Mohaček-Grošev Vlasta, Grdadolnik Jože, Hadži Dušan
Center of Excellence for Advanced Materials and Sensing Devices, Ruđer Bošković Institute , Bijenička c. 54, 10002 Zagreb, Croatia.
National Institute of Chemistry , Hajdrihova 19, 1000 Ljubljana, Slovenia.
J Phys Chem A. 2016 May 12;120(18):2789-96. doi: 10.1021/acs.jpca.5b12577. Epub 2016 Apr 29.
Low temperature Raman spectra of oxalic acid dihydrate (8-300 K) for both the polycrystalline and single crystal phase show strong variation with temperature in the interval from 1200 to 2000 cm(-1). Previous low temperature diffraction studies all confirmed the stability of the crystal P21/n phase with no indications of any phase transition, reporting the existence of a strong hydrogen bond between the oxalic acid and a water molecule. A new group of Raman bands in the 1200-1300 cm(-1) interval below 90 K is observed, caused by possible loss of the center of inversion. This in turn could originate either due to disorder in hydroxyl proton positions or due to proton transfer from carboxylic group to water molecule. The hypothesis of proton transfer is further supported by the emergence of new bands centered at 1600 and 1813 cm(-1), which can be explained with vibrations of H3O(+) ions. The broad band at 1600 cm(-1) looses intensity, while the band at 1813 cm(-1) gains intensity on cooling. The agreement between quantum calculations of vibrational spectra and experimentally observed Raman bands of hydronium ions in oxalic acid sesquihydrate crystal corroborates this hypothesis.
多晶相和单晶相的二水合草酸(8 - 300 K)的低温拉曼光谱在1200至2000 cm⁻¹区间随温度有强烈变化。先前的低温衍射研究均证实了晶体P21/n相的稳定性,没有任何相变迹象,报告了草酸与水分子之间存在强氢键。在90 K以下的1200 - 1300 cm⁻¹区间观察到一组新的拉曼谱带,这可能是由于反演中心的丧失所致。这反过来可能源于羟基质子位置的无序,或者是由于质子从羧基转移到水分子。质子转移的假设进一步得到了以1600和1813 cm⁻¹为中心的新谱带出现的支持,这可以用H₃O⁺离子的振动来解释。1600 cm⁻¹处的宽带强度减弱,而1813 cm⁻¹处的谱带在冷却时强度增加。草酸半水合物晶体中振动光谱的量子计算与实验观察到的水合氢离子拉曼谱带之间的一致性证实了这一假设。