Tris(μ-phenoxo) bridged Cd(II) polymer synthesised from a symmetrical tripodal ligand: A novel observation for heptadentate monocapped trigonal antiprismatic Schiff base complex

Inorganic Chemistry Communications

Volumn 10, Issue 1, 2007, Pages 40-44

  Chakraborty, Joy ^a   Samanta, Brajagopal ^a   Pilet, Guillaume ^b   Mitra, Samiran ^a  

^a JADAVPUR UNIVERSITY   (India)

^b UNIVERSITÉ CLAUDE BERNARD LYON 1   (France)

Author keywords

Cd(II) polymer; Tris( phenoxo) bridging; X ray crystal structure; (1,5) Dicyanamide

Indexed keywords

EID: 33845288045     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2006.09.002     Document Type: Article

References (46)

1. Zanello P., Tamburini S., Vigato P.A., and Mazzochim G.A. Coord. Chem. Rev. 77 (1987) 165
2. McKee V., and Tandon S.S. J. Chem. Soc. Chem. Commun. (1988) 1334
3. Vallina A.T., and Evans H.S. Polyhedron 21 (2002) 1177
4. Arnold P.L., Blake A.J., Wilson C., and Love J.B. Inorg. Chem. 43 (2004) 8206
5. Swiegers G.F., and Malefetse T.J. J. Chem. Rev. 100 (2000) 3483
6. Moulton B., and Zaworotko M. J. Chem. Rev. 101 (2001) 1629
7. Slagt V.F., Kamer P.C.J., van Leeuwen P.W.N.M., and Reek J.N.H. J. Am. Chem. Soc. 126 (2004) 1526
8. Hogg L., Leigh D.A., Lusby P.J., Morelli A., Parsons S., and Wong J.K.Y. Angew. Chem., Int. Ed. 43 (2004) 218
9. Kanesato M., Ngassapa F.N., and Yokoyama T. Anal. Sci. 16 (2000) 781
10. Kanesato M., Ngassapa F.N., and Yokoyama T. Anal. Sci. 17 (2001) 471
11. Keypour H., Salehzadeh S., Pritchard R.G., and Parish R.V. Polyhedron 19 (2000) 1633
12. Wang J., Xu X., Chen J., Luo Q., Shen M.C., Huang X., and Wu Q. Inorg. Chim. Acta 256 (1997) 121
13. Xu X.-Y., Chen J.-L., Luo Q.-H., Shen M.-C., and Huang X.-Y. Q-J Wu. Polyhedron 16 (1996) 223
14. Djebbar-Sid S., Benali-Baitich O., and Deloume J.P. Polyhedron 16 (1997) 2175
15. Keypour H., and Stotter D.A. Inorg. Chim. Acta 33 (1979) 141
16. Keypour H., Pritchard R.G., and Parish R.V. Trans. Met. Chem. 23 (1998) 609
17. Keypour H., and Salehzadeh S. Transition Met. Chem. 25 (2000) 205
18. Blackman A.G. Polyhedron 24 (2005) 1
19. Brewer G., Luckett C., May L., Beatty A.M., and Scheidt W.R. Inorg. Chim. Acta 357 (2004) 2390
20. Costes J.-P., Novitchi G., and Lebrun C. J. Alloy Comp. 374 (2004) 377
21. Xu X.-Y., Luo Q.-H., Shen M.-C., Huang X.-Y., and Wu Q.-J. Polyhedron 16 (1997) 915
22. Saha M.K., Dey D.K., Choudhury C.R., Dey S.K., Mitra S., and Lehmann C.W. Chem. Lett. 32 (2003) 1136
23. Datta A., Choudhury C.R., Talukder P., Mitra S., Dahlenburg L., and Matsushita T. J. Chem. Res. (2003) 642
24. Karmakar R., Choudhury C.R., Bravic G., Sutter J.P., and Mitra S. Polyhedron 23 (2004) 649
25. Dey S.K., Mondal N., Vicente R., El Fallah M.S., Escuer A., Solans X., Gramlich V., and Mitra S. Inorg. Chem. 43 (2004) 2427
26. Claramunt A., Escuer A., Mautner F.A., and Vicente N.S.R. J. Chem. Soc., Dalton Trans. (2000) 2627
27. Vigato P.A., Tamburini S., and Fenton D.E. Coord. Chem. Rev. 106 (1990) 105
28. Bailey N.A., Rodriguez de Barbarin C.O., Fenton D.E., Hellier P.C., Kanesato M., and Leeson P.B. J. Chem. Soc., Dalton Trans. (1995) 765
29. Ngwenya M., Chen D., and Martell A. J. Reibenspies Inorg. Chem. 30 (1991) 2732
30. Fenton D.E. Pure Appl. Chem. 58 (1986) 1437
31. Jacobson K.B., and Turner J.E. Toxicology 60 (1980) 1
32. Hidalgo H.A., Koppa V., and Bryan E.S. FEBS Lett. 64 (1976) 159
33. Dakternieks D. Coord. Chem. Rev. 98 (1990) 288
34. Marchetti P.S., Bank S., Bell T.W., Kennedy M.A., and Ellis P.D. J. Am. Chem. Soc. 111 (1989) 2063
35. Thom V.J., Hosken G.D., and Hancock R.D. Inorg. Chem. 24 (1985) 3378
36. D.T. Richens, Annual Reports on the Progress of Chemistry, 86 (sect. A), The Royal Society of Chemistry, Cambridge, 1989, p. 66.
37. Adam K.R., Dancey K.P., Leong A.J., Lindoy L.F., McCool B.J., McPartlin M., and Tasker P.A. J. Am. Chem. Soc. 110 (1988) 8471
38. Drew M.G.B., Mcfall S., and Nelson S. J. Chem. Soc., Dalton Trans. (1979) 575
39. Adam K.R., Arshad S.P.H., Baldwin D.S., Duckworth P.A., Leong A.J., McCool B.J., Tailor B.A., and Tasker P.A. Inorg. Chem. 33 (1994) 1194
40. Drew M.G.B., Howarth O.W., Morgan G.G., and Nelson J. J. Chem. Soc., Dalton Trans. (1994) 3149
41. Bencini A., Bianch A., Castello M., Varia M.D., Garcia-Espana E., Micheloni M., and Paoletti P. Inorg. Chem. 28 (1989) 347
42. TEXSAN, TEXRAY Structure Analysis Package, Molecular Structure Corporation, The Woodlands, TX USA, 1989.
43. -1, F(0 0 0) = 1640. A prismatic single crystal of 1 was selected and mounted on a Nonius Kappa CCD diffractometer with MoKα radiation (λ = 0.71069 Å). The lattice constants were refined by least-square refinement using 6343 reflections (1.00°<θ<27.1°). No absorption correction was applied to the data sets. Data processing was performed by the Kappa CCD analysis software [32]. The structure has been solved by direct methods using SIR97 program [33] combined to Fourier difference syntheses and refined against F using reflections with [I/σ(I) > 3] (CRYSTALS program [34]). All non-hydrogen atomic positions were located in difference Fourier maps and refined anisotropically.
44. Nonius COLLECT, DENZO, SCALEPACK, SORTAV: Kappa CCD Program us B.V., Delft, The Netherlands 1999.
45. Cascarano G., Altomare A., Giacovazzo C., Guagliardi A., Moliterni A.G., Burla M.C., Polidori G., and Camalli M. Acta Crystallogr. A 52 (1996) C-79
46. Watkin D.J., Prout C.K., Carruthers J.R., and Betteridge P.W. CRYSTALS Issue 11. Chemical Crystallography Laboratory (1999), Oxford, UK