Anion effects on construction of ZnII compounds with a chelating ligand bis(2-pyridylmethyl)amine and their catalytic activities

Inorganica Chimica Acta

Volumn 366, Issue 1, 2011, Pages 337-343

  Kim, Youngmee ^a   Park, Byeong Kwon ^b   Eom, Geun Hee ^b   Kim, Soo Hyun ^b   Park, Hyun Min ^b   Choi, Young S ^c   Jang, Ho G ^c   Kim, Cheal ^b  

^a Ewha Womans University   (South Korea)

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

^c Korea University   (South Korea)

Author keywords

Bis(2 pyridylmethyl)amine; Catalyst; Geometric isomers; Transesterification; Zinc(II) complexes

Indexed keywords

AMIDES; CATALYST ACTIVITY; CATALYSTS; ISOMERS; LIGANDS; NEGATIVE IONS; TRANSESTERIFICATION; X RAY CRYSTALLOGRAPHY;

ANION EFFECTS; BIS(2-PYRIDYLMETHYL)AMINE; CATALYTIC TRANSESTERIFICATION; CHELATING LIGANDS; GEOMETRIC ISOMER; REACTION MECHANISM; UNSATURATED STRUCTURES; ZINC COMPLEX;

ZINC COMPOUNDS;

EID: 79251596466     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2010.11.029     Document Type: Article

References (41)

