Jensen Casper Vindahl, Vogt Emil, Poulsen Andras Sun, Kjaergaard Henrik G
Department of Chemistry, University of Copenhagen, 2100 Copenhagen-Ø, Denmark.
J Phys Chem A. 2024 Aug 8;128(31):6382-6391. doi: 10.1021/acs.jpca.4c02730. Epub 2024 Jul 31.
We have detected the methanol dimer, trimer, and tetramer at equilibrium conditions at room temperature in the gas phase using direct absorption Fourier transform infrared spectroscopy. The infrared intensity of the OH-stretching transitions are enhanced upon hydrogen bonding and are increasingly red-shifted with increasing cluster size, facilitating identification and quantification of the various clusters. We calculate the intensities of the bound OH-stretches, OH, for all clusters with a range of reduced dimensional vibrational models with different levels of electronic structure theory. Partial pressures of the clusters are obtained by scaling the measured integrated absorbance of the OH-stretching bands by the calculated intensities of the associated vibrational transitions. We estimate the methanol dimer equilibrium constant, , to be 0.033, at 298.15 K, which is comparable to that of the water dimer. For the methanol trimer and tetramer, we estimate equilibrium constants for aggregation of monomers of ∼ 0.04 and ∼ 0.6, respectively.
我们使用直接吸收傅里叶变换红外光谱法,在室温下的平衡条件下,于气相中检测到了甲醇二聚体、三聚体和四聚体。OH伸缩跃迁的红外强度在形成氢键时会增强,并且随着团簇尺寸的增加而越来越向红端移动,这有助于对各种团簇进行识别和定量。我们使用具有不同电子结构理论水平的一系列降维振动模型,计算了所有团簇中键合OH伸缩振动(OH)的强度。通过将OH伸缩带的测量积分吸光度按相关振动跃迁的计算强度进行缩放,得到团簇的分压。我们估计在298.15 K时甲醇二聚体的平衡常数为0.033,这与水二聚体的平衡常数相当。对于甲醇三聚体和四聚体,我们分别估计单体聚集的平衡常数约为0.04和约0.6。