Valence Isomerism between Sterically Protected Methylenephosphine P-Sulfide and 1,2-Thiaphosphirane

Kozo Toyota, Hiroaki Takahashi, Kazuho Shimura, Masaaki Yoshifuji

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)


Reaction of (diphenylmethylene)(2,4,6-tri-t-butylphenyl)phosphine with elemental sulfur afforded 3,3-diphenyl-2-(2,4,6-tri-t-butylphenyl)-1,2-thiaphosphirane 2-sulfide via methylenephosphine P-sulfide. Desulfurization reaction of the thiaphosphirane 2-sulfide with tris(dimethylamino)phosphine gave 3,3-diphenyl-2-(2,4,6-tri-r-butylphenyi)-l,2-thiaphosphirane. Valence isomerization occurred between the methylenephosphine P-sulfide and the thiaphosphirane by heat or by photo-irradiation. The structures of the methylenephosphine, the methylenephosphine P-sulfide, and the thiaphosphirane were analyzed by X-ray crystallography.

Original languageEnglish
Pages (from-to)141-145
Number of pages5
JournalBulletin of the Chemical Society of Japan
Issue number1
Publication statusPublished - 1996 Jan 1

ASJC Scopus subject areas

  • Chemistry(all)


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