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Activation and desoxygenation of CO, CO2, and SO2 with sulfur-rich azide and amide.

作者信息

Sellmann D, Geipel F, Heinemann F W

机构信息

Institut für Anorganische Chemie der Universität Erlangen-Nürnberg, Germany.

出版信息

Chemistry. 2000 Dec 1;6(23):4279-84. doi: 10.1002/1521-3765(20001201)6:23<4279::aid-chem4279>3.0.co;2-s.

DOI:10.1002/1521-3765(20001201)6:23<4279::aid-chem4279>3.0.co;2-s
PMID:11140957
Abstract

The azide and amide complexes (NBu4)[Ni(N3)('S3')] (2) and (NBu4)[NiN(SiMe3)2] (4) were found to react with CO, CO2, and SO2 under very mild conditions at temperatures down to -50 degrees C. Depending on the N oxidation state of the nitrogen ligands, addition or partial to complete desoxygenation of the oxides takes place. The reaction between 2 and CO gives (NBU4)[Ni(NCO)('S3')] (3). The reactions between 4 and CO, CO2, and SO2 afford selectively the cyano, isocyanato, and sulfinylimido complexes (NBu4)[Ni(X)('S3')] with X = CN- (5), NCO- (3), and NSO- (6). The silyl groups act as oxygen acceptors. Mechanisms are suggested which have in common the formation of reactive five-coordinate (NBu4)[Ni(L)(L')('S3')] intermediates. In these reactions, highly activated L and L' react with each other. The complexes were characterized by standard methods, and (NBu4)[Ni(CN)('S3')] (5) was also analyzed by X-ray crystallography.

摘要

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