메뉴 건너뛰기




Volumn , Issue 10, 1998, Pages 1595-1601

Synthesis of 3,4-diarylpyrroles and conversion into dodecaarylporphyrins; a new approach to porphyrins with altered redox potentials

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33748514809     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a801185k     Document Type: Article
Times cited : (71)

References (75)
  • 1
    • 0003946851 scopus 로고
    • ed. K. M. Smith, Elsevier, Amsterdam
    • Effects of peripheral substituents and central metals on the redox and optical properties of porphyrins have been extensively studied, see, Porphyrins and Metalloporphyrins, ed. K. M. Smith, Elsevier, Amsterdam 1975;
    • (1975) Porphyrins and Metalloporphyrins
  • 5
    • 0042404743 scopus 로고
    • P. G. Gassman, A. Ghosh and J. Almlof, J. Am. Chem. Soc., 1992, 114, 9990, where many references of electron deficient porphyrins are presented; for recent papers,
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9990
    • Gassman, P.G.1    Ghosh, A.2    Almlof, J.3
  • 34
    • 33748728035 scopus 로고    scopus 로고
    • However, these routes are not always useful for the preparation of p-substituted meso-non-substituted porphyrins, see, C. Kitamura and Y. Yamashita, J. Chem. Soc., Perkin Trans. 1, 1997, 1443.
    • (1997) J. Chem. Soc., Perkin Trans. 1 , pp. 1443
    • Kitamura, C.1    Yamashita, Y.2
  • 36
    • 0000248247 scopus 로고
    • John Wiley, New York
    • G. Jones, Organic Reactions, John Wiley, New York, 1967, 15, 204;
    • (1967) Organic Reactions , vol.15 , pp. 204
    • Jones, G.1
  • 44
    • 0003013648 scopus 로고
    • Synthesis of octaphenylporphyrin (4c) from 2a was reported in a preliminary report, see, N. Ono and K. Maruyama, Chem. Lett., 1988, 1511.
    • (1988) Chem. Lett. , pp. 1511
    • Ono, N.1    Maruyama, K.2
  • 63
    • 0024562778 scopus 로고
    • J. S. Lindsey and R. W. Wagner, J. Org. Chem., 1989, 54, 828, where modified procedures for tetrarylporphyrins are presented.
    • (1989) J. Org. Chem. , vol.54 , pp. 828
    • Lindsey, J.S.1    Wagner, R.W.2
  • 65
    • 0029798749 scopus 로고    scopus 로고
    • Recently, it was reported that porphyrins fused with acenaphthylene rings bring about remarkably red-shifted electronic absorption spectra, see, T. D. Lash and P. Chadraskar, J. Am. Chem. Soc., 1996, 118, 8767;
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 8767
    • Lash, T.D.1    Chadraskar, P.2
  • 71
    • 37049076050 scopus 로고
    • Oligothiophenes with donor and acceptor groups show better nonlinear optical activity than the corresponding phenylene derivatives, and now opto-electronic materials derived from thiophenes have been extensively studied; see, A. K.-Y. Jen, V. P. Rao, K. Y. Wong and K. J. Drost, J. Chem. Soc., Chem. Commun., 1993, 90;
    • (1993) J. Chem. Soc., Chem. Commun. , pp. 90
    • Jen, A.K.-Y.1    Rao, V.P.2    Wong, K.Y.3    Drost, K.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.