Modular "Click" Preparation of Bifunctional Polymeric Heterometallic Catalysts

被引:54
作者
Wang, Wenlong [1 ]
Zhao, Liyuan [1 ]
Lv, Hui [1 ]
Zhang, Guodong [1 ]
Xia, Chungu [1 ]
Hahn, F. Ekkehardt [2 ]
Li, Fuwei [1 ]
机构
[1] Chinese Acad Sci, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Univ Munster, Inst Anorgan & Analyt Chem, Corrensstr 30, D-48149 Munster, Germany
基金
中国国家自然科学基金;
关键词
bifunctional catalysts; catalyst design; click chemistry; cooperative catalysis; N-heterocyclic carbene; N-HETEROCYCLIC CARBENES; TRANSITION-METAL-COMPLEXES; POROUS ORGANIC POLYMERS; TRIFLUOROMETHYL KETONES; COOPERATIVE CATALYSIS; COORDINATION CHEMISTRY; TERMINAL ALKYNES; TANDEM CATALYSIS; CARBON-DIOXIDE; TRANSFORMATIONS;
D O I
10.1002/anie.201600999
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterobimetallic molecular complexes or strictly alternating metallated polymers are obtained by a click reaction between mononuclear metal complexes (secondary building units, SBUs) bearing NHCs functionalized with either p-azidophenyl or p-ethynylphenyl wingtips. With a copper-NHC complex as SBU the formation of molecular or polymeric compounds did not require any additives as the copper complex catalyzes the click reaction. Transmetallation from heterobimetallic Cu/Ag derivatives to Cu/Pd derivatives was achieved. The linker between the SBUs (flexible or rigid) influences the catalytic activity of the heterobimetallic compounds. The polymer with alternating copper-NHC and silver-NHC units and a flexible methylene-triazole bridge between them shows the highest activity in the catalytic alkynylation of trifluoromethyl ketones to give fluorinated propargylic alcohols.
引用
收藏
页码:7665 / 7670
页数:6
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