Firouzi A, Kumar D, Bull L M, Besier T, Sieger P, Huo Q, Walker S A, Zasadzinski J A, Glinka C, Nicol J
Department of Chemical Engineering, University of California, Santa Barbara 93106.
Science. 1995 Feb 24;267(5201):1138-43. doi: 10.1126/science.7855591.
A model that makes use of the cooperative organization of inorganic and organic molecular species into three dimensionally structured arrays is generalized for the synthesis of nanocomposite materials. In this model, the properties and structure of a system are determined by dynamic interplay among ion-pair inorganic and organic species, so that different phases can be readily obtained through small variations of controllable synthesis parameters, including mixture composition and temperature. Nucleation, growth, and phase transitions may be directed by the charge density, coordination, and steric requirements of the inorganic and organic species at the interface and not necessarily by a preformed structure. A specific example is presented in which organic molecules in the presence of multiply charged silicate oligomers self-assemble into silicatropic liquid crystals. The organization of these silicate-surfactant mesophases is investigated with and without interfacial silicate condensation to separate the effects of self-assembly from the kinetics of silicate polymerization.
一种利用无机和有机分子物种协同组织形成三维结构阵列的模型被推广用于纳米复合材料的合成。在该模型中,系统的性质和结构由离子对无机和有机物种之间的动态相互作用决定,因此通过可控合成参数(包括混合物组成和温度)的微小变化可以很容易地获得不同的相。成核、生长和相变可能由界面处无机和有机物种的电荷密度、配位和空间要求引导,而不一定由预先形成的结构引导。给出了一个具体例子,其中在多电荷硅酸盐低聚物存在下有机分子自组装成硅otropic液晶。研究了这些硅酸盐 - 表面活性剂中间相在有无界面硅酸盐缩合情况下的组织情况,以将自组装的影响与硅酸盐聚合动力学分开。