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首页> 外文期刊>European journal of inorganic chemistry >Impact of Spin State Transition on Vibrations of [Fe-(PM-BiA)(2)(NCS)(2)] and [Fe-(PM-PEA)(2)(NCS)(2)] Spin Crossover Compounds: Experimental and Theoretical Far IR and Raman Study
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Impact of Spin State Transition on Vibrations of [Fe-(PM-BiA)(2)(NCS)(2)] and [Fe-(PM-PEA)(2)(NCS)(2)] Spin Crossover Compounds: Experimental and Theoretical Far IR and Raman Study

机译:旋转状态过渡对[Fe-(PM-BIA)(2)(2)(2)(2)]和[Fe-(PM-PEA)(2)(2)(2)(2)]旋转交叉化合物的影响:实验 和理论远利和拉曼研究

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Far IR and Raman spectroscopy of [Fe-(PM-BiA) (2)(NCS)(2)] and [Fe-(PM-PEA)(2)(NCS)(2)] were performed to record the vibration modes of these complexes and their evolutions during spin state transition. THz spectroscopy was used to measure the far IR absorption of these compounds down to 20 cm(-1). Using density functional theory calculations, we were able to retrieve and to visualize these vibrations in both highspin and low-spin states. In both compounds, Raman spectra recorded in the 800-2250 cm(-1) wavenumber range are well accounted for by our computations. For far IR vibration modes, most of the experimental absorption peaks above 100 cm(-1) are well reproduced. However, below 100 cm(-1), marked differences were recorded. For [Fe-(PM-BiA)(2)(NCS)(2)], we demonstrate that the interactions with surrounding molecules impact the computed far IR spectra non-negligibly and can partly correct this difference.
机译:进行[Fe-(PM-BIA)(2)(2)(2)]和[Fe-(PM-PEA)(2)(2)]的远程和拉曼光谱,以记录振动模式 这些复合物及其在旋转状态过渡期间的演变。 使用THz光谱学用于测量这些化合物的远程IR吸收至20cm(-1)。 使用密度泛函理论计算,我们能够检索并在高旋转状态下可视化这些振动。 在两个化合物中,记录在800-2250cm(-1)波数范围内的拉曼光谱由我们的计算很好地占据了。 对于远红外振动模式,大多数高于100cm(-1)的实验吸收峰是良好的再现。 但是,低于100厘米(-1),记录了显着的差异。 对于[Fe-(PM-BIA)(2)(2)(2)(2)],我们证明与周围分子的相互作用影响计算的远程IR光谱不可忽略的并且可以部分校正这种差异。

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