Complete active space self-consistent-field (CASSCF) and multiconfiguration second-order perturbation theory (CASPT2) calculations with atomic natural orbital basis sets were performed to investigate the S-loss direct dissociation of the 1 2Pi(X 2Pi), 2 2Pi(A 2Pi), 1 2Sigma+(B 2Sigma+), 1 4Sigma-, 1 2Sigma-, and 1 2Delta states of the OCS+ ion and the predissociations of the 1 2Pi, 2 2Pi, and 1 2Sigma+ states. Our calculations indicate that the S-loss dissociation products of the OCS(+) ion in the six states are the ground-state CO molecule plus the S+ ion in different electronic states. The CASPT2//CASSCF potential energy curves were calculated for the S-loss dissociation from the six states. The calculations indicate that the dissociation of the 1 4Sigma- state leads to the CO + S+ (4Su) products representing the first dissociation limit; the dissociations of the 1 2Pi, 1 2Sigma-, and 1 2Delta states lead to the CO + S+(2Du) products representing the second dissociation limit; and the dissociations of the 2 2Pi and 1 2Sigma+ states lead to the CO + S+(2Pu) products representing the third dissociation limit. Seams of the 1 2Pi-1 4Sigma-, 2 2Pi-1 4Sigma-, 2 2Pi-1 2Sigma-, 2 2Pi-1 2Delta, and 1 2Sigma(+)-1 4Sigma- potential energy surface intersections were calculated at the CASPT2 level, and the minima along the seams were located. The calculations indicate that within the experimental energy range (15.07-16.0 eV) the 2 2Pi(A 2Pi) state can be predissociated by 1 4Sigma- forming the S+(4Su) ion and can undergo internal conversion to 1 2Pi followed by the direct dissociation of 1 2Pi forming S+(2Du) and that within the experimental energy range (16.04-16.54 eV) the 1 2Sigma+(B 2Sigma+) state can be predissociated by 1 4Sigma- forming the S+(4Su) ion and can undergo internal conversion to 2 2Pi followed by the predissociation of 2 2Pi by 1 2Sigma- and 1 2Delta forming the S+(2Du) ion. These indications are in line with the experimental fact that both the 4Su and 2Du states of the S+ ion can be formed from the 2 2Pi and 1 2Sigma+ states of the OCS+ ion.
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http://dx.doi.org/10.1063/1.2222357 | DOI Listing |
Chem Sci
January 2025
College of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 China
The naturally sluggish redox kinetics and limited utilization associated with the sulfur conversion in Zn/S electrochemistry hinder its real application. Herein, we report an phase reconstruction strategy that activates the catalytic activity of vanadium oxides for invoking redox-catalysis to manipulate reversible sulfur conversion. It was identified that the VO@C/S precursor derived from metal organic frameworks could be transformed into VO ·HO@C/S by a facile electrochemical induction process.
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December 2024
Key Laboratory of Physical Oceanography, Ministry of Education, Ocean University of China, Qingdao 266100, China.
Volatile sulfur compounds, such as dimethyl sulfide (DMS), carbonyl sulfide (OCS), and carbon disulfide (CS), significantly influence atmospheric chemistry and climate change. Despite the oceans being an important source of these sulfides, the limited understanding of their biogeochemical cycles in seawater introduces considerable uncertainties in quantifying their oceanic emissions and assessing atmospheric OCS budgets. To address this issue, we conducted a comprehensive field survey in the tropical eastern Indian Ocean (EIO) to examine the spatial distributions, source-sink dynamics, and sea-air exchange fluxes of marine DMS, OCS, and CS.
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October 2024
ETH Zürich, Institute of Molecular Physical Science, CH-8093 Zürich, Switzerland.
The reactions of He with OCS and CO have been studied at collision energies between ∼ ⋅ 200 mK and ∼ ⋅ 30 K by merging a beam of Rydberg He atoms with rotationally cold (∼3.5 K) seeded supersonic expansions containing either OCS or CO or a mixture of OCS (mole fraction 23.2%) and CO (76.
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J Phys Chem A
June 2024
Hefei National Research Center for Physical Science at Microscale and Department of Chemical Physics, University of Science and Technology of China, Hefei 230026, China.
The development of the velocity map ion imaging (VMI) technique has greatly advanced the study of photodissociation dynamics. The high-resolution imaging study of the photodissociation allows for the acquisition of precise and detailed information on the fragments. This information can further provide more insight into the energy partition and potential pathways involved in the photodissociation process.
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