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loại xúc tác nhôm có thành phần đơn mới cho phản ứng giữa các epoxit và carbon dioxide đã được chế tạo. Các xúc tác được cấu thành từ các phức nhôm–salen clorua với các nhóm trialkylammonium gắn trực tiếp vào các vòng thơm của ligand salen. Với các epoxit đầu mút, các xúc tác đã thúc đẩy sự hình thành các carbonat vòng dưới điều kiện phản ứng nhẹ (25–35 °C; 1–10 bar áp suất carbon dioxide). Tuy nhiên, với epoxit cyclohexene dưới cùng điều kiện phản ứng, các xúc tác tương tự đã thúc đẩy sự hình thành polycarbonate. Các xúc tác có thể được thu hồi từ hỗn hợp phản ứng và tái sử dụng.","\u003Cjats:p>Two new one-component aluminium-based catalysts for the reaction between epoxides and carbon dioxide have been prepared. The catalysts are composed of aluminium–salen chloride complexes with trialkylammonium groups directly attached to the aromatic rings of the salen ligand. With terminal epoxides, the catalysts induced the formation of cyclic carbonates under mild reaction conditions (25–35 °C; 1–10 bar carbon dioxide pressure). 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phản ứng khử nitơ bằng ánh sáng của vinyl azides để tạo ra 2\u003Cjats:italic>H\u003C\u002Fjats:italic>-azirines bằng cách sử dụng một phản ứng lưu thông ánh sáng được báo cáo và so sánh với quá trình hình thành 2\u003Cjats:italic>H\u003C\u002Fjats:italic>-azirines thông qua nhiệt. Về mặt quang hóa, vòng của 2\u003Cjats:italic>H\u003C\u002Fjats:italic>-azirines đã được mở ra để tạo ra các nitrile ylides, mà đã tham gia vào một phản ứng [3 + 2]-cycloaddition với các hợp chất 1,3-dipolarophiles. Khi diisopropyl azodicarboxylate hoạt động như là dipolarophile, các 1,3,4-triazole có thể được truy cập trực tiếp bắt đầu từ vinyl azide tương ứng.\u003C\u002Fjats:p>","\u003Cjats:p>The photodenitrogenation of vinyl azides to 2\u003Cjats:italic>H\u003C\u002Fjats:italic>-azirines by using a photoflow reactor is reported and compared with thermal formation of 2\u003Cjats:italic>H\u003C\u002Fjats:italic>-azirines. Photochemically, the ring of the 2\u003Cjats:italic>H\u003C\u002Fjats:italic>-azirines was opened to yield the nitrile ylides, which underwent a [3 + 2]-cycloaddition with 1,3-dipolarophiles. When diisopropyl azodicarboxylate serves as the dipolarophile, 1,3,4-triazoles become directly accessible starting from the corresponding vinyl azide.\u003C\u002Fjats:p>",{"VI":1938,"EN":1939},"[3 + 2]-Cycloaddition của nitrile ylides sau khi kích hoạt bằng ánh sáng vinyl azides trong điều kiện dòng chảy","[3 + 2]-Cycloadditions of nitrile ylides after photoactivation of vinyl azides under flow 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 hưởng steric và điện tử của sự thay thế xương sống trong các carbene dị vòng IMes (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) đã được điều tra bằng cách tổng hợp chuỗi phức chất [RhCl(CO)\u003Cjats:sub>2\u003C\u002Fjats:sub>(NHC)] để định lượng một cách thực nghiệm tham số điện tử Tolman (điện tử) và tỷ lệ thể tích chôn vùi (%\u003Cjats:italic>V\u003C\u002Fjats:italic>\u003Cjats:sub>bur\u003C\u002Fjats:sub>, steric). Các phức chất ruthenium–indenylidene tương ứng cũng đã được tổng hợp và kiểm tra trong các biến đổi metathesis chuẩn mực để thiết lập các mối tương quan có thể giữa khả năng phản ứng và các tham số điện tử, steric của NHC.\u003C\u002Fjats:p>","\u003Cjats:p>The steric and electronic influence of backbone substitution in IMes-based (IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene) \u003Cjats:italic>N\u003C\u002Fjats:italic>-heterocyclic carbenes (NHC) was probed by synthesizing the [RhCl(CO)\u003Cjats:sub>2\u003C\u002Fjats:sub>(NHC)] series of complexes to quantify experimentally the Tolman electronic parameter (electronic) and the percent buried volume (%\u003Cjats:italic>V\u003C\u002Fjats:italic>\u003Cjats:sub>bur\u003C\u002Fjats:sub>, steric) parameters. 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Quá trình tổng hợp dựa vào hợp chất polymer ổn định gắn với azide iod mà phục vụ cho việc thực hiện phản ứng 1,2-functionalization của alkenes trong quy trình dòng ống kính. Các hợp chất trung gian 2-iodo azides được thực hiện bước loại bỏ hỗ trợ polymer trung gian DBU, cho ra vinyl azides với hiệu suất tốt. Bước thứ ba liên quan đến việc hình thành vinyl triazoles thông qua phản ứng cycloaddition kiểu Huisgen xúc tác bằng đồng. Nhiệt cần thiết được tạo ra thông qua sự cảm ứng điện từ dựa trên đồng. Đồng không chỉ phục vụ như một vật liệu có thể gia nhiệt mà còn có hoạt tính xúc tác bên trong reactor dòng.\u003C\u002Fjats:p>","\u003Cjats:p>The multistep flow synthesis of vinyl azides and their application in the synthesis of vinyltriazoles is reported. The synthesis relies on a stable polymer-bound equivalent of iodine azide that serves to carry out 1,2-functionalization of alkenes in a telescope flow protocol. The intermediate 2-iodo azides are subjected to a DBU-mediated polymer-supported elimination step yielding vinyl azides in good yield. The third step involves the formation of vinyl triazoles by a copper-catalyzed Huisgen-\"click\" cycloaddition. The required heat is generated by electromagnetic induction based on copper. 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