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气相中的主客体化学:葫芦[6]脲与质子化水二聚体的复合物形成

Host-guest chemistry in the gas phase: complex formation of cucurbit[6]uril with proton-bound water dimer.

作者信息

Noh Dong Hun, Lee Shin Jung C, Lee Jong Wha, Kim Hugh I

机构信息

Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.

出版信息

J Am Soc Mass Spectrom. 2014 Mar;25(3):410-21. doi: 10.1007/s13361-013-0795-6. Epub 2014 Jan 17.

Abstract

The hydration of cucurbit[6]uril (CB[6]) in the gas phase is investigated using electrospray ionization traveling wave ion mobility mass spectrometry (ESI-TWIM-MS). Highly abundant dihydrated and tetrahydrated species of diprotonated CB[6] are found in the ESI-TWIM-MS spectrum. The hydration patterns of the CB[6] ion and the dissociation patterns of the hydrated CB[6] ion indicate that two water molecules are bound to each other, forming a water dimer in the CB[6] complex. Ion mobility studies combined with the structures calculated by density functional theory suggest that the proton-bound water dimer is present as a Zundel-like structure in the CB[6] portal, forming a hydrogen bond network with carbonyl groups of the CB[6]. When a large guest molecule is bound to a CB[6] portal, water molecules cannot bind to the portal. In addition, the strong binding energy of the water dimer blocks the portal, hindering the insertion of the long alkyl chain of the guest molecule into the CB[6] cavity. With small alkali metal cations, such as Li(+) and Na(+), a single water molecule interacts with the CB[6] portal, forming hydrogen bonds with the carbonyl groups of CB[6]. A highly stable Zundel-like structure of the proton-bound water dimer or a metal-bound water molecule at the CB[6] portal is suggested as an initial hydration process for CB[6], which is only dissolved in aqueous solution with acid or alkali metal ions.

摘要

采用电喷雾电离行波离子迁移率质谱法(ESI-TWIM-MS)对葫芦[6]脲(CB[6])在气相中的水合作用进行了研究。在ESI-TWIM-MS谱图中发现了双质子化CB[6]的高度丰富的二水合物和四水合物种。CB[6]离子的水合模式和水合CB[6]离子的解离模式表明,两个水分子相互结合,在CB[6]配合物中形成一个水二聚体。离子迁移率研究结合密度泛函理论计算的结构表明,质子结合的水二聚体以类似祖德耳(Zundel)的结构存在于CB[6]的入口处,与CB[6]的羰基形成氢键网络。当一个大的客体分子与CB[6]的入口结合时,水分子不能与该入口结合。此外,水二聚体的强结合能阻塞了入口,阻碍了客体分子的长烷基链插入CB[6]的空腔。对于小的碱金属阳离子,如Li(+)和Na(+),单个水分子与CB[6]的入口相互作用,与CB[6]的羰基形成氢键。质子结合的水二聚体或CB[6]入口处金属结合的水分子的高度稳定的类似祖德耳的结构被认为是CB[6]的初始水合过程,CB[6]仅在有酸或碱金属离子的水溶液中溶解。

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