Redox chemistry of a dimanganese(II,III) complex with an unsymmetric ligand: Water binding, deprotonation and accumulative light-induced oxidation

European Journal of Inorganic Chemistry

Volumn , Issue 24, 2006, Pages 5033-5047

  Anderlund, Magnus F ^a   Högblom, Joakim ^b   Shi, Wei ^a   Huang, Ping ^a   Eriksson, Lars ^c   Weihe, Högni ^d   Styring, Stenbjörn ^a   Åkermark, Björn ^c   Lomoth, Reiner ^a   Magnuson, Ann ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b LUND UNIVERSITY   (Sweden)

^c STOCKHOLM UNIVERSITY   (Sweden)

^d UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Bioinorganic chemistry; EPR spectroscopy; IR spectroscopy; Ligand exchange; Manganese

Indexed keywords

BINARY ALLOYS; BIOCHEMISTRY; ELECTRON SPIN RESONANCE SPECTROSCOPY; ELECTRON TRANSITIONS; MANGANESE COMPOUNDS; OXIDATION; PARAMAGNETIC RESONANCE; SPECTROELECTROCHEMISTRY; ULTRAVIOLET VISIBLE SPECTROSCOPY;

BIOINORGANIC CHEMISTRY; DINUCLEAR MANGANESE COMPLEX; EPR SPECTROSCOPY; INDUCED OXIDATIONS; IR-SPECTROSCOPY; LIGAND EXCHANGES; LIGHT-INDUCED; REDOX CHEMISTRY; SYNTHESISED; WATER BINDING;

LIGANDS;

EID: 33845897085     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200600676     Document Type: Article

References (80)

