Construction of Cd(II) compounds with a chelating ligand 2,2′-dipyridiylamine (Hdpa): Anion effect, catalytic activities and luminescence

Polyhedron

Volumn 29, Issue 2, 2010, Pages 773-786

  Park, Byeong Kwon ^a   Eom, Geun Hee ^a   Kim, Soo Hyun ^a   Kwak, Han ^a   Yoo, Seung Man ^a   Lee, Yu Jin ^a   Kim, Cheal ^a   Kim, Sung Jin ^b   Kim, Youngmee ^b  

^a Seoul National University of Science and Technology   (South Korea)

^b Ewha Womans University   (South Korea)

Author keywords

2,2 Dipyridylamine; Anion effect; Cd(II) complexes; Luminescence; Transesterification

Indexed keywords

EID: 73649097268     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2009.10.024     Document Type: Article

References (46)

1. Moler D.B., Li H., Chen B., Reineke T.M., O'Keeffe M., and Yaghi O.M. Acc. Chem. Res. 34 (2001) 319
2. Moulton B., and Zaworotko M.J. Chem. Rev. 101 (2001) 1629
3. Evans O.R., and Lin W. Acc. Chem. Res. 35 (2002) 511
4. Erxleben A. Coord. Chem. Rev. 246 (2003) 203
5. Barnett S.A., and Champness N.R. Coord. Chem. Rev. 246 (2003) 145
6. Carlucci L., Ciani G., and Proserpio D.M. Coord. Chem. Rev. 246 (2003) 247
7. Roesky H.W., and Andruh M. Coord. Chem. Rev. 236 (2003) 91
8. Luan X.J., Wang Y.-Y., Li D.-S., Liu P., Hu H.-M., Shi Q.-Z., and Peng S.-M. Angew. Chem., Int. Ed. 44 (2005) 3864
9. Ding B.-B., Weng Y.-Q., Mao Z.-W., Lam C.-K., Chen X.-M., and Ye B.-H. Inorg. Chem. 44 (2005) 8836
10. Angeloni A., Crawford P.C., Orpen A.G., Podesta T.J., and Shore B.J. Chem. Eur. J. 10 (2004) 3783
11. Balamurugan V., Hundal M.S., and Mukherjee R. Chem. Eur. J. 10 (2004) 1683
12. Wang Y., Yu J., Li Y., Shi Z., and Xu R. Chem. Eur. J. 9 (2003) 5048
13. Braga D., Grepioni F., and Desiraju G.R. Chem. Rev. 98 (1998) 1375
14. Janiak C., and Scharmann T.G. Polyhedron 22 (2003) 1123
15. Brammer L., Bruton E.A., and Sherwood P. Cryst. Growth Des. 1 (2001) 277
16. Desiraju G.R. Acc. Chem. Res. 35 (2002) 565
17. Janiak C. Dalton Trans. (2003) 2781
18. Carlucci L., Ciani G., Proserpio D.M., and Rizzato S. Chem. Eur. J. 5 (1999) 237
19. Wu H.-P., Janiak C., Rheinwald G., and Lang H. J. Chem. Soc., Dalton Trans. (1999) 183
20. Ni Z., and Vittal J. Cryst. Growth Des. 1 (2001) 195
21. Du M., Bu X.-H., Guo Y.-M., Liu H., Batten S.R., Ribas J., and Mak T.C.W. Inorg. Chem. 41 (2002) 4904
22. Ryu J.Y., Han J.H., Lee J.Y., Hong S.J., Choi S.H., Kim C., Kim S.-J., and Kim Y. Inorg. Chim. Acta 358 (2005) 3659
23. Gianfranco L.C., Ciani G., Proserpio D.M., and Rizzato S. CrystEngCommun 5 (2003) 190 and references therein
