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关于一种具有光开关杯芳烃的主客体复合物上客体置换反应的动力学研究。

A kinetic study of guest displacement reactions on a host-guest complex with a photoswitchable calixarene.

作者信息

Letzel Matthias C, Schäfer Christian, Novara Francesca R, Speranza Maurizio, Rozhenko Alexander B, Schoeller Wolfgang W, Mattay Jochen

机构信息

Fakultät für Chemie, Universität Bielefeld, Postfach 100131, 33501 Bielefeld, Germany.

出版信息

J Mass Spectrom. 2008 Nov;43(11):1553-64. doi: 10.1002/jms.1464.

Abstract

The displacement processes of several guests, incorporated in a calixarene host system, were investigated in the gas phase by electrospray ionization-Fourier transform-ion cyclotron resonance (ESI-FT-ICR) mass spectrometry. The complexes resulting from a resorcin[4]arene host with ammonia and sec-butylamine guests were isolated in an ICR-cell, separately using both states of the photoswitch as well as two reference systems for the open and closed forms of the photoswitchable host. The isolated complexes were forced to exchange the guest by using methylamine, ethylamine and sec-butylamine, resulting in different reaction rates for all the measured systems. Especially, the reaction rates of both states of the photoswitch are dependent on the provided guest. Potential side effects like proton exchanges were examined by an H/D-exchange experiment. The results were investigated and supported by quantum chemical calculations (DFT).

摘要

通过电喷雾电离-傅里叶变换离子回旋共振(ESI-FT-ICR)质谱法,在气相中研究了杯芳烃主体体系中几种客体的置换过程。使用光开关的两种状态以及光开关主体开放和闭合形式的两个参考体系,分别在ICR池中分离出由间苯二酚[4]芳烃主体与氨和仲丁胺客体形成的配合物。通过使用甲胺、乙胺和仲丁胺迫使分离出的配合物进行客体交换,所有测量体系均产生了不同的反应速率。特别是,光开关两种状态的反应速率取决于所提供的客体。通过H/D交换实验研究了质子交换等潜在副作用。结果通过量子化学计算(DFT)进行了研究和支持。

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