Variable coordination modes of benzaldehyde thiosemicarbazones - Synthesis, structure, and electrochemical properties of some ruthenium complexes

European Journal of Inorganic Chemistry

Volumn , Issue 29, 2008, Pages 4538-4546

  Dutta, Swati ^a   Basuli, Falguni ^a   Castineiras, Alfonso ^b   Peng, Shie Ming ^c   Lee, Gene Hsiang ^c   Bhattacharya, Samaresh ^a  

^a JADAVPUR UNIVERSITY   (India)

^b UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^c NATIONAL TAIWAN UNIVERSITY   (Taiwan)

Author keywords

Coordination modes; N ligands; Ruthenium; S ligands; Thiosemicarbazones

Indexed keywords

AMINES; CHELATION; CHLORINE COMPOUNDS; CRYSTAL STRUCTURE; CYCLIC VOLTAMMETRY; LIGANDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHENOLS; SYNTHESIS (CHEMICAL);

COORDINATION MODES; CRYSTALS STRUCTURES; DIMERIC COMPLEXES; MONOMERIC COMPLEXES; N LIGANDS; N-LIGANDS; N-S DONORS; S LIGANDS; S-DONOR LIGANDS; THIOSEMICARBAZONES;

RUTHENIUM COMPOUNDS;

EID: 54249090712     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200800547     Document Type: Article

References (72)

