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Volumn 75, Issue 11, 2002, Pages 2359-2370

Facile formation of stable crystals with gold-like metallic luster from organic molecules: 1-Aryl-2-(2-thienyl)-5-[5-(tricyanoethenyl)-2-thienyl]pyrroles

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; BRONZE; DERIVATIVES; GOLD; PHYSICAL PROPERTIES; SHEET METAL;

EID: 0346106097     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.75.2359     Document Type: Article
Times cited : (42)

References (25)
  • 1
    • 34547768200 scopus 로고
    • ed by T. A. Skotheim, Marcel Dekker, Inc., New York
    • "Handbook of Conducting Polymers, Volumes 1 & 2," ed by T. A. Skotheim, Marcel Dekker, Inc., New York (1986).
    • (1986) Handbook of Conducting Polymers, Volumes 1 & 2 , vol.1-2
  • 2
    • 23144432306 scopus 로고    scopus 로고
    • Electronic properties of polythiophenes
    • ed by D. Fichou, Wiley-VCH
    • S. Hotta and K. Ito, Electronic properties of polythiophenes in "Handbook of Oligo- and Polythiophenes," ed by D. Fichou, Wiley-VCH (1999), pp. 45-88.
    • (1999) Handbook of Oligo- and Polythiophenes , pp. 45-88
    • Hotta, S.1    Ito, K.2
  • 3
    • 0001172127 scopus 로고
    • Polyacetylene: New concepts and new phenomena
    • ed by T. A. Skotheim, Marcel Dekker, Inc., New York
    • A. J. Heeger, Polyacetylene: New concepts and new phenomena in "Handbook of Conducting Polymers," ed by T. A. Skotheim, Marcel Dekker, Inc., New York (1986), Vol. 2, pp. 729-756.
    • (1986) Handbook of Conducting Polymers , vol.2 , pp. 729-756
    • Heeger, A.J.1
  • 13
    • 37049079491 scopus 로고
    • Hitherto, many derivatives of 2-(tricyanoethenyl)thiophene have been reported mainly in order to develop efficient second-order nonlinear optical chromophores. For example, a) V. P. Rao, A. K.-Y. Jen, K. Y. Wong, and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 1118. b) A. K.-Y. Jen, V. P. Rao, K, J. Drost, K. Y. Wong, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1994, 2057. c) K. Onitsuka, H. Urayama, K. Sonogashira, and F. Ozawa, Chem. Lett., 1995, 1019. d) V. P. Rao, A. K.-Y. Jen, and Y. Cai, J. Chem. Soc. Chem. Commun., 1996, 1273. e) C.-F. Shu, W. J. Tsai, J.-Y. Chen, A. K.-Y. Jen, and Y. Zhang, Chem. Commun., 1996, 2279. f) C. R. Bu, H. Li, D. Van Derveer, and F. A. Mintz, Tetrahedron Lett., 37, 7331 (1996).
    • (1993) J. Chem. Soc., Chem. Commun. , pp. 1118
    • Rao, V.P.1    Jen, A.K.-Y.2    Wong, K.Y.3    Drost, K.J.4
  • 14
    • 37049075685 scopus 로고
    • Hitherto, many derivatives of 2-(tricyanoethenyl)thiophene have been reported mainly in order to develop efficient second-order nonlinear optical chromophores. For example, a) V. P. Rao, A. K.-Y. Jen, K. Y. Wong, and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 1118. b) A. K.-Y. Jen, V. P. Rao, K, J. Drost, K. Y. Wong, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1994, 2057. c) K. Onitsuka, H. Urayama, K. Sonogashira, and F. Ozawa, Chem. Lett., 1995, 1019. d) V. P. Rao, A. K.-Y. Jen, and Y. Cai, J. Chem. Soc. Chem. Commun., 1996, 1273. e) C.-F. Shu, W. J. Tsai, J.-Y. Chen, A. K.-Y. Jen, and Y. Zhang, Chem. Commun., 1996, 2279. f) C. R. Bu, H. Li, D. Van Derveer, and F. A. Mintz, Tetrahedron Lett., 37, 7331 (1996).
    • (1994) J. Chem. Soc., Chem. Commun. , pp. 2057
    • Jen, A.K.-Y.1    Rao, V.P.2    Drost, K.J.3    Wong, K.Y.4    Cava, M.P.5
  • 15
    • 0002612563 scopus 로고
    • Hitherto, many derivatives of 2-(tricyanoethenyl)thiophene have been reported mainly in order to develop efficient second-order nonlinear optical chromophores. For example, a) V. P. Rao, A. K.-Y. Jen, K. Y. Wong, and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 1118. b) A. K.-Y. Jen, V. P. Rao, K, J. Drost, K. Y. Wong, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1994, 2057. c) K. Onitsuka, H. Urayama, K. Sonogashira, and F. Ozawa, Chem. Lett., 1995, 1019. d) V. P. Rao, A. K.-Y. Jen, and Y. Cai, J. Chem. Soc. Chem. Commun., 1996, 1273. e) C.-F. Shu, W. J. Tsai, J.-Y. Chen, A. K.-Y. Jen, and Y. Zhang, Chem. Commun., 1996, 2279. f) C. R. Bu, H. Li, D. Van Derveer, and F. A. Mintz, Tetrahedron Lett., 37, 7331 (1996).
