期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 8, 页码 3293-3303出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja413060u
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资金
- European Research Council
The tetramethylene-bridged PMes(2)/B(C6F5)(2) frustrated Lewis pair (FLP) 8 was prepared by hydroboration of Mes(2)P-(CH2)(2)CH=CH2 with HB(C6F5)(2). It is an active FLP that splits dihydrogen under mild conditions and, consequently, serves as a metal-free hydrogenation catalyst for a variety of substrates. It also reacts typically with terminal acetylenes. The C-4-bridged FLP 23 was prepared by HB(C6F5)(2) hydroboration of 1-dimesitylphosphino-2-vinylferrocene. It represents a rare example of a FLP where the equilibrium between the open form and the closed internal P/B adduct form is experimentally observable. It also shows a variety of typical FLP reactions, including dihydrogen splitting. The FLPs 8 and 23 (open form) and many precursors and products were characterized by X-ray diffraction.
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