Nickel(II) complexes of tpa ligands with 6-phenyl substituents (Ph ntpa). Structure and H2O2-reactivity

Bulletin of the Chemical Society of Japan

Volumn 83, Issue 5, 2010, Pages 530-538

  Tano, Tetsuro ^a   Doi, Yoshitaka ^b   Inosako, Masayuki ^b   Kunishita, Atsushi ^a   Kubo, Minoru ^c   Ishimaru, Hirohito ^c   Ogura, Takashi ^c   Sugimoto, Hideki ^a   Itoh, Shinobu ^a,d  

^a OSAKA UNIVERSITY   (Japan)

^b Osaka Prefecture University   (Japan)

^c UNIVERSITY OF HYOGO   (Japan)

^d INSTITUTE FOR MOLECULAR SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROXYLATION; BIPYRAMIDAL STRUCTURES; DECOMPOSITION PROCESS; DONOR GROUPS; HIGH-SPIN GROUND STATE; LIGAND SUBSTITUENTS; LOW TEMPERATURES; METHYL AMINE; NICKEL COMPLEX; OCTAHEDRAL GEOMETRY; PHENYL SUBSTITUENTS; REDOX POTENTIALS;

HYDROXYLATION; NICKEL; NICKEL ALLOYS; NICKEL COMPOUNDS; REDOX REACTIONS;

LIGANDS;

EID: 77952365423     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.20090346     Document Type: Article

References (45)

