Trotter J 1984Indian J. Pure Appl. Phys. 22 249",{"VOID":1804},"10.1007\u002FBF02900724","2025-01-23T12:23:56.935+00:00",[30],"https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF02900724",[1809,1824],{"id":1810,"sortIndex":32,"researcher":28,"roles":1811,"affiliations":1812,"properties":1821,"displayName":1823,"givenName":28,"familyName":28},"6e612ea6-446b-4e5a-a571-ac3600accdbd",[964],[1813],{"id":1814,"sortIndex":32,"affiliation":1815,"properties":28},"2628307d-b3c4-4e2e-9422-6a73ca0c63c4",{"id":1814,"createTime":28,"updateTime":28,"relativeEntities":1816,"slug":28,"properties":1817,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1820,"statistic":28},[],{"title":1818},{"EN":1819},"Department of Crystallography and Biophysics, University of Madras, Madras, India",[],{"title":1822},{"VI":1823},"B K Sinha",{"id":1825,"sortIndex":40,"researcher":28,"roles":1826,"affiliations":1827,"properties":1834,"displayName":1836,"givenName":28,"familyName":28},"d01e87d2-3b33-46b3-b7a9-eda44aa1bf9a",[964],[1828],{"id":1814,"sortIndex":32,"affiliation":1829,"properties":28},{"id":1814,"createTime":28,"updateTime":28,"relativeEntities":1830,"slug":28,"properties":1831,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1833,"statistic":28},[],{"title":1832},{"EN":1819},[],{"title":1835},{"VI":1836},"Vasantha Pattabhi",{"url":1807,"publisher":1838,"properties":1879},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1839,"slug":872,"properties":1840,"entityType":25,"verifyStatus":882,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1844,"manageAffiliations":1848,"indexDatabases":1859,"url":28,"thumbnailPath":28,"statistic":1874,"gsStatistic":28,"type":55,"analyzePriority":28},[],{"issn":1841,"title":1842,"eissn":1843},{"VOID":877},{"EN":879},{"VOID":875},[1845],{"id":885,"createTime":28,"updateTime":28,"relativeEntities":1846,"label":1847,"description":28,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":888},[1849,1854],{"id":891,"createTime":28,"updateTime":28,"relativeEntities":1850,"slug":28,"properties":1851,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1853,"statistic":28},[],{"title":1852},{"EN":895},[],{"id":898,"createTime":28,"updateTime":28,"relativeEntities":1855,"slug":28,"properties":1856,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1858,"statistic":28},[],{"title":1857},{"EN":902},[904],[1860,1867],{"id":907,"indexDatabase":1861,"url":913,"indexYears":914,"academicFieldIds":1866,"indexDatabaseRanking":917},{"id":786,"createTime":28,"updateTime":28,"relativeEntities":1862,"label":1863,"description":1864,"key":792,"publicationTags":1865,"standard":28},[],{"EN":789,"VI":789},{"EN":789,"VI":791},[794],[916],{"id":919,"indexDatabase":1868,"url":931,"indexYears":28,"academicFieldIds":1873,"indexDatabaseRanking":28},{"id":921,"createTime":28,"updateTime":28,"relativeEntities":1869,"label":1870,"description":1871,"key":928,"publicationTags":1872,"standard":28},[],{"EN":924,"VI":924},{"EN":926,"VI":927},[930,813],[816],{"impactFactor":32,"impactFactorByYear":1875,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":48,"totalPublicationByYear":1876,"totalCitation":32,"totalCitationByYear":1877,"totalCitationPerPublication":32,"totalCitationPerPublicationByYear":1878,"hindexLast5Year":32,"hindex":32},{},{"1979