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Volumn 70, Issue 4, 2005, Pages 1276-1280

Reaction of triarylphosphine radical cations generated from photoinduced electron transfer in the presence of oxygen

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; ELECTRON TRANSITIONS; OXIDATION; OXYGEN; PHOTOLYSIS; PHOTOREACTIVITY; POSITIVE IONS; REACTION KINETICS;

EID: 13844313026     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049032l     Document Type: Article
Times cited : (59)

References (43)
  • 1
    • 0000490453 scopus 로고
    • and references therein
    • Yasui, S. Rev. Heteroatom Chem. 1995, 12, 145-161 and references therein.
    • (1995) Rev. Heteroatom Chem. , vol.12 , pp. 145-161
    • Yasui, S.1
  • 21
    • 13844307523 scopus 로고    scopus 로고
    • note
    • + in V.
  • 23
    • 0343021975 scopus 로고
    • Acetonitrile was refluxed over calcium hydride for at least 10 h and distilled. The solvent purified in this way still contains about 0.1% water. See, Yasui, S.; Shioji, K.; Ohno, A.; Yoshihara, M. Chem. Lett. 1993, 1393-1396.
    • (1993) Chem. Lett. , pp. 1393-1396
    • Yasui, S.1    Shioji, K.2    Ohno, A.3    Yoshihara, M.4
  • 35
    • 13844312228 scopus 로고    scopus 로고
    • note
    • -1, which was independently determined by the Stern-Volmer analysis.
  • 37
    • 13844316207 scopus 로고    scopus 로고
    • note
    • Although no experimental data are available, we are tempted to speculate that the peroxy radical 3 attacks the phosphine 1 to give the phosphoranyl radical with TBP geometry. This step would be subjected to a steric effect by the ortho substituent since the C-P-C angle becomes smaller.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.