Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Weak Forces in Inorganic Lattices: Anion Roles in Lattice Assembly

  • Lee, Young-Hoon (Department of Chemistry, Kyungpook National University) ;
  • Park, Yu-Chul (Department of Chemistry, Kyungpook National University) ;
  • Harrowfield, Jack M. (Laboratoire de Chimie Supramoleculaire, ISIS-ULP) ;
  • Thuery, Pierre (CEA Saclay, DSM/DRECAM/SCM (CNRS URA 331)) ;
  • Kim, Yang (Department of Chemistry and Advanced Materials, Kosin University)
  • Published : 2007.08.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Lehn, J.-M. Supramolecular Chemistry: Concepts and Perspectives VCH: Weinheim, 1995
  2. Henry, M. Chem. Phys. Chem. 2002, 3, 561 https://doi.org/10.1002/1439-7641(20020715)3:7<561::AID-CPHC561>3.0.CO;2-E
  3. Meyer, E. A.; Castellano, R. K.; Diederich, F. Angew. Chem. Int. Ed. 2003, 42, 1210 https://doi.org/10.1002/anie.200390319
  4. Park, S. B.; Yoon, I.; Seo, J.; Kim, H. J.; Kim, J. S.; Lee, S. S. Bull. Korean Chem. Soc. 2006, 27, 713 https://doi.org/10.5012/bkcs.2006.27.5.713
  5. Hunter, C. A. Angew. Chem. Int. Ed. 2004, 43, 5310 https://doi.org/10.1002/anie.200301739
  6. Hunter, C. A.; Chessari, G.; Packer, M. J.; Zonta, C.; Low, C. M. R.; Vinter, J. G. Chem. Eur. J. 2002, 8, 2860 https://doi.org/10.1002/1521-3765(20020703)8:13<2860::AID-CHEM2860>3.0.CO;2-N
  7. Harrowfield, J. M.; Matt, D. J. Incl. Phenom. Macrocyclic Chem. 2004, 50, 133 https://doi.org/10.1007/s10847-004-0288-0
  8. Dunitz, J. D.; Gavezzotti, A. Angew. Chem. Int. Ed. 2005, 44, 1766 https://doi.org/10.1002/anie.200460157
  9. Maitland, G. C.; Rigby, M.; Smith, E. B.; Wakeham, W. A. Intermolecular Forces: Their Origin and Determination Oxford University Press: New York, 1987
  10. J. Molecular Structure (THEOCHEM) Thakkit, A., Ed.; 2002; Vol. 591 –special issue on intermolecular forces
  11. Desiraju, G. R.; Steiner, T. The Weak Hydrogen Bond, IUCr Monographs on Crystallography, No. 9, Oxford University Press: New York, 1999
  12. Janiak, C. J. Chem. Soc., Dalton Trans. 2000, 3885
  13. Scudder, M. C.; Dance, I. G. J. Chem. Soc., Dalton Trans. 2001, 789 and references therein
  14. Jennings, W. B.; Farrell, B. M.; Malone, J. F. Acc. Chem. Res. 2001, 34, 885 https://doi.org/10.1021/ar0100475
  15. McMurtrie, J.; Dance, I. G. Cryst. Eng. Comm. 2005, 7, 216 and references therein. See also references 1-4 https://doi.org/10.1039/b500289c
  16. Henry, M.; Hosseini, M. W. New J. Chem. 2004, 28, 897 https://doi.org/10.1039/b402213k
  17. Comba, P.; Curtis, N. F.; Lawrance, G. A.; Sargeson, A. M.; Skelton, B. W.; White, A. H. Inorg. Chem. 1986, 25, 4260 https://doi.org/10.1021/ic00243a040
  18. Bernhardt, P. V.; Lawrance, G. A. Coord. Chem. Rev. 1990, 104, 297 https://doi.org/10.1016/0010-8545(90)80045-U
  19. Lawrance, G. A.; Manning, T. M.; Maeder, M.; Martinez, M.; O'Leary, M. A.; Patalinghug, W. C.; Skelton, B. W.; White, A. H. J. Chem. Soc., Dalton Trans. 1992, 1635 and following papers
  20. Harrowfield, J. M.; Jang, G. H.; Kim, Y.; Thuery, P.; Vicens, J. J. Chem. Soc., Dalton Trans. 2002, 1241
  21. Harrowfield, J. M.; Kim, J. Y.; Kim, Y.; Lee, Y. H.; Thuery, P. Polyhedron 2005, 24, 1569 https://doi.org/10.1016/j.poly.2005.04.013
  22. Bernhardt, P. V.; Cho, J. H.; Harrowfield, J. M.; Kim, J. Y.; Kim, Y.; Sujandi; Thuery, P.; Yoon, D. C. Polyhedron 2006, 25, 1811 https://doi.org/10.1016/j.poly.2005.11.024
  23. Kappa-CCD Software, Nonius BV, Delft, The Netherlands, 1998
  24. Otwinowski, Z.; Minor, W. Methods Enzymol. 1997, 276, 307 https://doi.org/10.1016/S0076-6879(97)76066-X
  25. Sheldrick, G. M. SHELXS-97 and SHELXL-97 University of Gottingen: Germany, 1997
  26. Sheldrick, G. M. SHELXTL, Version 5.1 University of Gottingen: Germany, distributed by Bruker AXS, Madison, WI, USA, 1999
  27. Kang, S. J.; Ozawa, T. C. Balls & Sticks available from: http://www.toycrate.org
  28. Bosnich, B.; Poon, C. K.; Tobe, M. L. Inorg. Chem. 1965, 4, 1102 https://doi.org/10.1021/ic50030a003
  29. Choi, M.-H.; Kim, B.-J.; Kim, I.-C.; Kim, S.-H.; Kim, Y.; Harrowfield, J. M.; Lee, M.-K.; Mocerino, M.; Rukmini, E.; Skelton, B. W.; White, A. H. J. Chem. Soc., Dalton Trans. 2001, 707 and references therein
  30. See Harrowfield, J. M.; Lugan, N.; Shahverdizadeh, G. H.; Soudi, A. A.; Thuery, P. Eur. J. Inorg. Chem. 2006, 389 and references therein
  31. Bernhardt, P. V.; Dyahningtyas, T. E.; Han, S. C.; Harrowfield, J. M.; Kim, I.-C.; Kim, Y.; Koutsantonis, G. A.; Thuery, P. Polyhedron 2004, 23, 869 and references therein https://doi.org/10.1016/j.poly.2003.12.014
  32. Harrowfield, J. M.; Lugan, N.; Marandi, F.; Shahverdizadeh, G. H.; Soudi, A. A. Aust. J. Chem. 2006, 59, 400 https://doi.org/10.1071/CH06131
  33. Letard, J.-F.; Guionneau, P.; Nguyen, O.; Sanchez Costa, J.; Marcen, S.; Chastanet, G.; Marchivie, M.; Goux-Capes, L. Chem. Eur. J. 2005, 11, 4582 https://doi.org/10.1002/chem.200500112

Cited by

  1. Hirshfeld surface analysis of crystal packing in aza-aromatic picrate salts vol.16, pp.21, 2014, https://doi.org/10.1039/C4CE00095A
  2. Functionalised azetidines as ligands: species derived by selective alkylation at substituent-nitrogen vol.2009, pp.3, 2007, https://doi.org/10.1039/b812298a