
handle: 20.500.11850/515006
The cyano(triphenylsilyl)phosphanide anion was prepared as a sodium salt from 2-phosphaethynolate. The electronic structure of this new cyano(silyl)phosphanide was studied via computational methods and its reactivity investigated using various electrophiles and Lewis acids, demonstrating its P- and N-nucleophilicity. The ambident reactivity is in agreement with computations. The silyl group also shows lability and therefore the cyano(silyl)phosphanide can be considered as a phosphacyanamide synthon, [PCN]2−, and serves as building block for the transfer of a PCN moiety.
ISSN:1433-7851
ISSN:1521-3773
ISSN:0570-0833
2-phosphaethynolate; anions; cyanophosphines; heterocumulene; phosphorus
2-phosphaethynolate; anions; cyanophosphines; heterocumulene; phosphorus
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