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杯芳烃与二茂铌二氯化物之间的主客体相互作用

Host-Guest Interactions between Calixarenes and Cp(2)NbCl(2).

作者信息

Morales Alexis, Santana Alberto, Althoff Gerhard, Melendez Enrique

机构信息

Department of Chemistry, University of Puerto Rico, Mayagüez, PR 00681.

出版信息

J Organomet Chem. 2011 Jul 1;696(13):2519-2527. doi: 10.1016/j.jorganchem.2011.03.021.

Abstract

The possible inclusion complexes of Cp(2)NbCl(2) into calixarenes hosts have been investigated. The existence of a true inclusion complex in the solid state was confirmed by a combination of NMR, ab-initio calculations, thermogravimetric analysis, FTIR, Raman and PXRD. Ab-initio calculations, (1)H NMR solution and solid state (13)C CP MAS NMR results demonstrated that p-sulfonic calix[6]arene does form an inclusion complex with Cp(2)NbCl(2). Raman spectroscopy showed, for the inclusion compound of p-sulfonic calix[6]arene-Cp(2)NbCl(2), a band between 500-850 cm(-1) characteristic of Nb-O vibration. This result suggests that Nb(V) may engage in coordination with the oxygen of the sulfonate group, as part of the host-guest interaction. However, it is important to mention that the niobocene dichloride (Cp(2)NbCl(2)) dissolves in water and undergoes oxidation and hydrolysis processes to yield Cp(2)NbCl(2)(OH) species. For that reason this band does not exclude that the Nb-O band belongs to Cp(2)NbCl(2)(OH). Solid State (13)C CP MAS NMR and solution (1)H NMR spectroscopies together with ab-initio results showed that Cp(2)NbCl(2) is included in the p-sulfonic calix[6]arene cavity, with both Cp rings inside the cavity. In contrast, the solution (1)H NMR results demonstrated that calix[6]arene does not form inclusion complex with Cp(2)NbCl(2) in CDCl(3) solution. Cp(2)NbCl(2) is not included in the calix[6]arene cavity, possibly due to the lack of sulfonate heads which promote Nb-O interactions and assist the inclusion of Cp(2)NbCl(2) into the cavity.

摘要

已对二氯二茂铌(Cp₂NbCl₂)与杯芳烃主体形成的可能包合物进行了研究。通过核磁共振(NMR)、从头算计算、热重分析、傅里叶变换红外光谱(FTIR)、拉曼光谱和粉末X射线衍射(PXRD)相结合的方法,证实了固态中存在真正的包合物。从头算计算、¹H NMR溶液和固态¹³C交叉极化魔角旋转(CP MAS)NMR结果表明,对磺酸基杯[6]芳烃确实与Cp₂NbCl₂形成了包合物。拉曼光谱显示,对于对磺酸基杯[6]芳烃 - Cp₂NbCl₂包合物,在500 - 850 cm⁻¹之间有一条Nb - O振动特征带。该结果表明,作为主客体相互作用的一部分,Nb(V)可能与磺酸根基团的氧发生配位。然而,需要指出的是,二氯二茂铌(Cp₂NbCl₂)可溶于水,并经历氧化和水解过程,生成Cp₂NbCl₂(OH)物种。因此,该谱带不能排除Nb - O谱带属于Cp₂NbCl₂(OH)的可能性。固态¹³C CP MAS NMR和溶液¹H NMR光谱以及从头算结果表明,Cp₂NbCl₂被包含在对磺酸基杯[6]芳烃的空腔中,两个茂环都在空腔内。相比之下,溶液¹H NMR结果表明,杯[6]芳烃在CDCl₃溶液中不与Cp₂NbCl₂形成包合物。Cp₂NbCl₂不被包含在杯[6]芳烃的空腔中,可能是由于缺乏促进Nb - O相互作用并协助Cp₂NbCl₂进入空腔的磺酸根基。

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