Syntheses and crystal structures of two cobalt carboxylate-phosphonates with 4,4′-bipyridine as a secondary metal linker

European Journal of Inorganic Chemistry

Volumn , Issue 18, 2004, Pages 3706-3711

  Song, Jun Ling ^a   Prosvirin, Andrey V ^b   Zhao, Han Hua ^b   Mao, Jiang Gao ^a  

^a FUJIAN INSTITUTE OF RESEARCH ON THE STRUCTURE OF MATTER   (China)

^b TEXAS A AND M UNIVERSITY   (United States)

Author keywords

Cobalt phosphonates; Crystal structure; Hydrothermal synthesis; Inorganic organic hybrids; Open frameworks

Indexed keywords

CARBOXYLATION; COBALT COMPOUNDS; COBALT DEPOSITS; CRYSTAL STRUCTURE; LIGANDS;

BIPYRIDINES; COBALT PHOSPHONATE; CRYSTALS STRUCTURES; DIMERIC UNITS; INORGANIC-ORGANIC HYBRID; MONOCLINIC SPACE GROUPS; OPEN FRAMEWORKS; PHOSPHONATES; SECONDARY METALS; SYNTHESIS AND CRYSTAL STRUCTURE;

HYDROTHERMAL SYNTHESIS;

4,4' BIPYRIDINE; CARBOXYLIC ACID; COBALT CARBOXYLATE PHOSPHONATE; COBALT COMPLEX; DIMER; LIGAND; METAL COMPLEX; PHOSPHONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BINDING; CHEMICAL COMPOSITION; CHEMICAL STRUCTURE; CROSS LINKING; CRYSTAL STRUCTURE; CRYSTALLIZATION; METAL BINDING; SYNTHESIS; THERMAL ANALYSIS;

EID: 4844222534     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejic.200400212     Document Type: Article

References (41)

