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Volumn 9, Issue 26, 2007, Pages 5417-5420

Synthesis, structure, and properties of benzoquinone dimer and trimers bearing t-Bu substituents

Author keywords

[No Author keywords available]

Indexed keywords

BENZOQUINONE DERIVATIVE; POLYMER;

EID: 38349187385     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702289u     Document Type: Article
Times cited : (21)

References (26)
  • 1
    • 85050430499 scopus 로고
    • Patai, S, Rappoport, Z, Eds, Wiley: Chichester, UK
    • The Chemistry of the Quinonoid Compounds; Patai, S., Rappoport, Z., Eds.; Wiley: Chichester, UK, 1988.
    • (1988) The Chemistry of the Quinonoid Compounds
  • 17
    • 38349113952 scopus 로고    scopus 로고
    • Although QQ is a known compound Hewgill, F. R, Hewitt, D. G. J. Chem. Soc, Sect. C 1967, 723, its redox behavior and precise molecular structure was not investigated
    • Although QQ is a known compound (Hewgill, F. R.; Hewitt, D. G. J. Chem. Soc., Sect. C 1967, 723.), its redox behavior and precise molecular structure was not investigated.
  • 21
    • 38349130954 scopus 로고    scopus 로고
    • As seen in the X-ray structure of polymorphs of substituted bipyrrole, the bond length linking two π moieties is sensitively altered depending on the dihedral angle: the pyrrole-pyrrole bond length of the anti conformer, where the dihedral angle Φ = 180°, is 1.4362(17) Â, whereas that of the syn conformer, where Φ = 40°, is 1.4490
    • As seen in the X-ray structure of polymorphs of substituted bipyrrole, the bond length linking two π moieties is sensitively altered depending on the dihedral angle: the pyrrole-pyrrole bond length of the anti conformer, where the dihedral angle Φ = 180°, is 1.4362(17) Â, whereas that of the syn conformer, where Φ = 40°, is 1.4490
  • 22
    • 0033577868 scopus 로고    scopus 로고
    • Å (Merz, A.; Kronberger, J.; Dunsch, L.; Neudeck, A.; Petr, A.; Parkanyi, L. Angew. Chem., Int. Ed. 1999, 38, 1442).
    • Å (Merz, A.; Kronberger, J.; Dunsch, L.; Neudeck, A.; Petr, A.; Parkanyi, L. Angew. Chem., Int. Ed. 1999, 38, 1442).
  • 25
    • 38349177047 scopus 로고    scopus 로고
    • Consequently, acidity and reactivity toward amines of these compound were observed to be significantly different. Bron, J.: Simmons, E. L. J. Phys. Chem. 1976, 80, 185.
    • Consequently, acidity and reactivity toward amines of these compound were observed to be significantly different. Bron, J.: Simmons, E. L. J. Phys. Chem. 1976, 80, 185.
  • 26
    • 38349098383 scopus 로고    scopus 로고
    • Versus SCE, in acetonitrile. Liu, Y.-C.; Zhang, M.-X.; Yang, L.; Liu, Z.-L. J. Chem. Soc., Perkin Trans. 2 1992, 1919.
    • Versus SCE, in acetonitrile. Liu, Y.-C.; Zhang, M.-X.; Yang, L.; Liu, Z.-L. J. Chem. Soc., Perkin Trans. 2 1992, 1919.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.