journal article·2005-11-01

Structure of a Cyclodextrin Functionalized Anionic Clay: XRD Analysis, Spectroscopy, and Computer Simulations

L. Mohanambe, S. Vasudevan

Langmuir· Volume 21· Issue 23
Publisher page

Abstract

Carboxy-methyl beta-cyclodextrin (CMCD) cavities have been intercalated within the galleries of anionic clay, Mg-Al layered double hydroxide (LDH). The cyclodextrin functionalized LDH has been reported to adsorb neutral and nonpolar guest molecules. X-ray diffraction, IR, and Raman vibrational spectroscopy and (13)C CPMAS NMR have been used to characterize the confined CMCD molecules, whereas molecular dynamics simulations have been used to probe the interlayer arrangement and orientation of the intercalated species. Spectroscopic measurements as well as MD simulations show that there is no significant change in the geometry of the CMCD cavity on intercalation. Within the galleries of the anionic clay, the CMCD anions are arranged as bilayers with the carboxy methyl substituents, located at the narrower opening of the bucket-like cyclodextrin toroid, anchored to the LDH sheet. This arrangement leaves the wider opening of the CMCD anion facing away from the layers allowing the interior of the cyclodextrin cavity to be accessible to guest molecules. Finally, the hydrophobicity of the anchored cyclodextrin cavity has been characterized using fluorescence from pyrene included within it.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Clay minerals and soil interactions · Mesoporous Materials and Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore-560012, India

References (55)

Show source-provided references
1. Intercalation Chemistry · 1982
2. Alberti, G.; Costantino, U. InComprehensive Supramolecular ChemistryAlberti, G., Bein, T., Atwood, J. L., Eds.; Wiley: Chichester, U.K., 1996; Vol. 7, p 1.
3. Gluech D. S. · Inorg. Chem. · 1993 · 32 · 189310.1021/ic00062a005 ↗
4. Aranda P. · Adv. Mater. · 1990 · 2 · 54510.1002/adma.19900021108 ↗
5. Jeevanandam P. · Chem. Mater. · 1998 · 10 · 127610.1021/cm9706006 ↗
6. Vogtle F. · 1991
7. Steed J. W. · 2000
8. Kijima T. · Nature · 1984 · 310 · 4510.1038/310045a0 ↗
9. Kijima T. · Nature · 1986 · 322 · 53310.1038/322533a0 ↗
10. Zhao H. · J. Chem. Soc., Dalton Trans. · 1997 · 11 · 196110.1039/a607604a ↗
11. Zhao H. · J. Inclusion Phenom. · 1998 · 316 · 317
12. Zhao H. · Clays Clay Miner. · 1998 · 46 · 71210.1346/CCMN.1998.0460612 ↗
13. Khan I. K. · J. Mater. Chem. · 2002 · 12 · 319110.1039/B204076J ↗
14. Constantino V. R. L. · J. Inorg. Chem. · 1995 · 34 · 88310.1021/ic00108a020 ↗
15. Miyata S. · Clays Clay Miner. · 1977 · 25 · 1410.1346/CCMN.1977.0250103 ↗
16. Miyata S. · Clays Clay Miner. · 1983 · 31 · 30510.1346/CCMN.1983.0310409 ↗
17. Miyata S. · Clays Clay Miner. · 1975 · 23 · 36910.1346/CCMN.1975.0230508 ↗
18. De Roy, A.; Forano, C.; El Malki, K.; Bessi, J. P. InExpanded Clays andOther Microporous Solids; Occelli, M. L., Robson, H. E., Eds.; Van Nostrand Reinhold: New York,1992; Vol. 2, p 108.10.1007/978-1-4684-8866-1_7 ↗
19. Cavani F. · Catal. Today · 1991 · 11 · 17310.1016/0920-5861(91)80068-K ↗
20. Newman S. · New J. Chem. · 1998 · 22 · 10510.1039/a708319j ↗
21. Vaccari A. · Appl. Clay Sci. · 1999 · 14 · 16110.1016/S0169-1317(98)00058-1 ↗
22. Rives V. · Coord. Chem. Rev. · 1999 · 181 · 6110.1016/S0010-8545(98)00216-1 ↗
23. Choy J. H. · J. Am. Chem. Soc. · 1999 · 121 · 139910.1021/ja981823f ↗
24. Choy J. H. · Angew. Chem., Int. Ed. · 2000 · 39 · 4042
25. Mohanambe L. · J. Phys. Chem. B · 2005 · 109 · 1186510.1021/jp0522516 ↗
26. Mohanambe L. · Inorg. Chem. · 2005 · 44 · 212810.1021/ic050039a ↗
27. Mohanambe L. · Inorg. Chem. · 2004 · 43 · 642110.1021/ic0495721 ↗
28. Zeng Q. H. · J. Phys. Chem. B · 2004 · 108 · 10033
29. Miroslav P. · J. Colloid Interface Sci. · 2001 · 236 · 131
30. Jianwei, W.; Andrey, G. K.; Kirkpatrick, R. J.; Xiaoqiang, H.Chem.Mater.2001,13, 145−15010.1021/cm000441h ↗
31. Andrey G. K. · Am. Mineral. · 2000 · 85 · 1052
32. Newman S. P. · J. Phys. Chem. B · 1998 · 102 · 671910.1021/jp981426r ↗
33. Newman S. P. · Langmuir · 2002 · 18 · 293910.1021/la0114528 ↗
34. Meyn M. · Inorg. Chem. · 1990 · 29 · 520110.1021/ic00351a013 ↗
35. Cerius · 2001
36. Bellotto M. · J. Phys. Chem. · 1996 · 100 · 8534
37. Rappe A. K. · J. Phys. Chem. · 1991 · 95 · 335810.1021/j100161a070 ↗
38. Lindner K. · Carbohydr. Res. · 1982 · 99 · 10310.1016/S0008-6215(00)81901-1 ↗
39. Szejtli J. · 1982
40. Mayo S. L. · J. Phys. Chem. · 1990 · 94 · 8909
41. Newman S. P. · 2001
42. Haile J. M. · 1992
43. Hoover W. H. · Phy. Rev. A · 1985 · 31
44. User · 2001
45. Allen, M. P.; Tildesley, D. J. InComputer simulation of Liquids; Oxford University Press: New York, 1987; p 385.
46. Choy J. H. · J. Phys. Chem. Solids · 2004 · 65 · 50910.1016/j.jpcs.2003.08.036 ↗
47. Connors K. · 1996 · 3 · 234
48. Szejtli · 1996 · 3 · 17
49. Szejtli · 1996 · 3 · 12
50. Hineno M. · Carbohydr. Res. · 1977 · 56 · 21910.1016/S0008-6215(00)83344-3 ↗
51. Tu A. T. · Carbohydr. Res. · 1979 · 76 · 23910.1016/0008-6215(79)80023-3 ↗
52. Kalyanasundaram K. · J. Am. Chem. Soc. · 1977 · 99 · 203910.1021/ja00449a004 ↗
53. Koyanagi M. · J. Mol. Spectrosc. · 1968 · 25 · 27310.1016/S0022-2852(68)80043-8 ↗
54. Robinson G. W. · J. Chem. Phys. · 1967 · 46 · 57210.1063/1.1840705 ↗
55. Bernard Valeur · 200110.1002/3527600248 ↗