1. L. M. Berreau, Comments Inorg. Chem. 2007, 28, 123.
2. G. K. Ingle, R. W. Watkins, A. M. Arif, L. M. Berreau, J. Coord. Chem. 2008, 61, 61.
3. A. G. Blackman, Eur. J. Inorg. Chem. 2008, 2633.
4. K. D. Karlin, S. Kaderli, A. D. Zuberbühler, Acc. Chem. Res. 1997, 30, 139.
5. M.-A. Kope, K. D. Karlin, in Biomimetic Oxidations Catalyzed by Transition Metal Complexes, ed. by B. Meunier, Imperial College Press, London, 2000, pp. 309362.
6. L. Q. Hatcher, K. D. Karlin, J. Biol. Inorg. Chem. 2004, 9, 669.
7. M. Costas, M. P. Mehn, M. P. Jensen, L. Que, Jr., Chem. Rev. 2004, 104, 939.
8. X. Shan, L. Que, Jr., J. Inorg. Biochem. 2006, 100, 421.
9. L. Que, Jr., Acc. Chem. Res. 2007, 40, 493.
10. M. Suzuki, Acc. Chem. Res. 2007, 40, 609.
11. S. Yamaguchi, H. Masuda, Sci. Technol. Adv. Mater. 2005, 6, 34.
12. E. Y. Tshuva, S. J. Lippard, Chem. Rev. 2004, 104, 987.
13. L.M.Mirica, X. Ottenwaelder, T. D. P. Stack, Chem. Rev. 2004, 104, 1013.
14. E. A. Lewis, W. B. Tolman, Chem. Rev. 2004, 104, 1047.
15. C.-L. Chuang, K. T. Lim, Q. Chen, J. Zubieta, J. W. Canary, Inorg. Chem. 1995, 34, 2562.
16. C.-L. Chuang, K. Lim, J. W. Canary, Supramol. Chem. 1995, 5, 39.
17. D. Maiti, H. R. Lucas, A. A. N. Sarjeant, K. D. Karlin, J. Am. Chem. Soc. 2007, 129, 6998.
18. A. Kunishita, M. Kubo, H. Ishimaru, T. Ogura, H. Sugimoto, S. Itoh, Inorg. Chem. 2008, 47, 12032.
19. T. Fujii, A. Naito, S. Yamaguchi, A. Wada, Y. Funahashi, K. Jitsukawa, S. Nagatomo, T. Kitagawa, H. Masuda, Chem. Commun. 2003, 2700.
20. S. Hikichi, M. Yoshizawa, Y. Sasakura, M. Akita, Y. Moro-oka, J. Am. Chem. Soc. 1998, 120, 10567.
21. S. Itoh, H. Bandoh, S. Nagatomo, T. Kitagawa, S. Fukuzumi, J. Am. Chem. Soc. 1999, 121, 8945.
22. K. Shiren, S. Ogo, S. Fujinami, H. Hayashi, M. Suzuki, A. Uehara, Y. Watanabe, Y. Moro-oka, J. Am. Chem. Soc. 2000, 122, 254.
23. B. S. Mandimutsira, J. L. Yamarik, T. C. Brunold, W. Gu, S. P. Cramer, C. G. Riordan, J. Am. Chem. Soc. 2001, 123, 9194.
24. S. Itoh, H. Bandoh, M. Nakagawa, S. Nagatomo, T. Kitagawa, K. D. Karlin, S. Fukuzumi, J. Am. Chem. Soc. 2001, 123, 11168.
25. R. Schenker, B. S. Mandimutsira, C. G. Riordan, T. C. Brunold, J. Am. Chem. Soc. 2002, 124, 13842.
26. S. Yao, E. Bill, C. Milsmann, K. Wieghardt, M. Driess, Angew. Chem., Int. Ed. 2008, 47, 7110.
27. K. Fujita, R. Schenker, W. Gu, T. C. Brunold, S. P. Cramer, C. G. Riordan, Inorg. Chem. 2004, 43, 3324.
28. M. T. Kieber-Emmons, R. Schenker, G. P. A. Yap, T. C. Brunold, C. G. Riordan, Angew. Chem., Int. Ed. 2004, 43, 6716.
29. R. Schenker, M. T. Kieber-Emmons, C. G. Riordan, T. C. Brunold, Inorg. Chem. 2005, 44, 1752.
30. M. T. Kieber-Emmons, J. Annaraj, M. S. Seo, K. M. V. Heuvelen, T. Tosha, T. Kitagawa, T. C. Brunold, W. Nam, C. G. Riordan, J. Am. Chem. Soc. 2006, 128, 14230.
31. J. Cho, R. Sarangi, J. Annaraj, S. Y. Kim, M. Kubo, T. Ogura, E. I. Solomon, W. Nam, Nat. Chem. 2009, 1, 568.
32. S. Hikichi, H. Okuda, Y. Ohzu, M. Akita, Angew. Chem., Int. Ed. 2009, 48, 188.
33. W. L. F. Armarego, D. D. Perrin, Purification of Laboratory Chemicals, 4th ed., Butterworth-Heinemann, Oxford, 1996.
34. Z. Tyeklár, R. R. Jacobson, N. Wei, N. N. Murthy, J. Zubieta, K. D. Karlin, J. Am. Chem. Soc. 1993, 115, 2677.
35. M. P. Jensen, E. L. Que, X. Shan, E. Rybak-Akimova, L. Que, Jr., Dalton Trans. 2006, 3523.
36. M. M. Makowska-Grzyska, E. Szajna, C. Shipley, A. M. Arif, M. H. Mitchell, J. A. Halfen, L. M. Berreau, Inorg. Chem. 2003, 42, 7472.
37. M. Ito, K. Sakai, T. Tsubomura, Y. Takita, Bull. Chem. Soc. Jpn. 1999, 72, 239.
38. SIR92: A. Altomare, G. Cascarano, C. Giacovazzo, A. Guagliardi, M. C. Burla, G. Polidori, M. Camalli, J. Appl. Crystallogr. 1994, 27, 435.
39. Crystal Structure: Crystal Structure Analysis Package version 3.8.1, Molecular Structure Corp. and Rigaku Corp., 2005.
40. E. Szajna, P. Dobrowolski, A. L. Fuller, A. M. Arif, L. M. Berreau, Inorg. Chem. 2004, 43, 3988.
41. L. Que, Jr., W. B. Tolman, Angew. Chem., Int. Ed. 2002, 41, 1114.
42. 16O was unsuccessful.
43. A. Kunishita, Y. Doi, M. Kubo, T. Ogura, H. Sugimoto, S. Itoh, Inorg. Chem. 2009, 48, 4997.
44. K. Honda, J. Cho, T. Matsumoto, J. Roh, H. Furutachi, T. Tosha, M. Kubo, S. Fujinami, T. Ogura, T. Kitagawa, M. Suzuki, Angew. Chem., Int. Ed. 2009, 48, 3304.
45. S. Itoh, Curr. Opin. Chem. Biol. 2006, 10, 115.