二维势面波包动力学分析了d2和d8四方配合物发光光谱中的振动结构

PhysChemComm Pub Date : 2000-01-01 DOI:10.1039/B008386K
M. Triest, S. Masson, J. Grey, C. Reber
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引用次数: 1

摘要

四边形反式reo2(乙烯基咪唑)4+配合物和正方形平面Pd(SCN)42?和Pt (SCN) 42吗?配合物在两种主要的振动模式下都表现出振动级数。在第一个复合体中,振动过程涉及高频和低频金属?配位模式。在方形平面配合物中,两种振动模式具有相似的频率。在中等分辨率下,通常在实验中观察到,这些化合物提供了缺失模式(或MIME)效应的一个例子。二维表面上的波包动力学以一种直观和吸引人的方式解释了光谱特征。不同的影响是由描述每个复合体的二维模型的两种模式之间的不同频率比引起的。从光谱中确定的发射态结构揭示了Pd(SCN)42?沿弯曲法向坐标的类似变化。和Pt (SCN) 42吗?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vibronic structure in the luminescence spectra of tetragonal d2 and d8 complexes analyzed by wavepacket dynamics on two-dimensional potential surfaces
The luminescence spectra of the tetragonal trans-ReO2(vinylimidazole)4+ complex and the square planar Pd(SCN)42? and Pt(SCN)42? complexes all show vibronic progressions in two predominant vibrational modes. In the first complex, the vibronic progressions involve high-frequency and low-frequency metal?ligand modes. In the square planar complexes, the two vibrational modes have similar frequencies. At the intermediate resolution, often observed experimentally, these compounds provide an example of the missing mode (or MIME) effect. Wavepacket dynamics on two-dimensional surfaces explain in a visual and intuitively appealing way the spectroscopic features. The distinct effects are caused by the different frequency ratios between the two modes of the two-dimensional models describing each complex. The emitting state structure determined from the spectra reveals similar changes along a bending normal coordinate for Pd(SCN)42? and Pt(SCN)42?
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