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Volumn , Issue 10, 1996, Pages 867-868

Preparation of one structural isomer of tetra-substituted phthalocyanine, 1,8,15,22-tetra(3′-pentoxy)phthalocyanine, and a crystal structure of its nickel(II) complex

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Indexed keywords


EID: 0002179688     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1996.867     Document Type: Article
Times cited : (33)

References (20)
  • 1
    • 0002261892 scopus 로고
    • H. Schultz, H. Lehmann, M. Rein, and M. Hanack, in Struct. and Bonding (Berlin), 74, 41(1991); P. Gregory, High-Technology Applications of Organic Colorants, Plenum Press, New York (1991); T. J. Marks, Science, 227, 881(1985); R. O. Loutfy, A. M. Hor, and A. Rucklidge, J. Imaging Sci., 31, 31(1987).
    • (1991) Struct. and Bonding (Berlin) , vol.74 , pp. 41
    • Schultz, H.1    Lehmann, H.2    Rein, M.3    Hanack, M.4
  • 2
    • 0004079885 scopus 로고
    • Plenum Press, New York
    • H. Schultz, H. Lehmann, M. Rein, and M. Hanack, in Struct. and Bonding (Berlin), 74, 41(1991); P. Gregory, High-Technology Applications of Organic Colorants, Plenum Press, New York (1991); T. J. Marks, Science, 227, 881(1985); R. O. Loutfy, A. M. Hor, and A. Rucklidge, J. Imaging Sci., 31, 31(1987).
    • (1991) High-Technology Applications of Organic Colorants
    • Gregory, P.1
  • 3
    • 0022011006 scopus 로고
    • H. Schultz, H. Lehmann, M. Rein, and M. Hanack, in Struct. and Bonding (Berlin), 74, 41(1991); P. Gregory, High-Technology Applications of Organic Colorants, Plenum Press, New York (1991); T. J. Marks, Science, 227, 881(1985); R. O. Loutfy, A. M. Hor, and A. Rucklidge, J. Imaging Sci., 31, 31(1987).
    • (1985) Science , vol.227 , pp. 881
    • Marks, T.J.1
  • 4
    • 0023145467 scopus 로고
    • H. Schultz, H. Lehmann, M. Rein, and M. Hanack, in Struct. and Bonding (Berlin), 74, 41(1991); P. Gregory, High-Technology Applications of Organic Colorants, Plenum Press, New York (1991); T. J. Marks, Science, 227, 881(1985); R. O. Loutfy, A. M. Hor, and A. Rucklidge, J. Imaging Sci., 31, 31(1987).
    • (1987) J. Imaging Sci. , vol.31 , pp. 31
    • Loutfy, R.O.1    Hor, A.M.2    Rucklidge, A.3
  • 13
    • 0042665307 scopus 로고    scopus 로고
    • note
    • 3) δ 1.38 (t, 24H, J = 7.3 Hz), 2.32 - 2.45 (m, 16H), 4.89 - 4.94 (m, 4H), 7.64 (d, 4H, J = 8.1 Hz), 8.12 (t, 4H, J = 7.8 Hz), 9.06 (d, 4H, J = 7.3 Hz).
  • 14
    • 0043166275 scopus 로고    scopus 로고
    • note
    • With the purification by reprecipitation and column chromatography, the relative yield of the isomer I considerably increased (10 - 15%). For HPLC analyses, the reaction mixtures without the purification were used. The relative yield was calculated from the relative peak height of the isomer I for those of all isomers.
  • 15
    • 0041663396 scopus 로고    scopus 로고
    • note
    • 6) δ 0.90 (t, 24H, J = 7.6 Hz), 1.18 - 1.93 (m, 16H), 4.28 - 4.32(m, 4H), 6.93 (d, 4H, J = 8.1 Hz), 7.53 (t, 4H, J = 7.8 Hz), 8.97 (d, 4H, J = 7.6 Hz).
  • 16
    • 0043166273 scopus 로고    scopus 로고
    • note
    • w = 0.138.
  • 18
    • 0041663395 scopus 로고    scopus 로고
    • M. Ashida, N. Uyeda, and E. Suito, Bull. Chem. Soc. Jpn., 39, 2616(1966); C. J. Brown, J. Chem. Soc., 1968, 2488.
    • J. Chem. Soc. , vol.1968 , pp. 2488
    • Brown, C.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.