Chhantyal-Pun Rabi, Welz Oliver, Savee John D, Eskola Arkke J, Lee Edmond P F, Blacker Lucy, Hill Henry R, Ashcroft Matilda, Khan M Anwar H, Lloyd-Jones Guy C, Evans Louise, Rotavera Brandon, Huang Haifeng, Osborn David L, Mok Daniel K W, Dyke John M, Shallcross Dudley E, Percival Carl J, Orr-Ewing Andrew J, Taatjes Craig A
School of Chemistry, The University of Bristol , Cantock's Close BS8 1TS, U.K.
Combustion Research Facility, Mail Stop 9055, Sandia National Laboratories , Livermore, California 94551-0969, United States.
J Phys Chem A. 2017 Jan 12;121(1):4-15. doi: 10.1021/acs.jpca.6b07810. Epub 2016 Dec 22.
The Criegee intermediate acetone oxide, (CH)COO, is formed by laser photolysis of 2,2-diiodopropane in the presence of O and characterized by synchrotron photoionization mass spectrometry and by cavity ring-down ultraviolet absorption spectroscopy. The rate coefficient of the reaction of the Criegee intermediate with SO was measured using photoionization mass spectrometry and pseudo-first-order methods to be (7.3 ± 0.5) × 10 cm s at 298 K and 4 Torr and (1.5 ± 0.5) × 10 cm s at 298 K and 10 Torr (He buffer). These values are similar to directly measured rate coefficients of anti-CHCHOO with SO, and in good agreement with recent UV absorption measurements. The measurement of this reaction at 293 K and slightly higher pressures (between 10 and 100 Torr) in N from cavity ring-down decay of the ultraviolet absorption of (CH)COO yielded even larger rate coefficients, in the range (1.84 ± 0.12) × 10 to (2.29 ± 0.08) × 10 cm s. Photoionization mass spectrometry measurements with deuterated acetone oxide at 4 Torr show an inverse deuterium kinetic isotope effect, k/k = (0.53 ± 0.06), for reactions with SO, which may be consistent with recent suggestions that the formation of an association complex affects the rate coefficient. The reaction of (CD)COO with NO has a rate coefficient at 298 K and 4 Torr of (2.1 ± 0.5) × 10 cm s (measured with photoionization mass spectrometry), again similar to rate for the reaction of anti-CHCHOO with NO. Cavity ring-down measurements of the acetone oxide removal without added reagents display a combination of first- and second-order decay kinetics, which can be deconvolved to derive values for both the self-reaction of (CH)COO and its unimolecular thermal decay. The inferred unimolecular decay rate coefficient at 293 K, (305 ± 70) s, is similar to determinations from ozonolysis. The present measurements confirm the large rate coefficient for reaction of (CH)COO with SO and the small rate coefficient for its reaction with water. Product measurements of the reactions of (CH)COO with NO and with SO suggest that these reactions may facilitate isomerization to 2-hydroperoxypropene, possibly by subsequent reactions of association products.
克里吉中间体丙酮氧化物((CH)COO)是在氧气存在下通过2,2 - 二碘丙烷的激光光解形成的,并通过同步辐射光电离质谱和腔衰荡紫外吸收光谱进行表征。使用光电离质谱和准一级方法测量了克里吉中间体与SO反应的速率系数,在298 K和4 Torr下为(7.3 ± 0.5) × 10 cm³ s⁻¹,在298 K和10 Torr(氦缓冲气)下为(1.5 ± 0.5) × 10 cm³ s⁻¹。这些值与直接测量的反式-CHCHOO与SO的速率系数相似,并且与最近的紫外吸收测量结果高度一致。在293 K和稍高压力(10至100 Torr)下,在氮气中通过腔衰荡测量(CH)COO的紫外吸收衰减来测量该反应,得到的速率系数甚至更大,范围为(1.84 ± 0.12) × 10至(2.29 ± 0.08) × 10 cm³ s⁻¹。在4 Torr下用氘代丙酮氧化物进行的光电离质谱测量表明,与SO反应存在反式氘动力学同位素效应,k/k = (0.53 ± 0.06),这可能与最近关于缔合络合物的形成影响速率系数的建议一致。(CD)COO与NO反应在298 K和4 Torr下的速率系数为(2.1 ± 0.5) × 10 cm³ s⁻¹(用光电离质谱测量),同样与反式-CHCHOO与NO反应的速率相似。在不添加试剂的情况下对丙酮氧化物去除的腔衰荡测量显示出一级和二级衰减动力学的组合,可以通过解卷积来推导(CH)COO的自反应及其单分子热衰变的值。推断在293 K下的单分子衰变速率系数为(305 ± 70) s⁻¹,与臭氧分解的测定结果相似。目前的测量结果证实了(CH)COO与SO反应的速率系数很大,而其与水反应的速率系数很小。(CH)COO与NO和与SO反应的产物测量表明,这些反应可能通过缔合产物的后续反应促进异构化为2 - 氢过氧丙烯。