221 related articles for article (PubMed ID: 33283439)
1. Criegee Intermediates Beyond Ozonolysis: Synthetic and Mechanistic Insights.
Hassan Z; Stahlberger M; Rosenbaum N; Bräse S
Angew Chem Int Ed Engl; 2021 Jul; 60(28):15138-15152. PubMed ID: 33283439
[TBL] [Abstract][Full Text] [Related]
2. Criegee Intermediates: What Direct Production and Detection Can Teach Us About Reactions of Carbonyl Oxides.
Taatjes CA
Annu Rev Phys Chem; 2017 May; 68():183-207. PubMed ID: 28463651
[TBL] [Abstract][Full Text] [Related]
3. Perspective: Spectroscopy and kinetics of small gaseous Criegee intermediates.
Lee YP
J Chem Phys; 2015 Jul; 143(2):020901. PubMed ID: 26178082
[TBL] [Abstract][Full Text] [Related]
4. Regional and global impacts of Criegee intermediates on atmospheric sulphuric acid concentrations and first steps of aerosol formation.
Percival CJ; Welz O; Eskola AJ; Savee JD; Osborn DL; Topping DO; Lowe D; Utembe SR; Bacak A; McFiggans G; Cooke MC; Xiao P; Archibald AT; Jenkin ME; Derwent RG; Riipinen I; Mok DW; Lee EP; Dyke JM; Taatjes CA; Shallcross DE
Faraday Discuss; 2013; 165():45-73. PubMed ID: 24600996
[TBL] [Abstract][Full Text] [Related]
5. Structure-dependent reactivity of Criegee intermediates studied with spectroscopic methods.
Jr-Min Lin J; Chao W
Chem Soc Rev; 2017 Dec; 46(24):7483-7497. PubMed ID: 28840926
[TBL] [Abstract][Full Text] [Related]
6. Research frontiers in the chemistry of Criegee intermediates and tropospheric ozonolysis.
Taatjes CA; Shallcross DE; Percival CJ
Phys Chem Chem Phys; 2014 Feb; 16(5):1704-18. PubMed ID: 24096945
[TBL] [Abstract][Full Text] [Related]
7. Direct Probing of Criegee Intermediates from Gas-Phase Ozonolysis Using Chemical Ionization Mass Spectrometry.
Berndt T; Herrmann H; Kurtén T
J Am Chem Soc; 2017 Sep; 139(38):13387-13392. PubMed ID: 28853879
[TBL] [Abstract][Full Text] [Related]
8. Infrared detection of Criegee intermediates formed during the ozonolysis of β-pinene and their reactivity towards sulfur dioxide.
Ahrens J; Carlsson PT; Hertl N; Olzmann M; Pfeifle M; Wolf JL; Zeuch T
Angew Chem Int Ed Engl; 2014 Jan; 53(3):715-9. PubMed ID: 24402798
[TBL] [Abstract][Full Text] [Related]
9. Unimolecular Decay of Criegee Intermediates to OH Radical Products: Prompt and Thermal Decay Processes.
Lester MI; Klippenstein SJ
Acc Chem Res; 2018 Apr; 51(4):978-985. PubMed ID: 29613756
[TBL] [Abstract][Full Text] [Related]
10. Characterization and Quantification of Particle-Bound Criegee Intermediates in Secondary Organic Aerosol.
Campbell SJ; Wolfer K; Gallimore PJ; Giorio C; Häussinger D; Boillat MA; Kalberer M
Environ Sci Technol; 2022 Sep; 56(18):12945-12954. PubMed ID: 36054832
[TBL] [Abstract][Full Text] [Related]
11. Observation of the simplest Criegee intermediate CH2OO in the gas-phase ozonolysis of ethylene.
Womack CC; Martin-Drumel MA; Brown GG; Field RW; McCarthy MC
Sci Adv; 2015 Mar; 1(2):e1400105. PubMed ID: 26601145
[TBL] [Abstract][Full Text] [Related]
12. Online Quantification of Criegee Intermediates of α-Pinene Ozonolysis by Stabilization with Spin Traps and Proton-Transfer Reaction Mass Spectrometry Detection.
Giorio C; Campbell SJ; Bruschi M; Tampieri F; Barbon A; Toffoletti A; Tapparo A; Paijens C; Wedlake AJ; Grice P; Howe DJ; Kalberer M
J Am Chem Soc; 2017 Mar; 139(11):3999-4008. PubMed ID: 28201872
[TBL] [Abstract][Full Text] [Related]
13. Isolating α-Pinene Ozonolysis Pathways Reveals New Insights into Peroxy Radical Chemistry and Secondary Organic Aerosol Formation.
Zhao Z; Zhang W; Alexander T; Zhang X; Martin DBC; Zhang H
Environ Sci Technol; 2021 May; 55(10):6700-6709. PubMed ID: 33913707
[TBL] [Abstract][Full Text] [Related]
14. Impact of the water dimer on the atmospheric reactivity of carbonyl oxides.
Anglada JM; Solé A
Phys Chem Chem Phys; 2016 Jun; 18(26):17698-712. PubMed ID: 27308802
[TBL] [Abstract][Full Text] [Related]
15. Direct observation of the gas-phase Criegee intermediate (CH2OO).
Taatjes CA; Meloni G; Selby TM; Trevitt AJ; Osborn DL; Percival CJ; Shallcross DE
J Am Chem Soc; 2008 Sep; 130(36):11883-5. PubMed ID: 18702490
[TBL] [Abstract][Full Text] [Related]
16. Substituent Effects on the Electronic Spectroscopy of Four-Carbon Criegee Intermediates.
Liu T; Zou M; Caracciolo A; Sojdak CA; Lester MI
J Phys Chem A; 2022 Sep; 126(38):6734-6741. PubMed ID: 36108247
[TBL] [Abstract][Full Text] [Related]
17. Enthalpies of formation for Criegee intermediates: A correlation energy convergence study.
Begley JM; Aroeira GJR; Turney JM; Douberly GE; Schaefer HF
J Chem Phys; 2023 Jan; 158(3):034302. PubMed ID: 36681629
[TBL] [Abstract][Full Text] [Related]
18. Pressure dependence of stabilized Criegee intermediate formation from a sequence of alkenes.
Drozd GT; Donahue NM
J Phys Chem A; 2011 May; 115(17):4381-7. PubMed ID: 21476564
[TBL] [Abstract][Full Text] [Related]
19. Exploring the chemical kinetics of partially oxidized intermediates by combining experiments, theory, and kinetic modeling.
Hoyermann K; Mauß F; Olzmann M; Welz O; Zeuch T
Phys Chem Chem Phys; 2017 Jul; 19(28):18128-18146. PubMed ID: 28681879
[TBL] [Abstract][Full Text] [Related]
20. Detection and identification of Criegee intermediates from the ozonolysis of biogenic and anthropogenic VOCs: comparison between experimental measurements and theoretical calculations.
Giorio C; Campbell SJ; Bruschi M; Archibald AT; Kalberer M
Faraday Discuss; 2017 Aug; 200():559-578. PubMed ID: 28580994
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]