Polarizable stilbazole-based organometallic complexes and polymers

Juan Burdeniuk, David Milstein

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Oxidative addition reactions of trans-4′-bromo-4-stilbazole (1) to Pd(PMe3)4, Pd(PEt3)4, and Pd(PiPr3)3 yield the corresponding PdII complexes (5). The quaternary complexes (6 and 7) are obtained by methylation and protonation of 5. Bromide abstraction from 5 leads to the charged polymers 9. Comparison of the spectroscopic properties (UV, IR, NMR) of these complexes, as well as those of the gold complex 4, with those of the parent organic compounds indicates that there is considerable metal participation in the conjugated systems. The oscillator strength (f) for the π-π* transition of the various compounds has been determined. The Pd and Au complexes have considerably higher f values than the parent bromostilbazoles, while palladium complexes exhibit a lower energy π-π* transition than the latter. The nature of the phosphine ligand in the palladium complex has a minor effect on conjugation.

Original languageEnglish
Pages (from-to)213-220
Number of pages8
JournalJournal of Organometallic Chemistry
Volume451
Issue number1-2
DOIs
Publication statusPublished - Jun 1 1993

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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