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首页> 外文期刊>New Journal of Chemistry >Synthesis and crystal structure of nitrosoruthenium complexes cis-[Ru(NO)Py2Cl2(OH)] and cis-[Ru(NO)Py2Cl2(H2O)]Cl. Photoinduced transformations of cis-[Ru(NO)Py2Cl2(OH)]
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Synthesis and crystal structure of nitrosoruthenium complexes cis-[Ru(NO)Py2Cl2(OH)] and cis-[Ru(NO)Py2Cl2(H2O)]Cl. Photoinduced transformations of cis-[Ru(NO)Py2Cl2(OH)]

机译:亚硝基钌配合物顺式[[Ru(NO)Py2Cl2(OH)]和顺式[Ru(NO)Py2Cl2(H2O)] Cl的合成及晶体结构。顺式[Ru(NO)Py2Cl2(OH)]的光诱导转变

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摘要

The interaction of K-2[Ru(NO)Cl-5] with an excess of pyridine followed by concentration of the reaction solution afforded two crystalline modifications of cis-[Ru(NO)Py2Cl2(OH)] (1a and 1b). The treatment of this hydroxocomplex with hydrochloric acid gave an aquacomplex cis-[Ru(NO)Py2Cl2(H2O)]Cl (2). The prepared complexes were characterized by elemental analysis, X-ray diffraction, infrared and H-1 NMR spectroscopies. Infrared and Raman spectroscopies provided evidence that irradiation of cis-[Ru(NO)Py2Cl2(OH)] (lambda similar to 450 nm, T = 80 K) resulted in photoisomerization with the formation of metastable states MS1 (isonitrosyl complex) and MS2 (eta(2)-coordination of the NO). The population of the MS1 state amounts to 60%. Differential scanning calorimetry (DSC) was used to determine the activation parameters for MS1: E-a = 65.2(3) kJ mol(-1), k(0) = 1.05(7) x 10(14) s(-1). These experimental data agree well with DFT calculations.
机译:K-2 [Ru(NO)Cl-5]与过量吡啶的相互作用,然后浓缩反应溶液,得到了顺-[Ru(NO)Py2Cl2(OH)]的两种晶体修饰(1a和1b)。用盐酸处理这种羟基络合物,得到水络合物顺式[[Ru(NO)Py2Cl2(H2O)] Cl(2)。通过元素分析,X射线衍射,红外和H-1 NMR光谱对制备的复合物进行表征。红外和拉曼光谱法提供的证据表明,顺-[Ru(NO)Py2Cl2(OH)](λ类似于450 nm,T = 80 K)的照射导致光致异构化,并形成了亚稳态MS1(异亚硝基复合物)和MS2( eta(2)-NO的配位)。 MS1州的人口达到60%。差示扫描量热法(DSC)用于确定MS1的激活参数:E-a = 65.2(3)kJ mol(-1),k(0)= 1.05(7)x 10(14)s(-1)。这些实验数据与DFT计算非常吻合。

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