pH-controlled the formation of 4-sulfocalix[4]arene-based 1D and 2D coordination polymers

Inorganic Chemistry Communications

Volumn 10, Issue 11, 2007, Pages 1257-1261

  Lin, Rong Guang ^a   Long, La Sheng ^a   Huang, Rong Bin ^a   Zheng, Lan Sun ^a  

^a XIAMEN UNIVERSITY   (China)

Author keywords

4 Sulfocalix 4 arene; Coordination polymer; Manganese; pH Dependent

Indexed keywords

EID: 35348883319     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2007.08.003     Document Type: Article

References (57)

1. Lehn J.M. Supramolecular Chemistry (1995), VCH, Weinheim
2. Braga D., Grepioni F., and Desiraju G.R. Chem. Rev. 98 (1998) 1375
3. Blake A.J., Champness N.R., Hubberstey P., Li W.S., Withersby M.A., and Schröder M. Coordination Chemistry Reviews 183 (1999) 117
4. Hagrman P.J., Hagrman D., and Zubieta J. Angew. Chem., Int. Ed. 38 (1999) 2639
5. Moulton B., and Zaworotko M.J. Chem. Rev. 101 (2001) 1629
6. Evans O.R., and Lin W. Acc. Chem. Res. 35 (2002) 511
7. Desiraju G.R. Acc. Chem. Res. 35 (2002) 565
8. Rao C.N.R., Natarajan S., and Vaidhyanathan R. Angew. Chem., Int. Ed. 43 (2004) 1466
9. Kitagawa S., Kitaura R., and Noro S. Angew. Chem., Int. Ed. 43 (2004) 2334
10. Batten S.R., and Robson R. Angew. Chem., Int. Ed. 37 (1998) 1460
11. Yaghi O.M., Li G., and Li H. Nature 37 (1995) 703
12. Carder G.B., Venkataraman D., Moore J.S., and Lee S. Nature 374 (1995) 792
13. Yaghi O.M., Li H., David C., Richardson D., and Groy T.L. Acc. Chem. Res. 31 (1998) 474
14. Leininger S., Olenyuk B., and Stang P.J. Chem. Rev. 100 (2000) 853
15. Atwood J.L., Barbour L.J., Hardie M.J., and Raston C.L. Coordin. Chem. Rev. 222 (2001) 3
16. Dalgarno S.J., Atwood J.L., and Raston C.L. Chem. Commun. (2006) 4567
17. Bott S.G., Coleman A.W., and Atwood J.L. J. Am. Chem. Soc. 110 (1988) 610
18. Johnson C.P., and Atwood J.L. Inorg. Chem. 35 (1996) 2602
19. Atwood J.L., Orra G.W., Means N.C., Hamada F., Zhang H.M., Bott S.G., and Robinson K.D. Inorg. Chem. 31 (1992) 603
20. Drljaca A., Hardie M.J., and Raston C.L. J. Chem. Soc., Dalton Trans. (1999) 3639
21. Drljaca A., Hardie M.J., Raston C.L., and Spiccia L. Chem. Eur. J. 5 (1999) 2295
22. Airey S., Drljaca A., Hardie M.J., and Raston C.L. Chem. Commun. (1999) 1137
23. Drljaca A., Hardie M.J., Ness T.J., and Raston C.L. Eur. J. Inorg. Chem. (2000) 2221
24. Hardie M.J., Johnson J.A., Raston C.L., and Webb H.R. Chem. Commun. (2000) 849
25. Dalgarno S.J., and Raston C.L. J. Chem. Soc., Dalton Trans. (2003) 287
26. Dalgarno S.J., Fisher J., and Raston C.L. Chem. Eur. J. 12 (2006) 2772
27. Dalgarno S.J., Atwood J.L., and Raston C.L. Cryst. Growth Des. 6 (2006) 175
28. Drljaca A., Hardie M.J., Johnson J.A., Raston C.L., and Webb H.R. Chem. Commun. (1999) 1135
29. Atwood J.L., Barbour L.J., Dalgarno S., Raston C.L., and Webb H.R. J. Chem. Soc., Dalton Trans. (2002) 4351
30. Atwood J.L., Ness T.N., Nichols P.J., and Raston C.L. Cryst. Growth Des. 2 (2002) 171
31. Webb H.R., Hardie M.J., and Raston C.L. Chem. Eur. J. 7 (2001) 3616
32. Dalgarno S.J., and Raston C.L. Chem. Commun. (2002) 2216
33. Liu Y., Guo D.S., Zhang H.Y., Kang S., and Song H.B. Cryst. Growth Des. 6 (2006) 1399
34. Orr G.W., Barbour L.J., and Atwood J.L. Science 285 (1999) 1043
35. Holliday B.J., and Mirkin C.A. Angew. Chem., Int. Ed. Engl. 40 (2001) 2022
36. Maeda K., Mochizuki H., Watanabe M., and Yashima E. J. Am. Chem. Soc. 128 (2006) 7639
37. Gautam R.D. Angew. Chem., Int. Ed. Engl. 34 (1995) 2311
38. Matsumoto N., Motoda Y., Matsuo T., Nakashima T., Re N., Dahan F., and Tuchagues J.-P. Inorg. Chem. 38 (1999) 1165
39. Lee J.W., Kim K., and Kim K. Chem. Commun. (2001) 1042
40. Braga D., Maini L., Polito M., Tagliavini E., and Grepioni F. Coordin. Chem. Rev. 246 (2003) 53
41. Niklas N., Hampelb F., and Alsfasser R. Chem. Commun. (2003) 1586
42. Yang J.-H., Zheng S.-L., Yu X.-L., and Chen X.-M. Cryst. Growth Des. 4 (2004) 831
43. Zheng P.-Q., Ren Y.-P., Long L.-S., Huang R.-B., and Zheng L.-S. Inorg. Chem. 44 (2005) 1190
44. Forster P.M., Stock N., and Cheetham A.K. Angew. Chem., Int. Ed. 44 (2005) 7608
45. Dalgarno S.J., Atwood J.L., and Raston C.L. Cryst. Growth Des. 6 (2006) 174
46. Suh M.P., Shim B.Y., and Yoon T.-S. Inorg. Chem. 33 (1994) 5509
47. Battistuzzi G., Borsari M., Menabue L., Saladini M., and Sola M. Inorg. Chem. 35 (1996) 4239
48. Dalgarno S.J., Hardie M.J., and Raston C.L. Cryst. Growth Des. 4 (2004) 227
49. Zhou Z.-H., Deng Y.-F., and Wan H.-L. Cryst. Growth Des. 5 (2005) 1109
50. Go Y.B., Wang X., Anokhina E.V., and Jacobson A.J. Inorg. Chem. 44 (2005) 8265
51. Zhang G.Q., Yang G.Q., and Ma J.S. Cryst. Growth Des. 6 (2006) 375
52. Lu W.-G., Jiang L., Feng X.-L., and Lu T.-B. Cryst. Growth Des. 6 (2006) 564
53. -1 (KBr): 3207s, 2921m, 2851m, 1634m, 1597m, 1448m, 1276m, 1159s, 1121s, 1043s, 896w, 797w, 736w, 660m, 624m, 562m. (It was mentioned that, when the amount of starting materials of the reaction was amplified to four times, and the solution of the reaction was fully evaporated, the yield for complexes 1 to 3 is about 63.7%, 50.4% and 47.8%, respectively).
54. 2 = 2155.
55. Iki H., Kijima H., Hamachi I., and Shinkai S. Supramol. Chem. 4 (1995) 223
56. +] at pH 5 equals to the total concentration of ammonia added in the reaction.
57. 2 = 0.2424.