Rhodium Carbene Complexes as Versatile Catalyst Precursors for Si-H Bond Activation

被引:51
作者
Krueger, Anneke [1 ]
Albrecht, Martin [1 ]
机构
[1] Univ Coll Dublin, Sch Chem & Chem Biol, Dublin 4, Ireland
基金
瑞士国家科学基金会;
关键词
carbenes; ligand cooperativity; mesoionic complexes; rhodium; silane activation; siloxanes; N-HETEROCYCLIC CARBENES; SILANE ALCOHOLYSIS; HETEROGENEOUS CATALYSIS; COORDINATION CHEMISTRY; HOMOGENEOUS CATALYSIS; OXIDATIVE ADDITION; CARBONYL-COMPOUNDS; SILICON-HYDROGEN; BUILDING-BLOCKS; DONOR LIGANDS;
D O I
10.1002/chem.201102197
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rhodium(III) complexes comprising monoanionic C,C,C-tridentate dicarbene ligands activate Si?H bonds and catalyse the hydrolysis of hydrosilanes to form silanols and siloxanes with concomitant release of H2. In dry MeNO2, selective formation of siloxanes takes place, while changing conditions to wet THF produces silanols exclusively. Silyl ethers are formed when ROH is used as substrate, thus providing a mild route towards the protection of alcohols with H2 as the only by-product. With alkynes, comparably fast hydrosilylation takes place, while carbonyl groups are unaffected. Further expansion of the Si?H bond activation to dihydrosilanes afforded silicones and polysilyl ethers. Mechanistic investigations using deuterated silane revealed deuterium incorporation into the abnormal carbene ligand and thus suggests a ligand-assisted mechanism involving heterolytic Si?H bond cleavage.
引用
收藏
页码:652 / 658
页数:7
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