Pouliquen G, Amiel C, Tribet C
Physico-chimie des Polymères et Milieux Dispersés, UMR 7615 CNRS and University Paris 6, ESPCI, 10 rue Vauquelin, F-75005 Paris, France.
J Phys Chem B. 2007 May 24;111(20):5587-95. doi: 10.1021/jp070798+. Epub 2007 May 1.
In aqueous solutions, beta-cyclodextrin (CD) and cyclodextrin-containing polymers (PolCD) associate with azobenzene-modified polyacrylate (AMP). Inclusion complexes in solution of CD (or PolCD) and AMP, and the viscosity of these mixtures, have been studied as a function of the composition of AMP and concentrations of samples. AMPs are random copolymers containing a low fraction of a light-responsive hydrophobic moieties (<10 mol % of 6-[4-alkylamido]phenylazobenzene acrylamide), and a charged hydrophilic unit, sodium acrylate. PolCDs are beta-cyclodextrin randomly conjugated with epichlorohydrin and fractionated to yield copolymers of average number of CD per chain equal to 50. In dilute solutions, the composition of complexes has been investigated by capillary electrophoresis and UV-vis spectrometry. Association between PolCD and AMP appears more complex than the conventional Benesi-Hildebrand scheme. We identified a tight (quantitative) binding regime followed by a gradual increase of the density of AMP-bound PolCD upon increasing the concentration of PolCD. At higher concentrations, the formation of large clusters has been characterized by the increase of viscosity by several decades. Light-triggered trans-conformation of the azobenzene moieties of AMPs leads to a marked photoswitch of viscosity. Reversible viscosity swings by up to 6-fold were achieved by alternative exposure to UV and visible lights. In contrast, the composition of PolCD/AMP complexes in dilute regime does not respond to light, though subtle modifications of the structures of complexes are reflected by variation of electrophoretic mobilities and UV spectra. The properties of interpolymer clusters and photoviscosity are accordingly the result of modification of the dynamics of association. In practice, the low concentration of photochrome makes it possible to obtain rapid responses in samples having a thickness of the order of cm. The data reported provide guidelines for the formulations of CD/polymer systems, specifically, viscosity enhancers, which should show promising developments in pharmaceuticals or cosmetics.
在水溶液中,β-环糊精(CD)和含环糊精聚合物(PolCD)与偶氮苯改性聚丙烯酸酯(AMP)缔合。研究了CD(或PolCD)与AMP在溶液中的包合物以及这些混合物的粘度与AMP组成和样品浓度的关系。AMPs是含有低比例光响应疏水基团(<10摩尔%的6-[4-烷基酰胺基]苯基偶氮苯丙烯酰胺)和带电荷亲水单元丙烯酸钠的无规共聚物。PolCDs是β-环糊精与环氧氯丙烷随机共轭并分级得到的每条链平均CD数等于50的共聚物。在稀溶液中,通过毛细管电泳和紫外-可见光谱研究了络合物的组成。PolCD与AMP之间的缔合似乎比传统的贝内西-希尔德布兰德方案更为复杂。我们确定了一种紧密(定量)结合模式,随后随着PolCD浓度的增加,与AMP结合处的PolCD密度逐渐增加。在较高浓度下,大聚集体的形成表现为粘度增加了几十倍。AMPs中偶氮苯基团的光触发反式构象导致粘度发生显著的光开关变化。通过交替暴露于紫外光和可见光,实现了高达6倍的可逆粘度变化。相比之下,稀溶液中PolCD/AMP络合物组成对光无响应,尽管络合物结构的细微变化通过电泳迁移率和紫外光谱的变化得以体现。聚合物聚集体的性质和光致粘度因此是缔合动力学变化的结果。实际上,光致变色剂的低浓度使得在厚度约为厘米的样品中能够获得快速响应。所报道的数据为CD/聚合物体系的配方提供了指导方针,特别是粘度增强剂,这在制药或化妆品领域应会有良好的发展前景。