scholarly journals Vinylene-bridged donor–acceptor type porous organic polymers for enhanced photocatalysis of amine oxidative coupling reactions under visible light

RSC Advances ◽  
2021 ◽  
Vol 11 (53) ◽  
pp. 33653-33660
Author(s):  
Bang Wu ◽  
Xinyue Jiang ◽  
Yang Liu ◽  
Qiu-Yan Li ◽  
Xinsheng Zhao ◽  
...  
Keyword(s):  
Visible Light ◽  
Oxidative Coupling ◽  
Coupling Reactions ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Photocatalytic Activities ◽  
Highly Effective ◽  
Donor Acceptor ◽  
Oxidative Coupling Reactions

Two vinylene-bridged D–A structural POPs are constructed by the electron-rich triarylamine and electron-deficient tricyanomesitylene, which exhibited highly effective photocatalytic activities for aerobic oxidative coupling of amines to imine.

scholarly journals Advances in visible light-mediated oxidative coupling reactions

2015 ◽  
Vol 36 (9) ◽  
pp. 1428-1439 ◽  
Author(s):  
Guoting Zhang ◽  
Changliang Bian ◽  
Aiwen Lei
Keyword(s):  
Visible Light ◽  
Oxidative Coupling ◽  
Coupling Reactions ◽  
Oxidative Coupling Reactions

Visible-Light-Driven Oxidative Coupling Reactions of Amines by Photoactive WS2 Nanosheets

ACS Catalysis ◽  
2016 ◽  
Vol 6 (5) ◽  
pp. 2754-2759 ◽  
Author(s):  
Faizan Raza ◽  
Jung Hyun Park ◽  
Hye-Rim Lee ◽  
Hye-In Kim ◽  
Su-Ji Jeon ◽  
...  
Keyword(s):  
Visible Light ◽  
Oxidative Coupling ◽  
Coupling Reactions ◽  
Visible Light Driven ◽  
Ws2 Nanosheets ◽  
Oxidative Coupling Reactions

An Unprecedented Cyano-Induced Sodium Nitrite-Catalyzed C(sp3)-H and C(sp2)-H Coupling Reaction

2018 ◽  
Vol 15 (7) ◽  
pp. 989-994 ◽  
Author(s):  
Ling Li ◽  
Bo Su ◽  
Yuxiu Liu ◽  
Qingmin Wang
Keyword(s):  
Sodium Nitrite ◽  
Oxidative Coupling ◽  
High Resolution Mass Spectrometry ◽  
Coupling Reaction ◽  
13C Nmr Spectroscopy ◽  
Coupling Reactions ◽  
Reaction Conditions ◽  
1H And 13C Nmr ◽  
Oxidative Coupling Reaction ◽  
Oxidative Coupling Reactions

Aim and Objective: During the investigation of sodium nitrite-catalyzed oxidative coupling reaction of aryls, an unprecedented C(sp2)-H and C(sp3)-H coupling of substituted 2-aryl acetonitrile was found. Materials and Methods: The structure of the coupled product was confirmed by 1H and 13C NMR spectroscopy and high-resolution mass spectrometry (HRMS), and comparison of its derivatives with known compounds. The effects of methoxy group in the benzene ring on the reaction were evaluated. Results: The optimized reaction conditions are summarized as follows: CF3SO3H/substrate = 1.5 equiv., NaNO2/substrate = 0.3 equiv., CH3CN as solvent. 2-(4-Methoxyphenyl)acetonitrile and 2-(3,4,5- trimethoxyphenyl)acetonitrile could also generate C(sp2)-H and C(sp3)-H coupling. The coupling reaction occurred as a typical radial mechanism. Conclusion: An unprecedented cyano-induced, NaNO2-catalyzed oxidative C(sp3)-H and C(sp2)-H coupling was reported. The reaction proceeded under very mild conditions, using O2 in the air as terminal oxidant. The unique oxidative manner might provide more inspiration for the development of intriguing oxidative coupling reactions.

scholarly journals Eosin Y dye-based porous organic polymers for highly efficient heterogeneous photocatalytic dehydrogenative coupling reaction

RSC Advances ◽  
2017 ◽  
Vol 7 (1) ◽  
pp. 408-414 ◽  
Author(s):  
Chang-An Wang ◽  
Yan-Wei Li ◽  
Xue-Li Cheng ◽  
Jian-Ping Zhang ◽  
Yin-Feng Han
Keyword(s):  
Coupling Reaction ◽  
Eosin Y ◽  
Organic Polymers ◽  
Porous Organic Polymers ◽  
Bottom Up ◽  
Highly Efficient ◽  
Dehydrogenative Coupling ◽  
Highly Effective

Eosin Y dye has been successfully embedded into a nanoporous network EY-POPs through a bottom-up strategy. The polymers could be used as highly effective and reusable heterogeneous organo-photocatalyst for the dehydrogenative coupling reaction.

Catalytic oxidative coupling promoted by bismuth TEMPOxide complexes

2018 ◽  
Vol 54 (8) ◽  
pp. 916-919 ◽  
Author(s):  
R. J. Schwamm ◽  
M. Lein ◽  
M. P. Coles ◽  
C. M. Fitchett
Keyword(s):  
Oxidative Coupling ◽  
Coupling Reactions ◽  
Oxidative Coupling Reactions

Bismuth(iii) TEMPOxide complexes are active catalysts for oxidative coupling reactions to generate TEMPO silylethers.

scholarly journals Enantioselective Iron/Bisquinolyldiamine Ligand-Catalyzed Oxidative Coupling Reaction of 2-Naphthols

Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 852 ◽  
Author(s):  
Lin-Yang Wu ◽  
Muhammad Usman ◽  
Wen-Bo Liu
Keyword(s):  
Oxidative Coupling ◽  
Coupling Reaction ◽  
Iron Complex ◽  
Coupling Reactions ◽  
Oxidative Coupling Reaction ◽  
Oxidative Coupling Reactions

An iron-catalyzed asymmetric oxidative homo-coupling of 2-naphthols for the synthesis of 1,1′-Bi-2-naphthol (BINOL) derivatives is reported. The coupling reaction provides enantioenriched BINOLs in good yields (up to 99%) and moderate enantioselectivities (up to 81:19 er) using an iron-complex generated in situ from Fe(ClO4)2 and a bisquinolyldiamine ligand [(1R,2R)-N1,N2-di(quinolin-8-yl)cyclohexane-1,2-diamine, L1]. A number of ligands (L2–L8) and the analogs of L1, with various substituents and chiral backbones, were synthesized and examined in the oxidative coupling reactions.

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