130 related articles for article (PubMed ID: 38109698)
1. Roaming in the Unimolecular Decay of
Liu T; Lester MI
J Phys Chem A; 2023 Dec; 127(51):10817-10827. PubMed ID: 38109698
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. OH Roaming and Beyond in the Unimolecular Decay of the Methyl-Ethyl-Substituted Criegee Intermediate: Observations and Predictions.
Liu T; Elliott SN; Zou M; Vansco MF; Sojdak CA; Markus CR; Almeida R; Au K; Sheps L; Osborn DL; Winiberg FAF; Percival CJ; Taatjes CA; Caravan RL; Klippenstein SJ; Lester MI
J Am Chem Soc; 2023 Sep; 145(35):19405-19420. PubMed ID: 37623926
[TBL] [Abstract][Full Text] [Related]
4. Communication: Real time observation of unimolecular decay of Criegee intermediates to OH radical products.
Fang Y; Liu F; Barber VP; Klippenstein SJ; McCoy AB; Lester MI
J Chem Phys; 2016 Feb; 144(6):061102. PubMed ID: 26874475
[TBL] [Abstract][Full Text] [Related]
5. Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates.
Vansco MF; Caravan RL; Zuraski K; Winiberg FAF; Au K; Trongsiriwat N; Walsh PJ; Osborn DL; Percival CJ; Khan MAH; Shallcross DE; Taatjes CA; Lester MI
J Phys Chem A; 2020 May; 124(18):3542-3554. PubMed ID: 32255634
[TBL] [Abstract][Full Text] [Related]
6. Four-Carbon Criegee Intermediate from Isoprene Ozonolysis: Methyl Vinyl Ketone Oxide Synthesis, Infrared Spectrum, and OH Production.
Barber VP; Pandit S; Green AM; Trongsiriwat N; Walsh PJ; Klippenstein SJ; Lester MI
J Am Chem Soc; 2018 Aug; 140(34):10866-10880. PubMed ID: 30074392
[TBL] [Abstract][Full Text] [Related]
7. UV spectroscopic characterization of dimethyl- and ethyl-substituted carbonyl oxides.
Liu F; Beames JM; Green AM; Lester MI
J Phys Chem A; 2014 Mar; 118(12):2298-306. PubMed ID: 24621008
[TBL] [Abstract][Full Text] [Related]
8. Selective deuteration illuminates the importance of tunneling in the unimolecular decay of Criegee intermediates to hydroxyl radical products.
Green AM; Barber VP; Fang Y; Klippenstein SJ; Lester MI
Proc Natl Acad Sci U S A; 2017 Nov; 114(47):12372-12377. PubMed ID: 29109292
[TBL] [Abstract][Full Text] [Related]
9. Direct observation of unimolecular decay of CH3CH2CHOO Criegee intermediates to OH radical products.
Fang Y; Liu F; Klippenstein SJ; Lester MI
J Chem Phys; 2016 Jul; 145(4):044312. PubMed ID: 27475366
[TBL] [Abstract][Full Text] [Related]
10. Deep tunneling in the unimolecular decay of CH
Fang Y; Liu F; Barber VP; Klippenstein SJ; McCoy AB; Lester MI
J Chem Phys; 2016 Dec; 145(23):234308. PubMed ID: 28010089
[TBL] [Abstract][Full Text] [Related]
11. Unraveling Conformer-Specific Sources of Hydroxyl Radical Production from an Isoprene-Derived Criegee Intermediate by Deuteration.
Hansen AS; Liu Z; Chen S; Schumer MG; Walsh PJ; Lester MI
J Phys Chem A; 2020 Jun; 124(24):4929-4938. PubMed ID: 32449860
[TBL] [Abstract][Full Text] [Related]
12. Direct production of OH radicals upon CH overtone activation of (CH3)2COO Criegee intermediates.
Liu F; Beames JM; Lester MI
J Chem Phys; 2014 Dec; 141(23):234312. PubMed ID: 25527940
[TBL] [Abstract][Full Text] [Related]
13. Infrared-driven unimolecular reaction of CH₃CHOO Criegee intermediates to OH radical products.
Liu F; Beames JM; Petit AS; McCoy AB; Lester MI
Science; 2014 Sep; 345(6204):1596-8. PubMed ID: 25258077
[TBL] [Abstract][Full Text] [Related]
14. Hydroxyacetone Production From C
Taatjes CA; Liu F; Rotavera B; Kumar M; Caravan R; Osborn DL; Thompson WH; Lester MI
J Phys Chem A; 2017 Jan; 121(1):16-23. PubMed ID: 28001404
[TBL] [Abstract][Full Text] [Related]
15. Calculation of the absolute photoionization cross-sections for C1-C4 Criegee intermediates and vinyl hydroperoxides.
Huang C; Yang B; Zhang F
J Chem Phys; 2019 Apr; 150(16):164305. PubMed ID: 31042918
[TBL] [Abstract][Full Text] [Related]
16. Unimolecular Decay of the Dimethyl-Substituted Criegee Intermediate in Alkene Ozonolysis: Decay Time Scales and the Importance of Tunneling.
Drozd GT; Kurtén T; Donahue NM; Lester MI
J Phys Chem A; 2017 Aug; 121(32):6036-6045. PubMed ID: 28692269
[TBL] [Abstract][Full Text] [Related]
17. UV spectroscopic characterization of an alkyl substituted Criegee intermediate CH3CHOO.
Beames JM; Liu F; Lu L; Lester MI
J Chem Phys; 2013 Jun; 138(24):244307. PubMed ID: 23822244
[TBL] [Abstract][Full Text] [Related]
18. Two Pathways for Dissociation of Highly Energized syn-CH3CHOO to OH Plus Vinoxy.
Wang X; Bowman JM
J Phys Chem Lett; 2016 Sep; 7(17):3359-64. PubMed ID: 27513186
[TBL] [Abstract][Full Text] [Related]
19. Electronic spectroscopy of methyl vinyl ketone oxide: A four-carbon unsaturated Criegee intermediate from isoprene ozonolysis.
Vansco MF; Marchetti B; Lester MI
J Chem Phys; 2018 Dec; 149(24):244309. PubMed ID: 30599734
[TBL] [Abstract][Full Text] [Related]
20. Tunneling effects in the unimolecular decay of (CH
Fang Y; Barber VP; Klippenstein SJ; McCoy AB; Lester MI
J Chem Phys; 2017 Apr; 146(13):134307. PubMed ID: 28390384
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