1. IR spectroelectrochemistry of 5: a) J. H. Alstrum-Acevedo, M. Kyle Brennaman, T. J. Meyer, Inorg. Chem. 2005, 44, 6802-6827;
2. b) S. Chakraborty, T. J. Wadas, H. Hester, R. Schmehl, R. Eisenberg, Inorg. Chem. 2005, 44, 6865-6878.
3. a) J. H. A. Nugent (Ed.), Special Issue on Photosynthetic Water Oxidation, BBA-Bioenergetics, Elsevier, Amsterdam, 2001, p. 1503;
4. b) J. Barber, BBA-Bioenergetics 2004, 1655, 123-132.
5. a) B. A. Diner, G. T. Babcock, in Oxygenic Photosynthesis: The Light Reactions (Eds.: D. R. Ort, C. F. Yocum), Kluwer Academic Publishers, Dordrecht, 1996, pp. 213-247;
6. b) J. Barber, Curr. Opin. Struct. Biol. 2002, 12, 523-530;
7. c) R. D. Britt, in Oxygenic Photosynthesis: The Light Reactions (Eds.: D. R. Ort, C. F. Yocum), Kluwer Academic Publishers, Dordrecht, 1996, pp. 137-164.
8. a) K. N. Ferreira, T. M. Iverson, K. Maglaoui, J. Barber, S. Iwata, Science 2004, 303, 1831-1838;
9. b) B. Loll, J. Kern, W. Saenger, A. Zouni. J. Biesiadka, Nature 2005, 438, 1040-1044.
10. W. C. Hoganson, G. T. Babcock, Science 1997, 277, 1953-1956.
11. a) B. Kok, B. Forbush, M. McGloin, Photochem. Photobiol. 1970, 11, 457-475;
12. b) B. Forbush, B. Kok, M. McGloin, Photochem. Photobiol. 1971, 14, 307-321.
13. M. Haumann, P. Liebisch, C. Müller, M. Barra, M. Grabolle, H. Dau, Science 2005, 310, 1019-1021.
14. a) S. Mukhopadhyay, S. K. Mandal, S. Bhaduri, W. H. Armstrong, Chem. Rev. 2004, 104, 3981-4026;
15. b) J. H. Robblee, R. M. Cinco, V. K. Yachandra, BBA-Bioenergetics 2001, 1503, 7-23;
16. c) H. Dau, L. Iuzzolino, J. Dittmer, BBA-Bioenergetics 2001, 1503, 24-39;
17. d) D. Kuzek, R. J. Pace, BBA-Bioenergetics 2001, 1503, 123-137.
18. M. Haumann, C. Müller, P. Liebisch, L. Iuzzolino, J. Dittmer, M. Grabolle, T. Neisius, W. Meyer-Klaucke, H. Dau, Biochemistry 2005, 44, 1894-1908.
19. a) Y. Naruta, M. Sasayama, T. Sasaki, Angew. Chem. Int. Ed. Engl. 1994, 33, 1839-1841;
20. b) M. Watkinson, A. Whiting, C. A. McAuliffe, J. Chem. Soc., Chem. Commun. 1994, 18, 2141-2142;
21. c) W. Ruettinger, M. Yagi, K. Wolf, S. Bernasek, G. C. Dismukes, J. Am. Chem. Soc. 2000, 122, 10353-10357.
22. a) J. Limburg, J. S. Vrettos, L. M. Liable-Sands, A. C. Rheingold, R. H. Crabtree, G. W. Brudvig, Science 1999, 283, 1524-1527;
23. b) A. K. Poulsen, A. Rompel, C. J. McKenzie, Angew. Chem. Int. Ed. 2005, 44, 6916-6920.
24. a) L. Sun, H. Berglund, R. Davydov, T. Norrby, L. Hammarström, P. Korall, A. Börje, C. Philouze, K. Berg, A. Tran, M. Andersson, G. Stenhagen, J. Mårtensson, M. Almgren, S. Styring, B. Åkermark, J. Am. Chem. Soc. 1997, 119, 6996-7004;
25. b) A. Magnuson, Y. Frapart, M. Abrahamsson, O. Horner, B. Åkermark, L. Sun, J.-J. Girerd, L. Hammarström, S. Styring, J. Am. Chem. Soc. 1999, 121, 89-96;
26. c) L. Sun, L. Hammarström, B. Åkermark, S. Styring, Chem. Soc. Rev. 2001, 30, 36-49.
27. L. Sun, M. Raymond, A. Magnuson, D. LeGourrierec, M. Tamm, M. Abrahamsson, P. Huang Kenéz, J. Mårtensson, G. Stenhagen, L. Hammarström, S. Styring, S. Åkermark, J. Inorg. Biochem. 2000, 78, 15-22.
28. M. Borgström, N. Shaikh, O. Johansson, M. F. Anderlund, S. Styring, B. Åkermark, A. Magnuson, L. Hammarström, J. Am. Chem. Soc. 2005, 127, 17504-17515.
