An unprecedented iron(III) complex supported by an asymmetric N-capped tripodal ligand incorporating the NO2S donor set

Inorganica Chimica Acta

Volumn 363, Issue 6, 2010, Pages 1297-1300

  Tong, Lok H ^a,b   Wong, Yee Lok ^a   Pascu, Sofia I ^c   Dilworth, Jonathan R ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF GENEVA   (Switzerland)

^c University of Bath   (United Kingdom)

Author keywords

Asymmetric tripodal ligand; Crystal structure; Iron(III) complex

Indexed keywords

CHELATION; CRYSTAL STRUCTURE; LIGANDS; X RAY CRYSTALLOGRAPHY;

1-METHYLIMIDAZOLE; BIPYRAMIDAL GEOMETRIES; COORDINATION ENVIRONMENT; DONOR SETS; TETRADENTATE LIGANDS; TRIPODAL LIGANDS; X-RAY CRYSTALLOGRAPHIC ANALYSIS;

IRON COMPOUNDS;

EID: 77949487265     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2009.09.010     Document Type: Article

References (46)

1. For phosphyl transfer enzymes, see:. Chandrasekaran A., Timosheva N.V., Day R.O., and Holmes R.R. Inorg. Chem. 42 (2003) 3285
2. Timosheva N.V., Chandrasekaran A., and Holmes R.R. Inorg. Chem. 43 (2004) 7403
3. For vanadium haloperoxidase, see:. Colpas G.J., Hamstra B.J., Kampf J.W., and Pecoraro V.L. J. Am. Chem. Soc. 118 (1996) 3469
4. Hamstra B.J., Houseman A.L.P., Colpas G.J., Kampf J.W., LoBrutto R., Frasch W.D., and Pecoraro V.L. Inorg. Chem. 36 (1997) 4866
5. Schneider C.J., Penner-Hahn J.E., and Pecoraro V.L. J. Am. Chem. Soc. 130 (2008) 2712
6. A recent review on nitrogen fixation using triamidoamine ligands, see:. Schrock R.R. Angew. Chem., Int. Ed. 47 (2008) 5512
7. For polymerisation catalysts, see:. Schrodi Y., Schrock R.R., and Bonitatebus Jr. P.J. Organometallics 20 (2001) 3560
8. Michalczyk L., de Gala S., and Bruno J.W. Organometallics 20 (2001) 5547
9. Kim Y., Kapoor P.N., and Verkade J.G. Inorg. Chem. 41 (2002) 4834
10. Kim Y., and Verkade J.G. Organometallics 21 (2002) 2395
11. Kim Y., Jnaneshwara G.K., and Verkade J.G. Inorg. Chem. 42 (2003) 1437
12. Bull S.D., Davidson M.G., Johnson A.L., Robinson D.E.J.E., and Mahon M.F. Chem. Commun. (2003) 1750
13. Redshaw C., Rowan M.A., Homden D.M., Dale S.H., Elsegood M.R.J., Matsui S., and Matsuura S. Chem. Commun. (2006) 3329
14. Gendler S., Segal S., Goldberg I., Goldschmidt Z., and Kol M. Inorg. Chem. 45 (2006) 4783
15. Chmura A.J., Chuck C.J., Davidson M.G., Jones M.D., Lunn M.D., Bull S.D., and Mahon M.F. Angew. Chem., Int. Ed. 46 (2007) 2280
16. For other types of catalysis, see:. Kirillov A.M., Haukka M., Kirillova M.V., and Pombeiro A.J.L. Adv. Synth. Catal. 347 (2005) 1435
17. Chen J., and Woo L.K. J. Organomet. Chem. 601 (2000) 57
18. Waterman R. Organometallics 26 (2007) 2492
19. Franczyk T.S., Czerwinski K.R., and Raymond K.N. J. Am. Chem. Soc. 114 (1992) 8138
