Complexation and photodimerization of anthracene-2-sulfonate in the presence of per-6-aminocyclodextrins
作者： Seizo Tamagaki , Kazuyuki Fukuda , Hideyuki Maeda , Norimasa Mimura , Waichiro Tagaki
DOI: 10.1039/P29950000389
关键词:
摘要: The stoichiometry of molecular complexation anthracene-2-sulfonate (AS) with hexakis-, heptakis and octakis-(6-amino-2,3-di-O-methyl-6-deoxy)cyclodextrins (α-, β- γ-PACDs) has been investigated by UV, fluorescence, circular dichroism spectrophotometry; in neutral alkaline media only β-PACD gives the 2 : inclusion complex, while sufficiently acidic all PACDs form complexes benefitting greatly from electrostatic interactions. relative rates for PACD-promoted photodimerization are closely related to modes.
rsc.org
sci-hub.se 参考文章(21)
Hans Joerg Schneider, Thomas Schiestel, Patrick Zimmermann, Host-guest supramolecular chemistry. 34. The incremental approach to noncovalent interactions: coulomb and van der Waals effects in organic ion pairs Journal of the American Chemical Society. ,vol. 114, pp. 7698- 7703 ,(1992) , 10.1021/JA00046A015
Takashi Tamaki, Tomokuni Kokubu, Kunihiro Ichimura, Regio- and stereoselective photodimerization of anthracene derivatives included by cyclodextrins Tetrahedron. ,vol. 43, pp. 1485- 1494 ,(1987) , 10.1016/S0040-4020(01)90264-9
Yoshihisa Inoue, Tadao Hakushi, Yu Liu, Linhui Tong, Baojian Shen, Daosen Jin, Thermodynamics of molecular recognition by cyclodextrins. 1. Calorimetric titration of inclusion complexation of naphthalenesulfonates with .alpha.-, .beta.-, and .gamma.-cyclodextrins: enthalpy-entropy compensation Journal of the American Chemical Society. ,vol. 115, pp. 475- 481 ,(1993) , 10.1021/JA00055A017
Akio Iwama, Toshihiro Toyoda, Misaku Yoshida, Tetsuo Otsubo, Yoshiteru Sakata, Soichi Misumi, None, Layered compounds. LII. Syntheses of eleven anthracenophanes. Bulletin of the Chemical Society of Japan. ,vol. 51, pp. 2988- 2994 ,(1978) , 10.1246/BCSJ.51.2988
Kazuaki Harata, Hisashi Uedaira, The Circular Dichroism Spectra of the β-Cyclodextrin Complex with Naphthalene Derivatives Bulletin of the Chemical Society of Japan. ,vol. 48, pp. 375- 378 ,(1975) , 10.1246/BCSJ.48.375
Joshua Boger, Richard J. Corcoran, Jean-Marie Lehn, Cyclodextrin chemistry. Selective modification of all primary hydroxyl groups of α- and β-cyclodextrins Helvetica Chimica Acta. ,vol. 61, pp. 2190- 2218 ,(1978) , 10.1002/HLCA.19780610622
Waichiro Tagaki, Kazutaka Yano, Kenji Yamanaka, Hiroshi Yamamoto, Tomohiro Miyasaka, Polyaminocyclodextrins as remarkably active catalysts for the decarboxylation of oxalacetate Tetrahedron Letters. ,vol. 31, pp. 3897- 3900 ,(1990) , 10.1016/S0040-4039(00)97500-2
Friedrich Cramer, Über Einschlußverbindungen, I. Mitteil.: Additionsverbindungen der Cycloamylosen Chemische Berichte. ,vol. 84, pp. 851- 854 ,(1951) , 10.1002/CBER.19510840912
Andrée Gadelle, Jacques Defaye, Selective Halogenation at Primary Positions of Cyclomaltooligosaccharides and a Synthesis of Per-3,6-anhydro Cyclomaltooligosaccharides Angewandte Chemie International Edition in English. ,vol. 30, pp. 78- 80 ,(1991) , 10.1002/ANIE.199100781
Mario N. Berberan-Santos, Josette Canceill, Jean Claude Brochon, Ludovic Jullien, Jean Marie Lehn, Jacques Pouget, Patrick Tauc, Bernard Valeur, Multichromophoric cyclodextrins. 1. Synthesis of O-naphthoyl-.beta.-cyclodextrins and investigation of excimer formation and energy hopping Journal of the American Chemical Society. ,vol. 114, pp. 6427- 6436 ,(1992) , 10.1021/JA00042A021