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Titlebook: Hydrogen-Bonded Liquids; John C. Dore,José Teixeira Book 1991 Springer Science+Business Media Dordrecht 1991 bonding.chemistry.electrolyte

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51#
發(fā)表于 2025-3-30 09:30:20 | 只看該作者
52#
發(fā)表于 2025-3-30 15:38:32 | 只看該作者
53#
發(fā)表于 2025-3-30 17:12:48 | 只看該作者
X-Ray Diffraction Studies of Liquidsental methods is given. The steps to convert the raw data into a reduced intensity function are also described. The structural description of molecular liquids as given by Fourier transformation is then analysed with a special reference to hydrogen-bonded liquids.
54#
發(fā)表于 2025-3-30 23:57:32 | 只看該作者
Structural Analysis of Liquid Formic Acid Using Neutron Diffractionuctural information. The bond lengths obtained from the intramolecular analysis are consistent with those obtained by other methods. The intermolecular structure consists of molecules linked extensively through hydrogen bonds of bond length 1.8. to form long chains.
55#
發(fā)表于 2025-3-31 03:35:10 | 只看該作者
Properties of H-Bonding in the Infrared Spectral Rangelimited to the study of the hydrogen stretching bands perturbed by this interaction. It is shown that their profile is generated by complex relaxation processes in which several oscillators, coupled by anharmonic forces, are simultanously relaxing. These processes are very fast, and the liquid acts, in essence, as a static disordered medium.
56#
發(fā)表于 2025-3-31 05:28:30 | 只看該作者
57#
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Nato Science Series C:http://image.papertrans.cn/h/image/430420.jpg
58#
發(fā)表于 2025-3-31 16:25:20 | 只看該作者
1389-2185 ded liquids‘ would be an appropriate topic. One of its attractions, was that there was much new material coming from widely disparate investigations and it woul978-94-010-5445-4978-94-011-3274-9Series ISSN 1389-2185
59#
發(fā)表于 2025-3-31 18:31:49 | 只看該作者
60#
發(fā)表于 2025-4-1 00:20:30 | 只看該作者
Methods for Calculating Intermolecular Potential Energy Surfacesethod gives a more detailed description of the interaction than the supermolecule approach, and consequently provides more physical insight into the nature of the interaction. Both of these methods require calculations to be carried out at a wide range of dimer geometries if a full description of th
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