Carbonyl oxide species play a key role in tropospheric oxidation of organic molecules and in low-temperature combustion processes. In the late 1940s, Criegee first postulated the participation of carbonyl oxides, now often called "Criegee intermediates," in ozonolysis of alkenes. However, despite decades of effort, no gas phase Criegee intermediate has before been observed. As a result, knowledge of gas phase carbonyl oxide reactions has heretofore been inferred by indirect means, with derived rate coefficients spanning orders of magnitude. We have directly detected the primary Criegee intermediate, formaldehyde oxide (CH2OO), in the chlorine-initiated gas-phase oxidation of dimethyl sulfoxide (DMSO). This work not only establishes that the Criegee intermediate is formed in DMSO oxidation also but opens the possibility for explicit kinetics studies on this critical atmospheric species.
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http://dx.doi.org/10.1021/ja804165q | DOI Listing |
J Phys Chem A
December 2024
Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
To better understand the key kinetic mechanisms controlling heterogeneous oxidation in organic aerosols, submicron particles composed of an alkene and a saturated carboxylic acid are exposed to ozone in a variable-temperature flow tube reactor. Effective uptake coefficients (γ) are obtained from the multiphase reaction kinetics, which are quantified by Vacuum Ultraviolet Photoionization Aerosol Mass Spectrometry. For aerosols composed of only of alkenes, γ doubles (from 6 × 10 to 1.
View Article and Find Full Text PDFJ Phys Chem A
December 2024
Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
A chlorine-substituted Criegee intermediate, ClCHOO, is photolytically generated using a diiodo precursor, detected by VUV photoionization at 118 nm, and spectroscopically characterized via ultraviolet-visible (UV-vis)-induced depletion of / = 80 under jet cooled conditions. UV-vis excitation resonant with a π* ← π transition yields a significant ground state depletion, indicating a strong electronic transition and rapid photodissociation. The broad absorption spectrum peaks at 350 nm and is attributed to contributions from both (∼70%) and (∼30%) conformers of ClCHOO based on spectral simulations using a nuclear ensemble method.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
Criegee intermediates (CIs) play an important role in atmospheric chemistry as a transient source of the OH radical through their formation by the ozonolysis of unsaturated organic compounds. Here, we report thermally initiated formation of the smallest CI (CHOO) in the oxidation of ethane (CHCH) that may be relevant to combustion and flames. The SiO/SiC oxidation microreactor is heated to 1800 K and has a short residence time of ∼100 μs.
View Article and Find Full Text PDFOrg Lett
December 2024
Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, United States.
As part of our investigations into C-C bond scission and functionalization, we report a halodealkenylation in which the C(sp)-C(sp) bonds of alkenes are cleaved and C(sp)-halide bonds are formed, via a radical intermediate. These transformations occur through Criegee ozonolysis and Fe-catalyzed reductive coupling assisted by vitamin C as a stoichiometric reductant. We applied this strategy to the formal synthesis of ()-γ-tocopherol.
View Article and Find Full Text PDFAnal Methods
December 2024
Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, China.
The transformation of renewable feedstocks into aromatic chemicals holds immense potential for advancing a green, low-carbon economy and fostering sustainable development. Herein, we present a novel approach for the conversion of isoeugenol, a renewable lignin derivative, into the valuable flavoring agent vanillin, utilizing ozone as an environmentally benign oxidant. The process optimization was significantly enhanced by the integration of Attenuated Total Reflectance Infrared (ATR-IR) monitoring.
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