":40,"1985":40,"1986":42,"1989":40},{},{},{"pages":1880,"volume":1882},{"VOID":1881},"229-234",{"VOID":1883},"98","1987-03-01",1987,[917,930],{"id":1888,"createTime":1889,"updateTime":1890,"relativeEntities":1891,"slug":1892,"properties":1893,"entityType":957,"verifyStatus":26,"verifyTime":1890,"verifyNote":958,"languages":28,"translateLanguages":28,"viewCount":32,"primaryUrl":1902,"fullTextUrl":28,"authors":1903,"publicationType":1018,"publisherRelationship":1945,"citationCount":28,"citationInfo":28,"publishDate":1992,"publishYear":1993,"citationAnalyzeStatus":882,"lastCitationAnalyze":28,"indexDatabases":1994,"openAccess":28,"references":28,"isForceReanalyzing":1069},"00a681e9-b3b4-42e9-a650-c3fc609fadde","2023-12-28T22:53:48.978+00:00","2025-02-02T01:37:23.621+00:00",[],"Laser-vaporization-A-versatile-method-for-studying-metal-clusters",{"abstract":1894,"title":1896,"references":1898,"doi":1900},{"EN":1895},"Vaporizing solid samples of metals and semiconductors with a YAG Laser is a method well suited for producing molecules and clusters of those materials. The clusters are examined by either laser-induced fluorescence (LIF) or mass spectroscopic methods. The technique is valuable for both gas phase and matrix studies. The method is described and some applications, studying either the structure of small metal molecules or their reactions, are reviewed, with emphasis on our recent results from the LIF studies of LiBe, Al2 and the reaction of Al with oxygen, yielding A12O. For larger clusters, Ion Cyclotron Resonance is an extremely valuable method, as we demonstrate by its application to the reactions of small charged silicon clusters with strong oxidising agents.",{"EN":1897},"Laser vaporization: A versatile method for studying metal clusters",{"VOID":1899},"Abe H and Kolb D M 1983Ber. Bunsenges. Phys. Chem. 87 523\nBauschlicher C W, Partridge H, Longhoff S R, Taylor P R and Walch S P 1987J. Chem. Phys. 86 7\nBondybey V E 1982aJ. Phys. Chem. 86 3396\nBondybey V E 1982bJ. Chem. Phys. 77 3771\nBondybey V E 1984Chem. Phys. Lett. 109 436\nBondybey V E 1985Science 227 125\nBondybey V E 1989Matrix spectroscopy (ed.) L Andrews and M Moskovits (Amsterdam: North Holland) p. 107\nBondybey V E and Bearder S S 1974 (unpublished results)\nBondybey V E and English J H 1977J. Chem. Phys. 67 3405\nBondybey V E and English J H 1978J. Chem. Phys. 68 4641\nBondybey V E and English J H 1980J. Chem. Phys. 73 42\nBondybey V E and English J H 1981J. Chem. Phys. 74 6978\nBondybey V E and English J H 1982J. Chem. Phys. 76 2165\nBondybey V E and English J H 1983Chem. Phys. Lett. 94 443\nBondybey V E and English J H 1984J. Chem. Phys. 80 568\nBondybey V E, Schwartz G P and English J H 1983J. Chem. Phys. 78 11\nBauchler A, Stauffer J L, Klemperer W and Wharton L 1963J. Chem. Phys. 55 2574\nCai M F, Carter C, Miller T A and Bondybey V E 1990 (to be submitted)\nCai M F, Dzugan T P and Bondybey V E 1989aChem. Phys. Lett. 155 430\nCai M F, Miller T A and Bondybey V E 1989bChem. Phys. Lett. 158 475\nDietz T G, Duncan M A, Powers D E and Smalley R J 1981J. Chem. Phys. 74 6511\nDouglas M A, Hauge R H and Margrave J L 1983aJ. Phys. Chem. 87 2945\nDouglas M A, Hauge R H and Margrave J L 1983bHigh Temp. Sci. 16 35\nFischer I, Bondybey V E, Rosmus P and Werner H J 1990Chem. Phys. (in print)\nGole J L, English J H and Bondybey V E 1982J. Phys. Chem. 86 2560\nHarrison R J and Handy N C 1986Chem. Phys. Lett. 98 97\nHeimbrook L A, Rasanen M and Bondybey V E 1987J. Mol. Struct. 