The first synthesis of a gable bis-phthalocyanine

Tetrahedron Letters

Volumn 45, Issue 52, 2004, Pages 9577-9580

  Asano, Yoshiaki ^a   Kobayashi, Nagao ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Dimers; Fluorescene; Nitriles; Phthalocyanines

Indexed keywords

MONOMER; NITRILE; PHTHALOCYANINE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; FLUORESCENCE; QUANTUM YIELD; SYNTHESIS;

EID: 9644260720     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.10.148     Document Type: Article

References (35)

1. N. Kobayashi Coord. Chem. Rev. 227 2002 129 152
2. J. Jiang, K. Kasuga, and D.P. Arnold S.H. Nalwa Supramolecular Photosensitive and Electroactive Materials 2001 Academic New York Chapter 2, pp 113-210
3. C. Ercolani, and B. Floris C.C. Leznoff A.B.P. Lever Phthalocyanines- Properties and Applications 1993 VCH Weinheim, New York Chapter 1, pp 1-41
4. C.C. Leznoff, H. Lam, S.M. Marcussio, W.A. Nevin, P. Janda, and N. Kobayashi J. Chem. Soc., Chem. Commun. 1987 699 701
5. N. Kobayashi J. Chem. Soc., Chem. Commun. 1991 1203 1205
6. D. Lelievre, L. Bosio, J. Simon, J.J. Andre, and F. Bensebaa J. Am. Chem. Soc. 114 1992 4475 4479
7. D. Lelievre, O. Damette, and J. Simon J. Chem. Soc., Chem. Commun. 1993 939 940
8. N. Kobayashi, H. Lam, W.A. Nevin, P. Janda, C.C. Leznoff, T. Koyama, A. Monden, and H. Shirai J. Am. Chem. Soc. 116 1994 879 890
9. T.F. Bauman, A.G.M. Barrett, and B.M. Hoffman Inorg. Chem. 36 1997 5661 5665
10. M.J. Cook, and M.J. Heeney Chem. Eur. J. 6 2000 3958 3967
11. E.M. Garcia-Frutos, F. Fernandez-Lazaro, E.M. Matya, P. Vazquez, and T. Torres J. Org. Chem. 65 2000 6841 6846
12. N. Kobayashi, T. Fukuda, and D. Lelievre Inorg. Chem. 39 2000 3632 3637
13. N. Kobayashi, A. Muranaka, and V.N. Nemykin Tetrahedron Lett. 42 2001 913 915
14. N. Kobayashi, Y. Higashi, and T. Osa J. Chem. Soc., Chem. Commun. 1994 1785 1786
15. N. Kobayashi, Y. Higashi, and T. Osa Chem. Lett. 1994 1813 1816
16. G. Torre, M.V. Martinez-Diaz, P.R. Ashton, and T. Torres J. Org. Chem. 63 1998 8888 8893
17. K. Ishii, N. Kobayashi, Y. Higashi, T. Osa, D. Lelievre, J. Simon, and S. Yamauchi Chem. Commun. 1999 969 970
18. N. Kobayashi, and H. Ogata Eur. J. Inorg. Chem. 2004 906 914
19. A. Florey, and P. Vogel Helv. Chim. Acta 58 1975 1488 1492
20. L.F. Fieser, and K.L. Williamson Organic Experiments 8th ed. 1988 Houghton Miffin Boston Chapter 40
21. C. Moureu, and J.C. Bongrand Ann. Chim. (Paris) 14 1920 5 10
22. A.T. Blomquist, and E.C. Winslow J. Org. Chem. 10 1945 149 158
23. A.J. Saggiomo J. Org. Chem. 22 1957 1171 1175
24. E. Ciganek, and C.G. Krespan J. Org. Chem. 33 1968 541 544
25. J.S. Meek, and R.D. Stacy J. Am. Chem. Soc. 26 1959 300 302
26. B. Konig, B. Knieriem, and A. de Meijere Chem. Ber. 126 1993 1643 1650
27. 4: C, 38.3; H, 2.14; N, 0.00; Found: C, 38.2; H, 2.15; N, 0.00
28. G.P. Ellis, and T.M. Romney-Alexsander Chem. Rev. 87 1987 779 794
29. J. Zanon, A. Klapars, and S.L. Buchwald J. Am. Chem. Soc. 125 2003 2890 2891
30. H. Krempl, R. Mattmer, and M. Hanack Synthesis 12 2000 1705 1708
31. 0.5: C, 73.9; H, 3.67; N, 15.7; Found: C, 73.6; H, 3.68; N, 15.5
32. Two types of gable porphyrin have been reported J.N.H. Reek, A.P.A.H. Schenning, A.W. Bosman, E.W. Meijer, and M.J. Crossley Chem. Commun. 1998 11 12
33. S. Ito, K. Nakamoto, H. Uno, T. Murashima, and N. Ono Chem. Commun. 2001 2696 2697
34. +, found: 1387.9
35. -4 mol/L