Sulfate binding in zinc(II) complexes of a monopyridylurea ligand N-(1-naphthyl)-N′-(3-pyridyl)urea

Inorganic Chemistry Communications

Volumn 13, Issue 9, 2010, Pages 1103-1107

  Huang, Xiaojuan ^a   Yang, Zaiwen ^a,b   Yang, Xiao Juan ^a   Zhao, Qilong ^a,b   Xia, Yana ^a,b   Wu, Biao ^a  

^a LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Fluorescence; Hydrogen bonded frameworks; N (1 naphthyl) N (3 pyridyl)urea; Sulfate binding

Indexed keywords

EID: 77955428038     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2010.06.037     Document Type: Article

References (50)

1. See, for examples: A. Bianchi, K. Bowman-James, E. García- España, Supramolecular Chemistry of Anions 1997 Wiley-VCH New York
2. J.M. Llinares, D. Powell, and K. Bowman-James Coord. Chem. Rev. 240 2003 57
3. P.D. Beer, and P.A. Gale Angew. Chem. Int. Ed. 40 2001 486
4. J.W. Steed Chem. Soc. Rev. 38 2009 506
5. J.W. Pflugrath, and F.A. Quiocho Nature 314 1985 257
6. A.K.H. Hirsch, F.R. Fischer, and F. Diederich Angew. Chem. Int. Ed. 46 2007 338
7. I. Ravikumar, P.S. Lakshminarayanan, M. Arunachalam, E. Sureshb, and P. Ghosh Dalton Trans. 2009 4160
8. R. Custelcean, and B.A. Moyer Eur. J. Inorg. Chem. 2007 1321
9. B. Wu, X.-J. Yang, C. Janiak, and P.G. Lassahn Chem. Commun. 2003 902
10. D. Seidel, V. Lynch, and J.L. Sessler Angew. Chem. Int. Ed. 41 2002 1422
11. D.R. Turner, E.C. Spencer, J.A.K. Howard, D.A. Tocher, and J.W. Steed Chem. Commun. 2004 1352
12. K.J. Wallace, R. Daari, W.J. Belcher, L.O. Abouderbala, M.G. Boutelle, and J.W. Steed J. Organomet. Chem. 666 2003 63
13. C.R. Bondy, P.A. Gale, and S.J. Loeb J. Am. Chem. Soc. 126 2004 5030
14. D.R. Turner, M.B. Hursthouse, M.E. Light, and J.W. Steed Chem. Commun. 2004 1354
15. D.R. Turner, B. Smith, A.E. Goeta, I.R. Evans, D.A. Tocher, J.A.K. Howarda, and J.W. Steed Cryst. Eng. Comm. 6 2004 633
16. R. Custelcean, B.A. Moyer, V.S. Bryantsev, and B.P. Hay Cryst. Growth Des. 6 2006 555
17. K.M. Mullen, and P.D. Beer Chem. Soc. Rev. 38 2009 1701
18. C. Caltagirone, and P.A. Gale Chem. Soc. Rev. 38 2009 520
19. R. Custelcean Chem. Commun. 2008 295
20. R. Custelcean, J. Bosano, P.V. Bonnesen, V. Kertesz, and B.P. Hay Angew. Chem. Int. Ed. 48 2009 4025
21. R. Custelcean, and P. Remy Cryst. Growth Des. 9 2009 1985
22. B. Wu, X. Huang, Y. Xia, X.-J. Yang, and C. Janiak Cryst. Eng. Comm. 9 2007 676
23. Y. Xia, B. Wu, Y. Liu, Z. Yang, X. Huang, L. He, and X.-J. Yang Cryst. Eng. Comm. 11 2009 1849
24. B. Wu, J. Liang, J. Yang, C. Jia, X.-J. Yang, H. Zhang, N. Tang, and C. Janiak Chem. Commun. 2008 1762
