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Raman and infrared band shapes of the NH +...X-hydrogen bond in trimethylaminium halide crystals
The infrared and Raman band profile and band-width of the crystalline halides (CH 3) 3NH +X − in the v(NH) stretching vibration region are analyzed with the help of the temperature dependence and of the isotopic substitution effect. While the infrared v(NH) band-width is several times larger than th...
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Published in: | Chemical physics letters 1974-07, Vol.27 (1), p.111-113 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The infrared and Raman band profile and band-width of the crystalline halides (CH
3)
3NH
+X
− in the
v(NH) stretching vibration region are analyzed with the help of the temperature dependence and of the isotopic substitution effect. While the infrared
v(NH) band-width is several times larger than the Raman linewidth in the pure substance, the widths are about the same in the isotopic diluted system (CH
3)
3NH
+Cl
−/(CH
3)
3ND
+Cl
−. This result is explained by induced cooperative effects increasing strongly the anharmonicity of the electrical moment and not that of the polarizability of the NH oscillators. |
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ISSN: | 0009-2614 1873-4448 |
DOI: | 10.1016/0009-2614(74)80456-2 |