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Volumn 11, Issue 1, 2005, Pages 354-360

Synthesis, characterization, and properties of subporphyrazines: A new class of nonplanar, aromatic macrocycles with absorption in the green region

Author keywords

Absorption; Macrocycles; Subphthalocyanines; Subporphyrazines; UV Vis spectroscopy

Indexed keywords

ABSORPTION COEFFICIENTS; HYPSOCHROMIC SHIFTS; MESOMORPHIC BEHAVIOR; OPTICAL POLARISING MICROSCOPY;

EID: 19944425987     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200400787     Document Type: Article
Times cited : (75)

References (50)
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    • b) "Synthesis and Spectroscopic Properties of Phthalocyanine Analogs": N. Kobayashi in The Porphyrin Handbook, Vol.15 (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, CA, 2003, pp. 161-262;
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    • (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, CA
    • c) "Design and Synthesis of Low-Symmetry Phthalocyanines and Related Systems": M. S. Rodríguez-Morgade, G. de la Torre, T. Torres in The Porphyrin Handbook, Vol. 15 (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, CA, 2003, pp. 125-159;
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    • Rodríguez-Morgade, M.S.1    De La Torre, G.2    Torres, T.3
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    • 11244299503 scopus 로고    scopus 로고
    • (Imperial Chemical Industries PLC, UK), Brit. UK Pat. Appl. GB 95-12755
    • a) P. Hunt, (Imperial Chemical Industries PLC, UK), Brit. UK Pat. Appl. GB 95-12755, CAN 124:234870, 1996;
    • (1996) CAN , vol.124 , pp. 234870
    • Hunt, P.1
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    • a) C. G. Claessens, T. Torres, Angew. Chem. 2002, 114, 2673; Angew. Chem. Int. Ed. 2002, 41, 2561;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2561
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    • b) T. Fukuda, J. R. Stork, R. J. Potucek, M. M. Olmstead, B. C. Noll, N. Kobayashi, W. S. Durfee, Angew. Chem. 2002, 114, 2677; Angew. Chem. Int. Ed. 2002, 41, 2565.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2565
  • 31
    • 0028921649 scopus 로고
    • To the best of our knowledge, only two examples of subporphyrazines have been reported; however, the electronic properties described for these compounds do not match the data obtained in the present study for this type of compound. See a) J. Rauschnabel, M. Hanack, Tetrahedron Lett. 1995, 36, 1629;
    • (1995) Tetrahedron Lett. , vol.36 , pp. 1629
    • Rauschnabel, J.1    Hanack, M.2
  • 38
    • 11244296845 scopus 로고    scopus 로고
    • note
    • Similar to the synthesis of subphthalocyanines, in which phthalimides are obtained as byproducts, the main impurity found in subporphyrazine synthesis is the corresponding succinimide.
  • 49
    • 0001019915 scopus 로고    scopus 로고
    • (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, CA
    • "meso-Azaporphyrins and their Analogues": N. Kobayashi in The Porphyrin Handbook, Vol. 2 (Eds.: K. M. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, CA, 2000, pp. 301-360.
    • (2000) The Porphyrin Handbook , vol.2 , pp. 301-360
    • Kobayashi, N.1
  • 50
    • 11244285042 scopus 로고    scopus 로고
    • (ES Pat. Appl.), 2004016
    • Some of the results presented here have been patented by us for this purpose: T. Torres, M. S. Rodríguez-Morgade, (ES Pat. Appl.), 2004016.
    • Torres, T.1    Rodríguez-Morgade, M.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.