Matsugi Akira, Takahashi Kazuo
National Institute of Advanced Industrial Science and Technology (AIST) , 16-1 Onogawa, Tsukuba, Ibaraki 305-8569, Japan.
Department of Materials and Life Sciences, Sophia University , 7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8554, Japan.
J Phys Chem A. 2017 Jul 6;121(26):4881-4890. doi: 10.1021/acs.jpca.7b04086. Epub 2017 Jun 27.
The thermal decomposition reactions of 2,3,3,3- and trans-1,3,3,3-tetrafluoropropenes (TFPs) have been studied both experimentally and computationally to elucidate their kinetics and mechanism. The experiments were performed by observing the temporal profiles of HF produced in the decomposition of the tetrafluoropropenes behind shock waves at temperatures of 1540-1952 K (for 2,3,3,3-TFP) or 1525-1823 K (for trans-1,3,3,3-TFP) and pressure of 100-200 kPa in Ar bath. The reaction pathways responsible for the profiles were explored based on quantum chemical calculations. The decomposition of 2,3,3,3-TFP was predicted to proceed predominantly via direct 1,2-HF elimination to yield CHCCF, while trans-1,3,3,3-TFP was found to decompose to HF and a variety of isomeric CHF products including CHCCF, CFCCHF, CCHCF, and CFCHCF. The CHF isomers can subsequently decompose to either CF + CHCF or CFCC + HF products. Multichannel RRKM/master equation calculations were performed for the identified decomposition channels. The observed formation rates and apparent yields of HF are shown to be consistent with the computational predictions.
已通过实验和计算研究了2,3,3,3-和反式-1,3,3,3-四氟丙烯(TFP)的热分解反应,以阐明其动力学和反应机理。实验是通过观察在氩气浴中温度为1540 - 1952 K(对于2,3,3,3-TFP)或1525 - 1823 K(对于反式-1,3,3,3-TFP)、压力为100 - 200 kPa的冲击波后四氟丙烯分解产生的HF的时间分布来进行的。基于量子化学计算探索了导致这些分布的反应途径。预计2,3,3,3-TFP的分解主要通过直接1,2-HF消除生成CHCCF,而发现反式-1,3,3,3-TFP分解为HF和多种异构CHF产物,包括CHCCF、CFCCHF、CCHCF和CFCHCF。CHF异构体随后可分解为CF + CHCF或CFCC + HF产物。对确定的分解通道进行了多通道RRKM/主方程计算。观察到的HF生成速率和表观产率与计算预测结果一致。