Synthesis, crystal structure, and physicochemical properties of the new metal-organic framework - The iron(III) complex with benzene- 1,3,5-tricarboxylate

Russian Chemical Bulletin

Volumn 63, Issue 4, 2014, Pages 862-869

  Sotnik, S A ^a   Kolotilov, S V ^a   Kiskin, M A ^b   Dobrokhotova, Zh V ^b   Gavrilenko, K S ^c   Novotortsev, V M ^b   Eremenko, I L ^b   Imshennik, V K ^d   Maksimov, Yu V ^d   Pavlishchuk, V V ^a  

^a L V PISARZHEVSKII INSTITUTE OF PHYSICAL CHEMISTRY   (Ukraine)

^b KURNAKOV INSTITUTE OF GENERAL AND INORGANIC CHEMISTRY   (Russian Federation)

^c TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV   (Ukraine)

^d SEMENOV INSTITUTE OF CHEMICAL PHYSICS   (Russian Federation)

Author keywords

Benzene 1,3,5 tricarboxylate; Henry reaction; Iron(III); Metal organic framework; M ssbauer spectroscopy; Sorption; Sorption kinetics; X ray diffraction

Indexed keywords

EID: 84918793971     PISSN: 10665285     EISSN: 15739171     Source Type: Journal    
DOI: 10.1007/s11172-014-0522-x     Document Type: Article

References (29)

1. H.-C. Zhou, J. R. Long, O. M. Yaghi, Chem. Rev., 2012, 112, 673.
2. E. Chelebaeva, J. Larionova, Y. Guari, R. A. S. Ferreira, L. D. Carlos, F. A. A. Paz, A. Trifonov, C. Guérin, Inorg. Chem., 2008, 47, 775.
3. S. V. Kolotilov, M. A. Kiskin, I. L. Eremenko, V. M. Novotortsev, Curr. Inorg. Chem., 2013, 3, 144.
4. M.-H. Xie, X.-L. Yang, Y. He, J. Zhang, B. Chen, C.-D. Wu, Chem. Eur. J. 2013, 19, 14316.
5. H. Wu, Q. Gong, D. H. Olson, J. Li, Chem. Rev., 2012, 112, 836.
6. R. B. Getman, Y.-S. Bae, C. E. Wilmer, R. Q. Snurr, Chem. Rev., 2012, 112, 703.
7. J.-R. Li, J. Sculley, H.-C. Zhou, Chem. Rev., 2012, 112, 869.
8. D. N. Dybtsev, A. L. Nuzhdin, H. Chun, K. P. Bryliakov, E. P. Talsi, V. P. Fedin, K. Kim, Angew. Chem., Int. Ed. Engl., 2006, 45, 916.
9. S. A. Sotnik, I. L. Eremenko, V. V. Pavlishchuk, K. S. Gavrilenko, Teor. Eksp. Khim., 2013, 49, 94
10. [Theor. Exp. Chem. (Engl. Transl.), 2013, 49].
11. M. Yoon, R. Srirambalaji, K. Kim, Chem. Rev., 2012, 112, 1196.
12. L. E. Kreno, K. Leong, O. K. Farha, M. Allendorf, R. P. Van Duyne, J. T. Hupp, Chem. Rev., 2012, 112, 1105.
13. Y. Cui, Y. Yue, G. Qian, B. Chen, Chem. Rev., 2012, 112, 1126.
14. T. B. Čeliè, M. Rangus, K. Lázár, V. Kaučič, N. Z. Logar, Angew. Chem., Int. Ed. Engl., 2012, 51, 12490.
15. L. Xie, S. Liu, C. Gao, R. Cao, J. Cao, C. Sun, Z. Su, Inorg. Chem., 2007, 46, 7782.
16. A. L. Spek, PLATON, A Multipurpose Crystallographic Tool, Utrecht University, Utrecht, 1998.
17. A. V. Pavlishchuk, S. V. Kolotilov, M. Zeller, L. K. Thompson, I. O. Fritsky, A. W. Addison, A. D. Hunter, Eur. J. Inorg. Chem., 2010, 4851.
18. D. S. Nesterov, E. N. Chygorin, V. N. Kokozay, V. V. Bon, R. Boèa, Y. N. Kozlov, L. S. Shulpina, J. Jezierska, A. Ozarowski, A. J. L. Pombeiro, G. B. Shulpin, Inorg. Chem., 2012, 51, 9110.
19. D. Enders, M. R. M. Huttl, J. Runsink, G. Raabe, B. Wendt, Angew. Chem., Int. Ed. Engl., 2007, 46, 467.
20. K. Motokura, M. Tada, Y. Iwasawa, Angew. Chem., 2008, 120, 9370.
21. J.-R. Li, R. J. Kuppler, H.-C. Zhou, Chem. Soc. Rev., 2009, 38, 1477.
22. R. M. Alosmanov, Vestn. Mosk. Univ., Ser. Khim., 2011, 52, 145
23. [Vestn. Mosk. Univ., Ser. Khim. (Engl. Transl.), 2011, 52].
24. F.-C. Wui, R.-L. Tseng, R.-S. Juang, Wat. Res., 2001, 35, 613.
25. Y. S. Ho, G. McKay, Wat. Res., 2000, 34, 735.
26. K. Schlichte, T. Kratzke, S. Kaskel, Microp. Mesop. Mater., 2004, 73, 81.
27. A. Weissberger, E. S. Proskauer, J. A. Riddick, E. E. Toops, Organic Solvents, Interscience Publishers Inc., New York, 1955, 552 pp.
28. SMART (Control) and SAINT (Integration) Software, Version 5.0, Bruker AXS Inc., Madison, WI, 1997.
29. G. M. Sheldrick, SHELXS-97 and SHELXL97, Program for the Refinement of Crystal Structure, University of Göttingen, Gö ttingen (Germany), 1997.