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Volumn 118, Issue 9, 1996, Pages 2275-2282

Reactivity and efficiency of singlet- and triplet-excited states in intermolecular hydrogen abstraction reactions

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; AZO COMPOUND;

EID: 0029932129     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9535118     Document Type: Article
Times cited : (62)

References (60)
  • 24
    • 0003352065 scopus 로고
    • Charney, D. R.; Dalton, J. C.; Hautala, R. R.; Snyder, J. J.; Turro, N. J. J. Am. Chem. Soc. 1974, 96, 1407: Tominaga, K.; Yamauchi, S.; Hirota, N. J. Phys. Chem. 1988, 92, 5160; Ohara, K.; Hirota, N.; Steren, C. A.; van Willigen, H. Chem. Phys. Lett. 1995, 232, 169.
    • (1988) J. Phys. Chem. , vol.92 , pp. 5160
    • Tominaga, K.1    Yamauchi, S.2    Hirota, N.3
  • 25
    • 0011987475 scopus 로고
    • Charney, D. R.; Dalton, J. C.; Hautala, R. R.; Snyder, J. J.; Turro, N. J. J. Am. Chem. Soc. 1974, 96, 1407: Tominaga, K.; Yamauchi, S.; Hirota, N. J. Phys. Chem. 1988, 92, 5160; Ohara, K.; Hirota, N.; Steren, C. A.; van Willigen, H. Chem. Phys. Lett. 1995, 232, 169.
    • (1995) Chem. Phys. Lett. , vol.232 , pp. 169
    • Ohara, K.1    Hirota, N.2    Steren, C.A.3    Van Willigen, H.4
  • 36
    • 0001200678 scopus 로고
    • Quenching of singlet- and triplet-excited bicyclic azoalkanes by hydrogen donors results in the formation of (oxidation-sensitive) hydrazines as photoproducts, which indicates that the quenching mechanism is hydrogen abstraction in both cases: Engel, P. S.; Kitamura, A.; Keys, D. E. J. Org. Chem. 1987, 52, 5015. Engel, P. S.; Keys, D. E.; Kitamura, A. J. Am. Chem. Soc. 1985, 107, 4964.
    • (1987) J. Org. Chem. , vol.52 , pp. 5015
    • Engel, P.S.1    Kitamura, A.2    Keys, D.E.3
  • 37
    • 0000340978 scopus 로고
    • Quenching of singlet- and triplet-excited bicyclic azoalkanes by hydrogen donors results in the formation of (oxidation-sensitive) hydrazines as photoproducts, which indicates that the quenching mechanism is hydrogen abstraction in both cases: Engel, P. S.; Kitamura, A.; Keys, D. E. J. Org. Chem. 1987, 52, 5015. Engel, P. S.; Keys, D. E.; Kitamura, A. J. Am. Chem. Soc. 1985, 107, 4964.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 4964
    • Engel, P.S.1    Keys, D.E.2    Kitamura, A.3
  • 55
    • 33751157551 scopus 로고
    • (e) For the Norrish-type II reaction see: Sauers, R. R.: Edberg, L. A. J. Org. Chem. 1994, 59, 7061. Sengupta, D.; Sumathi, R.; Chandra, A. K. J. Photochem. Photobiol. A: Chem. 1991, 60, 149.
    • (1994) J. Org. Chem. , vol.59 , pp. 7061
    • Sauers, R.R.1    Edberg, L.A.2
  • 57
    • 0001527994 scopus 로고
    • 12a however, the intermediary ketyl radical may further abstract a hydrogen atom from a second stannane molecule to form directly the photoreduction product 2-propanol. cf.: Chatgilialoglu, C.: Ingold, K. U.; Scaiano, J. C. J. Am. Chem. Soc. 1981, 103, 7739.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 7739
    • Chatgilialoglu, C.1    Ingold, K.U.2    Scaiano, J.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.