Organometallic synthesis, reactivity and catalysis in the solid state using well-defined single-site species

被引:48
作者
Pike, Sebastian D. [1 ]
Weller, Andrew S. [1 ]
机构
[1] Univ Oxford, Dept Chem, Oxford UK1 3TA, England
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2015年 / 373卷 / 2037期
基金
英国工程与自然科学研究理事会;
关键词
solid state; organometallic; reactivity; catalysis; TRIPODAL (POLYPHOSPHINE)METAL COMPLEXES; HETEROGENEOUS ASYMMETRIC HYDROGENATION; OXIDATIVE-ADDITION; CRYSTAL TRANSFORMATION; COORDINATION CHEMISTRY; MONOVALENT RHODIUM; HYBRID SOLIDS; H BONDS; N-C; ACTIVATION;
D O I
10.1098/rsta.2014.0187
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Acting as a bridge between the heterogeneous and homogeneous realms, the use of discrete, well-defined, solid-state organometallic complexes for synthesis and catalysis is a remarkably undeveloped field. Here, we present a review of this topic, focusing on describing the key transformations that can be observed at a transition-metal centre, as well as the use of well-defined organometallic complexes in the solid state as catalysts. There is a particular focus upon gas-solid reactivity/catalysis and single-crystal-to-single-crystal transformations.
引用
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页数:24
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