Spectroscopic detection is an important method to monitor alkoxy radicals in atmospheric photochemistry studies. In this work, we report the first observation of the laser-induced fluorescence (LIF) spectra of isobutoxy, 2-methyl-1-butoxy, and 3-methyl-1-butoxy in supersonic jet-cooled condition. Ground state unimolecular decomposition and isomerization as well as excited state relaxation dynamics of isobutoxy were discussed in combination with the theoretical calculations. Analysis of the experimental and theoretical results showed that methyl substitution on the β carbon of the alkoxy radicals changed the LIF spectra of alkoxy radicals significantly. The competition between the ground state reactions and the photoexcitation process depended strongly on the radical structure and hence affected the involvement of alkoxy radicals in the photochemical reactions in the upper troposphere. This study will help to understand the dynamic role of alkoxy radicals in the atmosphere.
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http://dx.doi.org/10.1021/jp4016239 | DOI Listing |
Phys Chem Chem Phys
January 2025
The Fritz Haber Center for Molecular Dynamics, Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
Peroxy radicals are key intermediates in many atmospheric processes. Reactions between such radicals are of particular interest as they can lead to accretion products capable of participating in new particle formation (NPF). These reactions proceed through a tetroxide intermediate, which then decomposes to a complex of two alkoxy radicals and O, with spin conservation dictating that the complex must be formed in the triplet state.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Physical Chemistry, Gdańsk University of Technology, Narutowicza 11/12, Gdańsk, 80-233, Poland.
The study investigated the degradation of 3-methoxy-1-propanol (3M1P) by OH using the M06-2X/6-311++G(d, p) level, with CCSD(T) single-point corrections. We focused on hydrogen atom abstraction from various alkyl groups within the molecule. The rate coefficient for 3M1P degradation was calculated from the sum of the rate coefficients corresponding to the removal of H-atoms from primary (-CH), secondary (-CH-), tertiary (-CH< ), and alcohol (-ΟH) groups.
View Article and Find Full Text PDFJ Org Chem
January 2025
Department of Chemistry, Birla Institute of Technology and Science Pilani, Pilani Campus, Rajasthan 333031, India.
A convenient and efficient transition-metal-free method has been developed for the C(sp)-H alkoxylation/aryloxylation of 1,4-quinones by direct cross-dehydrogenative coupling with readily available alcohols and phenols in the presence of TEMPO under simple and mild conditions. The method allowed the installation of a wide range of alkoxy/aryloxy groups, exhibited high functional group tolerance, showed a broad substrate scope, afforded good to excellent yields of products in a simple one-pot operation, and could be performed on a gram scale. Mechanistic investigation indicated the involvement of the radical pathway.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
P. Roy and Diana T. Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 S. 34th St., Philadelphia, Pennsylvania 19104, United States.
Photocatalytic C-H activation is an emerging area of research. While cerium chloride photocatalysts have been extensively studied, the role of alcohol additives in these systems remains a subject of ongoing discussion. It was demonstrated that the photocatalyst [NEt][CeCl] () produces •Cl and added alcohols exhibit zero-order kinetics.
View Article and Find Full Text PDFJ Phys Chem A
December 2024
Department of Chemistry, University of Rochester, Rochester, New York 14627-0216, United States.
Decay processes of exciplexes of cyanoanthracenes with alkylbenzene donors were compared to those with alkoxybenzenes. For the three decay processes of exciplexes, the radiative rate constant () of alkoxy derivatives is slightly lower than those of alkylbenzenes at the same average exciplex energy. However, the corresponding deactivation rate constants, intersystem crossing () and nonradiative decay (), are considerably higher.
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