We present the first direct study on the thermal unimolecular decomposition of allyl radicals. Experiments have been performed behind shock waves, and the experimental conditions covered temperatures ranging from 1125 K up to 1570 K and pressures between 0.25 and 4.5 bar. Allyl radicals have been generated by thermal decomposition of allyl iodide, and H-atom resonance absorption spectroscopy has been used to monitor the reaction progress. A marked pressure dependence of the rate constant has been observed which is in agreement with the results from a master equation analysis. However, our experimental results as well as our Rice-Ramsperger-Kassel-Marcus calculations seem to contradict the results of Deyerl et al. (J. Chem. Phys. 1999, 110, 1450) who investigated the unimolecular decomposition of allyl radicals upon photoexcitation and tried to deduce specific rate constants for the unimolecular dissociation in the electronic ground state. At pressures around 1 bar we extracted the following rate equation: k(T) = 5.3 x 10(79)(T/K)(-19.29) exp[(-398.9 kJ/mol)/RT] s(-1). The uncertainty of the rate constant calculated from this equation is estimated to be 30%.
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Polymers (Basel)
December 2024
Industrial Chemistry Laboratory, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, 15771 Athens, Greece.
Well-defined amorphous/semi-crystalline statistical copolymers of n-dodecyl isocyanate, DDIC, and allyl isocyanate, ALIC, were synthesized via coordination polymerization using the chiral half-titanocene complex CpTiCl(O-(S)-2-Bu) as an initiator. In the frame of the terminal model, the monomer reactivity ratios of the statistical copolymers were calculated using both well-known linear graphical methods and the computer program COPOINT. The molecular and structural characteristics of the copolymers were also calculated.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Chinese Academy of Sciences), Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, 200032, Shanghai, China.
Organolithium reagents, known for their low cost, ready availability, and high reactivity, allow fast cross-coupling under ambient conditions. However, their direct cross-coupling with fluoroalkyl electrophiles remains a formidable challenge due to the easy formation of thermo-unstable fluoroalkyl lithium species during the reaction, which are prone to decomposition via rapid α/β-fluoride elimination. Here, we exploit heteroatom-stabilized allylic anions to harness the exceptional reactivity of organolithium reagents, enabling the compatibility of difluoroalkyl halides and facilitating versatile and precise fluorine functionality introduction under mild conditions.
View Article and Find Full Text PDFPhys Chem Chem Phys
October 2024
Department of Chemistry, KU Leuven, Celestijnenlaan, 200F, Leuven 3001, Belgium.
In this study, we revisited the mechanism of isoprene oxidation by OH radicals, focusing on the formation of hydroperoxyaldehydes (HPALDs) in the reactions following O-addition at the α-position to ,'-OH-allyl radical products of the 1,6-H shift of the 1st-generation -δ-OH-isoprenylperoxy radicals. Utilizing high-level quantum chemical calculations and a master equation approach, we provide theoretical confirmation that the formation of δ-HPALDs dominates by far and show that production of β-HPALDs by the mechanism proposed by Wennberg (, 2018, , 3337-3390) is negligible. Besides the dominance of the δ-HPALD formation channel, our investigation also reveals a novel though minor reaction channel resulting in the formation of an allylic δ-hydroperoxy acid and OH radical.
View Article and Find Full Text PDFThe catalytic pyrolysis of guaiacol-based lignin monomers, vanillin, syringol, and eugenol over commercial HZSM-5 has been investigated using Photoelectron Photoion Coincidence (PEPICO) spectroscopy to unveil the reaction mechanism by detecting reactive intermediates, such as quinone methides and ketenes, and products. shares the decomposition mechanism with guaiacol due to prompt and efficient decarbonylation, which allows us to control this reaction leading to a phenol selectivity increase by switching to a faujasite catalyst and decreasing the Si/Al ratio. first demethylates to 3-methoxycatechol, which mainly dehydroxylates to - and -guaiacol.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2024
School of Petrochemical Engineering, Changzhou University, Changzhou 213164, Jiangsu, China.
Poly(aryl ether) materials are used in a wide range of applications in the communications and microelectronics fields for their outstanding mechanical and dielectric properties. In order to further improve the comprehensive performance, this work reports a series of cross-linkable poly(aryl ether)s (UCL-PAEn) containing trifluoroisopropyl and perfluorobiphenyl structures using 2,2-bis(4-hydroxyphenyl)hexafluoropropane, 2,2'-diallyl bisphenol A, and perfluorobiphenyl as starting materials. Their chemical structures and the effect of changes in the allyl content on the properties are thoroughly investigated.
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