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Phosphide delivery to a cyclotrisilene.


ABSTRACT: The reactivity of the 2-phosphaethynolate anion (PCO(-)) towards a cyclic trisilene (cSi3(Tip)4) is reported. The result is the net activation of the P-C and Si-Si multiple bonds of the precursors affording a heteroatomic bicyclo[1.1.1]pentan-2-one analogue ([P(CO)Si3(Tip)4](-); 1). This reaction can be interpreted as the formal addition of a phosphide and a carbonyl across the Si-Si double bond. Photolytic decarbonylation of 1 results in the incorporation of the phosphide vertex into the cyclotrisilene scaffold, yielding a congener of the cyclobutene anion with considerable allylic character.

SUBMITTER: Robinson TP 

PROVIDER: S-EPMC4506556 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

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Phosphide delivery to a cyclotrisilene.

Robinson Thomas P TP   Cowley Michael J MJ   Scheschkewitz David D   Goicoechea Jose M JM  

Angewandte Chemie (International ed. in English) 20141121 2


The reactivity of the 2-phosphaethynolate anion (PCO(-)) towards a cyclic trisilene (cSi3(Tip)4) is reported. The result is the net activation of the P-C and Si-Si multiple bonds of the precursors affording a heteroatomic bicyclo[1.1.1]pentan-2-one analogue ([P(CO)Si3(Tip)4](-); 1). This reaction can be interpreted as the formal addition of a phosphide and a carbonyl across the Si-Si double bond. Photolytic decarbonylation of 1 results in the incorporation of the phosphide vertex into the cyclot  ...[more]

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