Zwier Timothy S
Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, Indiana 47907-2084, USA.
J Phys Chem A. 2006 Mar 30;110(12):4133-50. doi: 10.1021/jp056390z.
Molecules with several flexible coordinates have potential energy surfaces with a large number of minima and many transition states separating them. A general experimental protocol is described that is capable of studying conformational isomerization in such circumstances, measuring the product quantum yields following conformation-specific infrared excitation, and measuring energy thresholds for isomerization of specific X --> Y reactant-product isomer pairs following excitation via stimulated emission pumping (SEP). These methods have been applied to a series of molecules of varying size and conformational complexity, including 3-indolepropionic acid (IPA), meta-ethynylstyrene, N-acetyltryptophan methyl amide (NATMA), N-acetyltryptophan amide (NATA), and melatonin. Studies of isomerization in solute-solvent complexes are also described, including a measurement of the barrier to isomerization in the IPA-H2O complex, and a unique isomerization reaction in which a single water molecule is shuttled between H-bonding sites on the trans-formanilide (TFA) molecule.
具有多个灵活坐标的分子具有势能面,其上有大量极小值以及许多将它们分隔开的过渡态。本文描述了一种通用的实验方案,该方案能够在这种情况下研究构象异构化,测量构象特异性红外激发后的产物量子产率,并通过受激发射泵浦(SEP)激发后测量特定X→Y反应物-产物异构体对异构化的能量阈值。这些方法已应用于一系列大小和构象复杂度各异的分子,包括3-吲哚丙酸(IPA)、间乙炔基苯乙烯、N-乙酰色氨酸甲酯酰胺(NATMA)、N-乙酰色氨酸酰胺(NATA)和褪黑素。还描述了溶质-溶剂络合物中的异构化研究,包括测量IPA-H₂O络合物中异构化的势垒,以及一个独特的异构化反应,其中单个水分子在反式甲酰苯胺(TFA)分子的氢键位点之间穿梭。