Department of Chemistry and Biochemistry, California State University Northridge, 18111 Nordhoff St., Northridge, CA 91330-8262, USA.
Phys Chem Chem Phys. 2018 Nov 14;20(44):27949-27958. doi: 10.1039/c8cp04903c.
The chemical mechanisms of the OH radical, Cl-atom and O3 initiated oxidation of (Z)-CF3CH[double bond, length as m-dash]CHCl were studied at 296 ± 1 K in 10-700 Torr air of N2/O2 diluent. Cl atoms add to the [double bond splayed left]C[double bond, length as m-dash]C[double bond splayed right] double bond: 12 ± 5% to the terminal carbon and 85 ± 5% to the central carbon. In 700 Torr of air the products are CF3CHClCHO, HCOCl, CF3COCl, CF3CHO, (E)-CF3CH[double bond, length as m-dash]CHCl, CF3C(O)CHCl2, and CF3CHClCOCl. The yield of (E) isomer was dependent on total pressure, but independent of O2 partial pressure; consistent with isomerization occurring via Cl atom elimination from the chemically activated rather than the thermalized CF3CHCHCl-Cl adduct. The rate constant for (Z)-CF3CH[double bond, length as m-dash]CHCl + Cl was measured at low pressure (10-15 Torr) and found to be indistinguishable from that determined at 700 Torr total pressure, whereas the low pressure rate constant for (E)-CF3CH[double bond, length as m-dash]CHCl was 36% smaller. G4MP2 ab initio calculations showed that the (E) isomer is 1.2 kcal mol-1 more stable than the (Z) isomer. Cl atom elimination from the adduct will preferentially form the (E) isomer and hence the rate of CF3CH[double bond, length as m-dash]CHCl loss will be more sensitive to pressure for the (Z) than the (E) isomer. Reaction of (Z)-CF3CH[double bond, length as m-dash]CHCl with OH radicals gives CF3CHO, HCOCl, (E)-CF3CH[double bond, length as m-dash]CHCl, and HCl. A significant chlorine atom elimination channel was observed experimentally, and supported by computational results. The oxidation products of the reaction of O3 with (Z)- and (E)-CF3CH[double bond, length as m-dash]CHCl were determined with no evidence of isomerization. The results are discussed with respect to the atmospheric chemistry and environmental impact of (Z)- and (E)-CF3CH[double bond, length as m-dash]CHCl.
在氮气/氧气稀释剂中的 10-700 托空气下,于 296±1 K 研究了(Z)-CF3CH[双键,长度为破折号]CHCl 被 OH 自由基、Cl 原子和 O3 引发的氧化的化学机制。Cl 原子加成到[双键张开左]C[双键,长度为破折号]C[双键张开右]双键:终端碳原子上的 12±5%,中心碳原子上的 85±5%。在 700 托的空气中,产物为 CF3CHClCHO、HCOCl、CF3COCl、CF3CHO、(E)-CF3CH[双键,长度为破折号]CHCl、CF3C(O)CHCl2 和 CF3CHClCOCl。(E)异构体的产率取决于总压力,但与 O2 分压无关;与 Cl 原子从化学活化而不是热化的 CF3CHCHCl-Cl 加合物中消除一致。在低压(10-15 托)下测量了(Z)-CF3CH[双键,长度为破折号]CHCl + Cl 的速率常数,发现与在 700 托总压力下测定的速率常数没有区别,而(E)-CF3CH[双键,长度为破折号]CHCl 的低压速率常数小 36%。G4MP2 从头算计算表明,(E)异构体比(Z)异构体稳定 1.2 kcal mol-1。从加合物中消除 Cl 原子将优先形成(E)异构体,因此 CF3CH[双键,长度为破折号]CHCl 的损失速率对(Z)异构体的压力比(E)异构体更敏感。(Z)-CF3CH[双键,长度为破折号]CHCl 与 OH 自由基反应生成 CF3CHO、HCOCl、(E)-CF3CH[双键,长度为破折号]CHCl 和 HCl。实验中观察到一个显著的氯原子消除通道,并得到计算结果的支持。(Z)-和(E)-CF3CH[双键,长度为破折号]CHCl 与 O3 反应的氧化产物已确定,没有异构化的证据。结果与(Z)-和(E)-CF3CH[双键,长度为破折号]CHCl 的大气化学和环境影响有关。