Affiliation:
1. Karlsruhe Institute of Technology (KIT) Institute of Inorganic Chemistry (AOC) Engesserstr. 15 76131 Karlsruhe Germany
Abstract
AbstractPhosphaketenes of divalent group 14 compounds can potentially serve as precursors for the synthesis of heavy multiple‐bond systems. We have employed the dtbpCbz substituent (dtbpCbz=1,8‐bis(3,5‐ditertbutylphenyl)‐3,6‐ditertbutylcarbazolyl) to prepare such phosphaketenyltetrylenes [(dtbpCbz)EPCO] (E=Ge, Sn, Pb). While the phosphaketenyltetrylenes are stable at ambient conditions, they can be readily decarbonylated photolytically. For the germylene and stannylene derivatives, dimeric diphosphene‐type products [(dtbpCbz)EP]2 (E=Ge, Sn) were obtained. In contrast, photolysis of the phosphaketenylplumbylene, via isomerisation of the [(dtbpCbz)PbP] intermediate to [(dtbpCbz)PPb], afforded an unsymmetric and incompletely decarbonylated product [(dtbpCbz)2Pb2P2CO] formally comprising a [(dtbpCbz)PPb] and a [(dtbpCbz)PbPCO] moiety.
Funder
China Scholarship Council
Subject
General Chemistry,Biochemistry,Organic Chemistry
Cited by
3 articles.
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