DOI QR코드

DOI QR Code

Synthesis, Structures and Properties of Two Metal-organic Frameworks Derived from 3-Nitro-1,2-benzenedicarboxylic Acid

  • Xu, Wen-Jia (College of Chemistry and Chemical Engineering, Guangxi University for Nationalities) ;
  • Zhang, Ling-Yu (College of Chemistry and Chemical Engineering, Guangxi University for Nationalities) ;
  • Tang, Jin-Niu (College of Chemistry and Chemical Engineering, Guangxi University for Nationalities) ;
  • Wang, Dai-Yin (College of Chemistry and Chemical Engineering, Guangxi University for Nationalities) ;
  • Pan, Gang-Hong (College of Chemistry and Chemical Engineering, Guangxi University for Nationalities) ;
  • Feng, Yu (College of Chemistry and Chemical Engineering, Guangxi University for Nationalities)
  • Received : 2013.04.15
  • Accepted : 2013.05.16
  • Published : 2013.08.20

Abstract

Two metal-organic frameworks based on the connectivity co-effect between rigid benzenedicarboxylic acid and bridging ligand have been synthesized $[Zn_2(3-NO_2-bdc)_2(4,4'-bpy)_2H_2O]_n$ (1), $[Co(3-NO_2-bdc)(4,4'-bpy)H_2O]_n$ (2) (where $3-NO_2-bdcH_2$ = 3-nitro-1,2-benzenedicarboxylic acid, 4,4'-bpy = 4,4'-bipyridine). The two novel complexes were characterized by IR spectrum, elemental analysis, fluorescent properties, thermogravimetric analysis, single-crystal X-ray diffraction and powder X-ray diffraction (PXRD). X-ray structure analysis reveals that 1 and 2 are two-dimensional (2D) network structures. Complex 1 and complex 2 belong to triclinic crystal with P-1 space group. The luminescence measurements reveal that two complexes exhibit good fluorescent emissions in the solid state at room temperature. Also, thermal decomposition process and powder X-ray diffraction of complexes were investigated.

Keywords

References

  1. Henninger, S. K.; Habib, H. A.; Janiak, C. J. Am. Chem. Soc. 2009, 131, 2776-2777. https://doi.org/10.1021/ja808444z
  2. Habib, H. A.; Hoffmann, A.; Hoppe, H. A.; Janiak, C. Dalton Trans. 2009, 1742-1751.
  3. Habib, H. A.; Sanchiz, J.; Janiak, C. Dalton Trans. 2008, 4877- 4884.
  4. Janiak, C. Dalton Trans. 2003, 2781-2804.
  5. Higuchi, M.; Tanaka, D.; Horike, S.; Sakamoto, H.; Nakamura, K.; Takashima, Y.; Hijikata, Y.; Yanai, N.; Kim, J.; Kato, K.; Kubota, Y.; Takata, M.; Kitagawa, S. J. Am. Chem. Soc. 2009, 131, 10336- 10337. https://doi.org/10.1021/ja900373v
  6. Zhou, Y. L.; Zeng, M. H.; Wei, L. Q.; Li, B. W.; Kurmoo, M. Chem. Mater. 2010, 22, 4295-4303. https://doi.org/10.1021/cm1011229
  7. Li, K. H.; Olson, D. H.; Seidel, J.; Emge, T. J.; Gong, H. W.; Zeng, H. P.; Li, J. J. Am. Chem. Soc. 2009, 131, 10368-10369. https://doi.org/10.1021/ja9039983
  8. Zeng, M. H.; Wang, Q. X.; Tan, Y. X.; Hu, S.; Zhao, H. X.; Long, L. S.; Kurmoo, M. J. Am. Chem. Soc. 2010, 132, 2561-2563. https://doi.org/10.1021/ja908293n
  9. Xu, G. C.; Ding, Y. J.; Okamura, T. A.; Huang, Y. Q.; Bai, Z. S.; Hua, Q.; Liu, G. X.; Sun, W. Y.; Ueyama, N. Cryst. Growth Des. 2009, 9, 395-403. https://doi.org/10.1021/cg800600g
  10. Wang, Y.; Huang, Y. Q.; Liu, G. X.; Okamura, T. A.; Doi, M.; Sheng, Y. W.; Sun, W. Y.; Ueyama, N. Chem. Eur. J. 2007, 13, 7523-7531. https://doi.org/10.1002/chem.200700133
  11. Fan, J.; Hanson, B. E. Chem. Commun. 2005, 2327-2329.
  12. Fan, J.; Yee, G. T.; Wang, G.; Hanson, B. E. Inorg. Chem. 2006, 45, 599-608. https://doi.org/10.1021/ic051286h
  13. Zheng, Y. Z.; Xue, W.; Tong, M. L.; Chen, X. M.; Zheng, S. L. Inorg. Chem. 2008, 47, 11202-11212. https://doi.org/10.1021/ic801498n
  14. Fan, L. L.; Li, C. J.; Meng, Z. S.; Tong, M. L. Eur. J. Inorg. Chem. 2008, 25, 3905-3909.
  15. Liu, W. T.; Ou, Y. C.; Xie, Y. L.; Lin, Z. J.; Tong, M. L. Eur. J. Inorg. Chem. 2009, 28, 4213-4218.
  16. Yaghi, O. M.; O'Keeffe, M.; Ockwig, N. W.; Chae, H. K.; Eddadoudi, M.; Kim, J. Nature 2003, 423, 705. https://doi.org/10.1038/nature01650
  17. Higashi, T. Program for Absorption Correction, Rigaku Corporation: Tokyo, Japan, 1995.
  18. Sheldrick, G. M. SHELXTL V5.1 software reference manual. Bruker AXS, Inc, Madison, Wisconsin, USA, 1997.
  19. Guilera, G.; Steed, J. W. Chem. Commun. 1999, 1563-1564.
  20. Fabbrizzi, L.; Licchelli, M.; Rabaioli, G.; Taglietti, A. Coord. Chem. Rev. 2000, 205, 85. https://doi.org/10.1016/S0010-8545(00)00239-3
  21. Evans, R. C.; Douglas, P.; Winscom, C. J. Coord. Chem. Rev. 2006, 250, 2093. https://doi.org/10.1016/j.ccr.2006.02.007
  22. Chen, W.; Wang, J. Y.; Chen, C.; Yue, Q.; Yuan, H. M.; Chen, J. X.; Wang, S. N. Inorg. Chem. 2003, 42, 944-946. https://doi.org/10.1021/ic025871j
  23. Bauer, C. A.; Timofeeva, T. V.; Settersten, T. B.; Patterson, B. D.; Liu, V. H.; Simmons, B. A.; Allendorf, M. D. J. Am. Chem. Soc. 2007, 129, 7136-7144. https://doi.org/10.1021/ja0700395

Cited by

  1. Assembly and Catalytic Properties of a 3D (4,6)-connected Cobalt-organic Framework with fsh Topology vol.35, pp.2, 2014, https://doi.org/10.5012/bkcs.2014.35.2.651