25. F. Zhuge, B. Wu, J. Liang, J. Yang, Y. Liu, C. Jia, C. Janiak, N. Tang, and X.-J. Yang Inorg. Chem. 48 2009 10249
26. B. Wu, J. Liang, Y. Zhao, M. Li, S. Li, Y. Liu, Y. Zhang, and X.-J. Yang Cryst. Eng. Comm. 2010 10.1039/b920777e
27. X. Huang, Y. Xia, H. Zhang, Z. Yan, Y. Tang, X.-J. Yang, and B. Wu Inorg. Chem. Commun. 11 2008 450
28. - 1): 3368 (N-H), 3091, 1721 (C?O), 1542, 1494, 1196, 1125, 1018 (S-O), 794, 767, 650.
29. K. Nakamoto Infrared and Raman Spectra of Inorganic and Coordination Compounds 6th ed. 2009 John Wiley & Sons, Inc Hoboken, New Jersey
30. P.S. Corbin, S.C. Zimmerman, P.A. Thiessen, N.A. Hawryluk, and T.J. Murray J. Am. Chem. Soc. 123 2001 10475
31. 2- anion in compound 2 are distributed over two positions with an occupancy of 0.637 on one position. The hydrogen atoms on the carbon (C33) and oxygen (O7) of methanol were not included due to such disordering and the location of the carbon atom at a two-fold axis.
32. L. Yang, D.R. Powell, and R.P. Houser Dalton Trans. 2007 955
33. B. Wu, X. Huang, J. Liang, Y. Liu, X.-J. Yang, and H.-M. Hu Inorg. Chem. Commun. 10 2007 563
34. C. Jia, J. Liang, J. Yang, X. Huang, X.-J. Yang, B. Wu, and N. Tang Z. Anorg. Allg. Chem. 634 2008 1210
35. R. Custelcean, P. Remy, P.V. Bonnesen, D.-E. Jiang, and B.A. Moyer Angew. Chem. Int. Ed. 47 2008 1866
36. D.R. Turner, B. Smith, E.C. Spencer, A.E. Goeta, I.R. Evans, D.A. Tocher, J.A.K. Howarda, and J.W. Steed New J. Chem. 29 2005 90
37. R. Custelcean, V. Sellin, and B.A. Moyer Chem. Commun. 2007 1541
38. L. Carlucci, G. Ciani, D.M. Proserpio, and S. Rizzato Cryst. Eng. Comm. 5 2003 190
39. D. Yuan, Y. Xu, M. Hong, W. Bi, Y. Zhou, and X. Li Eur. J. Inorg. Chem. 2005 1182
40. S. Ferrer, F. Lloret, I. Bertomeu, G. Alzuet, J. Borrás, S. García-Granda, M. Liu-González, and J.G. Haasnoot Inorg. Chem. 41 2002 5821
41. Z. Huang, H.-B. Song, M. Du, S.-T. Chen, and X.-H. Bu Inorg. Chem. 43 2004 931
42. C.-Y. Niu, B.-L. Wu, X.-F. Zheng, H.-Y. Zhang, H.-W. Hou, Y.-Y. Niu, and Z.-J. Li Cryst. Growth Des. 8 2008 1566
43. L. Carlucci, G. Ciani, and D.M. Proserpio Cryst. Growth Des. 5 2005 37
44. D.K. Kumar, A. Das, and P. Dastidar Cryst. Growth Des. 7 2007 205
45. D.K. Kumar, A. Das, and P. Dastidar Cryst. Eng. Comm. 8 2006 805
46. N.N. Adarsh, D.K. Kumar, and P. Dastidar Cryst. Eng. Comm. 10 2008 1565
47. G. Bergamini, P. Ceroni, M. Maestri, S.-K. Lee, J.V. Heyst, and F. Vögtle Inorg. Chim. Acta 360 2007 1043
48. M. Mei, and S. Wu New J. Chem. 25 2001 471
49. W.-G. Lu, L. Jiang, X.-L. Feng, and T.-B. Lu Cryst. Growth Des. 6 2006 564
50. F. Li, Y. Wang, G. Li, Y. Sun, X. Gu, and E. Gao Inorg. Chem. Commun. 10 2007 767