文献类型：期刊文献

英文题名：Aggregation and Host-Guest Interactions in Dansyl-Substituted Poly(acrylate)s in the Presence of β-Cyclodextrin and a β-Cyclodextrin Dimer in Aqueous Solution: A UV-Vis, Fluorescence, ¹H NMR, and Rheological Study

作者：Wang, Jie[2];Duc-Truc Pham[1];Kee, Tak W.[1];Clafton, Scott N.[1];Guo, Xuhong[2];Clements, Philip[1];Lincoln, Stephen F.[1];Prud'homme, Robert K.[4];Easton, Christopher J.[3]

机构：[1]Univ Adelaide, Sch Chem & Phys, Adelaide, SA 5005, Australia;[2]E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China;[3]Australian Natl Univ, Res Sch Chem, Canberra, ACT 0200, Australia;[4]Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA

年份：2011

卷号：44

期号：24

起止页码：9782

外文期刊名：MACROMOLECULES

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000298198600035)】；

基金：We gratefully acknowledge Australian Research Council funding, NSFC Grant 20774028 and 20774030, 111 Project Grant B08021, Shanghai Shuguang Plan Project 06SG35, Shanghai Pujiang Talent Project 07PJ14022, and the China Scholarship Council for supporting this work.

语种：英文

摘要：A UV-vis, steady-state, and time-resolved fluorescence 2D H-1 NOESY NMR spectroscopic and rheological study of new poly(acrylate)s 3% randomly substituted with either N-(2-aminoethyl)-, N-(6-aminohexyl)-, or N-(12-aminododecyl)-5-dansyl-sulfonamide to give the substituted polymers PAADSen, PAADShn, and PAADSddn, respectively, is reported. Their dansyl substituent aggregation and complexation by beta-cyclodextrin, beta CD, and its covalently linked dimer N,N'-bis(6(A)-deoxy-6(A)-beta-cyclodextrin)urea, 66 beta CD(2)ur, is also reported. The beta CD complexation of the dansyl substituents is characterized by apparent complexation constants, K = 89, 105, and 55 dm(3) mol(-1) for PAADSen, PAADShn, and PAADSddn, respectively, and the analogous complexations by 66 beta CD(2)ur are characterized by K = 3.04 x 10(3), 3.42 x 10(4), and 2.42 x 10(5) dm(3) mol(-1) at pH 7.0 in aqueous 0.10 mol dm(-3) NaCl at 298.2 K. Under the same conditions the dansyl substituent shows three fluorescence decay constants assigned to the aggregated (tau(1) = 2.2, 2.5, and 3.2 ns), single (tau(2) = 5.0, 5.3, and 9.5 ns), beta CD (tau(3) = 13.2, 11.7 ns, and undetected), and 66 beta CD(2)ur complexed dansyl substituent states (tau(3) = 13.9, 20.8, and 19.3 ns) where the values in each data set correspond to PAADSen, PAADShn, and PAAddn solutions, respectively. 2D H-1 NOESY NMR spectroscopy provides additional insight into dansyl substituent complexation by beta CD and 66 beta CD(2)ur, as do rheological studies. These data are interpreted in terms of the factors affecting dansyl substituent fluorescence quenching and the impact of tether length on dansyl substituent aggregation, complexation, and network formation.