Formation of the spirocyclic, Si-centered cage cations [ClP(NSiMe3)2Si(NSiMe3)2P5]+ and [P5(NSiMe3)2Si(NSiMe3)2P5]2+

被引：8
|
作者：
Holthausen, M. H. [1 ]
Weigand, J. J. [1 ]
机构：
[1] Tech Univ Dresden, Fachrichtung Chem & Lebensmittelchem, Anorgan Mol Chem, D-01062 Dresden, Germany
来源：
DALTON TRANSACTIONS | 2016年 / 45卷 / 05期
关键词：
P-P BOND; WHITE PHOSPHORUS; P-4; TETRAHEDRON; PHOSPHAZENES; ACTIVATION; ELEMENTS; COORDINATION; COMPLEXES; INSERTION; SILYLENE;
D O I：
10.1039/c5dt01512j
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
On account of our interest in P-4 activation by phosphenium ion insertion into P-P bonds we have developed synthetic routes to bicyclic N-P-Si-heterocycle 7 and probed its reactivity towards GaCl3 and P-4. A GaCl3-induced rearrangement of 7 leads to the in situ formation of spirocyclic, Si-centered phosphenium ions. Their insertion into P-P bonds of one or two P-4 tetrahedra yields polyphosphorus cages [ClP(NSiMe3)(2)Si(NSiMe3)(2)P-5](+) (19(+)) and [P-5(NSiMe3)(2)Si(NSiMe3)(2)P-5](2+) (13(2+)).
引用
收藏
页码：1953 / 1961
页数：9
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