Colmenero Francisco, Escribano Rafael
Instituto de Estructura de la Materia (IEM-CSIC) , C/ Serrano, 113, 28006 Madrid , Spain.
J Phys Chem A. 2019 May 16;123(19):4241-4261. doi: 10.1021/acs.jpca.9b01354. Epub 2019 May 6.
A precise and complete thermodynamic, Raman spectroscopic, and ultraviolet-visible (UV-vis) optical characterization of the deltic, squaric, and croconic cyclic oxocarbon acids is obtained using theoretical solid-state methods employing very demanding calculation parameters. The computed fundamental thermodynamic properties include the isobaric specific heat, the entropy, the enthalpy, and the Gibbs free energy as a function of temperature. The calculated specific heats at 298.15 K of the deltic, squaric, and croconic acids are 89.7, 111.2, and 133.2 J mol K, respectively, and the corresponding entropies are 98.3, 117.3, and 136.5 J mol K. The only value of these properties known from experimental measurements is the specific heat of the squaric acid, which differs from the computed value at 315 K by about 4.9%. The calculated values of the thermodynamic properties are then used to determine the thermodynamic properties of formation of these materials in terms of the elements. As an application of the calculated thermodynamic properties of formation, the Gibbs free energies of reaction and associated reaction constants are evaluated for the reactions of thermal decomposition and complete combustion of the squaric and croconic acids and the reaction of interconversion between them. The only available experimental values of these properties, namely, the enthalpies of combustion of squaric and croconic acids at room temperature, are reproduced theoretically with high accuracy. The Raman spectra of these materials are also computed using density functional perturbation theory. The analysis of the theoretical Raman spectra of these materials points out to significant differences with respect to their usual empirical assignment. Therefore, the Raman spectra of these materials are fully reassigned. Finally, the ultraviolet-visible (UV-vis) optical properties of the deltic, squaric, and croconic acids are computed. The UV-vis absorption spectrum of the croconic acid in the spectral region 225-425 nm and the UV absorption spectrum of the squaric acid in the region 200-350 nm, which had previously been measured experimentally, are well reproduced. The corresponding spectrum for the deltic acid and the reflectivity, optical conductivity, dielectric, refractive index, and loss optical functions of the three materials, which had never been published as far as we know, are reported as a function of the wavelength of incident radiation in the range 200-750 nm. The origin of the peaks in the absorption spectra, which had not been analyzed so far, is unveiled here by examining the interband electronic transitions in these materials.
使用采用非常严格计算参数的理论固态方法,对δ型、方型和呫吨型环状含氧羧酸进行了精确而完整的热力学、拉曼光谱和紫外可见(UV-vis)光学表征。计算得到的基本热力学性质包括等压比热、熵、焓以及作为温度函数的吉布斯自由能。在298.15 K时,δ型、方型和呫吨型酸的计算比热分别为89.7、111.2和133.2 J·mol⁻¹·K⁻¹,相应的熵分别为98.3、117.3和136.5 J·mol⁻¹·K⁻¹。从实验测量中已知的这些性质的唯一值是方酸的比热,其在315 K时与计算值相差约4.9%。然后,利用计算得到的热力学性质值来确定这些材料基于元素的生成热力学性质。作为生成热力学性质计算的应用,对方酸和呫吨酸的热分解和完全燃烧反应以及它们之间的相互转化反应的反应吉布斯自由能和相关反应常数进行了评估。这些性质仅有的可用实验值,即方酸和呫吨酸在室温下的燃烧焓,可以通过理论高精度再现。还使用密度泛函微扰理论计算了这些材料的拉曼光谱。对这些材料理论拉曼光谱的分析指出了与它们通常的经验归属存在显著差异。因此,对这些材料的拉曼光谱进行了全面重新归属。最后,计算了δ型、方型和呫吨型酸的紫外可见(UV-vis)光学性质。呫吨酸在225 - 425 nm光谱区域的紫外可见吸收光谱以及方酸在200 - 350 nm区域的紫外吸收光谱,此前已通过实验测量,得到了很好的再现。据我们所知,从未发表过的δ型酸的相应光谱以及这三种材料的反射率、光导率、介电常数、折射率和损耗光学函数,作为入射辐射波长在200 - 750 nm范围内的函数进行了报道。通过研究这些材料中的带间电子跃迁,揭示了迄今为止尚未分析的吸收光谱中峰的起源。