Copper(II) assisted hydrolysis of 2,4,6-tris(pyrazol-1-yl)-1,3,5-triazine. Crystal and molecular structure of catena-[CuL(H2O)Cl]n (L = 2,4-dione-1,3,5-(1H)-triazin-1-amido)

Inorganica Chimica Acta

Volumn 374, Issue 1, 2011, Pages 637-642

  Manzur, Jorge ^a,c   Acuña, Carolina ^a   Vega, Andrés ^b,c   García, Ana María ^a  

^a DEPARTAMENTO DE FÍSICA   (Chile)

^b UNIVERSIDAD ANDRÉS BELLO   (Chile)

^c CENTER FOR THE DEVELOPMENT OF NANOSCIENCE AND NANOTECHNOLOGY CEDENNA   (Chile)

Author keywords

1,3,5 Triazine; Copper complex; Hydrolysis; Molecular structure

Indexed keywords

CRYSTAL STRUCTURE; CRYSTALS; HYDROLYSIS; LIGANDS; MOLECULAR STRUCTURE;

1 ,3 ,5-TRIAZINES; ANIONIC LIGANDS; COPPER COMPLEXES; COVALENT CHAINS; CRYSTAL AND MOLECULAR STRUCTURE; HYDROLYSIS PRODUCTS; MULTIDENTATE LIGANDS; PARTIAL HYDROLYSIS;

COPPER COMPOUNDS;

EID: 79960554377     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2011.03.031     Document Type: Article

References (45)

