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Volumn 71, Issue 26, 2006, Pages 9602-9608

Ring opening of 2,5-didehydrothiophene: Matrix photochemistry of C 4H2S isomers

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIZATION; ETHYNYLTHIOKETENES; MATRIX-ISOLATED DIETHYNYL SULFIDE; POTENTIAL ENERGY SURFACE;

EID: 33845924448     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061678l     Document Type: Article
Times cited : (14)

References (50)
  • 35
    • 33845964865 scopus 로고    scopus 로고
    • Nonetheless, the experiment involving the argon matrix helps resolve the matrix site splitting. See Supporting Information for details
    • Nonetheless, the experiment involving the argon matrix helps resolve the matrix site splitting. See Supporting Information for details.
  • 41
    • 33845938725 scopus 로고    scopus 로고
    • 1 transition, i.e., a combination of in-plane and out-of-plane π → π* transitions of 5. Currently, it is uncertain how the observed photochemistry has any relevance to this electronic transition of 5 and/or to the incomplete photoconversion of 5 to 6. (As judged by the IR experiments, the photostationary mixture includes approximately 25% of the initial amount of 5.)
    • 1 transition, i.e., a combination of in-plane and out-of-plane π → π* transitions of 5. Currently, it is uncertain how the observed photochemistry has any relevance to this electronic transition of 5 and/or to the incomplete photoconversion of 5 to 6. (As judged by the IR experiments, the photostationary mixture includes approximately 25% of the initial amount of 5.)
  • 43
    • 33845963571 scopus 로고    scopus 로고
    • According to an Natural Resonance Theory (NRT) analysis, the thiirane structure is recognized as a minor resonance contributor of diethynyl sulfide (3). See Supporting Information for details.
    • According to an Natural Resonance Theory (NRT) analysis, the thiirane structure is recognized as a minor resonance contributor of diethynyl sulfide (3). See Supporting Information for details.
  • 45
    • 33845928416 scopus 로고    scopus 로고
    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Zakrzewski, V. G, Montgomery, J. A, Jr, Stratmann, R. E, Burant, J. C, Dapprich, S, Millam, J. M, Daniels, A. D, Kudin, K. N, Strain, M. C, Farkas, O, Tomasi, J, Barone, V, Cossi, M, Cammi, R, Mennucci, B, Pomelli, C, Adamo, C, Clifford, S, Ochterski, J, Petersson, G. A, Ayala, P. Y, Cui, Q, Morokuma, K, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Cioslowski, J, Ortiz, J. V, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Gomperts, R, Martin, R. L, Fox, D. J, Keith, T, Al-Laham, M. A, Peng, C. Y, Nanayakkara, A, Gonzalez, C, Challacombe, M, Gill, P. M. W, Johnson, B. G, Chen, W, Wong, M. W, Andres, J. L, Head-Gordon, M, Replogle, E. S, Pople, J. A. Gaussian 98, revision A.6; Gaussian, Inc, Pittsburgh, PA, 1998
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Zakrzewski, V. G.; Montgomery, J. A., Jr.; Stratmann, R. E.; Burant, J. C.; Dapprich, S.; Millam, J. M.; Daniels, A. D.; Kudin, K. N.; Strain, M. C.; Farkas, O.; Tomasi, J.; Barone, V.; Cossi, M.; Cammi, R.; Mennucci, B.; Pomelli, C.; Adamo, C.; Clifford, S.; Ochterski, J.; Petersson, G. A.; Ayala, P. Y.; Cui, Q.; Morokuma, K.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Cioslowski, J.; Ortiz, J. V.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Gonzalez, C.; Challacombe, M.; Gill, P. M. W.; Johnson, B. G.; Chen, W.; Wong, M. W.; Andres, J. L.; Head-Gordon, M.; Replogle, E. S.; Pople, J. A. Gaussian 98, revision A.6; Gaussian, Inc.: Pittsburgh, PA, 1998.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.