20. Chuang C.-L., dos Santos O., Xu X., and Canary J.W. Inorg. Chem. 36 (1997) 967
21. Tobey S.L., Jones B.D., and Anslyn E.V. J. Am. Chem. Soc. 125 (2003) 4026
22. Brennan B.A., Alms G., Nelson M.J., Durney L.T., and Scarrow R.C. J. Am. Chem. Soc. 118 (1996) 9194
23. Scarrow R.C., Strickler B.S., Ellison J.J., Shoner S.C., Kovacs J.A., Cummings J.G., and Nelson M.J. J. Am. Chem. Soc. 120 (1998) 9237
24. Heinrich L., Li Y., Vaissermann J., Chottard G., and Chottard J.-C. Angew. Chem., Int. Ed. 38 (1999) 3526
25. Werth M.T., Tang S.-F., Formicka G., Zeppezauer M., and Johnson M.K. Inorg. Chem. 34 (1995) 218
26. Cornman C.R., Jantzi K.L., Wirgau J.I., Stauffer T.C., Kampf J.W., and Boyle P.D. Inorg. Chem. 37 (1998) 5851
27. Ochs C., Hahn F.E., and Fröhlich R. Chem. Eur. J. 6 (2000) 2193
28. Rosa D.T., Krause Bauer J.A., and Baldwin M.J. Inorg. Chem. 40 (2001) 1606
29. Hahn F.E., Ochs C., Lügger T., and Fröhlich R. Inorg. Chem. 43 (2004) 6101
30. Wong Y.-L., Cowley A.R., and Dilworth J.R. Inorg. Chim. Acta 357 (2004) 4358
31. Cornman C.R., Stauffer T.C., and Boyle P.D. J. Am. Chem. Soc. 119 (1997) 5986
32. Jang H.G., Cox D.D., and Que Jr. L. J. Am. Chem. Soc. 113 (1991) 9200
33. Jo D.-H., Chiou Y.-M., and Que Jr. L. Inorg. Chem. 40 (2001) 3181
34. Rodriguez M.-C., Morgenstern-Badarau I., Cesario M., Guilhem J., Keita B., and Nadjo L. Inorg. Chem. 35 (1996) 7804
35. Viswanathan R., Palaniandavar M., Balasubramanian T., and Muthiah T.P. Inorg. Chem. 37 (1998) 2943
36. Velusamy M., Mayilmurugan R., and Palaniandavar M. Inorg. Chem. 43 (2004) 6284
37. Li F., Wang M., Li P., Zhang T., and Sun L. Inorg. Chem. 46 (2007) 9364
38. Ogo S., Wada S., Watanabe Y., Iwase M., Wada A., Harata M., Jitsukawa K., Masuda H., and Einaga H. Angew. Chem., Int. Ed. 37 (1998) 2102
39. Ogo S., Yamahara R., Roach M., Suenobu T., Aki M., Ogura T., Kitagawa T., Masuda H., Fukuzumi S., and Watanabe Y. Inorg. Chem. 41 (2002) 5513
40. Hsu H.-F., Dong Y., Shu L., Young Jr. V.G., and Que Jr. L. J. Am. Chem. Soc. 121 (1999) 5230
41. Tong L.H., Wong Y.-L., Pascu S.I., and Dilworth J.R. Dalton Trans. (2008) 4784
42. Tyler L.A., Noveron J.C., Olmstead M.M., and Mascharak P.K. Inorg. Chem. 39 (2000) 357
43. Otwinowski Z., and Minor W. In: Carter C.W., and Sweet R.M. (Eds). Processing of X-ray Diffraction Data Collected in Oscillation Mode. Methods Enzymology vol. 276 (1997), Academic Press, New York
44. Altomare A., Cascarano G., Giacovazzo G., Guagliardi A., Burla M.C., Polidori G., and Camalli M. J. Appl. Crystallogr. 27 (1994) 435
45. D.J. Watkin, C.K. Prout, J.R. Carruthers, P.W. Betteridge, R.I. Cooper, Crystals, Issue 11, Chemical Crystallography Laboratory, University of Oxford, 2001.
46. Bashkin J.S., Huffman J.C., and Christou G. J. Am. Chem. Soc. 108 (1986) 5038