Two 3-D Cd^II/Zn^II complexes based on mixed 1,1-cyclobutanedicarboxylate and 4,4′-bipyridine ligands

References

• (a) M. Du, C.-P. Li, C.-S. Liu, S.-M. Fang. Coord. Chem. Rev., 257, 1282 (2013); (b) J.-R. Li, J. Sculley, H.-C. Zhou. Chem. Rev., 112, 869 (2012); (c) C.-P. Li, J.-M. Wu, M. Du. Chem. Eur. J., 18, 12437 (2012).
   Web of Science ®Google Scholar
• (a) H.-R. Fu, F. Wang, J. Zhang. Dalton Trans., 43, 4668 (2014); (b) B. Bhattacharya, R. Dey, P. Pachfule, R. Banerjee, D. Ghoshal. Cryst. Growth Des., 13, 731 (2013); (c) M.P. Suh, H.J. Park, T.K. Prasad, D.W. Lim. Chem. Rev., 112, 782 (2012).
   PubMed Web of Science ®Google Scholar
• L. Duan, Z.H. Wu, J.P. Ma, X.W. Wu, Y.B. Dong. Inorg. Chem., 49, 11164 (2010).
   PubMed Web of Science ®Google Scholar
• (a) L. Ma, C. Abney, W. Lin. Chem. Soc. Rev., 38, 1248 (2009); (b) R.K. Das, A. Aijaz, M.K. Sharma, P. Lama, P.K. Bharadwaj. Chem. Eur. J., 18, 6866 (2012).
   PubMed Web of Science ®Google Scholar
• (a) O.K. Farha, J.T. Hupp. Acc. Chem. Res., 43, 1166 (2010); (b) J.D. Rocca, D. Liu, W. Lin. Acc. Chem. Res., 44, 957 (2011).
   PubMed Web of Science ®Google Scholar
• (a) M. Kurmoo. Chem. Soc. Rev., 38, 1353 (2009); (b) S. Sanda, S. Parshamoni, A. Adhikary, S. Konar. Cryst. Growth Des., 13, 5442 (2013).
   PubMed Web of Science ®Google Scholar
• (a) Y. Cui, Y. Yue, G. Qian, B. Chen. Chem. Rev., 112, 1126 (2012); (b) A. Santra, P.K. Bharadwaj. Cryst. Growth Des., 14, 1476 (2014); (c) L.-H. Cao, Y.-L. Wei, Y. Yang, H. Xu, S.-Q. Zang, H.-W. Hou, T.C.W. Mak. Cryst. Growth Des., 14, 1827 (2014).
   PubMed Web of Science ®Google Scholar
• (a) B. Bhattacharya, R. Dey, D.K. Maity, D. Ghoshal. CrystEngComm, 15, 9457 (2013); (b) C.-P. Li, M. Du. Chem. Commun., 47, 5958 (2011); (c) D.J. Tranchemontagne, J.L. Mendoza-Cortés, M. O’Keeffe, O.M. Yaghi. Chem. Soc. Rev., 38, 1257 (2009); (d) S. Natarajan, P. Mahata. Chem. Soc. Rev., 38, 2304 (2009).
   Web of Science ®Google Scholar
• For examples: (a) J. Zhang, L. Wojtas, R.W. Larsen, M. Eddaoudi, M.J. Zaworotko. J. Am. Chem. Soc., 131, 17040 (2009); (b) M. Higuchi, D. Tanaka, S. Horike, H. Sakamoto, K. Nakamura, Y. Takashima, Y. Hijikata, N. Yanai, J. Kim, K. Kato, Y. Kubota, M. Takata, S. Kitagawa. J. Am. Chem. Soc., 131, 10336 (2009); (c) Q.-X. Yao, Z.-F. Ju, X.-H. Jin. J. Zhang. Inorg. Chem., 48, 1266 (2009).
   PubMed Web of Science ®Google Scholar
• For examples: (a) Y. Zheng, Z. Fu, H. Chen, C. Liu, S. Liao, J. Dai. Chem. Commun., 48, 8114 (2012); (b) Y. Hijikata, S. Horike, D. Tanaka, J. Groll, M. Mizuno, J. Kim, M. Takata, S. Kitagawa. Chem. Commun., 47, 7632 (2011); (c) J. Tao, M.-L. Tong, J.-X. Shi, X.-M. Chen, S.W. Ng. Chem. Commun., 2043 (2000).
   PubMed Web of Science ®Google Scholar
• For examples: (a) S.M. Keltie, P.A. Gale, M.E. Light, M. Tromp. J. Coord. Chem., 66, 3058 (2013); (b) F. Guo, J. Xu, X. Zhang, B. Zhu. Inorg. Chim. Acta, 363, 3790 (2010); (c) H.-L. Zhu, W. Xu, J.-L. Lin, J. Zhang, Y.-Q. Zheng. J. Coord. Chem., 64, 2088 (2011).
