Marushkevich Kseniya, Khriachtchev Leonid, Räsänen Markku
Laboratory of Physical Chemistry, University of Helsinki, P.O. Box 55, FIN-00014, Finland.
Phys Chem Chem Phys. 2007 Nov 21;9(43):5748-51. doi: 10.1039/b712647f.
Conformers of formic acid (FA) are studied by IR spectroscopy in solid hydrogen. The higher-energy cis-FA conformer is prepared by vibrational excitation of the ground-state trans-FA conformer. The quantum yield of the trans to cis conformational process in solid hydrogen appears about two orders of magnitude smaller than in solid argon, which is explained by efficient coupling of the vibrationally excited trans form with the host vibrations deactivating the conformational change. The trans to cis conformational process is efficiently promoted by excitation of the hydrogen-matrix rovibrational transitions (host excitation), which confirms the strong coupling between vibrations of the host and embedded molecule. These results demonstrate a unique process of conformational reorganization mediated by vibrational excitation of the host. The tunneling decay of the cis-FA monomer in solid hydrogen is found to be 4 times faster than in solid argon but 30 times slower than in solid neon, and this is discussed in terms of the matrix solvation effect.
通过红外光谱对固态氢中的甲酸(FA)构象异构体进行了研究。通过基态反式FA构象异构体的振动激发制备了高能顺式FA构象异构体。固态氢中反式到顺式构象过程的量子产率似乎比固态氩中的小约两个数量级,这是由于振动激发的反式构象与主体振动的有效耦合使构象变化失活所致。通过氢基质转动-振动跃迁的激发(主体激发)有效地促进了反式到顺式的构象过程,这证实了主体与嵌入分子振动之间的强耦合。这些结果证明了由主体的振动激发介导的独特构象重组过程。发现固态氢中顺式FA单体的隧穿衰减比固态氩中的快4倍,但比固态氖中的慢30倍,并根据基质溶剂化效应进行了讨论。