Synthesis, Kinetics, and Photochemistry of the Chromium(III) DicyanoaquoEDTA Complex.

Abstract

The complex Cr(Y)(CN)2(H2O)(3-) resembles the various cyano-aquo and cyano-amine complexes of Cr(III) in that the thermal reaction is one of cyanide aquation, the rate increasing with decreasing pH. Unlike the other cases, however, there does not appear to be appreciable contribution to the rate from a path involving -CrCNH. It is possible that the aquation is assisted by internal protonation of a cyano groupd through hydrogen boding from a non-coordinated but protonated carboxyl group. While the cyano-ammine complexes show primarily ammonia photoaquation, the photochemistry of our complex is one of cyanide aquation only. A likely explanation, however, is that labilization of other ligands is either blocked, or if it does occur, is unobservable under our conditions. Both the quantum yield behavior and the emission behavior are consistent with the photolysis and emission rules proposed for Cr(III) complexes.

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Document Details

Document Type
Technical Report
Publication Date
Feb 01, 1983
Accession Number
ADA124302

Entities

People

  • Arthur W. Adamson
  • Marc Cimolino
  • Zhong Chen

Organizations

  • University of Southern California

Tags

Communities of Interest

  • C4I
  • Energy and Power Technologies
  • Weapons Technologies

DTIC Thesaurus Topics

  • Absorption
  • Absorption Spectra
  • Acid-Base Equilibrium
  • Alcohols
  • Buffers (Chemistry)
  • California
  • Chemical Synthesis
  • Chemistry
  • Chromium
  • Materials
  • Military Research
  • Quantum Yields
  • Sodium
  • Sodium Hydroxide
  • Standards
  • United States
  • Universities

Fields of Study

  • Chemistry

Readers

  • Chemistry (specifically Chemical Fluorescence)
  • Organic Chemistry

Technology Areas

  • Quantum Computing