Issue 16, 1974

Nucleophilic attack on co-ordinated phosphinoacetylenes: products from the hydrolysis of cis-PdCl2(Ph2PC[triple bond, length half m-dash]CCF3)2 and the X-ray structure of a 1-diphenylphosphino-3,3,3-trifluoropropen-2-olato complex

Abstract

The hydrolysis of cis-PdCl2(Ph2PC[triple bond, length half m-dash]CCF3)2 proceeds via nucleophilic attack at both phosphorus and alkyne sites yielding novel complexes containing 1-diphenylphosphino-3,3,3-trifluoropropen-2-olato, diphenyl-ethoxyphosphine, diphenylphosphinous acid, and β-keto phosphine ligands; a 1-diphenylphosphino-3,3,3-trifluoropropen-2-olato species has been fully characterised by an X-ray structure determination.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 668-669

Nucleophilic attack on co-ordinated phosphinoacetylenes: products from the hydrolysis of cis-PdCl2(Ph2PC[triple bond, length half m-dash]CCF3)2 and the X-ray structure of a 1-diphenylphosphino-3,3,3-trifluoropropen-2-olato complex

S. Jacobson, N. J. Taylor and A. J. Carty, J. Chem. Soc., Chem. Commun., 1974, 668 DOI: 10.1039/C39740000668

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