   Web of Science ®Google Scholar
• For examples: (a) X.-J. Zheng, L.-P. Jin, S. Gao, S.-Z. Lu. New J. Chem., 29, 798 (2005); (b) T.K. Maji, M. Ohba, S. Kitagawa. Inorg. Chem., 44, 9225 (2005); (c) T.K. Maji, W. Kaneko, M. Ohba, S. Kitagawa. Chem. Commun., 4613 (2005).
   Web of Science ®Google Scholar
• For examples: (a) E.-Y. Choi, K. Park, C.-M. Yang, H. Kim, J.-H. Son, S.W. Lee, Y.H. Lee, D. Min, Y.-U. Kwon. Chem. Eur. J., 10, 5535 (2004); (b) M. Dinca, J.R. Long. J. Am. Chem. Soc., 127, 9376 (2005); (c) C. Serre, C. Mellot-Draznieks, S. Surble, N. Audebrand, Y. Filinchuk, G. Ferey. Science, 315, 1828 (2007).
   PubMed Web of Science ®Google Scholar
• (a) L. Sun, J.-F. Song, R.-S. Zhou, J. Zhang, L. Wang, K.-L. Cui, X.-Y. Xu. J. Coord. Chem., 67, 822 (2014); (b) M. Hu, M. Chen, X.-G. Yang, S.-M. Fang, C.-S. Liu. J. Coord. Chem., 64, 3928 (2011); (c) M. Hu, Q. Zhang, L.-M. Zhou, S.-M. Fang, C.-S. Liu. Inorg. Chem. Commun., 13, 1548 (2010); (d) S.-M. Fang, Q. Zhang, M. Hu, E.C. Sanudo, M. Du, C.-S. Liu. Inorg. Chem., 49, 9617 (2010).
   Web of Science ®Google Scholar
• For examples: (a) Y. Rodríguez-Martín, M. Hernández-Molina, J. Sanchiz, C. Ruiz-Pérez, F. Lloret, M. Julve. Dalton Trans., 2359 (2003); (b) F.S. Delgado, C.A. Jimenez, P. Lorenzo-Luis, J. Pasan, O. Fabelo, L. Canadillas-Delgado, F. Lloret, M. Julve, C. Ruiz-Pérez. Cryst. Growth Des., 12, 599 (2012); (c) T.K. Maji, S. Sain, G. Mostafa, T.-H. Lu, J. Ribas, M. Monfort, N.R. Chaudhuri. Inorg. Chem., 42, 709 (2003); (d) W.-B. Yu, Y.-F. Han, Y.-J. Lin, G.-X. Jin. Chem. Eur. J., 17, 1863 (2011).
   Web of Science ®Google Scholar
• For examples: (a) M. Déniz, J. Pasán, O. Fabelo, L. Cañadillas-Delgado, F. Lloret, M. Julvec, C. Ruiz-Pérez. New J. Chem., 34, 2515 (2010); (b) M. Déniz, J. Pasán, O. Fabelo, L. Cañadillas-Delgado, P. Lorenzo-Luis, F. Lahoz, D. López, C. Yuste, M. Julve, C. Ruiz-Pérez. C. R. Chimie, 15, 911 (2012); (c) J. Pasán, J. Sanchiz, F. Lloret, M. Julve, C. Ruiz-Pérez. CrystEngComm, 9, 478 (2007).
   Web of Science ®Google Scholar
• For examples: (a) J. Pasán, J. Sanchiz, C. Ruiz-Pérez, F. Lloret, M. Julve. Inorg. Chem., 44, 7794 (2005); (b) J. Pasan, J. Sanchiz, C. Ruiz-Pérez, F. Lloret, M. Julve. Eur. J. Inorg. Chem., 4081 (2004); (c) L. Canadillas-Delgado, C. Yuste, M. Julve, F. Lloret, C. Ruiz-Pérez. Cryst. Growth Des., 12, 4505 (2012); (d) E. Gao, M. Zhu, L. Liu, Y. Huang, L. Wang, C. Shi, W. Zhang, Y. Sun. Inorg. Chem., 49, 3261 (2010).
   PubMed Web of Science ®Google Scholar
• (a) R. Baldomá, M. Monfort, J. Ribas, X. Solans, M.A. Maestro. Inorg. Chem., 45, 8144 (2006); (b) Z. Rzaczynska, A. Bartyzel, T. Glowiak. Polyhedron, 22, 2595 (2003); (c) M.-X. Li, H. Dai, M. Shao, L. Shi, K.-H. Lin, Z.-X. Cheng, L.-H. Weng. Chin. J. Chem. (Engl.), 24, 487 (2006); (d) M. Yodoshi, M. Mototsuji, N. Okabe. Acta Crystallogr. Sect. E, 63, m634 (2007); (e) K.-Y. Choi, K.-J. Kim. Struct. Chem., 19, 741 (2008).