1. D.B. Moler, H. Li, B. Chen, T.M. Reineke, M. O'Keeffe, and O.M. Yaghi Acc. Chem. Res. 34 2001 319
2. B. Moulton, and M.J. Zaworotko Chem. Rev. 101 2001 1629
3. O.R. Evans, and W. Lin Acc. Chem. Res. 35 2002 511
4. A. Erxleben Coord. Chem. Rev. 246 2003 203
5. S.A. Barnett, and N.R. Champness Coord. Chem. Rev. 246 2003 145
6. L. Carlucci, G. Ciani, and D.M. Proserpio Coord. Chem. Rev. 246 2003 247
7. H.W. Roesky, and M. Andruh Coord. Chem. Rev. 236 2003 91
8. X.J. Luan, Y.-Y. Wang, D.-S. Li, P. Liu, H.-M. Hu, Q.-Z. Shi, and S.-M. Peng Angew. Chem., Int. Ed. 44 2005 3864
9. B.-B. Ding, Y.-Q. Weng, Z.-W. Mao, C.-K. Lam, X.-M. Chen, and B.-H. Ye Inorg. Chem. 44 2005 8836
10. A. Angeloni, P.C. Crawford, A.G. Orpen, T.J. Podesta, and B.J. Shore Chem. Eur. J. 10 2004 3783
11. V. Balamurugan, M.S. Hundal, and R. Mukherjee Chem. Eur. J. 10 2004 1683
12. Y. Wang, J. Yu, Y. Li, Z. Shi, and R. Xu Chem. Eur. J. 9 2003 5048
13. D. Braga, F. Grepioni, and G.R. Desiraju Chem. Rev. 98 1998 1375
14. C. Janiak Dalton Trans. 2003 2781
15. L. Carlucci, G. Ciani, D.M. Proserpio, and S. Rizzato Chem. Eur. J. 5 1999 237
16. H.-P. Wu, C. Janiak, G. Rheinwald, and H. Lang J. Chem. Soc. 1999 183
17. Z. Ni, and J. Vittal Cryst. Growth Des. 1 2001 195
18. M. Du, X.-H. Bu, Y.-M. Guo, H. Liu, S.R. Batten, J. Ribas, and T.C.W. Mak Inorg. Chem. 41 2002 4904
19. J.Y. Ryu, J.H. Han, J.Y. Lee, S.J. Hong, S.H. Choi, C. Kim, S.-J. Kim, and Y. Kim Inorg. Chim. Acta 358 2005 3659
20. A.J. Blake, N.R. Champness, P. Hubberstey, W.-S. Li, M.A. Withersby, and M. Schröder Coord. Chem. Rev. 183 1999 117
21. M.C. Hong, Y.J. Zhao, W.P. Su, R. Cao, M. Fujita, Z.Y. Zhou, and A.S.C. Chan J. Am. Chem. Soc. 122 2000 4819
22. J.F. Ma, J.F. Liu, X. Yan, H.Q. Jia, and Y.H. Lin J. Chem. Soc. 2000 2403
23. Y.M. Lee, S.J. Hong, H.J. Kim, S.H. Lee, H. Kwak, C. Kim, S.-J. Kim, and Y. Kim Inrog. Chem. Commun. 10 2007 287
24. H. Kwak, S.H. Lee, S.H. Kim, Y.M. Lee, E.Y. Lee, B.K. Park, E.Y. Kim, C. Kim, S.-J. Kim, and Y. Kim Eur. J. Inorg. Chem. 2008 408
25. J. Glerup, P.A. Goodson, D.J. Hodgson, K. Michelsen, K.M. Nielsen, and H. Welbe Inorg. Chem. 31 1992 4611
26. B.K. Park, S.H. Lee, E.Y. Lee, H. Kwak, Y.M. Lee, Y.J. Lee, J.Y. Jun, C. Kim, S.-J. Kim, and Y. Kim J. Mol. Struct. 890 2008 123
27. Bruker, shelxtl/pc, Version 6.12 for Windows XP. 2001, Bruker AXS Inc., Madison, Wisconsin, USA.
28. D. Seebach, E. Hungerbuhler, R. Naef, D. Schnurrenberger, B. Weidmann, and M. Zuger Synthesis 1982 138
29. M.-H. Lin, and T.V. RajanBabu Org. Lett. 2 2000 997
30. G.A. Grasa, R.M. Kissling, and S.P. Nolan Org. Lett. 4 2002 3583
31. G.A. Grasa, T. Guveli, R. Singh, and S.P. Nolan J. Org. Chem. 68 2003 2812
32. R.L.E. Furlan, E.G. Mata, and O.A. Mascaretti Tetrahedron Lett. 39 1998 2257
33. C.E. Rehberg, and C.H. Fisher J. Org. Chem. 12 1947 226
34. Y. Kim, S.-J. Kim, S.H. Choi, J.H. Han, S.H. Nam, J.H. Lee, H.J. Kim, C. Kim, D.W. Kim, and H.G. Jang Inorg. Chim. Acta 359 2006 2534
35. J.Y. Kwon, Y. Kim, S.-J. Kim, S.H. Lee, H. Kwak, and C. Kim Inorg. Chim. Acta 361 2008 1885
36. L. Xu, Y. Kim, S.-J. Kim, H.J. Kim, and C. Kim Inrog. Chem. Commun. 10 2007 586
37. Y.J. Song, H. Kwak, Y.M. Lee, S.H. Kim, S.H. Lee, B.K. Park, J.Y. Jun, S.M. Yu, C. Kim, S.-J. Kim, and Y. Kim Polyhedron 28 2009 1241
38. S.H. Kim, B.K. Park, Y.J. Song, S.M. Yu, H.G. Koo, E.Y. Kim, J.I. Poong, J.H. Lee, C. Kim, S.-J. Kim, and Y. Kim Inorg. Chim. Acta 362 2009 4119
39. H. Kwak, S.H. Lee, S.H. Kim, Y.M. Lee, B.K. Park, Y.J. Lee, J.Y. Jun, C. Kim, S.-J. Kim, and Y. Kim Polyhedron 28 2009 553
40. G.W. Nyce, J.A. Lamboy, E.F. Connor, R.M. Waymouth, and J.L. Hedrick Org. Lett. 4 2002 3587
41. D. Tashiro, Y. Kawasaki, S. Sakaguchi, and Y. Ishii J. Org. Chem. 62 1997 8141