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光致键联异构化在镍、钯和铂二硝基配合物单晶中的应用——光结晶学研究。

Photoactivated linkage isomerism in single crystals of nickel, palladium and platinum di-nitro complexes--a photocrystallographic investigation.

机构信息

Department of Chemistry, University of Bath, Claverton Down, Bath, UK.

出版信息

Dalton Trans. 2012 Nov 14;41(42):13173-9. doi: 10.1039/c2dt30314k.

Abstract

Low temperature, single crystal photocrystallographic studies have been carried out on four square planar Group 10 complexes [Ni(PEt(3))(2)(NO(2))(2)] 1, [Pd(PPh(3))(2)(NO(2))(2)] 2, [Pd(AsPh(3))(2)(NO(2))(2)] 3 and [Pt(PPh(3))(2)(NO(2))(2)] 4, in which the two nitro groups adopt the trans configuration. Irradiation with UV light, at 100 K, of single crystals of complexes 1-3 photoisomerise from the η(1)-NO(2) nitro form to the η(1)-ONO nitrito form occurred. Complex 1 underwent 25% conversion to the nitrito form before crystal decomposition occurred. 2 and 3 underwent 46% and 39% conversion, respectively, to the nitrito form when a photostationary state was reached. While under the same experimental conditions 4 showed no isomerisation. The photocrystallographic results can be correlated with the results of DFT calculations and with the observed trends in the solution UV/visible absorption spectroscopy obtained for these complexes. The results suggest that while steric factors in the isomerization processes are important there may also be a kinetic effect relating to the lability of the metal involved.

摘要

低温下,对四个平面正方形 Group 10 配合物 [Ni(PEt(3))(2)(NO(2))(2)] 1、[Pd(PPh(3))(2)(NO(2))(2)] 2、[Pd(AsPh(3))(2)(NO(2))(2)] 3 和 [Pt(PPh(3))(2)(NO(2))(2)] 4 进行了单晶光结晶学研究,其中两个硝基采用反式构型。在 100 K 下,用紫外光照射单晶,配合物 1-3 从 η(1)-NO(2)硝基形式光异构化为 η(1)-ONO 亚硝酰基形式。在晶体分解之前,配合物 1 经历了 25%的转化为亚硝酰基形式。当达到光稳定状态时,2 和 3 分别经历了 46%和 39%的转化为亚硝酰基形式。而在相同的实验条件下,4 没有发生异构化。光结晶学结果可以与 DFT 计算结果以及这些配合物在溶液紫外/可见吸收光谱中观察到的趋势相关联。结果表明,虽然在异构化过程中立体因素很重要,但可能也存在与涉及的金属的不稳定性有关的动力学效应。

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