Protonation of Cobalt Tetraneopentoxyphthalocyanine as a Function of Oxidation State

Abstract

The protonation of cobalt tetraneopentoxy-phthalocyanine (CoTNPc) has been studies as a function of the oxidation state of this species. Data are reported for phthalocyanine cobalt (I), cobalt (II), and cobalt (III) cation radical species, usually dissolved in dichlorobenzene (DCB). Up to four stepwise protonation processes were observed using trifluoroacetic (TFAA), hydrochloric or sulphuric acid. These were followed by recording the electronic spectra of these species as a function of acid concentration. Analysis of these spectra, which usually displayed isosbestic points, yielded stoichiometry and stability constant data and allowed for the identification of the spectra of the species generated. The spectra are discussed in terms of a previously model for protonation of phthalocyanine species. Electronic spectroscopic data are reported for protonated phthalocyanine radical species, for the first time. The basicity of these species decreases from the cobalt(I) species to the COBALT(III) radical cation species, in order of increasing oxidation state.

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Document Details

Document Type
Technical Report
Publication Date
Mar 03, 1992
Accession Number
ADA247898

Entities

People

  • Alfred Beverley Philip Lever
  • P. A. Bernstein

Organizations

  • University of York

Tags

Communities of Interest

  • C4I
  • Energy and Power Technologies
  • Space

DTIC Thesaurus Topics

  • Absorption
  • Absorption Spectra
  • Chemical Engineering
  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Engineering
  • Ground State
  • Materials Science
  • Military Research
  • North Carolina
  • Oxidation
  • Phthalocyanines
  • Q Band
  • Spectra
  • Spectroscopy
  • United States

Fields of Study

  • Chemistry

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies
  • Organic Chemistry

Technology Areas

  • Microelectronics