1. [1a] A. K. Cheetham, G. Ferey, T. Loiseau, Angew. Chem. Int. Ed. 1999, 38, 3269.
2. [1b] J. Zhu, X. Bu, P. Feng, G. D. Stucky, J. Am. Chem. Soc. 2000, 122, 11563.
3. A. Clearfield, in New Developments in Ion Exchange Materials (Eds.: M. Abe, T. Kataoka, T. Suzuki), Kodansha, Ltd., Tokyo, 1991.
4. G. Cao, H.-G. Hong, T. E. Mallouk, Acc. Chem. Res. 1992, 25, 420.
5. G. Alberti, Comprehensive Supramolecular Chemistry (Ed: J. M. Lehn), Pergamon/Elsevier Science, Ltd., Oxford, U. K., 1996, vol. 7.
6. A. Clearfield, in Progress in Inorganic Chemistry (Ed.: K. D. Karlin), John Wiley & Sons, New York, 1998, vol. 47, pp. 371-510.
7. L. A. Vermeulen, in Progress in Inorganic Chemistry, vol. 44 ("Molecular Level Artificial Photosynthetic Materials") (Ed.: G. J. Meyer), John Wiley & Sons, New York, 1997, p. 143.
8. S. G. Carling, D. Visser, R. K. Kremer, J. Solid State Chem. 1993, 106, 111.
9. B. Bujoli, O. Pena, P. Palvadeau, J. Le Bideau, C. Payen, J. Rouxel, Chem. Mater. 1993, 5, 583.
10. C. Bellitto, F. Federici, A. Altomare, R. Rizzi, S. A. Ibrahim, Inorg. Chem. 2000, 39, 1803.
11. P. Rabu, P. Janvier, B. Bujoli, J. Mater. Chem. 1999, 9, 1323.
12. S. O. H Gutschke, D. J. Price, A. K. Powell, P. T. Wood, Angew. Chem. Int. Ed. 1999, 38, 1088.
13. [12a] P. Yin, L.-M. Zheng, S. Gao, X.-Q. Xin, Chem. Commun. 2001, 2346.
14. [12b] L.-M. Zheng, S. Gao, H.-H. Song, S. Decurtins, A. J. Jacobson, X.-Q. Xin, Chem. Mater. 2002, 14, 3143.
15. [12c] L.-M. Zheng, P. Yin, X.-Q. Xin, Inorg. Chem. 2002, 41, 4084.
16. [13a] R.-B. Fu, X.-T. Wu, S-M. Hu, J.-J. Zhang, Z.-Y. Fu, W.-X. Du, Inorg. Chem. Commun. 2003, 6, 827.
17. [13b] R.-B. Fu, X.-T. Wu, S-M. Hu, J.-J. Zhang, Z.-Y. Fu, W.-X. Du, S.-Q. Xia, Eur. J. Inorg. Chem. 2003, 1798.
18. [13c] R.-B. Fu, S-M. Hu, Z.-Y. Fu, J.-J. Zhang, W.-X. Du, X.-T. Wu, New J. Chem. 2003, 27, 230.
19. [14a] P. Yin, S. Gao, L.-M. Zheng, Z.-M. Wang, X.-Q. Xin, Chem. Commun. 2003, 1076.
20. [14b] S.-S. Bao, L.-M. Zheng, Y.-J. Liu, W. Xu, S.-H. Feng, Inorg. Chem. 2003, 42, 5037.
21. [14c] P. Yin, S. Gao, L.-M. Zheng, Z.-M. Wang, X.-Q. Xin, Chem. Mater. 2003, 15, 3233.
22. [15a] F. Fredoueil, M. Evain, D. Massiot, M. Bujoli-Doeuff, P. Janvier, A. Clearfield, B. Bujoli, J. Chem. Soc., Dalton Trans. 2002, 1508.
23. [15b] S. Drumel, P. Janiver, P. Barboux, M. Bujoli-Doeuff, B. Bujoli, Inorg. Chem. 1995, 34, 148.
24. [16a] J.-G. Mao, Z. Wang, A. Clearfield, Inorg. Chem. 2002, 41, 2334.
25. [16b] J.-G. Mao, Z. Wang, A. Clearfield, J. Chem. Soc., Dalton Trans. 2002, 4541.
26. [16c] J.-G. Mao, Z. Wang, A. Clearfield, Inorg. Chem. 2002, 41, 3713.
27. [16d] C. Lei, J.-G. Mao, Y.-Q. Sun, H.-Y. Zeng, A. Clearfield, Inorg. Chem. 2003, 42, 6157.
28. [17a] N. Stock, S. A. Frey, G. D. Stucky, A. K. Cheetham, J. Chem. Soc., Dalton Trans. 2000, 4292.
29. [17b] S. Ayyappan, G. D. Delgado, A. K. Cheetham, G. Ferey, C. N. R. Rao, J. Chem. Soc., Dalton Trans. 1999, 2905.
30. [17c] A. Distler, S. C. Sevov, Chem. Commun. 1998, 959.
31. [18a] E. Burkholder, V. Golub, C. J. O'Connor, J. Zubieta, Chem. Commun. 2003, 2128.
32. [18b] E. Finn, R. C. Burkholder, J. Zubieta, Chem. Commun. 2001, 1852.
33. [18c] R. C. Finn, J. Zubieta, Inorg. Chem. 2001, 40, 2466.
34. [18d] R. C. Finn, E. Burkholder, J. Zubieta, Inorg. Chem. 2001, 40, 3745.
35. J.-G. Mao, A. Clearfield, Inorg. Chem. 2002, 41, 2319.
36. [20a] A. Turner, P. A. Jaffrès, E. J. MacLean, D. Villemin, V. McKee, G. B. Hix, Dalton Trans. 2003, 1314.
37. [20b] H. Jankovics, M. Daskalakis, C. P. Raptopoulou, A. Terzis, V. Tangoulis, J. Giapintzakis, T. Kiss, A. Salifoglou, Inorg. Chem. 2002, 41, 3366.
38. K. Moedritzer, R. R. Irani, J. Org. Chem. 1966, 31, 1603.
39. B. Zhang, D. M. Poojary, A. Clearfield, G.-Z. Peng, Chem. Mater. 1996, 8, 1333.
40. [23a] G. M. Sheldrick, Program SADABS, University Göttingen, 1995.
41. [23b] G. M. Sheldrick, SHELXTL - Crystallographic Software Package, version 5.1, Bruker-AXS, Madison, WI, USA, 1998.