abstraction reaction
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Author(s):  
J. Espinosa-Garcia

In this paper we study the gas-phase hydrogen abstraction reaction between fluorine atoms and silane in a three-step process: potential energy surface, kinetics and dynamics. Firstly, we developed for the...


Author(s):  
Juan-Carlos Lizardo-Huerta ◽  
Sonia Taamalli ◽  
Kanika Sood ◽  
Laurent Gasnot ◽  
Florent Louis ◽  
...  

2021 ◽  
Vol 1201 ◽  
pp. 113257
Author(s):  
Dorra Khiri ◽  
Sonia Taamalli ◽  
Duy Quang Dao ◽  
Thanh-Binh Nguyen ◽  
Laurent Gasnot ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2015
Author(s):  
Christine Elian ◽  
Vlasta Brezová ◽  
Pauline Sautrot-Ba ◽  
Martin Breza ◽  
Davy-Louis Versace

Two new photopolymerizable vinyl (2-(allyloxy) 1,4-naphthoquinone, HNQA) and epoxy (2-(oxiran-2yl methoxy) 1,4-naphthoquinone, HNQE) photoinitiators derived from lawsone were designed in this paper. These new photoinitiators can be used as one-component photoinitiating systems for the free-radical photopolymerization of acrylate bio-based monomer without the addition of any co-initiators. As highlighted by the electron paramagnetic resonance (EPR) spin-trapping results, the formation of carbon-centered radicals from an intermolecular H abstraction reaction was evidenced and can act as initiating species. Interestingly, the introduction of iodonium salt (Iod) used as a co-initiator has led to (1) the cationic photopolymerization of epoxy monomer with high final conversions and (2) an increase of the rates of free-radical polymerization of the acrylate bio-based monomer; we also demonstrated the concomitant thiol–ene reaction and cationic photopolymerizations of a limonene 1,2 epoxide/thiol blend mixture with the HNQA/Iod photoinitiating system.


2020 ◽  
Vol 124 (46) ◽  
pp. 9626-9637
Author(s):  
Özlem Yönder ◽  
Gunnar Schmitz ◽  
Christof Hättig ◽  
Rochus Schmid ◽  
Paulo Debiagi ◽  
...  

2020 ◽  
Vol 500 (1) ◽  
pp. 1188-1200
Author(s):  
Killian Leroux ◽  
Lahouari Krim

ABSTRACT Methanol, which is one of the most abundant organic molecules in the interstellar medium, plays an important role in the complex grain surface chemistry that is believed to be a source of many organic compounds. Under energetic processing such as ultraviolet (UV) photons or cosmic rays, methanol may decompose into CH4, CO2, CO, HCO, H2CO, CH3O and CH2OH, which in turn lead to complex organic molecules such as CH3OCHO, CHOCH2OH and HOCH2CH2OH through radical recombination reactions. However, although molecular oxygen and its detection, abundance and role in the interstellar medium have been the subject of many debates, few experiments on the oxidation of organic compounds have been carried out under interstellar conditions. The present study shows the behaviour of solid methanol when treated by UV light and thermal processing in oxygen-rich environments. Methanol has been irradiated in the absence and presence of O2 at different concentrations in order to study how oxidized complex organic molecules may form and also to investigate the O-insertion reaction in the C–H bound to form methanediol HOCH2OH through a CH3OH + O(1D) solid-state reaction. The adding of O2 in the thermal and photochemical reaction of solid methanol leads to the formation of O3, H2O and HO2, in addition to three main organics, HCOOH, CHOCHO and HOCH2OH. We show that in an O2-rich environment, species such as CO, CH4, HCO, CH3OH and CHOCH2OH are oxidized into CO2, CH3OH, HC(O)OO, HOCH2OH and CHOCHO, respectively, while HCOOH might be formed through the H2CO + O(3P) → (OH + HCO)cage → HCOOH hydrogen-abstraction reaction.


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