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首页> 外文期刊>The Journal of Chemical Physics >THE INFRARED PHOTODISSOCIATION SPECTRA OF FE-N(CH3OH)(M) COMPLEXES AND THEIR DEUTERATED ANALOGS NEAR 10-MU
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THE INFRARED PHOTODISSOCIATION SPECTRA OF FE-N(CH3OH)(M) COMPLEXES AND THEIR DEUTERATED ANALOGS NEAR 10-MU

机译:FE-N(CH3OH)(M)配合物的红外光解离谱及其在10-MU附近的氘化模拟物

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The infrared photodissociation spectra of Fe-n(CH3OH)(m), Fe-n(CH3OD)(m), Fe-n(CD3OH)(m), and Fe-n(CD3OD)(m) (n = 5-15; m = 1,2) have been recorded from 920-1090 cm(-1). Analysis of the spectral features indicates that in all cases, molecularly adsorbed methanol is the absorbing chromophore, with no evidence of methoxy formation. The observed frequencies for the C-O stretching vibration and other vibrational modes are shifted similar to 40 cm(-1) to the red of the corresponding fundamentals of gas-phase methanol. The spectral shifts and thus the magnitude of the cluster-methanol interaction are observed to be independent of iron cluster size over the size range studied, implying an insensitivity of the interaction to the underlying cluster structure. (C) 1996 American Institute of Physics. [References: 33]
机译:Fe-n(CH3OH)(m),Fe-n(CH3OD)(m),Fe-n(CD3OH)(m)和Fe-n(CD3OD)(m)的红外光解离光谱(n = 5- 15; m = 1,2)已记录在920-1090 cm(-1)处。光谱特征分析表明,在所有情况下,分子吸收的甲醇都是吸收发色团,没有甲氧基形成的迹象。观察到的C-O拉伸振动和其他振动模式的频率与气相甲醇的相应基本原理的红色相似地偏移了40 cm(-1)。在所研究的尺寸范围内,观察到光谱位移以及簇-甲醇相互作用的强度与铁簇的大小无关,这意味着相互作用对下面的簇结构不敏感。 (C)1996年美国物理研究所。 [参考:33]

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