29. a) I. Vass, S. Styring, Biochemistry 1991, 30, 830-839;
30. b) C. Tommos, G. T. Babcock, BBA-Bioenergetics 2000, 1458, 199-219;
31. c) P. Geijer, F. Morvaridi, S. Styring, Biochemistry 2001, 40, 10881-10891;
32. d) R. Radmer, G. Cheniae, Top. Photosynthesis 1977, 2, 303-348.
33. a) bpmp = 2,6-bis{[N,N-bis(2-pyridinemethyl)amino]methyl}-4-methylphenol;
34. b) H. Diril, H. R. Chang, M. J. Nilges, X. H. Zhang, J. A. Potenza, H. J. Schugar, S. S. Isied, D. N. Hendrickson, J. Am. Chem. Soc. 1989, 111, 5102-5114.
35. P. Huang, A. Magnuson, R. Lomoth, M. Abrahamsson, M. Tamm, L. Sun, B. van Rotterdam, J. Park, L. Hammarström, B. Åkermark, S. Styring, J. Inorg. Biochem. 2002, 91, 159-172.
36. G. Eilers, C. Zettersten, L. Nyholm, L. Hammarström, R. Lomoth, Dalton Trans. 2005, 1033-1041.
37. P. Huang, J. Högblom, M. F. Anderlund, L. Sun, A. Magnuson, S. Styring, J. Inorg. Biochem. 2004, 98, 733-745.
38. bpy = 2,2-bipyridine.
39. a) bhpp = 2,6-bis{[(2-hydroxy-3,5-di-tert-butylbenzyl)(2- pyridylmethyl)amino]methyl}-4-methylphenol;
40. b) R. Lomoth, P. Huang, J. Zheng, L. Sun, L. Hammarström, B. Åkermark, S. Styring, Eur. J. Inorg. Chem. 2002, 2965-2974.
41. C. Higushi, H. Sakiyama, H. Okawa, R. Isobe, D. E. Fenton, J. Chem. Soc., Dalton Trans. 1994, 7, 1097-1103.
42. B. C. Dave, R. S. Czernuszewicz, Inorg. Chim. Acta 1998, 281, 25-35.
43. P. Karsten, A. Neves, A. J. Bortoluzzi, J. Strahle, C. Maichle-Mossmer, Inorg. Chem. Commun. 2002, 5, 434-438.
44. a) L. Dubois, D.-F. Xiang, X.-S. Tan, J. Pécault, P. Jones, S. Baudron, L. LePape, J.-M. Latour, C. Baffert, S. Chardon-Noblat, M.-N. Collomb, A. Deronzier, Inorg. Chem. 2003, 42, 750-760;
45. b) L. Dubois, R. Caspar, L. Jacquamet, P.-E. Petit, M. F. Charlot, C. Baffert, M.-N. Collomb, A. Deronzier, J.-M. Latour, Inorg. Chem. 2003, 42, 4817-4827.
46. a) C. Fraser, L. Johnston, A. L. Rheingold, B. S. Haggerty, J. K. Williams, J. Whelan, B. Bosnich, Inorg. Chem. 1992, 31, 1835-1844;
47. b) R. Hutzelmann, K. Wieghardt, U. Florke, H. J. Haupt, D. C. Weatherburn, J. Bonvoisin, G. Blondin, J.-J. Girerd, J. Am. Chem. Soc. 1992, 114, 1681-1696;
48. c) P. Karsten, A. Neves, A. J. Bortoluzzi, M. Lanznaster, V. Drago, Inorg. Chem. 2002, 41, 4624-4626.
49. E. Lambert, B. Chabut, S. Chardon-Noblat, A. Deronzier, G. Chottard, A. Bousseksou, J. Tuchagues, J. Laugier, M. Bardet, J. M. Latour, J. Am. Chem. Soc. 1997, 119, 9424-9437.
50. M. Lubben, B. L. Feringa, J. Org. Chem. 1994, 59, 2227-2233.
51. I. D. Brown, D. Altermatt, Acta Crystalhgr., Sect. B: Struct. Sci. 1985, 41, 244-247.
52. a) R. M. Buchanan, K. J. Oberhausen, J. F. Richardson, Inorg. Chem. 1988, 27, 971-973;
53. b) H.-R. Chang, S. K. Larsen, P. D. W. Boyd, C. G. Pierpont, D. N. Hendrickson, J. Am. Chem. Soc. 1988, 110, 4565-4576.
54. H. Diril, H.-R. Chang, X. Zhang, S. K. Larsen, J. A. Potenza, C. G. Pierpont, H. J. Schugar, S. S. Isied, D. N. Hendrickson, J. Am. Chem. Soc. 1987, 109, 6207-6208.
55. G. Aromi, J. Telser, A. Ozarowski, L.-C. Brunel, H.-M. Stoeckli-Evans, J. Krzystek, Inorg. Chem. 2005, 44, 187-196.
