One-dimensional (1D) helical and 2D homochiral metal-organic frameworks built from a new chiral octahydrobinaphthalene-derived dicarboxylic acid

Inorganic Chemistry Communications

Volumn 11, Issue 9, 2008, Pages 948-950

  Ouyang, Xiang ^a   Chen, Zhenxia ^a   Liu, Xiaofeng ^a   Yang, Yongtai ^a   Deng, Mingli ^a   Weng, Linhong ^a   Zhou, Yaming ^a   Jia, Yu ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

Chiral ligand; Helical; Homochiral metal organic frameworks; Solvothermal reaction

Indexed keywords

EID: 50249144539     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2008.04.023     Document Type: Article

References (25)

1. Li H., Eddaoudi M., O'Keeffe M., and Yaghi O.M. Nature 402 (1999) 276
2. Férey G., Serre C., Draznieks C.M., Millange F., Surblé S., Dutour J., and Margiolaki I. Angew. Chem. Int. Ed. 43 (2004) 6296
3. Rowsell J.L.C., and Yaghi O.M. Angew. Chem. Int. Ed. 44 (2005) 4670
4. Dinca M., Dailly A., Liu Y., Brown C.M., Neumann D.A., and Long J.R. J. Am. Chem. Soc. 128 (2006) 16876
5. Farha O.K., Spokoyny A.M., Mulfort K.L., Hawthorne M.F., Mirkin C.A., and Hupp J.T. J. Am. Chem. Soc. 129 (2007) 12680
6. Kondo A., Noguchi H., Carlucci L., Proserpio D.M., Ciani G., Kajiro H., Ohba T., Kanoh H., and Kaneko K. J. Am. Chem. Soc. 129 (2007) 12362
7. Fujita M., Kwon Y.J., Washizu S., and Ogura K. J. Am. Chem. Soc. 116 (1994) 1151
8. Sawaki T., and Aoyama Y. J. Am. Chem. Soc. 121 (1999) 4793
9. Horcajada P., Serre C., Vallet-Regí M., Sebban M., Taulelle F., and Férey G. Angew. Chem. Int. Ed. 45 (2006) 5974
10. Min K.S., and Suh M.P. J. Am. Chem. Soc. 122 (2000) 6834
11. Seo J.S., Whang D., Lee H., Jun S.I., Oh J., Jeon Y.J., and Kim K. Nature 404 (2000) 982
12. Evans O.R., Ngo H.L., and Lin W. J. Am. Chem. Soc. 123 (2001) 10395
13. Hu A., Ngo H.L., and Lin W. J. Am. Chem. Soc. 125 (2003) 11490
14. Wu C.D., Hu A., Zhang L., and Lin W. J. Am. Chem. Soc. 127 (2005) 8940
15. Cui Y., Evans O.R., Ngo H.L., White P.S., and Lin W. Angew. Chem. Int. Ed. 41 (2002) 1159
16. Cram D.J., Helgeson R.C., Peacock S.C., Kaplan L.J., Domeier L.A., Moreau P., Koga K., Mayer J.M., Chao Y., et al. J. Org. Chem. 43 (1978) 1930
17. 2 (all data) = 0.1665 with GOF = 1.110.
18. -1.
19. Nakamoto K. Infrared and Raman Spectra of Inorganic and Coordination Compounds. fourth ed. (1986), Wiley Press, NY
20. -1, from 30 to 600 °C.
21. Yaghi O.M., O'Keeffe M., Ockwig N.W., Chae H.K., Eddaoudi M., and Kim J. Nature 423 (2003) 705
22. Evans O.R., Manke D.R., and Lin W. Chem. Mater. 14 (2002) 3866
23. Sun D., Ke Y., Collins D.J., Lorigan G.A., and Zhou H.C. Inorg. Chem. 46 (2007) 2725
24. The solid state photoluminescence spectra were performed on Hitachi F-4500.
25. G.M. Sheldrick, SHELXS 97, Program for X-ray Crystal Structure Solution and Refinement, University of Gottingen, Germany, 1997.