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Volumn 69, Issue 10, 2004, Pages 3538-3545

Photolysis of 3-(2-Formylphenyl)-3-chlorodiazirine in an Ar Matrix at Low Temperature

Author keywords

[No Author keywords available]

Indexed keywords

ARGON; AROMATIC COMPOUNDS; INFRARED SPECTROSCOPY; KETONES; LOW TEMPERATURE OPERATIONS; QUANTUM THEORY; ULTRAVIOLET RADIATION; ULTRAVIOLET SPECTROSCOPY;

EID: 2442631390     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049802t     Document Type: Article
Times cited : (8)

References (47)
  • 2
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    • (b) Sheridan, R. S. Organic Photochemistry; Padwa, A., Ed.; Dekker: New York, 1987; Vol. 8, pp 159-248.
    • (1987) Organic Photochemistry , vol.8 , pp. 159-248
    • Sheridan, R.S.1
  • 3
    • 2442552667 scopus 로고    scopus 로고
    • Brinker, U., Ed.; JAI Press: Greenwich, CT
    • (c) Sander, W.; Bettinger, H. F. In Advances in Carbene Chemistry; Brinker, U., Ed.; JAI Press: Greenwich, CT, 2001; Vol. 3, pp 160-203.
    • (2001) Advances in Carbene Chemistry , vol.3 , pp. 160-203
    • Sander, W.1    Bettinger, H.F.2
  • 5
    • 2442510757 scopus 로고    scopus 로고
    • Bertrand, Ed.; Fontis Media S.A.: Lausanne
    • (e) Sander, W. In Carbene Chemistry; Bertrand, Ed.; Fontis Media S.A.: Lausanne, 2002, pp 1-25.
    • (2002) Carbene Chemistry , pp. 1-25
    • Sander, W.1
  • 6
    • 0005712009 scopus 로고    scopus 로고
    • Brinder, U., Ed.; JAI Press: Greenwich, CT
    • (f) Maier, G.; Reisenauer, H. P. In Advances in Carbene Chemistry; Brinder, U., Ed.; JAI Press: Greenwich, CT, 2001; Vol. 3, pp 116-157.
    • (2001) Advances in Carbene Chemistry , vol.3 , pp. 116-157
    • Maier, G.1    Reisenauer, H.P.2
  • 10
    • 0006949456 scopus 로고
    • (Methoxycarbonyl)phenylcarbene gave the corresponding furan as a result of the interaction of the carbenic center with carbonyl oxygen. Murata, S.; Ohtawa, Y.; Tomioka, H. Chem. Lett. 1989, 853.
    • (1989) Chem. Lett. , pp. 853
    • Murata, S.1    Ohtawa, Y.2    Tomioka, H.3
  • 11
    • 0001194621 scopus 로고
    • Methylphenylcarbene generated o-quinodimethane as a result of 1,4-H migration from methyl hydrogen to the carbenic center. McMahon, R. J.; Chapman, O. L. J. Am. Chem. Soc. 1987, 109, 683.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 683
    • McMahon, R.J.1    Chapman, O.L.2
  • 23
    • 2442563268 scopus 로고    scopus 로고
    • note
    • 1/2 dependence. See refs 5 and 8a.
  • 24
    • 0002357673 scopus 로고
    • Brinker, U., Ed.; JAI Press: Greenwich, CT
    • Moss, R. A. In Advances in Carbene Chemistry; Brinker, U., Ed.; JAI Press: Greenwich, CT, 1994; Vol. 1, pp 59-88.
    • (1994) Advances in Carbene Chemistry , vol.1 , pp. 59-88
    • Moss, R.A.1
  • 25
    • 0043218317 scopus 로고
    • Intermolecular H atom abstractions of triplet carbenes have been shown to proceed by a QMT mechanism at very low temperature. See for reviews: (a) Platz, M. S. Acc. Chem. Res. 1988, 21, 236.
    • (1988) Acc. Chem. Res. , vol.21 , pp. 236
    • Platz, M.S.1
  • 28
    • 2442561169 scopus 로고    scopus 로고
    • Moss, A. M., Platz, M. S., Jones, M., Jr., Eds.; Wiley: New York
    • (d) Tomioka, H. In Reactive Intermediate Chemistry; Moss, A. M., Platz, M. S., Jones, M., Jr., Eds.; Wiley: New York, 2004; pp 375-461.
    • (2004) Reactive Intermediate Chemistry , pp. 375-461
    • Tomioka, H.1
  • 34
    • 2442479317 scopus 로고    scopus 로고
    • note
    • 12 at 20 K even for a classical H transfer reaction.5
  • 35
    • 2442506502 scopus 로고    scopus 로고
    • Moss, A. M., Platz, M. S., Jones, M., Jr., Eds.; Wiley: New York
    • It is well-known that halocarbenes have a singlet ground state. See, for instance: Jones, M. Jr.; Moss, R. A. In Reactive Intermediate Chemistry; Moss, A. M., Platz, M. S., Jones, M., Jr., Eds.; Wiley: New York, 2004; pp 273-328.
    • (2004) Reactive Intermediate Chemistry , pp. 273-328
    • Jones Jr., M.1    Moss, R.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.