Browse > Article
http://dx.doi.org/10.5012/bkcs.2005.26.6.892

A Novel Linking Schiff-Base Type Ligand (L: py-CH=N-C6H4-N=CH-py) and Its Zinc Coordination Polymers:Preparation of L, 2-Pyridin-3-yl-1H-benzoimidazol, trans-[Zn(H2O)4L2].(NO3)2.(MeOH)2[Zn(NO3)(H2O)2(L)].(NO3).(H2O)2 and [Zn(L)(OBC)(H2O)] (OBC = 4,4'-Oxybis(benzoate))  

Kim, Han-Na (Department of Chemistry (BK21), Institute of Basic Science, Sungkyunkwan University, Natural Science Campus)
Lee, Hee-K. (Department of Chemistry (BK21), Institute of Basic Science, Sungkyunkwan University, Natural Science Campus)
Lee, Soon-W. (Department of Chemistry (BK21), Institute of Basic Science, Sungkyunkwan University, Natural Science Campus)
Publication Information
Abstract
A long, bis(monodentate), linking Schiff-base ligand L (py-CH=N-$C_6H_4$-N=CH-py) was prepared from 1,4-phenylenediamine and 3-pyridinecarboxaldehyde by the Schiff-base condensation. Ligand L has two terminal pyridyl groups capable of coordinating to metals through their nitrogen atoms. In contrast, the same reaction between 1,2-phenylenediamine and 3-pyridinecarboxaldehyde produced a mixture of imidazol isomers (2-pyridin-3-yl-1H-benzoimidazole), which are connected to one another by the N-H…N hydrogen bonding to form a tetramer. From Zn($NO_3)_2{\cdot}6H_2O$ and ligand L under various conditions, one discrete molecule, trans- [Zn($H_2O)_4L_2]{\cdot}(NO_3)_2{\cdot}(MeOH)_2$, and two 1-D zinc polymers, [Zn$(NO_3)(H_2O)_2(L)]{\cdot}(NO_3){\cdot}(H_2O)_2$ and [Zn(L) (OBC)($H_2O$)], were prepared. In ligand L, the N$\ldots$N separation between the terminal pyridyl groups is 13.994 $\AA$, with their nitrogen atoms at the meta positions (3,3’) in a trans manner. The corresponding N$\ldots$N separations in its compounds range from 13.853 to 14.754 $\AA$.
Keywords
Linking Schiff-base ligand; Coordination polymer; Tetramer;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
Times Cited By Web Of Science : 15  (Related Records In Web of Science)
Times Cited By SCOPUS : 1
연도 인용수 순위
1 Kesanli, B.; Lin, W. Coord. Chem. Rev. 2003, 246, 305   DOI   ScienceOn
2 Lopez, S.; Kahraman, M.; Harmata, M.; Keller, S. W. Inorg. Chem. 1997, 36, 6138   DOI   ScienceOn
3 LaDuca Jr., R. L.; Desciak, M.; Laskoski, M.; Rarig Jr., R. S.; Zubieta, J. J. Chem. Soc. Dalton Trans. 2000, 2255
4 Choi, E.-Y.; Park, K.; Yang, C.-M.; Kim, H.; Son, J.-H.; Lee, S. W.; Lee, Y. H.; Min, D.; Kwon, Y.-U. Chem. Eur. J. 2004, 10, 5535   DOI   ScienceOn
5 Swiergers, G. F.; Malefetse, T. J. Coord. Chem. Rev. 2002, 225, 91   DOI   ScienceOn
6 Eddaoudi, M.; Kim, J.; Rosi, N.; Vodak, D.; Wachter, J.; O'Keeffe, M.; Yaghi, O. M. Science 2002, 295, 469   DOI   ScienceOn
7 Moulton, B.; Zaworotko, M. J. Chem. Rev. 2001, 101, 1629   DOI   ScienceOn
