Photoisomerizable heterodienes derived from a phosphine borane

Magnus Bebbington, Sébastien Bontemps, Ghenwa Bouhadir, Didier Bourissou

Research output: Contribution to journalArticleResearchpeer-review

Abstract

(Chemical Equation Presented) Stable relations: Reaction of phenylazide with a phosphine borane derivative gives rise to an intramolecularly stabilized phosphazide 1 (R = iPr, R′ = mesityl) that undergoes an unprecedented photoisomerization process associated with a change from an N α→B to an Nβ→B interaction (see scheme). The generality and possible reversibility of such phenomena are demonstrated with the related phosphazine adduct 2.

Original languageEnglish
Pages (from-to)3333-3336
Number of pages4
JournalAngewandte Chemie - International Edition
Volume46
Issue number18
DOIs
StatePublished - 2 Jul 2007

Fingerprint

phosphine
Boranes
Photoisomerization
Derivatives
phosphazine
phenylazide
3'-azido-2',3'-dideoxythymidine 5'-H-phoshonate

Keywords

  • Boranes
  • Isomerization
  • Phosphazides
  • Phosphorus heterocycles
  • Photochemistry

Cite this

Bebbington, Magnus ; Bontemps, Sébastien ; Bouhadir, Ghenwa ; Bourissou, Didier. / Photoisomerizable heterodienes derived from a phosphine borane. In: Angewandte Chemie - International Edition. 2007 ; Vol. 46, No. 18. pp. 3333-3336.
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Photoisomerizable heterodienes derived from a phosphine borane. / Bebbington, Magnus; Bontemps, Sébastien; Bouhadir, Ghenwa; Bourissou, Didier.

In: Angewandte Chemie - International Edition, Vol. 46, No. 18, 02.07.2007, p. 3333-3336.

Research output: Contribution to journalArticleResearchpeer-review

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