Abstract
Substituted diazenes react with zerovalent nickel phosphine complexes to form Π complexes or to eliminate dinitrogen to form nickel(II) species. Possible alternative mechanisms for the photochromic behavior of an azobenzene Π complex are suggested. Several cyano- and alkyl-substituted diazenes have been shown to eliminate dinitrogen and oxidatively add to the Ni(0) complexes. Evidence is presented to suggest that oxidative addition takes place through a Π intermediate. A new complex of bis(p-methylbenzoyl)diazene exhibits a fluxional behavior between square-planar and tetrahedral coordination about the nickel atom.
Original language | English (US) |
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Pages (from-to) | 1183-1189 |
Number of pages | 7 |
Journal | Inorganic chemistry |
Volume | 14 |
Issue number | 5 |
DOIs | |
State | Published - May 1 1975 |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry