Pure and Applied Chemistry

Pure Appl. Chem., 2013, Vol. 85, No. 2, pp. 397-404

http://dx.doi.org/10.1351/PAC-CON-12-08-11

Published online 2013-01-21

Supramolecular assembly in metal complexes: Two structural cases

References

• 1. J. W. Steed, J. L. Atwood. Supramolecular Chemistry, 2^nd ed., John Wiley, Chichester (2009).
• 2. J.-M. Lehn. Angew. Chem., Int. Ed. 27, 89 (1988).
• 3. J.-M. Lehn. Supramolecular Chemistry: Concepts and Perspectives, VCH, Weinheim (1995).
• 4. C. Dietrich-Buchecker, M. C. Jimenez-Molero, V. Sartor, J.-P. Sauvage. Pure Appl. Chem. 75, 1383 (2003). (http://dx.doi.org/10.1351/pac200375101383)
• 5. H. Dodziuk. Introduction to Supramolecular Chemistry, Kluwer Academic, Dordrecht (2002).
• 6. S. R. Batten, S. M. Neville, D. R. Turner. Coordination Polymers: Design, Analysis and Application, Royal Society of Chemistry, Cambridge (2009).
• 7. M.-C. Hong, L. Chen. Design and Construction of Coordination Polymers, John Wiley, Hoboken, NJ (2009).
• 8. G. R. Desiraju. Crystal Design: Structure and Function, John Wiley, Hoboken, NJ (2003).
• 9. M. C. Etter. J. Phys. Chem. 95, 4601 (1991). (http://dx.doi.org/10.1021/j100165a007)
• 10. G. R. Desiraju, T. Steiner. The Weak Hydrogen Bond in Structural Chemistry and Biology, Oxford University Press, Oxford (1999).
• 11. T. Steiner. Angew. Chem., Int. Ed. 41, 48 (2002). (http://dx.doi.org/10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U)
• 12. C. E. Wilmer, M. Leaf, C. Y. Lee, O. K. Farha, B. G. Hauser, J. T. Hupp, R. Q. Snurr. Nat. Chem. 4, 83 (2012). (http://dx.doi.org/10.1038/nchem.1192)
• 13. M. Fyfe, J. Stoddart. Acc. Chem. Res. 30, 393 (1997). (http://dx.doi.org/10.1021/ar950199y)
• 14. G. R. Desiraju. The Crystal as a Supramolecular Entity, John Wiley, Chichester (1996).
• 15. T. S. Moore, T. F. Winmill. J. Am. Chem. Soc. 101, 1635 (1912).
• 16. L. Pauling. The Nature of the Chemical Bond and the Structure of Molecules and Crystals: An Introduction to Modern Structural Chemistry, Cornell University Press, Ithaca, NY (1940).
• 17. P. Metrangolo, G. Resnati. Chem.—Eur. J. 7, 2511 (2001). (http://dx.doi.org/10.1002/1521-3765(20010618)7:12<2511::AID-CHEM25110>3.0.CO;2-T)
• 18. K. Biradha, M. Sarkar, L. Rajput. Chem. Commun. 4169 (2006). (http://dx.doi.org/10.1039/b606184b)
• 19. M. Ghazzali. Ph.D. Dissertation. Chalmers Tekniska Högskola, Göteborg, Sweden (2008).
• 20. L. Öhrström, V. Langer, M. Ghazzali. Acta Crystallogr., Sect. C 64, 277 (2008). (http://dx.doi.org/10.1107/S0108270108018039)
• 21. M. Ghazzali, V. Langer, K. Larsson, L. Öhrström. CrystEngComm 13, 5813 (2011). (http://dx.doi.org/10.1039/c1ce05527e)
• 22. S. Kitagawa, K. Uemura. Chem. Soc. Rev. 34, 109 (2005). (http://dx.doi.org/10.1039/b313997m)
