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丙二酸二乙酯对离子封装富勒烯M@C(M =空、锂、钠、钾、镁、钙和氯)的宾格尔-赫希加成反应

Bingel-Hirsch Addition of Diethyl Bromomalonate to Ion-Encapsulated Fullerenes M@C (M=Ø, Li, Na, K, Mg, Ca, and Cl).

作者信息

Besalú-Sala Pau, Luis Josep M, Solà Miquel

机构信息

Institut de Química Computacional i Catàlisi (IQCC) and Departament de Química, Universitat de Girona, C/ Maria Aurèlia Capmany 69, 17003, Girona, Catalonia, Spain.

出版信息

Chemistry. 2020 Nov 11;26(63):14481-14487. doi: 10.1002/chem.202003208. Epub 2020 Oct 6.

Abstract

In the last 30 years, fullerene-based materials have become popular building blocks for devices with a broad range of applications. Among fullerene derivatives, endohedral metallofullerenes (EMFs, M@C) have been widely studied owing to their unique properties and reactivity. For real applications, fullerenes and EMFs must be exohedrally functionalized. It has been shown that encapsulated metal cations facilitate the Diels-Alder reaction in fullerenes. Herein, the Bingel-Hirsch (BH) addition of ethyl bromomalonate over a series of ion-encapsulated M@C (M=Ø, Li, Na, K, Mg, Ca, and Cl; Ø@C stands for C without any endohedral metal) is quantum mechanically explored to analyze the effect of these ions on the BH addition. The results show that the incarcerated ion has a very important effect on the kinetics and thermodynamics of this reaction. Among the systems studied, K@C is the one that leads to the fastest BH reaction, whereas the slowest reaction is given by Cl@C.

摘要

在过去30年里,基于富勒烯的材料已成为具有广泛应用的器件的常用构建模块。在富勒烯衍生物中,内嵌金属富勒烯(EMFs,M@C)因其独特的性质和反应活性而受到广泛研究。对于实际应用而言,富勒烯和EMFs必须进行外表面官能化。研究表明,包封的金属阳离子可促进富勒烯中的狄尔斯-阿尔德反应。在此,用量子力学方法探究了丙二酸乙酯在一系列离子包封的M@C(M = Ø、Li、Na、K、Mg、Ca和Cl;Ø@C代表不含任何内嵌金属的C)上的宾格尔-赫希(BH)加成反应,以分析这些离子对BH加成反应的影响。结果表明,包封的离子对该反应的动力学和热力学有非常重要的影响。在所研究的体系中,K@C导致的BH反应最快,而Cl@C的反应最慢。

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