157 129\nJonsson B, Roos B O, Taylor P R and Siegbahn P E M 1981J. Chem. Phys. 74 4566\nKaldor U 1990Chem. Phys. 140 1\nKlotzbuecher W E and Ozin G A 1978J. Am. Chem. Soc. 100 2262\nKnight L B and Weltner W 1971J. Chem. Phys. 55 5066\nKonawalow D D and Fish J L 1984Chem. Phys. Lett. 104 211\nKundig E P, Moskovits M and Ozin G A 1975Nature (London) 254 503\nLamson S and Messmer R 1983Chem. Phys. Lett. 98 72\nLinevsky M J 1961J. Chem. Phys. 34 587\nLoomis F W and Nusbaum R E 1931Phys. Rev. 38 1447\nMakowiecki D M, Lynch D A and Carlson K D 1971J. Phys. Chem. 75 1963\nMandich M L, Bondybey V E and Reents W D 1987J. Chem. Phys. 86 4245\nMandich M L, Reents W D and Bondybey V E 1986J. Phys. Chem. 90 2315\nMasip J, Clotet A, Ricart J M, Illas F and Rubio J 1988Chem. Phys. Lett. 144 373\nMeinel H 1972Can. J. Phys. 50 158\nMichels H H, Hobbs R H and Wright L A 1985Chem. Phys. Lett. 118 67\nMoskovits M, Limm W and Mejean T 1985J. Chem. Phys. 82 4875\nOhez P, Jaegle P, Leach S and Velghe M 1969J. Appl. Phys. 40 2545\nPartridge H, Bauschlicher C W and Siegahn P E M 1983Chem. Phys. Lett. 97 198\nPetersson G A and Shirley W A 1989Chem. Phys. Lett. 160 494\nPewestorff W, Bonaĉic’-Koutecký, V and Koutecký J 1988J. Chem. Phys. 89 5794\nRasanen M, Heimbrook L A and Bondybey V E 1987aJ. Mol. Struct. 157 129\nRasanen M, Liu J Y, Dzugan T P and Bondybey V E 1987bChem. Phys. Lett. 142 308\nReents W D and Bondybey V E 1986Chem. Phys. Lett. 125 324\nReents W D, Mandich M L and Bondybey V E 1986Chem. Phys. Lett. 131 1\nRöeggen I, Morokuma K and Yamashita K 1987Chem. Phys. Lett. 140 349\nRoscoe H E, and Schuster A 1874J. Chem. Soc. 27 942\nRosmus P, Werner H-J, Reinsch E A and Larson M J 1986J. Electron. Spectr. 41 289\nSchlachta R, Fischer I, Rosmus P and Bondybey V E 1990Chem. Phys. Lett. 170 485\nSchmidt-Mink I, Mûller W and Meyer W 1985Chem. Phys. 92 263\nSnelson A 1970J. Phys. Chem. 74 2574\nSonchik S M, Andrews L and Carlson K D 1983J. Phys. Chem. 87 2004\nSunil K K and Jordan K D 1988J. Phys. Chem. 92 2774\nWagner E L 1974Theort. Chim. Acta. 32 395\nWerner H-J and Rosmus P 1985Comparison of ab initio quantum chemistry with experiments for small molecules — the state of the art, (ed.) R J Bartlett (Dordrecht: Reidel)\nTse J S 1988J. Mol. Struct. 165 21\nUpton T H 1986J. Phys. Chem. 90 754",{"VOID":1901},"10.1007\u002FBF02842088","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF02842088",[1904,1919,1932],{"id":1905,"sortIndex":32,"researcher":28,"roles":1906,"affiliations":1907,"properties":1916,"displayName":1918,"givenName":28,"familyName":28},"4c9c0b58-cdb5-46ed-83e5-361c085dbf3a",[964],[1908],{"id":1909,"sortIndex":32,"affiliation":1910,"properties":28},"09f73086-8b03-4f67-9258-a5409e2e8a2e",{"id":1909,"createTime":28,"updateTime":28,"relativeEntities":1911,"slug":28,"properties":1912,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1915,"statistic":28},[],{"title":1913},{"VI":1914},"Institut für Physikalische Chemie der TU München, Garching, Germany",[],{"title":1917},{"VI":1918},"V. E. 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