Comparing Reaction Routes for 3(RO•••OR′) Intermediates Formed in Peroxy Radical Self- and Cross-Reactions

被引:35
|
作者
Hasan, Galib [1 ,2 ]
Salo, Vili-Taneli [1 ,2 ]
Valiev, Rashid R. [1 ,2 ]
Kubecka, Jakub [1 ]
Kurten, Theo [1 ,2 ]
机构
[1] Univ Helsinki, Fac Sci, Inst Atmospher & Earth Syst Res, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Chem, FIN-00014 Helsinki, Finland
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2020年 / 124卷 / 40期
基金
芬兰科学院;
关键词
TRANSITION-STATE-THEORY; QUANTUM RRK THEORY; RATE CONSTANTS; OPTIMIZATION; HYDROCARBONS; MIGRATION; CHEMISTRY; MECHANISM; AEROSOLS; KINETICS;
D O I
10.1021/acs.jpca.0c05960
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Organic peroxy radicals (RO2) are key intermediates in the chemistry of the atmosphere. One of the main sink reactions of RO2 is the recombination reaction RO2 + R'O-2, which has three main channels (all with O-2 as a coproduct): (1) R-H=O + R'OH, (2) RO + R'O, and (3) ROOR'. The RO + R'O "alkoxy" channel promotes radical and oxidant recycling, while the ROOR' "dimer" channel leads to low-volatility products relevant to aerosol processes. The ROOR' channel has only recently been discovered to play a role in the gas phase. Recent computational studies indicate that all of these channels first go through an intermediate complex( 1)(RO center dot center dot center dot O-3(2)center dot center dot center dot OR'). Here, O-3(2) is very weakly bound and will likely evaporate from the system, giving a triplet cluster of two alkoxy radicals: (3)(RO center dot center dot center dot OR'). In this study, we systematically investigate the three reaction channels for an atmospherically representative set of RO + R'O radicals formed in the corresponding RO2+ R'O-2 reaction. First, we systematically sample the possible conformations of the RO center dot center dot center dot OR' clusters on the triplet potential energy surface. Next, we compute energetic parameters and attempt to estimate reaction rate coefficients for the three channels: evaporation/dissociation to RO + R'O, a hydrogen shift leading to the formation of R'(-H)=O + ROH, and "spin-flip" (intersystem crossing) leading to, or at least allowing, the formation of ROOR' dimers. While large uncertainties in the computed energetics prevent a quantitative comparison of reaction rates, all three channels were found to be very fast (with typical rates greater than 10 6 s(-1)). This qualitatively demonstrates that the computationally proposed novel RO2 + R'O-2 reaction mechanism is compatible with experimental data showing non-negligible branching ratios for all three channels, at least for sufficiently complex RO2.
引用
收藏
页码:8305 / 8320
页数:16
相关论文
共 19 条
  • [1] Computational Investigation of Substituent Effects on the Alcohol plus Carbonyl Channel of Peroxy Radical Self- and Cross-Reactions
    Hasan, Galib
    Salo, Vili-Taneli
    Almeida, Thomas Golin
    Valiev, Rashid R.
    Kurten, Theo
    JOURNAL OF PHYSICAL CHEMISTRY A, 2023, 127 (07): : 1686 - 1696
  • [2] Acetonyl Peroxy and Hydro Peroxy Self- and Cross-Reactions: Kinetics, Mechanism, and Chaperone Enhancement from the Perspective of the Hydroxyl Radical Product
    Zuraski, Kristen
    Hui, Aileen O.
    Grieman, Fred J.
    Darby, Emily
    Moller, Kristian H.
    Winiberg, Frank A. F.
    Percival, Carl J.
    Smarte, Matthew D.
    Okumura, Mitchio
    Kjaergaard, Henrik G.
    Sander, Stanley P.
    JOURNAL OF PHYSICAL CHEMISTRY A, 2020, 124 (40): : 8128 - 8143
  • [3] Accretion Product Formation from Self- and Cross-Reactions of RO2 Radicals in the Atmosphere
    Berndt, Torsten
    Scholz, Wiebke
    Mentler, Bernhard
    Fischer, Lukas
    Herrmann, Hartmut
    Kulmala, Markku
    Hansel, Armin
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (14) : 3820 - 3824
  • [4] Acetonyl Peroxy and Hydroperoxy Self- and Cross-Reactions: Temperature-Dependent Kinetic Parameters, Branching Fractions, and Chaperone Effects
    Zuraski, Kristen
    Grieman, Fred J.
    Hui, Aileen O.
    Cowen, Julia
    Winiberg, Frank A. F.
    Percival, Carl J.
    Okumura, Mitchio
    Sander, Stanley P.
    JOURNAL OF PHYSICAL CHEMISTRY A, 2023, 127 (37): : 7772 - 7792
  • [5] Kinetics and products of propargyl (C3H3) radical self- reactions and propargyl-methyl cross-combination reactions
    Fahr, A
    Nayak, A
    INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, 2000, 32 (02) : 118 - 124
  • [6] Self- and cross-reactions of β-hydroxyperoxy radicals of relevance to tropospheric monoterpene oxidation:: structure-activity relationships for rate coefficients
    Boyd, AA
    Villenave, E
    Lesclaux, R
    ATMOSPHERIC ENVIRONMENT, 2003, 37 (20) : 2751 - 2760
  • [7] Kinetic studies of reactions of the nitrate radical (NO3) with peroxy radicals (RO2):: an indirect source of OH at night?
    Vaughan, Stewart
    Canosa-Mas, Carlos E.
    Pfrang, Christian
    Shallcross, Dudley E.
    Watson, Laura
    Wayne, Richard P.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2006, 8 (32) : 3749 - 3760
  • [8] Kinetics and atmospheric implications of peroxy radical cross reactions involving the CH3C(O)O2 radical
    Villenave, E
    Lesclaux, R
    Seefeld, S
    Stockwell, WR
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D19) : 25273 - 25285
  • [9] Reassessing the photochemical production of methanol from peroxy radical self and cross reactions using the STOCHEM-CRI global chemistry and transport model
    Khan, M. A. H.
    Cooke, M. C.
    Utembe, S. R.
    Xiao, P.
    Derwent, R. G.
    Jenkin, M. E.
    Archibald, A. T.
    Maxwell, P.
    Morris, W. C.
    South, N.
    Percival, C. J.
    Shallcross, D. E.
    ATMOSPHERIC ENVIRONMENT, 2014, 99 : 77 - 84
  • [10] Gas-phase reactions between RO2 and NO, HO2 or CH3O2:: correlations between rate constants and the SOMO energy of the peroxy (RO2) radical
    King, MD
    Canosa-Mas, CE
    Wayne, RP
    ATMOSPHERIC ENVIRONMENT, 2001, 35 (12) : 2081 - 2088