Molecular organization of mono(p-hydroquinonyl)porphyrin through coordinate bond

Chemistry Letters

Volumn , Issue 6, 1996, Pages 497-498

  Miyaji, Hidekazu ^a   Kobuke, Yoshiaki ^a   Kondo, Jiro ^a  

^a SHIZUOKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0030487427     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1996.497     Document Type: Article

References (9)

1. G. McDermott, S. M. Prince, A. A. Freer, A. W. Hawthornthwaite-Lawless, M. Z. Papiz, R. J. Cogdell, and N. W. Isaacs, Nature, 374, 517 (1995).
2. T. Nozawa, K. Ohtomo, M. Suzuki, H. Nakagawa, Y. Shikama, H. Konami, and Z.-Y. Wang, Photosynth. Res., 41, 211 (1994).
3. Y. Kobuke and H. Miyaji, J. Am. Chem. Soc., 116, 4111 (1994).
4. H. Miyaji, Y. Kobuke, and J. Kondo, Proc. 12th Internat. Conf. Chem. Org. Solid State, in press.
5. Tetrakis(hydroquinonyl)porphyrin is reported: a) J. Dalton and L. R. Milgrom, J. Chem. Soc., Chem. Commun., 1979, 609.
6. b) A. C. Chan, J. Dalton, and L. R. Milgrom, J. Chem. Soc. Perkin Trans. 2, 1982, 707.
7. Preparation of mono(hydroquinonyl)porphyrin derivative is reported, although no isolation of the product is given: J. L. Sessler, M. R. Johnson, S. E. Creager, J. C. Fettinger, and J. A. Ibers, J. Am. Chem. Soc., 112, 9310 (1990).
8. em (CHC13) 649, 711 nm.
9. 3) 611, 662 nm.