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金属有机骨架作为光致变色客体分子的主体。

Metal-organic frameworks as hosts for photochromic guest molecules.

机构信息

Department of Chemistry, University of Cologne, Greinstr. 6, 50939 Cologne, Germany.

出版信息

Inorg Chem. 2013 Mar 4;52(5):2744-9. doi: 10.1021/ic302856b. Epub 2013 Feb 14.

Abstract

Several metal-organic framework compounds (MOF-5, MIL-68(Ga), MIL-68(In), MIL-53(Al)) were loaded with azobenzene (AZB), as confirmed by XRPD measurements and elemental analysis. By IR spectroscopy, it was shown that the light-induced trans/cis isomerization of AZB in these hybrid host-guest compounds is improved compared to that of solid AZB. A population of the excited cis state up to 30% has been obtained for AZB0.66@MIL-68(In). However, no light-induced trans/cis isomerization was observed for AZB0.5@MIL-53(Al). Structural models obtained from high-resolution synchrotron powder diffraction data show that AZB molecules are densely packed within the channels of MIL-53(Al) so that no trans/cis isomerization can occur. A different situation was observed for AZB in the larger channels of MIL-68(Ga). Thus, this investigation shows the influence of the host material on the switching behavior of the embedded AZB molecules.

摘要

几种金属有机骨架化合物(MOF-5、MIL-68(Ga)、MIL-68(In)、MIL-53(Al))被负载了偶氮苯(AZB),这一点通过 X 射线粉末衍射(XRPD)测量和元素分析得到了证实。通过红外光谱(IR)表明,与固态 AZB 相比,这些混合主客体化合物中 AZB 的光诱导顺反异构化得到了改善。在 AZB0.66@MIL-68(In)中,获得了高达 30%的激发顺式态的种群。然而,在 AZB0.5@MIL-53(Al)中没有观察到光诱导的顺反异构化。从高分辨率同步辐射粉末衍射数据获得的结构模型表明,AZB 分子在 MIL-53(Al)的通道中紧密堆积,因此不会发生顺反异构化。在更大的 MIL-68(Ga)通道中,AZB 的情况则有所不同。因此,这项研究表明了主体材料对嵌入的 AZB 分子的开关行为的影响。

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