Covalent Linking of Coordination-Organized Slipped Cofacial Porphyrin Dimers

Bulletin of the Chemical Society of Japan

Volumn 77, Issue 2, 2004, Pages 365-374

  Ohashi, Atsushi ^b   Satake, Akiharu ^a   Kobuke, Yoshiaki ^a,b  

^a NARA INSTITUTE OF SCIENCE AND TECHNOLOGY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

INTRAMOLECULAR METATHESIS; MOLECULAR LENGTH;

CHEMICAL BONDS; DIMERS; OLEFINS; ORGANIC SOLVENTS; SUBSTITUTION REACTIONS;

PORPHYRINS;

5,15 BIS[2 (ALLYLOXYCARBONYL)ETHYL]PORPHYRINATOZINC; BIS[3 (ALLYLOXY)PROPYL] 20 (1 METHYL 2 IMIDAZOLYL)PORPHYRINATOZINC; DIMER; PORPHYRIN DERIVATIVE; PYRIDINE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; COVALENT BOND; REACTION ANALYSIS; RING CLOSING METATHESIS; STRUCTURE ANALYSIS;

EID: 1542290071     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.77.365     Document Type: Article

References (22)

1. a) D. Holten, D. F. Bocian, and J. S. Lindsey, Acc. Chem. Res., 35, 57 (2002).
2. b) H. L. Anderson, Chem. Commun., 1999, 2323.
3. c) N. Aratani and A. Osuka, Bull. Chem. Soc. Jpn., 74, 1361 (2001).
4. d) P. D. Harvey, "The Porphyrin Handbook," ed by K. M. Kadish, K. M. Smith, and R. Guilard, Elsevier Science (2003), Vol. 18, pp. 63-250.
5. e) K. Ogawa and Y. Kobuke, "Self-Assembled Porphyrin Arrays," in "Encyclopedia of Nanoscience and Nanotechnology," ed by H. S. Nalwa, to be published in 2003, American Scientific Pub.
6. a) Y. Kobuke and H. Miyaji, J. Am. Chem. Soc., 116, 4111 (1994).
7. b) K. Ogawa and Y. Kobuke, Angew. Chem., Int. Ed., 39, 4070 (2000).
8. c) Y. Kobuke and K. Ogawa, Bull. Chem. Soc. Jpn., 76, 689 (2003).
9. a) K. Ogawa, T. Zhang, K. Yoshihara, and Y. Kobuke, J. Am. Chem. Soc., 124, 22 (2002).
10. Other systems based on porphyrin wires are also reported: b) S. M. Kuebler, R. G. Denning, and H. L. Anderson, J. Am. Chem. Soc., 122, 339 (2000).
11. c) T. E. O. Screen, J. R. G. Thorne, R. G. Denning, D. G. Bucknall, and H. L. Anderson, J. Am. Chem. Soc., 124, 9712 (2002).
12. R. Takahashi and Y. Kobuke, J. Am. Chem. Soc., 125, 2372 (2003).
13. a) A. Nomoto and Y. Kobuke, Chem. Commun., 2002, 1104.
14. b) A. Nomoto, H. Mitsuoka, H. Ozeki, and Y. Kobuke, Chem. Commun., 2003, 1074.
15. Review: T. M. Trnka and R. H. Grubbs, Acc. Chem. Res., 34, 18 (2001).
16. Supplied from Molecular Simulation Inc. Version 4.6 and "Universal" parameters were used.
17. J. Otera, N. Danoh, and H. Nozaki, J. Org. Chem., 56, 5307 (1991).
18. a) C. W. Lee and R. H. Grubbs, Org. Lett., 2, 2145 (2000).
19. b) D. Meng, D.-S. Su, A. Balog, P. Bertinato, E. J. Sorensen, S. J. Danishefsky, Y.-H. Zheng, T.-C. Chou, L. He, and S. B. Horwitz, J. Am. Chem. Soc., 119, 2733 (1997).
20. A. J. Phillips and A. D. Abell, Aldrichimica Acta, 32, 75 (1999).
21. P. M. Gannett, D. L. Nagel, P. J. Reilly, T. Lawson, J. Sharpe, and B. Toth, J. Org. Chem., 53, 1064 (1988).
22. R. W. Hoffmann and I. Muenster, Liebigs Ann. Recl., 1997, 1143.