Stimuli-responsive supramolecular micellar assemblies of cetylpyridinium chloride with cucurbit[5/7]urils

被引:41
作者
Choudhury, Sharmistha Dutta [1 ]
Barooah, Nilotpal [1 ]
Aswal, Vinod Kumar [2 ]
Pal, Haridas [1 ]
Bhasikuttan, Achikanath C. [1 ]
Mohanty, Jyotirmayee [1 ]
机构
[1] Bhabha Atom Res Ctr, Radiat & Photochem Div, Bombay 400085, Maharashtra, India
[2] Bhabha Atom Res Ctr, Div Solid State Phys, Bombay 400085, Maharashtra, India
关键词
CETYL PYRIDINIUM CHLORIDE; BETA-CYCLODEXTRIN; DIFFERENTIAL INTERACTION; CUCURBITURIL HOMOLOGS; THIAZOLE ORANGE; HOST; VESICLES; RECOGNITION; COMPLEXES; BROMIDE;
D O I
10.1039/c3sm52024b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This article demonstrates, for the first time, construction of novel cucurbituril (CB)-adorned supramolecular micellar assemblies of a cationic surfactant, cetylpyridinium chloride (CPC), through noncovalent host-guest interactions. The distinct cation receptor features and cavity dimensions of the CB5 and CB7 homologues assert that the macrocyclic hosts remain complexed with the CPC monomers and take part in the micelle formation, a unique observation in contrast to that of the classical host, beta-cyclodextrin. The cooperative contributions of the CB macrocycles in the micelle formation have been documented by the photochemical, surface tension, conductivity, DOSY NMR, and SANS measurements. The contrasting downward and upward shifts in the cmc of the CPC surfactant, respectively, with CB5 and CB7 hosts provide a unique opportunity for the controlled tuning of the micellization region for CPC from 0.57 to 1.6 mM, by using a combination of the macrocyclic hosts. The article also establishes the reversible response of these soft supramolecular micellar structures to thermal-stimuli, which projects their utility for on-demand smart drug-delivery vehicles.
引用
收藏
页码:3485 / 3493
页数:9
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