The molecular structure of [bis-(2-Tribromomethylsulfonyl-benzothiazole)-silver(I)- tetrafluoroborate·(acetone)][Ag{(C7H4NS)SO 2CBr3}2BF4·Me2CO]: A possible model for bromine elimination of silver halide fog centers

Journal of Imaging Science and Technology

Volumn 40, Issue 2, 1996, Pages 117-122

  Blair, John T ^a   Patel, Ranjan C ^b   Rogers, Robin D ^c   Whitcomb, David R ^a  

^a 3M COMPANY   (United States)

^b 3M Drug Delivery Systems   (United Kingdom)

^c NORTHERN ILLINOIS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BROMINE; CHELATION; CHEMICAL BONDS; CRYSTAL STRUCTURE; FREE RADICALS; IMAGING SYSTEMS; MOLECULAR STRUCTURE; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

LIGAND; SILVER HALIDES; SINGLE CRYSTAL X RAY ANALYSIS; TRIBROMOMETHYLSULFONYLBENZOTHIAZOLE;

SILVER COMPOUNDS;

EID: 0030103742     PISSN: 10623701     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (68)

1. (a) J. W. Reeves, US Patent 4,435,499.
2. (b) J. W. Reeves, US Patent 4,264,725.
3. (c) L. F. Costa, J. A. Van Allan, and F. Grum, US Patent 3,874,946.
4. (d) J. W. Van den Houte, DE Patent 2,306,020.
5. (e) A. Mori, T. Fukui, K. Kagami, and M. Suzuki, Japan Patent 05,127,296 A2.
6. (f) J. B. Philip and P. G. Skoug EP Patent 600,586 A1.
7. (g) D. B. Oliff and M. P. Kirk, EP Patent 600,587 A1.
8. (h) G. Gutman and E. J. Goettert, DE Patent 2,745,048.
9. S. Swain and R. E. Watts, US Patent 4, 756, 999.
10. (a) P.B. Gilman Jr., and J. D. Bass, DE Patent 2,159,631.
11. (b) Y. Nagaoka, H. Okusa, and S. Hirabayashi, Japan 03,198,043 A2.
12. (c) K. Endo, K. Yamamoto, E. Kanada, and S. Suzuki, Great Britain Patent 2,161,948 A1.
13. Y. Nagaoka, and S. Hirabayashi, Japan Patent 03,138,639 A2.
14. M. Yagihara, T. Matsushita, and Y. Idota, Japan Patent 61,095,353 A2.
15. (a) J. G. Smith, and R. C. Reed, US Patent 4,105,451.
16. (b) J. G. Smith and R. C. Reed, Res. Discl., 158, 68 (1977).
17. (c) R. A. De Mauriac and R. A. Landholm, US Patent 3,761,270.
18. U. L. Laridon, R. A. Van Brandt, and A. L. Poot, DE Patent 2,548,184.
19. (a) A. Giusti, G. Peyronel, and E. Gilberti, Spectrochim. Acta. 38A, 1185 (1982).
20. (b) A. S. Salameh, H. A. Tayim, and B. C. Uff, Polyhedron, 1, 543 (1982).
21. (c) M. Aresta and F. J. Ciminale, Chem. Soc., Dalton Trans. 1520 (1981).
22. (d) E. Koleva, Dokl. Bolg. Akad. Nauk. 33, 1481 (1980).
23. (e) S. N. Prajapati, I. M. Bhatt, and K. P. Soni, J. Inst. Chem., Calcutta, 48 (3): 123 (1976).
24. (f) M. Aresta, C. F. Nobile, F. Ciminale, and G. Bartoli, J. Chem. Soc., Dalton Trans. 1203 (1976).
25. (g) R. N. Dash and D. V. R. Rao, J. Indian Chem. Soc., 51: 787 (1974).
26. (h) Y. Ito, Y. Inubushi, M. Zenbayashi, S. Tomita, and T. Saegusa, J. Am. Chem. Soc. 95:4447 (1973).
27. (i) M. V. Artemenko, E. A. Chistyakova, K. F. Slyusarenko, and O. B. Pritula, Ukr. Khim. Zh. 38: 137 (1972).
28. T. Patel, R. K. Gartia, and D. Misra, Indian J. Phys. 47: 316 (1973).
29. (a) R. L. Bodner and A. I. Popov, Inorg. Chem. 11: 1410 (1972).
30. (b) T. Tsuda, S. Ohba, M.Takahashi, and M. Ito, Acta Cryst. C45: 887 (1989).
31. (c) I. Søtofte and K. Nielsen, Acta Chem. Scand. A37: 891 (1983).
32. H. Schmidbaur, A. Mair, G. Müller, J. Lachmann, and S. Gamper, Z. Naturforsch. 46b: 912 (1991).
33. (a) S. R. Cooper, Acc. Chem. Res. 21: 141 (1988).