24. Blake A.J., Champness N.R., Hubberstey P., Li W.-S., Withersby M.A., and Schröder M. Coord. Chem. Rev. 183 (1999) 117
25. Hong M.C., Zhao Y.J., Su W.P., Cao R., Fujita M., Zhou Z.Y., and Chan A.S.C. J. Am. Chem. Soc. 122 (2000) 4819
26. Ma J.F., Liu J.F., Yan X., Jia H.Q., and Lin Y.H. J. Chem. Soc., Dalton Trans. (2000) 2403
27. Ho K.-Y., Yu W.-Y., Cheung K.-K., and Che C.-M. Chem. Commun. (1998) 2101
28. Ho K.-Y., Yu W.-Y., Cheung K.-K., and Che C.-M. Dalton Trans. (1999) 1581
29. Gultneh Y., Khan A.R., Blaise D., Chaudhry S., Ahvazi B., Marvey B.B., and Butchre R.J. J. Inorg. Biochem. 75 (1999) 7
30. Kwak H., Lee S.H., Kim S.H., Lee Y.M., Lee E.Y., Park B.K., Kim E.Y., Kim C., Kim S.-J., and Kim Y. Eur. J. Inorg. Chem. (2008) 408
31. Lee Y.M., Hong S.J., Kim H.J., Lee S.H., Kwak H., Kim C., Kim S.-J., and Kim Y. Inorg. Chem. Commun. 10 (2007) 287
32. Griffith E.A.H., Li H.-Y., and Amma E.L. Inorg. Chim. Acta 148 (1988) 203
33. Bruker, shelxtl/pc, Version 6.12 for Windows XP, Bruker AXS Inc., Madison, Wisconsin, USA, 2001.
34. Song Y.J., Kwak H., Lee Y.M., Kim S.H., Lee S.H., Park B.K., Jun J.Y., Yu S.M., Kim C., Kim S.-J., and Kim Y. Polyhedron 28 (2009) 1241
35. Kim S.H., Park B.K., Song Y.J., Yu S.M., Koo H.G., Kim E.Y., Poong J.I., Lee J.H., Kim C., Kim S.-J., and Kim Y. Inorg. Chim. Acta 362 (2009) 4119
36. Kwak H., Lee S.H., Kim S.H., Lee Y.M., Park B.K., Lee Y.J., Jun J.Y., Kim C., Kim S.-J., and Kim Y. Polyhedron 28 (2009) 553
37. Nyce G.W., Lamboy J.A., Connor E.F., Waymouth R.M., and Hedrick J.L. Org. Lett. 4 (2002) 3587
38. Tashiro D., Kawasaki Y., Sakaguchi S., and Ishii Y. J. Org. Chem. 62 (1997) 8141
39. Kim Y., Kim S.-J., Choi S.H., Han J.H., Nam S.H., Lee J.H., Kim H.J., Kim C., Kim D.W., and Jang H.G. Inorg. Chim. Acta 359 (2006) 2534
40. Kwon J.Y., Kim Y., Kim S.-J., Lee S.H., Kwak H., and Kim C. Inorg. Chim. Acta 361 (2008) 1885
41. Xu L., Kim Y., Kim S.-J., Kim H.J., and Kim C. Inrog. Chem. Commun. 10 (2007) 586
42. Park B.K., Lee S.H., Lee E.Y., Kwak H., Lee Y.M., Lee Y.J., Jun J.Y., Kim C., Kim S.-J., and Kim Y. J. Mol. Struct. 890 (2008) 123
43. Allendrof M.D., Bauer C.A., Bhakta R.K., and Houk R.J.T. Chem. Soc. Rev. 38 (2009) 1330
44. Lee S.Y., Park S., Kim H.J., Jung J.H., and Lee S.S. Inorg. Chem. 47 (2008) 1913
45. Wei Y., Yu Y., and Wu K. Cryst. Growth Des. 7 (2007) 2262
46. Chen X.L., Zhang B., Hu H.-M., Fu F., Wu X.-L., Qin T., Yang M.-L., Xue G.-L., and Wang J.-W. Cryst. Growth Des. 8 (2008) 3706