1. a) M. J. M. Campbell, Coord. Chem. Rev. 1975, 15, 279;
2. b) S. B. Padhye, G. B. Kaffman, Coord. Chem. Rev. 1985, 63, 127;
3. c) I. Haiduc, C. Silvestru, Coord. Chem. Rev. 1990, 99, 253;
4. d) D. X. West, S. B. Padhye, P. B. Sonawane, Struct. Bonding (Berlin) 1992, 76, 1;
5. e) D. X. West, A. E. Liberta, S. B. Padhye, R. C. Chikate, P. B. Sonawane, A. S. Kumbhar, R. G. Yerande, Coord. Chem. Rev. 1993, 123, 49.
6. a) F. A. French, E. Blanz Jr, J. Med. Chem. 1970, 13, 1117;
7. b) A. C. Sartorellic, K. C. Agrawal, A. S. Tsiftsoglou, A. C. Moore, Adv. Enz. Reg. 1977, 15, 117;
8. c) K. C. Agrawal, A. C. Sartorelli, Prog. Med. Chem. 1978, 15, 321;
9. d) J. P. Scovill, D. L. Klayman, C. F. Franchino, J. Med. Chem. 1982, 25, 1261;
10. e) A. Kraker, S. Krezoski, J. Schneier, D. Mingel, H. Petering, J. Biol. Chem. 1985, 260, 13710;
11. f) A. E. Liberta, D. X. West, Biometals 1992, 5, 121;
12. g) D. Kovala-Demertzi, A. Domopaulou, M. A. Demertzis, C. P. Raptopoulou, A. Terzis, Polyhedron 1994, 13, 1917;
13. h) A. Papageorgiou, Z. Iakovidou, D. Mourelatos, E. Mioglou, L. Boutis, A. Kotsis, D. Kovala-Demertzi, D. X. Domopoulou, M. A. Demertzis, Anticancer Res. 1997, 17, 247;
14. i) M. C. Miller III, C. N. Stineman, J. R. Vance, D. X. West, I. H. Hall, Anticancer Res. 1998, 18, 4131;
15. j) D. Kovala-Demertzi, J. R. Miller, N. Kourkoumelis, S. K. Hajikakou, M. A. Demertzis, Polyhedron 1999, 18, 1005;
16. k) Z. Iakovidou, A. Papageorgiou, M. A. Demertzis, E. Mioglou, D. Mourelatos, A. Kotsis, P. N. Yadav, D. Kovala-Demertzi, Anticancer Drugs 2001, 12, 65.
17. a) F. Basuli, S. M. Peng, S. Bhattacharya, Inorg. Chem. 1997, 36, 5645;
18. b) F. Basuli, M. Ruf, C. G. Pierpont, S. Bhattacharya, Inorg. Chem. 1998, 37, 613;
19. c) F. Basuli, S. M. Peng, S. Bhattacharya, Inorg. Chem. 2000, 39, 1120;
20. d) I. Pal, F. Basuli, T. C. W. Mak, S. Bhattacharya, Angew. Chem. Int. Ed. 2001, 40, 2923;
21. e) S. Dutta, F. Basuli, S. M. Peng, G. H. Lee, S. Bhattacharya, New J. Chem. 2002, 26, 4623.
22. Y. P. Tion, C. Y. Duan, Z. L. Lu, X. Z. You, H. K. Fun, S. Kandasamy, Polyhedron 1996, 15, 2263.
23. a) A. Castineiras, E. Bermejo, D. X. West, A. K. EI-Sawaf, J. K. Swearingen, Polyhedron 1998, 17, 275;
24. b) A. Castineiras, M. Gil, E. Bermejo, D. X. West, Z. Naturforsch., Teil B 2000, 55, 863;
25. c) E. Bermejo, A. Castineiras, L. J. Ackerman, M. D. Owens, D. X. West, Z. Allg. Anorg. Chem. 2001, 627, 1966;
26. d) C. A. Brown, W. Kaminsky, K. A. Claborn, K. I. Goldberg, D. X. West, J. Brazilian Chem. Soc. 2002, 13, 10;
27. e) D. Mishra, S. Naskar, M. G. B. Drew, S. K. Chattopadhyay, Polyhedron 2005, 24, 1861;
28. f) D. Mishra, S. Naskar, M. G. B. Drew, S. K. Chattopadhyay, Inorg. Chim. Acta 2006, 359, 585;
29. g) T. S. Lobana, G. Bawa, A. Castineiras, R. J. Butcher, B. J. Liaw, C. W. Liu, Polyhedron 2006, 25, 2897.
30. F. Basuli, S. M. Peng, S. Bhattacharya, Inorg. Chem. 2001, 40, 1126.
31. a) J. J. Levison, S. D. Robinson, J. Chem. Soc. A 1970, 2947;
32. b) R. Young, G. Wilkinson, Inorg. Synth. 1977, 17, 79;
33. c) R. F. Winter, F. M. Hornung, Inorg. Chem. 1997, 36, 6197;
34. d) C. S. Yi, S. Y. Yun, I. A. Guzei, Organometallics 2004, 23, 5392;
35. e) T. Li, R. Churlaud, A. J. Lough, K. Abdur-Rashid, R. H. Morris, Organometallics 2004, 23, 6239;
36. f) R. CelenligilCetin, L. A. Watson, C. Guo, B. M. Foxman, O. V. Ozerov, Organometallics 2005, 24, 186.
37. a) S. Bhattacharya, C. G. Pierpont, Inorg. Chem. 1991, 30, 1511;
38. b) M. Menon, A. Pramanik, N. Bag, A. Chakravorty, J. Chem. Soc., Dalton Trans. 1995, 1417;
39. c) A. Pramanik, N. Bag, G. K. Lahiri, A. Chakravorty, J. Chem. Soc., Dalton Trans. 1990, 3823.
40. a) A. C. Skapski, P. G. H. Troughton, Chem. Commun. (London) 1968, 1230;
41. b) M. I. Bruce, J. Howard, I. W. Nowell, G. Shaw, P. Woodward, J. Chem. Soc., Chem. Commun. 1972, 1041;
42. c) L. D. Brown, S. D. Robinson, A. Sahajpal, J. A. Ibers, Inorg. Chem. 1977, 16, 2728.
43. a) S. K. Burley, G. A. Petsko, Science 1985, 229, 23;
44. b) H. C. Weiss, D. Blaser, R. Boese, B. M. Doughan, M. M. Haley, Chem. Commun. 1997, 1703;
45. c) N. N. L. Madhavi, A. K. Katz, H. L. Carrell, A. Nangia, G. R. Desiraju, Chem. Commun. 1997, 1953;
46. d) S. K. Burley, G. A. Petsko, Adv. Protein Chem. 1988, 39, 125;
47. e) M. Nishio, M. Hirota, Y. Umezawa, The CH-π Interactions (Evidence, Nature and Consequences), Wiley-VCH, New York, 1998;
48. f) Y. Umezawa, S. Tsuboyama, K. Honda, J. Uzawa, M. Nishio, Bull. Chem. Soc. Jpn. 1998, 71, 1207;
49. g) G. R. Desiraju, T. Steiner, The Weak hydrogen Bond (IUCr Monograph on Crystallography 9), Oxford Science Pub., 1999;
50. h) M. J. Hannon, C. L. Painting, N. W. Alcock, Chem. Commun. 1999, 2023;
51. i) B. J. Mcnelis, L. C. Nathan, C. J. Clark, J. Chem. Soc., Dalton Trans. 1999, 1831;
52. j) K. Biradha, C. Seward, M. J. Zaworotko, Angew. Chem. Int. Ed. 1999, 38, 492;
53. k) M. J. Calhorda, Chem. Commun. 2000, 801;
54. l) C. Janiak, S. Temizdemir, S. Dechert, Inorg. Chem. Commun. 2000, 3, 271;
55. m) C. Janiak, S. Temizdemir, S. Dechert, W. Deck, F. Girgsdies, J. Heinze, M. J. Kolm, T. G. Scarmann, O. M. Zipffel, Eur. J. Inorg. Chem. 2000, 1229;
56. n) T. Steiner, Angew. Chem. Int. Ed. 2002, 41, 48;
57. o) I. Dance, New J. Chem. 2003, 27, 22.
58. A. Amoedo, M. Graña, J. Martínez, T. Pereira, M. López-Torres, A. Fernández, J. J. Fernández, J. M. Vila, Eur. J. Inorg. Chem. 2002, 613.
59. a) H. Yamazaki, K. Aoki, J. Organomet. Chem. 1976, C54, 122;
60. b) G. R. Clark, J. Organomet. Chem. 1977, 134, 51.
61. T. S. Lobana, G. Bawa, A. Castineiras, R. J. Butcher, M. Zeller, Organometallics 2008, 27, 175.
62. 2)(H)] complex.
63. a) C. Mealli and D. M. Proserpio, CACAO Version 4.0, July, 1994, Firenze, Italy;
64. b) C. Mealli, D. M. Proserpio, J. Chem. Educ. 1990, 67, 399.
65. J. G. Tojal, T. Rojo, Polyhedron 1999, 18, 1123.
66. L. P. Hammett, Physical Organic Chemistry, 2nd ed., Mcgraw Hill, New York, 1970.
67. R. N. Mukherjee, O. A. Rajan, A. Chakravorty, Inorg. Chem. 1982, 21, 785.
68. A. Ahmed, S. D. Robinson, M. F. Uttley, J. Chem. Soc., Dalton Trans. 1972, 843.
69. a) D. T. Sawyer, J. L. Roberts Jr, Experimental Electrochemistry for Chemists, Wiley, New York, 1974, pp. 167-215;
70. b) M. Walter, L. Ramaley, Anal. Chem. 1973, 45, 165.
71. Chemical shifts are given in ppm and multiplicity of the signals along with the associated coupling constants (J in Hz) are given in parentheses. Overlapping signals are marked with an asterisk.
72. G. M. Sheldrick, SHELXS-97 and SHELXL-97, Fortran Programs for Crystal Structure Solution and Refinement, University of Gottingen, 1997.