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Thionylimide (HNSO) and its isomer thionitrous acid (HSNO) are important intermediates in atmospheric chemistry and biology, respectively. However, the chemical network linking HNSO and HSNO is not fully understood due to the absence of some high-energy isomers. Herein, we report the identification of -HNSO and -HONS during the photochemistry of -HNSO in a solid Ne matrix at 3 K. The characterization of both species with matrix-isolation IR spectroscopy is supported by D- and N-isotope labeling experiments and quantum chemical calculations at the CCSD(T)-F12B/VTZ-F12 level of theory using configuration-selective vibrational configuration interaction theory (VCI). Interestingly, spontaneous reactions via quantum mechanical tunneling (QMT) have been observed at 3 K for the → conformational rotation in HNSO and HOSN, as well as for the 1,3-hydrogen migration in -HONS (→ -HSNO). The QMT mechanism by the hydrogen atom is consistent with the kinetic isotope effects (KIEs) and the multidimensional instanton theory calculations.
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http://dx.doi.org/10.1021/jacs.5c08291 | DOI Listing |
J Am Chem Soc
August 2025
Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, China.
Thionylimide (HNSO) and its isomer thionitrous acid (HSNO) are important intermediates in atmospheric chemistry and biology, respectively. However, the chemical network linking HNSO and HSNO is not fully understood due to the absence of some high-energy isomers. Herein, we report the identification of -HNSO and -HONS during the photochemistry of -HNSO in a solid Ne matrix at 3 K.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
June 2016
Institut für Chemie, Universität Rostock, Albert-Einstein-Strasse 3a, 18059, Rostock, Deutschland.
A new synthetic approach enabled the generation of highly labile thionylimide, H-NSO, which was trapped by adduct formation with the bulky Lewis acid B(C6 F5 )3 and fully characterized. For comparison, a series of different Me3 Si-NSO Lewis acid adducts were studied. Treatment of Me3 Si-NSO with the silylium ion [Me3 Si](+) led to the formation of the hitherto unknown iminosulfonium ion [Me3 Si-N=S-O-SiMe3 ](+) , which could be isolated and fully characterized as a salt in the presence of weakly coordinating carborate anions.
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