L—组氨酸和色氨酸三元体系中稀土（Ⅲ）,钙（Ⅱ）的化学形态

在模拟生理条件下（３７℃,Ｉ＝０．１５ｍｏｌ／ＬＮａＣｌ）,用ｐＨ电位滴定与计算机模拟计算相结合的方法研究了镨（Ⅲ）、钆（Ⅲ）、铽（Ⅲ）、镱（Ⅲ）４ｔｋｈ ｔｑｄ ｆｆｆｆｙｂ ｂｂ ｔ ｑｇｈ （Ⅱ）、锌（Ⅱ）离子在Ｌ－组氨酸、色氨酸三元体系中的化学形态。讨论了稀土（Ⅲ）、钙（Ⅱ）和锌（Ⅱ）的物种分布特点。     

Preparation and Characterization of Ternary Europium ComplexDoped Thin SolGel Hybrid Film by Fluorescence Spectroscopy*

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅｌｏｗ－ｔｅｍｐｅｒａｔｕｒｅｐｒｏｃｅｓｓｉｎｇｏｆｔｈｅｓｏｌ－ｇｅｌｍａｔｅｒｉａｌｍａｋｅｓｉｔｐｏｓｓｉｂｌｅｔｏｅｎｔｒａｐｏｒｇａｎｉｃｓｐｅｃｉｅｓｅａｓｉｌｙｗｉｔｈｉｎａｒｉｇｉｄｇｌａｓｓｍａｔｒｉ...     

L-组氨酸和色氨酸三元体系中稀土(Ⅲ)、钙(Ⅱ)和锌(Ⅱ)的化学形态

在模拟生理条件下(37℃,I=0.15 mol/L NaCl),用pH电位滴定与计算机模拟计算相结合的方法研究了镨(Ⅲ)、钆(Ⅲ)、铽(Ⅲ)、镱(Ⅲ)4种稀土离子和钙(Ⅱ)、锌(Ⅱ)离子在L-组氨酸、色氨酸三元体系中的化学形态.讨论了稀土(Ⅲ)、钙(Ⅱ)和锌(Ⅱ)的物种分布特点.     

稀土与甘氨酰－L－亮氨酸的配位作用

用ｐＨ电位法测定了生理条件下（３７℃，Ｉ＝０．１５ｍｏｌ／Ｌ）和２５℃，Ｉ＝０．１０ｍｏｌ／Ｌ时甘氨酰－Ｌ－亮氨酸的质子化常数及其稀土配合物稳定常数，结果表明稀土可与该配体形成１：１配合物，并且配合物稳定性呈现明显“四分组效应”。讨论了钇的位置以及肽键对配合物稳定性的影响。     

两步溶胶-凝胶法于SiO2/聚合物杂化基质中原位合成铕的三元配合物及其发光性质

采用两步溶胶－凝胶过程制备了含铕的三元配合物的凝胶。荧光激发光谱证实于ＳｉＯ２基质中原位合成了铕的配合物。含铕配合物的杂化材料发出铕的特征荧光，与相应的纯配合物溶于乙醇相比，铕离子具有较长的荧光寿命。     

稀土与甘氨酰—L—亮氨酸的配位作用

用ｐＨ电位法测定了生理条件（３７℃，Ｉ＝０．１５ｍｏｌ／Ｌ）和２５℃，Ｉ＝０．１０ｍｏｌ／Ｌ时甘氨酰Ｌ－亮氨酸的质子化常数及其稀土配合物稳定常数。结果表明稀土可与该配体形成１：１配合物，并且配合物稳定性呈现明显“四分组效应”。讨论了钇的位置以及肽键对配合物稳定性的影响。     

Preparation and Luminescence Properties of the Ternary Europium Complex Incorporated into an Inorganic/Polymer Matrix by a Sol-Gel Method

Ternary europium complexes with thenoyltrifluoroacetone (TTA) and phenanthroline (phen) were incorporated into SiO₂/polymer matrix by a sol-gel method. The gels exhibit the characteristic emission bands of europium ion. In addition, Eu³⁺ presents a longer fluorescence lifetime in gel than in the corresponding pure complex powder. Concentration effects on the luminescence intensity were investigated. The reasons that are responsible for above results are also discussed in the context.     

Magnetic Fe3O4@mesoporous silica composites for drug delivery and bioadsorption

Magnetic Fe(3)O(4)@mesoporous silica (MS) composites were synthesized by generating Fe(3)O(4) nanoparticles in the mesoporous silica matrix using the sol-gel method in nitrogen atmosphere. The mesoporous silica hosts include SBA-15 particles owning highly ordered p6mm mesostructure, siliceous mesostructured cellular foams (MCFs), and fiber-like mesoporous silica (FMS) with unique pore structures. The X-ray diffraction (XRD), transmission electron microscopy (TEM), and N(2) adsorption/desorption results show that Fe(3)O(4) functionalized MCFs and FMS possess suitable mesoporous structure for the adsorption of both small-molecular drug and large biomolecules. The biocompatibility tests on L929 fibroblast cells using MTT assay reveal low cytotoxicity of these systems. These Fe(3)O(4)@mesoporous silica composites show sustained release properties for aspirin in vitro. The release of the aspirin molecules from the pores of the Fe(3)O(4)@mesoporous silica composites is basically a diffusive process. Fe(3)O(4)@MCFs and Fe(3)O(4)@FMS owning larger pore size are good candidates for the adsorption of bovine serum albumin (BSA). These magnetic composites can be potential vectors for drug delivery and bioadsorption.     

Tetra‐μ‐α‐alanine‐bis­[tetra­aqua­gadolinium(III)] hexaperchlorate

The title complex, [Gd₂(C₃H₇NO₂)₄(H₂O)₈](ClO₄)₆, contains centrosymmetric dimeric [Gd₂(Ala)₄(H₂O)₈]⁶⁺ cations (Ala is α‐alanine) and perchlorate anions. The four alanine mol­ecules act as bridging ligands linking two Gd³⁺ ions through their carboxylate O atoms. Each Gd³⁺ ion is also coordinated by four water mol­ecules, which complete an eightfold coordination in a square‐antiprism fashion. The perchlorate anions and the methyl groups of the alanine ligands are disordered.     

间甲基和邻氯苯甲酸稀土配合物发光性能的研究

本文研究了间甲基苯甲酸稀土配合物REL3(RE=Eu,Tb;HL=m-CH2C6H4CO2H)和邻氯苯甲酸稀土配合物REL3·H2O(RE=EU·Tb;HL=ClC6H4CO2H)的荧光性能,测量了配合物的激发和荧光光谱及其寿命,讨论了晶体结构对能级匹配、能量传递等光谱性质的影响.