• 23. A. L. Spek. Acta Crystallogr., Sect. D 65, 148 (2009). (http://dx.doi.org/10.1107/S090744490804362X)
• 24. D. M. Ciurtin, Y.-B. Dong, M. D. Smith, T. Barclay, H. C. zur Loye. Inorg. Chem. 40, 2825 (2001). (http://dx.doi.org/10.1021/ic0014336)
• 25. P. M. Lommerse, A. J. Stone, R. Taylor, F. H. Allen. J. Am. Chem. Soc. 118, 3108 (1996). (http://dx.doi.org/10.1021/ja953281x)
• 26. H. L. Nguyen, P. N. Horton, M. B. Hursthouse, A. C. Legon, D. W. Bruce. J. Am. Chem. Soc. 126, 16 (2004). (http://dx.doi.org/10.1021/ja036994l)
• 27. S. C. Nyburg, C. H. A. Faerman. Acta Crystallogr., Sect. B 41, 274 (1985). (http://dx.doi.org/10.1107/S0108768185002129)
• 28. G. R. Desiraju, R. Parthasarathi. J. Am. Chem. Soc. 111, 8725 (1989). (http://dx.doi.org/10.1021/ja00205a027)
• 29. S. L. Price, A. J. Stone, J. Lucas, R. S. Rowland, A. E. Thornley. J. Am. Chem. Soc. 116, 4910 (1994). (http://dx.doi.org/10.1021/ja00090a041)
• 30. J.-W. Zou, Y.-J. Jiang, M. Guo, G.-X. Hu, B. Zhang, H.-C. Liu, Q. S. Yu. Chem.—Eur. J. 11, 740 (2005). (http://dx.doi.org/10.1002/chem.200400504)
• 31. V. R. Pedireddi, D. S. Reddy, B. S. Goud, D. C. Craig, A. D. Rae, G. R. Desiraju. J. Chem. Soc., Perkin Trans. 2353 (1994).
• 32. N. Ramasubbu, R. Parthasarathy, P. Murray-Rust. J. Am. Chem. Soc. 108, 4308 (1986). (http://dx.doi.org/10.1021/ja00275a012)
• 33. T. Caronna, R. Liantonio, T. A. Logothetis, P. Metrangolo, T. Pilati, G. Resnati. J. Am. Chem. Soc. 126, 4500 (2004). (http://dx.doi.org/10.1021/ja039884n)
• 34. B. K. Saha, R. K. R. Jetti, L. S. Reddy, S. Aitipamula, A. Nangia. Cryst. Growth Des. 5, 887 (2005). (http://dx.doi.org/10.1021/cg049691r)
• 35. R. Paulini, K. Muller, F. Diederich. Angew. Chem., Int. Ed. 44, 1788 (2005). (http://dx.doi.org/10.1002/anie.200462213)
• 36. M. B. Andrews, C. L. Cahill. Dalton Trans. 41, 3911 (2012). (http://dx.doi.org/10.1039/c2dt11985d)
• 37. M. Ghazzali, V. Langer, C. Lopes, A. Eriksson, L. Öhrström. New J. Chem. 31, 1777 (2007). (http://dx.doi.org/10.1039/b704009a)
• 38. F. F. Awwadi, R. D. Willett, K. A. Peterson, B. Twamley. Chem.—Eur. J. 12, 8952 (2006). (http://dx.doi.org/10.1002/chem.200600523)
• 39. L. Brammer, F. Zordan, G. M. Espallargas, S. L. Purver, L. A. Marin, H. Adams, P. Sherwood. ACA Trans. 39, 114 (2004).
• 40. F. Zordan, L. Brammer, P. Sherwood. J. Am. Chem. Soc. 127, 5979 (2005). (http://dx.doi.org/10.1021/ja0435182)
• 41. G. A. Van Albada, M. Ghazzali, K. Al-Farhan, J. Reedijk. Inorg. Chem. Commun. 14, 1149 (2011). (http://dx.doi.org/10.1016/j.inoche.2011.04.010)
• 42. Cambridge Crystallographic Database Centre, CCDC, CSD version 5.33 November 2011 was used employing five filters; disorder free, errors free, organometallic, intermolecular with only 3.0–3.7 Å chlorides short contact distance.