56. a) S. R. Cooper, G. C. Dismukes, M. P. Klein, M. Calvin, J. Am. Chem. Soc. 1978, 100, 7248-7252;
57. b) M. Zheng, S. V. Khangulov, G. C. Dismukes, V. V. Barynin, Inorg. Chem. 1994, 33, 382-387;
58. c) J. S. Bashkin, A. R. Schake, J. B. Vincent, H.-R. Chang, Q. Li, J. C. Huffman, G. Christou, D. N. Hendrickson, J. Chem. Soc., Chem. Commun. 1988, 11, 700-702;
59. d) G. C. Dismukes, J. E. Sheats, J. A. Smegal, J. Am. Chem. Soc. 1987, 109, 7202-7203.
60. P. Huang, N. Shaikh, M. Anderlund, S. Styring, L. Hammarström, J. Inorg. Biochem. 2006, 100, 1139-1146.
61. -1 for manganese 1 and 2 respectively.
62. +/0 in acetonitrile (1.27 V vs. NHE in water). Potentials in nonaqueous solvents are frequently measured and reported versus the aqueous SCE. This introduces unknown junction potentials, however, and a comparison of such data with potentials obtained in other solvents like water is not meaningful even if the potentials are formally given versus the same reference electrode like SCE or NHE. Independent of this problem, electrochemical potentials are intrinsically solvent dependent and any comparison between data in different solvents can only be approximate;
63. b) I. Rubinstein, A. J. Bard, J. Am. Chem. Soc. 1981, 103, 512-516.
64. Electrolysis at 0.92 V appears to be a multielectron process presumably because of the oxidation of degradation products.
65. R. A. Marcus, J. Chem. Phys. 1965, 43, 679-701.
66. 2 - 1/ε) where r ≈ 5 Å is the molecular radius and R(≥2r) is the distance between the molecule and its image charge;
67. b) A. J. Bard, L. R. Faulkner, in Electrochemical Methods: Fundamentals and Applications, 2nd ed., Wiley, New York, 2001.
68. M. L. A. Abrahamsson, H. Berglund Baudin, A. Tran, C. Philouze, K. E. Berg, M. K. Raymond-Johansson, L. Sun, B. Åkermark, S. Styring, L. Hammarström, Inorg. Chem. 2002, 41, 1534-1544.
69. a) P. J. Pessiki, S. V. Khangulov, G. C. Dismukes, J. Am. Chem. Soc. 1994, 116, 891-897;
70. b) S. V. Khangulov, P. J. Pessiki, V. V. Barynin, D. E. Ash, G. C. Dismukes, Biochemistry 1995, 34, 2015-2025;
71. c) T. Howard, J. Telser, V. J. DeRose, Inorg. Chem. 2000, 39, 3379-3385;
72. d) S. Blanchard, G. Blondin, E. Rivière, M. Nierlich, J.-J. Girerd, Inorg. Chem. 2003, 42, 4568-4578.
73. K.-O. Schäfer, R. Bittl, W. Zweygart, F. Lendzian, G. Haselhorst, T. Weyhermüller, K. Wieghardt, W. Lubitz, J. Am. Chem. Soc. 1998, 120, 13104-13120.
74. 2 was not observed by visual inspection but cannot be excluded.
75. a) J. E. Sheats, R. S. Czernuszewitcz, G. C. Dismukes, A. L. Rheingold, V. Petrouleas, J.-A. Stubbe, W. H. Armstrong, R. H. Beer, S. J. Lippard, J. Am. Chem. Soc. 1987, 109, 1435-1444;
76. b) E. M. Boelrijk, S. V. Khangulov, C. G. Dismukes, Inorg. Chem. 2000, 39, 3009-3019.
77. J. Limburg, J. S. Vrettos, H. Chen, J. C. de Paula, R. H. Crabtree, G. W. Brudvig, J. Am. Chem. Soc. 2001, 123, 423-430.
78. G. M. Sheldrick, Acta Crystallogr., Sect. A: Found. Crystallogr. 1990, 46, 467-473.
79. G. M. Sheldrick, Computer Program for the Refinement of Crystal Structures, University of Göttingen, 1997.
80. R. Manchanda, G. W. Brudvig, R. H. Crabtree, New J. Chem. 1994, 18, 561-568.