Heavy cation effect on intersystem crossing between triplet and singlet phenylacyl and benzyl geminate radical pairs within zeolites

M. Warrier, N. J. Turro, Vaidhyanathan Ramamurthy

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

The difference in product selectivity observed between dibenzyl ketones and naphthyl esters in zeolites is due to the difference in spin of the radical pairs formed from these precursors. Heavy cations present in zeolites can enhance intersystem crossing between triplet and singlet geminate radical pairs. (C) 2000 Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)7163-7167
Number of pages5
JournalTetrahedron Letters
Volume41
Issue number37
StatePublished - Sep 3 2000
Externally publishedYes

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Zeolites
Cations
Ketones
Esters

Keywords

  • Dibenzyl ketone
  • Radical pairs
  • Spin
  • Zeolite

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Heavy cation effect on intersystem crossing between triplet and singlet phenylacyl and benzyl geminate radical pairs within zeolites. / Warrier, M.; Turro, N. J.; Ramamurthy, Vaidhyanathan.

In: Tetrahedron Letters, Vol. 41, No. 37, 03.09.2000, p. 7163-7167.

Research output: Contribution to journalArticle

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