   PubMed Web of Science ®Google Scholar
• (a) K.J. Barnham, M.I. Djuran, P.D.S. Murdoch, J.O. Ranford, P.J. Sadler. Inorg. Chem., 35, 1065 (1996); (b) K.J. Barnham, M.I. Djuran, U. Frey, M.A. Mazid, P.J. Sadler. J. Chem. Soc., Chem. Commun., 65 (1994); (c) E. Alessio, G. Mestroni, A. Bergamo, G. Sava. Met. Ions Biol. Syst., 42, 323 (2004); (d) E. Alessio, G. Mestroni, A. Bergamo, G. Sava. Curr. Top. Med. Chem., 4, 1525 (2004); (e) J.M. Redemaket-Lakhai, D. van den Bongard, D. Pluim, J.H. Beijnen, J.H.M. Schellens. Clin. Cancer Res., 10, 3717 (2004); (f) A.C. Hotze, M. Bacac, A.H. Velders, B.A. Jansen, H. Kooijman, A.L. Spek, J.G. Haasnnoot, J. Reedijk. J. Med. Chem., 46, 1743 (2003); (g) C. Tu, J. Lin, Y. Shao, Z. Guo. Inorg. Chem., 42, 5795 (2003); (h) W. Liu, X. Chen, M. Xie, L.Q. Ye, Y. Yu, S. Hou. J. Inorg. Biochem., 102, 1942 (2008); (i) K. Meelich, M. Galanski, V.B. Arion, B.K. Keppler. Eur. J. Inorg. Chem., 12, 2476 (2006).
   PubMed Web of Science ®Google Scholar
• (a) Z. Rzaczynska, A. Bartyzel, T. Glowiak. J. Coord. Chem., 56, 1525 (2003); (b) F.D. Rochon, G. Massarweh. Inorg. Chim. Acta, 359, 4095 (2006).
   Web of Science ®Google Scholar
• (a) S. Kitagawa, R. Kitaura, S. Noro. Angew. Chem. Int. Ed., 43, 2334 (2004); (b) P. Pachfule, C. Dey, T. Panda, R. Banerjee. CrystEngComm, 12, 2381 (2010).
   PubMed Web of Science ®Google Scholar
• Bruker AXS, SAINT Software Reference Manual, Madison, WI (1998).
   Google Scholar
• G.M. Sheldrick. SADABS, Siemens Area Detector Absorption Corrected Software, University of Göttingen, Germany (1996).
   Google Scholar
• (a) G.M. Sheldrick. SHELXTL NT Version 5.1. Program for Solution and Refinement of Crystal Structures, University of Göttingen, Germany (1997); (b) G.M. Sheldrick. Acta Cryst., A64, 112 (2008).
   Google Scholar
• (a) J.-M. Li, Y.-G. Zhang, J.-H. Chen, L. Rui, Q.-M. Wang, X.-T. Wu. Polyhedron, 19, 1117 (2000); (b) G.-L. Wen, Y.-Y. Wang, W.-H. Zhang, C. Ren, R.-T. Liu, Q.-Z. Shi. CrystEngComm, 12, 1238 (2010).
   Web of Science ®Google Scholar
• (a) L. Carlucci, G. Ciani, D.W. van Gudenberg, D.M. Proserpio, A. Sironi. Chem. Commun., 631 (1997); (b) A.M. Kirillov, S.W. Wieczorek, M.F.C.G. da Silva, J. Sokolnicki, P. Smolenski, A.J.L. Pombeiro. Cryst. Eng. Comm., 13, 6329 (2011); (c) A.C. Kathalikkattil, K.K. Bisht, N. Aliaga-Alcaide, E. Suresh. Cryst. Growth Des., 11, 1631 (2011).
   Web of Science ®Google Scholar
• C. Janiak. J. Chem. Soc., Dalton Trans., 3885 (2000).
   Google Scholar
• (a) H. Yersin, A. Vogler. Photochemistry and Photophysics of Coordination Compounds, Springer, Berlin (1987); (b) B. Valeur. Molecular Fluorescence: Principles and Applications, Wiley-VCH, Weinheim, Germany (2002).
   Google Scholar
• (a) N.W. Ockwig, O. Delgado-Friederichs, M. O’Keeffe, O.M. Yaghi. Acc. Chem. Res., 38, 176 (2005); (b) S.R. Batten, S.M. Neville, D.R. Turner. Coordination Polymers: Design Analysis and Application, Royal Society of Chemistry (RSC) Publishing, Cambridge (2008); (c) C.-P. Li, J. Chen, P.-W. Liu, M. Du. CrystEngComm, 15, 9713 (2013).
   PubMed Web of Science ®Google Scholar