Czímerová A, Iyi N, Bujdák J
Institute of Inorganic Chemistry, Slovak Academy of Sciences, Dúbravská Cesta 9, SK-84536 Bratislava, Slovakia.
J Colloid Interface Sci. 2008 Apr 1;320(1):140-51. doi: 10.1016/j.jcis.2007.10.055. Epub 2008 Jan 28.
Series of montmorillonites with systematically reduced layer charges represent a suitable model for studying various properties and interactions of layered inorganic compounds. The reduced-charge montmorillonites (RCMs) used in this study were prepared by a standard method of Li+-fixation in Nanocor montmorillonite at 100-300 degrees C. The layer charge gradually decreased with increasing temperature of RCM preparation. Li+-fixation led in some cases to the loss of expandability due to the formation of mixed swelling/nonswelling and homogeneous nonswelling phases. The interaction of two cationic dyes-rhodamine 3B (R3B) and oxazine 4 (Ox4)-with reduced-charge montmorillonites in dispersions was studied by means of UV/vis absorption and fluorescence spectroscopy. Montmorillonite with the highest charge density induced the formation of H-aggregates of the dye cations characterized by a sandwich-type structure. As the layer charge decreased, the amount of the H-aggregates was reduced in favor of H-dimers and monomers. RCMs with low charge density suppressed dye cation aggregation and mainly monomeric forms were detected. The process of energy transfer from R3B to Ox4 was detected as decreasing the emission from the energy donor and increasing the emission from the energy acceptor. The energy transfer was clearly influenced by the properties of RCM templates. The dye cations adsorbed at the surface of the highest-charge specimen formed H-aggregates, which were efficient luminescence quenchers. Fluorescence resonance energy transfer (FRET) gradually increased with the charge reduction to be optimal at the templates with medium layer charge. Substantial decrease of the layer charge and reduction of clay mineral swelling led to the decrease of both the luminescence and the efficiency of FRET. The relations of energy transfer processes to the layer charges and swelling properties of montmorillonite are analyzed in detail.
一系列层电荷系统降低的蒙脱石是研究层状无机化合物各种性质和相互作用的合适模型。本研究中使用的低电荷蒙脱石(RCMs)是通过在100 - 300℃下对Nanocor蒙脱石进行标准的Li + 固定方法制备的。随着RCM制备温度的升高,层电荷逐渐降低。在某些情况下,Li + 固定由于形成混合膨胀/非膨胀和均匀非膨胀相而导致膨胀性丧失。通过紫外/可见吸收光谱和荧光光谱研究了两种阳离子染料罗丹明3B(R3B)和恶嗪4(Ox4)与分散体中低电荷蒙脱石的相互作用。具有最高电荷密度的蒙脱石诱导形成具有三明治型结构的染料阳离子H - 聚集体。随着层电荷降低,H - 聚集体的数量减少,有利于H - 二聚体和单体的形成。低电荷密度的RCMs抑制染料阳离子聚集,主要检测到单体形式。检测到从R3B到Ox4的能量转移过程表现为能量供体的发射减少和能量受体的发射增加。能量转移明显受RCM模板性质的影响。吸附在最高电荷样品表面的染料阳离子形成H - 聚集体,它们是有效的发光猝灭剂。荧光共振能量转移(FRET)随着电荷降低而逐渐增加,在中等层电荷的模板处达到最佳。层电荷的大幅降低和粘土矿物膨胀的减少导致发光和FRET效率均降低。详细分析了能量转移过程与蒙脱石层电荷和膨胀性质的关系。