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氧代乙氧基钛簇合物[Ti16O16(OEt)32]的反应活性。基于纳米结构单元的杂化材料的通用前驱体。

Reactivity of titanium oxo ethoxo cluster [Ti16O16(OEt)32]. Versatile precursor of nanobuilding block-based hybrid materials.

作者信息

Fornasieri Giulia, Rozes Laurence, Le Calvé Stéphanie, Alonso Bruno, Massiot Dominique, Rager Marie Noëlle, Evain Michel, Boubekeur Kamal, Sanchez Clément

机构信息

Laboratoire de Chimie de la Matière Condensée, UMR CNRS 7574, Université Pierre et Marie Curie, 4 place Jussieu, 75252 Paris Cedex 05, France.

出版信息

J Am Chem Soc. 2005 Apr 6;127(13):4869-78. doi: 10.1021/ja043330i.

Abstract

Oxo alcoxo metallic clusters can be employed as inorganic nanobuilding blocks to obtain well-defined organic-inorganic hybrid materials. A better understanding of the surface reactivity of the clusters should allow optimization of the elaboration of hybrid materials through a better control of the hybrid interface. The oxo alcoxo cluster Ti(16)O(16)(OEt)32 presents a shell of labile ethoxy groups that can be selectively transalcoholyzed with preservation of the titanium oxo core, leading to new oxo alcoxo clusters Ti(16)O(16)(OEt)32-x(OR)x (R: alkyl, phenyl, styrenic, etc. groups). The reactivity of the Ti(16)O(16)(OEt)32 cluster toward aliphatic and aromatic alcohols is investigated to determine both the kinetics and the number of substituted titanium atoms, which are strongly dependent on the nature of the alcohol. Characterization of the organic modification of the cluster is performed in situ by liquid (13)C NMR measurements, using the molecular structures of two new clusters, Ti(16)O(16)(OEt)28(OnPr)4 and Ti(16)O(16)(OEt)(24)(OnPr)(8) (OnPr = propoxy groups), as references. The structures of these clusters have been established using single-crystal X-ray diffraction. Moreover, a complete spectroscopic assignment of each ethoxy group is proposed after combining crystallographic data, (13)C NMR T(1) relaxation measurements, and (1)H-(1)H, (1)H-(13)C 2D NMR experiments. Finally, the cluster is functionalized with polymerizable ligands via transalcoholysis and transesterification reactions using hydroxystyrene and acetoxystyrene.

摘要

氧代醇氧基金属簇可作为无机纳米构建块,用于制备结构明确的有机-无机杂化材料。更好地了解这些簇的表面反应性,应有助于通过更好地控制杂化界面来优化杂化材料的制备。氧代醇氧基簇Ti(16)O(16)(OEt)32具有一层不稳定的乙氧基壳层,该壳层可在保留钛氧核心的情况下被选择性地进行转醇解反应,从而生成新的氧代醇氧基簇Ti(16)O(16)(OEt)32-x(OR)x(R:烷基、苯基、苯乙烯基等基团)。研究了Ti(16)O(16)(OEt)32簇对脂肪族和芳香族醇的反应性,以确定反应动力学以及取代钛原子的数量,这两者都强烈依赖于醇的性质。通过液体(13)C NMR测量,以两个新簇Ti(16)O(16)(OEt)28(OnPr)4和Ti(16)O(16)(OEt)(24)(OnPr)(8)(OnPr = 丙氧基)的分子结构为参考,对簇的有机修饰进行原位表征。这些簇的结构已通过单晶X射线衍射确定。此外,在结合晶体学数据、(13)C NMR T(1)弛豫测量以及(1)H-(1)H、(1)H-(13)C二维NMR实验后,对每个乙氧基进行了完整的光谱归属。最后,通过使用羟基苯乙烯和乙酰氧基苯乙烯的转醇解和酯交换反应,用可聚合配体对该簇进行功能化。

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