    • (1995) Chem. Lett. , pp. 1019
    • Onitsuka, K.1    Urayama, H.2    Sonogashira, K.3    Ozawa, F.4
  • 16
    • 0347721268 scopus 로고    scopus 로고
    • Hitherto, many derivatives of 2-(tricyanoethenyl)thiophene have been reported mainly in order to develop efficient second-order nonlinear optical chromophores. For example, a) V. P. Rao, A. K.-Y. Jen, K. Y. Wong, and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 1118. b) A. K.-Y. Jen, V. P. Rao, K, J. Drost, K. Y. Wong, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1994, 2057. c) K. Onitsuka, H. Urayama, K. Sonogashira, and F. Ozawa, Chem. Lett., 1995, 1019. d) V. P. Rao, A. K.-Y. Jen, and Y. Cai, J. Chem. Soc. Chem. Commun., 1996, 1273. e) C.-F. Shu, W. J. Tsai, J.-Y. Chen, A. K.-Y. Jen, and Y. Zhang, Chem. Commun., 1996, 2279. f) C. R. Bu, H. Li, D. Van Derveer, and F. A. Mintz, Tetrahedron Lett., 37, 7331 (1996).
    • (1996) J. Chem. Soc. Chem. Commun. , pp. 1273
    • Rao, V.P.1    Jen, A.K.-Y.2    Cai, Y.3
  • 17
    • 0000269523 scopus 로고    scopus 로고
    • Hitherto, many derivatives of 2-(tricyanoethenyl)thiophene have been reported mainly in order to develop efficient second-order nonlinear optical chromophores. For example, a) V. P. Rao, A. K.-Y. Jen, K. Y. Wong, and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 1118. b) A. K.-Y. Jen, V. P. Rao, K, J. Drost, K. Y. Wong, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1994, 2057. c) K. Onitsuka, H. Urayama, K. Sonogashira, and F. Ozawa, Chem. Lett., 1995, 1019. d) V. P. Rao, A. K.-Y. Jen, and Y. Cai, J. Chem. Soc. Chem. Commun., 1996, 1273. e) C.-F. Shu, W. J. Tsai, J.-Y. Chen, A. K.-Y. Jen, and Y. Zhang, Chem. Commun., 1996, 2279. f) C. R. Bu, H. Li, D. Van Derveer, and F. A. Mintz, Tetrahedron Lett., 37, 7331 (1996).
    • (1996) Chem. Commun. , pp. 2279
    • Shu, C.-F.1    Tsai, W.J.2    Chen, J.-Y.3    Jen, A.K.-Y.4    Zhang, Y.5
  • 18
    • 0030574020 scopus 로고    scopus 로고
    • Hitherto, many derivatives of 2-(tricyanoethenyl)thiophene have been reported mainly in order to develop efficient second-order nonlinear optical chromophores. For example, a) V. P. Rao, A. K.-Y. Jen, K. Y. Wong, and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 1118. b) A. K.-Y. Jen, V. P. Rao, K, J. Drost, K. Y. Wong, and M. P. Cava, J. Chem. Soc., Chem. Commun., 1994, 2057. c) K. Onitsuka, H. Urayama, K. Sonogashira, and F. Ozawa, Chem. Lett., 1995, 1019. d) V. P. Rao, A. K.-Y. Jen, and Y. Cai, J. Chem. Soc. Chem. Commun., 1996, 1273. e) C.-F. Shu, W. J. Tsai, J.-Y. Chen, A. K.-Y. Jen, and Y. Zhang, Chem. Commun., 1996, 2279. f) C. R. Bu, H. Li, D. Van Derveer, and F. A. Mintz, Tetrahedron Lett., 37, 7331 (1996).
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7331
    • Bu, C.R.1    Li, H.2    Van Derveer, D.3    Mintz, F.A.4
  • 20
    • 0001281257 scopus 로고
    • A strategy for the synthesis of molecular crystals containing two-dimensional layers is discussed: Y.-L. Chang, M.-A. West, F. W. Fowler and J. W. Lauher, J. Am. Chem. Soc., 115, 5991 (1993). Its related papers: S. Coe, J. J. Kane, T. L. Nguyen, L. M. Toledo, E. Wininger, F. W. Fowler and J. W. Lauher, J. Am. Chem. Soc., 119, 86 (1997), and the references cited therein.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 5991
    • Chang, Y.-L.1    West, M.-A.2    Fowler, F.W.3    Lauher, J.W.4
  • 21
    • 0031043017 scopus 로고    scopus 로고
    • and the references cited therein
    • A strategy for the synthesis of molecular crystals containing two-dimensional layers is discussed: Y.-L. Chang, M.-A. West, F. W. Fowler and J. W. Lauher, J. Am. Chem. Soc., 115, 5991 (1993). Its related papers: S. Coe, J. J. Kane, T. L. Nguyen, L. M. Toledo, E. Wininger, F. W. Fowler and J. W. Lauher, J. Am. Chem. Soc., 119, 86 (1997), and the references cited therein.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 86
    • Coe, S.1    Kane, J.J.2    Nguyen, T.L.3    Toledo, L.M.4    Wininger, E.5    Fowler, F.W.6    Lauher, J.W.7


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