34. (b) P. J. Blower, J. A. Clarkson, S. C. Rawle, J. R. Hartman, R. E. Wolf, Jr., R. Yagbasan, S. G. Bott, and S. R. Cooper, Inorg. Chem. 28: 4040 (1989).
35. (c) J. Clarkson, R. Yagbasan, P. J. Blower, S. C. Rawle, and S. R. Cooper, J. Chem. Soc., Chem. Commun. 950 (1987).
36. (a) X.-M. Chen and T. C. W. Mak, J. Chem. Soc. Dalton Trans. 1219 (1991).
37. (b) v-M. Hedrich and H. Hartl, Acta Cryst. C39:533 (1983).
38. (c) v-M. Hedrich and H. Hartl, Acta Cryst. C39: 1649 (1983).
39. (d) R. G. Griffin, J. D. Ellett, Jr., M. Mehring, J. G. Bullitt, and J. S. Waugh, J. Chem. Phys. 57: 2147 (1972).
40. (e) P. Coggon and A. T. McPhail, J. Chem. Soc., Chem. Commun. 91 (1972).
41. (f) A. E. Blakeslee and J. L. Hoard, J. Am. Chem. Soc. 78: 3029 (1956).
42. (g) J. K. Mohana Rao and M. A. Viswamitra, Acta Cryst. B28: 1484 (1972).
43. (g) T. C. W. Mak, W-H, Yip, C. H. L. Kennard, G. Smith, and E. J. O'Reilly, Aust. J. Chem. 39: 541 (1986).
44. (h) B. T. Usubaliev, É. M Movsumov, I. R. Amiraslanov, A. I. Akhmedov, A. A. Musaev, and Kh. S. Mamedov, Zhurn. Strukturnoi Khimii 22: 98 (1981).
45. (a) M. Näveke, P. G. Jones, A. Blaschette, D. Schomburg, H. K. Cammenga, and M. Z. Epple, Z Anorg. Allg. Chem. 619: 1027 (1993).
46. (b) N. C. Baenziger and A. W. Struss, Inorg. Chem., 15: 1807 (1976).
47. (c) D. D. Desmarteau, S. S. Zuberi, W. T. Pennington, and B. B. Randolph, Eur. J. Solid State Chem. 29: 777 (1992).
48. G. Ferguson, C. Glidewell, I. Gosney, D. Lloyd, S. Metacalfe, and H. Lumbroso, J. Chem. Soc. Perkin Trans. II, 1829 (1988).
49. (a) W. Henderson, R. D. W. Kemmitt, L. J. S. Prouse, and D. R. Russell, J. Chem. Soc. Dalton Trans. 781 (1990).
50. (b) C. M. Lukehart, A. T. McPhail, D. R. McPhail, and M. D. Owen, J. Chem. Soc., Chem. Commun. 215 (1990).
51. (a) T. Laube, A. Weidenhaupt, and R. Hunziker, J. Am. Chem. Soc., 113: 2561 (1991).
52. (b) D. M. Van Seggen, O. P. Anderson, and S. H. Strauss, Inorg. Chem. 31: 2987 (1992).
53. (c) M. R. Colsman, T. D. Newbound, L. J. Marshall, M. D. Noirot, M. M. Miller, G. P. Wulfsberg, J. S. Frye, O. P. Anderson, and S. H. Strauss, J. Am. Chem. Soc. 112:2349 (1990).
54. (d) T. D. Newbound, M. R. Colsman, M. M. Miller, G. P. Wulfsberg, O. P. Anderson, and S. H. Strauss, J. Am Chem Soc 111: 3762 (1989).
55. (e) M. R. Colsman, M. D. Noirot, M. M. Miller, O.P. Anderson, and S. H. Strauss, J. Am. Chem. Soc., 110:6886 (1988).
56. (a) E. Horn, M. R. Snow, and E. R. T. Tiekink, Aust. J. Chem. 40: 761 (1987).
57. (b) A. Bondi, J. Phys. Chem. 68: 441 (1964).
58. L. J. Bellamy, The IR Spectra of Complex Molecules, 3rd ed., Chapman and Hall, London (1975).
59. (a) K. Itano, M. Nakano, and M. Hashimoto, US Patent 3,667,954.
60. (b) N. Fudaba and Y. Sumitomo, Japan Patent 50,014,332.
61. (c) Y. Hayashi, M. Saniada, and R. Hirohashi, Nihon Shashin Gakkaishi, 51: 495 (1988).
62. (d) Y. Tsujimoto, A. Noguchi, M. Sasaki, T. Kazami, and T. Saito, Japan Patent 50,089,018.
63. (e) C. Haessner, H. Mustroph, and J. Marx, DD Patent 153,443 Z.
64. (a) J. Belloni-Cofler, J. Amblard, J. L. Marignier, and M. Mostafavi, Endeavor, 15: 2 (1991).
65. (b) J. Belloni, M. Mostafavi, J. L. Marignier, and J. Amblard, J. Imaging Sci. 35: 68 (1991).
66. H. M. M. Wilson, Vibrational Spectroscopy. 7, 287 (1994).
67. G. Xue, Q. Dai, and S. Jiang, J. Am. Chem. Soc. 110: 2393 (1988).
68. J. S. Suh, N. H. Jang, D. H. Jeong, and M. Moskovits, J. Phys. Chem., 100: 805 (1995).