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异双金属钛有机框架中布朗斯特酸度的金属节点控制

Metal Node Control of Brønsted Acidity in Heterobimetallic Titanium-Organic Frameworks.

作者信息

Rubio-Gaspar Ana, Navalón Sergio, Tatay Sergio, Cirujano Francisco G, Fernández-Conde Carmen, Padial Natalia M, Martí-Gastaldo Carlos

机构信息

Functional Inorganic Materials Team, Instituto de Ciencia Molecular (ICMol), Universitat de València, Paterna, 46980 València, Spain.

Departamento de Química, Universitat Politècnica de València, 46022 València, Spain.

出版信息

J Am Chem Soc. 2023 Jan 23;145(7):3855-60. doi: 10.1021/jacs.2c12718.

Abstract

Compared to indirect framework modification, synthetic control of cluster composition can be used to gain direct access to catalytic activities exclusive of specific metal combinations. We demonstrate this concept by testing the aminolysis of epoxides with a family of isostructural mesoporous frameworks featuring five combinations of homometallic and heterobimetallic metal-oxo trimers (Fe, Ti, TiFe, TiCo, and TiNi). Only TiFe nodes display activities comparable to benchmark catalysts based on grafting of strong acids, which here originate from the combination of Lewis Ti and Brønsted Fe-OH acid sites. The applicability of MUV-101(Fe) to the synthesis of β-amino alcohols is demonstrated with a scope that also includes the gram scale synthesis of propranolol, a natural β-blocker listed as an essential medicine by the World Health Organization, with excellent yield and selectivity.

摘要

与间接的骨架修饰相比,簇组成的合成控制可用于直接获得特定金属组合之外的催化活性。我们通过测试一族具有同金属和异双金属金属-氧三聚体(Fe、Ti、TiFe、TiCo和TiNi)五种组合的同结构介孔骨架对环氧化物的氨解反应来证明这一概念。只有TiFe节点显示出与基于强酸接枝的基准催化剂相当的活性,这里的活性源自路易斯酸Ti和布朗斯特酸Fe-OH酸位点的组合。MUV-101(Fe)在β-氨基醇合成中的适用性通过一系列反应得到了证明,其中还包括克级规模合成普萘洛尔,这是一种被世界卫生组织列为基本药物的天然β-阻滞剂,产率和选择性都很高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adf7/9951219/d4d30edeb5d5/ja2c12718_0001.jpg

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