1. S.R. Batten, B.F. Hoskins, R. Robson, B. Moubaraki, and K.S. Murray Chem. Commun. 2000 1095
2. S.R. Batten, B.F. Hoskins, and R. Robson J. Am. Chem. Soc. 117 1995 5385
3. T. Kusukawa, and M. Fujita J. Am. Chem. Soc. 124 2002 13576
4. O. Ohmori, M. Kawano, and M. Fujita Angew. Chem., Int. Ed. 44 2005 1962
5. K. Kumazawa, K. Biradha, T. Kusukawa, T. Okano, and M. Fujita Angew. Chem., Int. Ed. 42 2003 3909
6. M. Yoshizawa, S. Miyagi, M. Kawano, K. Ishiguro, and M. Fujita J. Am. Chem. Soc. 126 2004 9172
7. M. Yoshizawa, J. Nakagawa, K. Kumazawa, M. Nagao, M. Kawano, T. Ozeki, and M. Fujita Angew. Chem., Int. Ed. 44 2005 1810
8. B.Q. Ma, and P. Coppens Chem. Commun. 2003 2290
9. M. Fujita, M. Tominaga, A. Hori, and B. Therrien Accounts Chem. Res. 38 2005 371
10. B. Therrien J. Organomet. Chem. 696 2011 637
11. E.M. Smolin, and L. Rapoport Triazines and Derivatives 1959 Interscience New York
12. R. Zibaseresht, and R.M. Hartshorn Aust. J. Chem. 58 2005 345
13. A. Majumder, C.R. Choudhury, S. Mitra, C. Marschner, and J. Baumgartner Z. Naturforsch. B60 2005 99
14. N.C. Thomas, B.L. Foley, and A.L. Rheingold Inorg. Chem. 27 1988 3426
15. J. Prasad, and N.C. Peterson Inorg. Chem. 10 1971 88
16. C.R. De Silva, J.F. Wang, M.D. Carducci, S.A. Rajapakshe, and Z.P. Zheng Inorg. Chim. Acta 357 2004 630
17. G.K. Pagenkopf, and D.W. Margerum Inorg. Chem. 7 1968 2514
18. L. Zhang, X.Q. Lu, Q. Zhang, C.-L. Chen, and B.-S. Kang Transition Met. Chem. 30 2005 76
19. P. Paul, B. Tyagi, A.K. Bilakhiya, M.M. Bhadbhade, E. Suresh, and G. Ramachandraiah Inorg. Chem. 37 1998 5733
20. E.I. Lerner, and S.J. Lippard J. Am. Chem. Soc. 98 1976 5397
21. E.I. Lerner, and S.I. Lippard Inorg. Chem. 16 1977 1546
22. J. Faus, M. Julve, J.M. Amigó, and T. Debaerdemaeker J. Chem. Soc., Dalton Trans. 1989 1681
23. Q.-H. Zhao, M.-S. Zhang, and R.-B. Fang J. Struct. Chem. 7 2006 764
24. J.V. Folgado, E. Escrivá, A. Beltrán-Porter, and D. Beltrán-Porter Transition Met. Chem. 11 1986 485
25. C.Y. Yang, X.-M. Chen, W.-H. Zhang, J. Chen, Y.-S. Yang, and M.-L. Gong J. Chem. Soc., Dalton Trans. 1996 1767
26. P. Gamez, P. de Hoog, O. Roubeau, M. Lutz, W.L. Driessen, A.L. Spek, and J. Reedijk Chem. Commun. 2002 1488
27. S. Demeshko, S. Dechert, and F. Meyer J. Am. Chem. Soc. 126 2004 4508
28. S.M. Neville, B.A. Leita, D.A. Offermann, M.B. Duriska, B. Moubaraki, K.W. Chapman, G.J. Halder, and K.S. Murray Eur. J. Inorg. Chem. 2007 1073
29. F. Gómez-de la Torre, A. De la Hoz, F. Jalón, B. Manzano, A. Otero, A. Rodríguez, C. Rodríguez-Pérez, A. Echevarría, and J. Elguero Inorg. Chem. 37 1998 6606
30. A. Echevarría, J. Elguero, A.L. Llamas-Saiz, C. Foces-Foces, G. Schultz, and I. Hargittai Struct. Chem. 5 1994 255
31. H. Reimlinger, A. Noels, J. Jadot, and A. van Overstraeten Chem. Ber. 103 1979 1954
32. A. Gelling, K.G. Orrell, A.G. Osborne, and V. Sik J. Chem. Soc., Dalton Trans. 1996 3371
33. R.M. Claramunt, P. Cornago, M. Cano, J.V. Heras, M.L. Gallego, E. Pinilla, and M.R. Torres Eur. J. Inorg. Chem. 2003 2693
34. I. Almena, E. Díez-Barra, A. De la Hoz, J. Ruiz, A. Sánchez-Migallón, and J. Elguero J. Heterocyclic Chem. 35 1998 1263
35. V. Milata, R.M. Claramunt, P. Cabildo, M.D. Santa María, P. Cornago, L. Infantes, F.H. Cano, and J. Elguero Heterocycles 55 2001 905
36. D. Azarifar, M.A. Zolfigol, and A. Forghaniha Heterocycles 63 2004 1897
37. A. Guerrero, F.A. Jalón, B.R. Manzano, A. Rodríguez, R.M. Claramunt, P. Cornago, V. Milata, and J. Elguero Eur. J. Inorg. Chem. 2004 549
38. D. Quiñonero, P.M. Dey, M.P. Carranza, A.M. Rodríguez, F.A. Jalón, and B.R. Manzano Dalton Trans. 39 2010 794
39. saintplus V6.22, Bruker AXS Inc., Madison, WI, USA.
40. G.M. Sheldrick shelxtl nt/2000 Version 6.10 2000 Bruker AXS Inc. Madison, WI, USA
41. sadabs V2.05, Bruker AXS Inc., Madison, WI, USA.
42. A.W. Addison, T.N. Rao, J. Reedijk, J. Van Rijn, and G.C. Vershcoor J. Chem. Soc., Dalton Trans. 1984 1349
43. (a) P.G. Slade, M. Raupach, and E.W. Radoslovich Acta Crystallogr., Sect. B29 1973 279
44. L.R. Falvello, L. Pascual, M. Tomas, and E.P. Urriolabeitia J. Am. Chem. Soc. 119 1997 11894
45. R.D. Hart, B.W. Skelton, and A.H. White Aust. J. Chem. 45 1992 1927