Abstract
A systematic study on the reactivity of the cyclo-P-4 complexes [(CpTa)-Ta-R(CO)2(eta(4)-P-4)] towards pnictogenium cations results in the formation of functionalised interpnictogen cations. Phosphenium ions insert into one of the P-P bonds to give ring-expanded cyclo-P5R2 products. In contrast, an arsenium-functionalised P4AsCy2 ligand displays an interesting borderline case between ring ...
Abstract
A systematic study on the reactivity of the cyclo-P-4 complexes [(CpTa)-Ta-R(CO)2(eta(4)-P-4)] towards pnictogenium cations results in the formation of functionalised interpnictogen cations. Phosphenium ions insert into one of the P-P bonds to give ring-expanded cyclo-P5R2 products. In contrast, an arsenium-functionalised P4AsCy2 ligand displays an interesting borderline case between ring expansion and coordination, while stibenium cations afford addition products. Tuning of the steric and electronic properties of the stibenium ion shows a drastic influence on the reaction outcome.
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