8 Swiergers, G. F.; Malefetse, T. J. Chem. Rev. 2000, 100, 3   DOI   ScienceOn
9 Calligaris, M.; Randaccio, L. Schiff Bases as Acyclic Polydentate Ligands in Comprehensive Coordination Chemistry; Wilikinson, G.; Gillard, R. D.; McCleverty, J. A., Eds.; Pergamon Press: New York, 1987; Vol. 2, pp 715-738
10 Vigato, P. A.; Tanburini, S. Coord. Chem. Rev. 2004, 248, 1717 and references therein   DOI   ScienceOn
11 Hernanddez-Molina, R.; Mederos, A. Acyclic and Macrocyclic Schiff Base Ligands in Comprehensive Coordination Chemistry II; McCleverty, J. A.; Meyer, T. J., Eds.; Pergamon Press: New York, 2004; Vol. 2, pp 411-446
12 Yaghi, O. M.; Li, H.; Davis, C.; Richardson, D.; Groy, T. L. Acc. Chem. Res. 1998, 31, 474   DOI   ScienceOn
13 Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. 1998, 37, 1460   DOI   ScienceOn
14 Zaman, M. B.; Smith, M. D.; Ciurtin, D. M.; zur Loye, H.-C. Inorg. Chem. 2002, 41, 4895   DOI   ScienceOn
15 Batten, S. R.; Champness, N. R. Coord. Chem. Rev. 2003, 246, 145   DOI   ScienceOn
16 Zaman, M. B.; Tomura, M.; Yamashita, Y. Org. Lett. 2000, 2, 273   DOI   ScienceOn
17 Rarig Jr., R. S.; Zubieta, J. Polyhedron 2003, 22, 177   DOI   ScienceOn
18 Bosch, E.; Barnes, C. L. New J. Chem. 2001, 25, 1376   DOI   ScienceOn
19 Withersby, M. A.; Blake, A. L.; Champness, N. R.; Cooke, P. A.; Hubberstey, P.; Li, W.-S.; Schroder, M. Inorg. Chem. 1999, 38, 2259   DOI   ScienceOn
20 Dong, Y.-B.; Smith, M. D.; Layland, R. C.; zur Loye, H.-C. Chem. Mater. 2000, 12, 1156   DOI   ScienceOn
21 Dong, Y.-B.; Smith, M. D.; zur Loye, H.-C. J. Solid State Chem. 2000, 155, 143   DOI   ScienceOn
22 Constable, E. C.; Morris, D.; Carr, S. New J. Chem. 1998, 287
23 Min, D.; Yoon, S. S.; Lee, J. H.; Suh, M.; Lee, S. W. Inorg. Chem. Commun. 2001, 4, 297   DOI   ScienceOn
24 Huh, H. S.; Min, D.; Lee, Y. K.; Lee, S. W. Bull. Korean Chem. Soc. 2002, 23, 619   DOI   ScienceOn
25 Min, D.; Yoon, S. S.; Jung, D. Y.; Lee, C. Y.; Kim, Y.; Han, W. S.; Lee, S. W. Inorg. Chim. Acta 2001, 324, 293   DOI   ScienceOn
26 Min, D.; Yoon, S. S.; Lee, S. W. Inorg. Chem. Commun. 2002, 5, 143   DOI   ScienceOn
27 Lee, S. W.; Kim, H. J.; Lee, Y. K.; Park, K.; Son, J.-H.; Kwon, Y.-U. Inorg. Chim. Acta 2003, 353, 151   DOI   ScienceOn
28 Janiak, C. Dalton Trans. 2003, 2781
29 Dong, Y.-B.; Smith, M. D.; zur Loye, H.-C. Inorg. Chem. 2000, 39, 4927 and references therein   DOI   ScienceOn
30 Bruker, SHELXTL, Structure Determination Software Programs; Bruker Analytical X-ray Instruments Inc.: Madison, Wisconsin, USA, 1997
31 Holman, K. T.; Hammud, H. H.; Isber, S.; Tabbal, M. Polyhedron 2005, 24, 221   DOI   ScienceOn
32 Cho. B.-Y.; Min, D.; Lee, S. W. Polyhedron submitted
33 Lee, H. K.; Min, D.; Cho, B.-Y.; Lee, S. W. Bull. Korean Chem. Soc. 2004, 25, 619