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University of Lethbridge

The monophosphaamidine functional group

Abstract

The synthesis and characterization of two new bulky N,P-monophosphaamidines (also known as C-aminophosphaalkenes) are described. These phosphorus analogues to amidines are shown to exhibit isomerism and tautomerism in solution that is characteristic tothe amidine functional group. In addition, the nature of the P=C-N system is examined using DFT techniques. Metal complexes of the title compounds with Group 6 metal carbonyls (L-M(CO)5, M=Cr,Mo,W) are also described. A new primary phosphane is reported that contains the sterically bulky, 2,6-diisoropylphenyl (Dip) group, along with mono and disilylated derivatives. Also included is the synthesis and characterization of a new bulky N,N',P-monophosphaguanidine.

Author and committee

dc:creator, dc:contributor.*
Authors
  • Masuda, Jason D.
  • University of Lethbridge. Faculty of Arts and Science

Subjects

dc:subject × 3

Identifiers

dc:identifier.*
Identifier
hdl:10133/191
OAI identifier oai:identifier
oai:opus.uleth.ca:10133/191

Chain of custody

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University of Lethbridge
Base URL
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Last updated
2026-07-27
Source record
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citation

Masuda, Jason D.; University of Lethbridge. Faculty of Arts and Science. The monophosphaamidine functional group. 2002.