Meso-trialkyl-substituted subporphyrins

Angewandte Chemie - International Edition

Volumn 49, Issue 2, 2010, Pages 321-324

  Hayashi, Shin Ya ^a   Inokuma, Yasuhide ^a   Easwaramoorthi, Shanmugam ^b   Kim, Kil Suk ^b   Kim, Dongho ^b   Osuka, Atsuhiro ^a  

^a KYOTO UNIVERSITY   (Japan)

^b Yonsei University   (South Korea)

Author keywords

Desulfurlzation; Fluorescence; Macrocycles; Porphyrinoids

Indexed keywords

ALKYL SUBSTITUENT; BENZYLIC; CHEMICAL EQUATIONS; MACROCYCLES; PORPHYRINOIDS;

CHEMICAL REACTIONS; DESULFURIZATION; FLUORESCENCE; OPTICAL PROPERTIES;

ELECTROCHEMICAL PROPERTIES;

EID: 73349117510     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200906005     Document Type: Article

References (21)

1. a) Y. Inokuma, A. Osuka, Dalton Trans. 2008, 2517-2526;
2. b) Y. Inokuma, J. H. Kwon, T. K. Ahn, M.-C. Yoon, D. Kim, A. Osuka, Angew. Chem. 2006, 118, 975-978;
3. Angew. Chem. Int. Ed. 2006, 45, 961-964;
4. c) E. Tsurumaki, S. Saito, K. S. Kim, J. M. Lim, Y. Inokuma, D. Kim, A. Osuka, J. Am. Chem. Soc. 2008, 130, 438-439.
5. a) N. Kobayashi, Y. Takeuchi, A. Matsuda, Angew. Chem. 2007, 119, 772-774;
6. Angew. Chem. Int. Ed. 2007, 46, 758-760;
7. b) Y. Takeuchi, A. Matsuda, N. Kobayashi, J. Am. Chem. Soc. 2007, 129, 8271-8281.
8. a) T. Torres, Angew. Chem. 2006, 118, 2900-2903;
9. Angew. Chem. Int. Ed. 2006, 45, 2834-2837;
10. b) R. Myśliborski, L. LatosGrazyński, L. Sztrenberg, T. Lis, Angew. Chem. 2006, 118, 3152-3156;
11. Angew. Chem. Int. Ed. 2006, 45, 3670-3674.
12. a) Y. Inokuma, Z. S. Yoon, D. Kim, A. Osuka, J. Am. Chem. Soc. 2007, 129, 4747-4761;
13. b) Y. Inokuma, S. Easwaramoorthi, S. Y. Jang, K. S. Kim, D. Kim, A. Osuka, Angew. Chem. 2008, 120, 4918-4921;
14. Angew. Chem. Int. Ed. 2008, 47, 4840-4843;
15. c) Y. Inokuma, S. Easwaramoorthi, Z. S. Yoon, D. Kim, A. Osuka, J. Am. Chem. Soc. 2008, 130, 12234-12235.
16. a) P. Rothemund, J. Am. Chem. Soc. 1935, 57, 2010-2011;
17. b) P. Rothemund, J. Am. Chem. Soc. 1936, 58, 625-627.
18. α atoms.
19. M. Nagai, H. Urimoto, K. Uetake, N. Sakikawa, R. D. Gonzalez, Bull. Chem. Soc. Jpn. 1989, 62, 557-562.
20. 3 indicated three peaks at δ = -15.0, -12.1, and -7.9 ppm, which were assigned for 2b, meso-tripentylsubchlorin, and meso-tripentylbacteriosubchlorin, respectively. The reduction products distribution varied depending on the activity of catalyst and reaction time (see the Supporting Information).
21. A. P. Kozikowski, W. Tückmantel, Y. Hu, J. Org. Chem. 2001, 66, 1287-1296.