The collision-induced rate coefficients of ortho-para conversion for the H + H reaction provide accurate information to probe the lifetime of cold environments in interstellar media. Rotationally resolved reaction probabilities are calculated at the low collision energy regime (0 < ≤ 0.3 eV) by employing the coupled three-dimensional (3D) time-dependent wave packet (TDWP) formalism in hyperspherical coordinates on a recently constructed ab initio ground adiabatic potential energy surface of H [ , , 204306] for the process H + H ( = 0, = 0-5) → H + H (' = 0, '). Cross-sections are then computed from the converged reaction probabilities as a function of total angular momentum () over the same energy regime and subsequently employed to obtain the rate constants for the ortho-to-para (O-P) and para-to-ortho (P-O) conversions and their ratio. The ratio of ortho-para conversion shows (a) appropriate convergence with the inclusion of a higher number of initial rotational states as well as a reasonable agreement with the results from a quantum statistical method and (b) a peak at lower temperature that could be due to the available collision energy for transitions involving lower rotational states ( = 0 → ' = 1).
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http://dx.doi.org/10.1021/acs.jpca.4c02243 | DOI Listing |
J Phys Chem A
October 2024
School of Physics and Physical Engineering, Qufu Normal University, Qufu 273165, P. R. China.
The collision-induced rate coefficients of ortho-para conversion for the H + H reaction provide accurate information to probe the lifetime of cold environments in interstellar media. Rotationally resolved reaction probabilities are calculated at the low collision energy regime (0 < ≤ 0.3 eV) by employing the coupled three-dimensional (3D) time-dependent wave packet (TDWP) formalism in hyperspherical coordinates on a recently constructed ab initio ground adiabatic potential energy surface of H [ , , 204306] for the process H + H ( = 0, = 0-5) → H + H (' = 0, ').
View Article and Find Full Text PDFSci Rep
September 2024
Faculty of Maritime and Transportation, Ningbo University, Ningbo, 315211, People's Republic of China.
The catalytic conversion of ortho-hydrogen (o-H) to para-hydrogen (p-H) serves as a crucial step in the storage of liquid hydrogen. A variety of iron-cobalt bimetallic catalysts (FCO) were synthesized using a precipitation method, incorporating diverse levels of Co doping into Fe-based catalysts. The effects of Co doping on the crystal structure, porosity, and magnetism of FCO catalysts were studied by XRD, N physical adsorption, FTIR, XPS, and VSM analyses.
View Article and Find Full Text PDFMolecular hydrogen (H) ortho-para conversion (O/P conversion) proceeds slowly at low temperatures accompanying a heat release. Thus, catalysts for accelerating this conversion rate are highly demanded in terms of the storage and utilization of liquid H. The catalysts for this purpose are experimentally screened by examining a broad range of materials covering magnetic, non-magnetic, metallic, and nonmetallic oxides.
View Article and Find Full Text PDFChempluschem
September 2024
Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
A set of At-astatoarenes were synthesized from corresponding trimethylgermyl arenes with an average radiochemical conversion (RCC) of ca. 50 % for electron-rich and approx. 70 % in case of electron-deficient arenes.
View Article and Find Full Text PDFMolecules
March 2024
School of Pharmacy, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
The (sp)-aryl sulfonate functional group is found in bioactive molecules, but their synthesis can involve extreme temperatures (>190 °C or flash vacuum pyrolysis) and strongly acidic reaction conditions. Inspired by the 1917 Tyrer industrial process for a sulfa dye that involved an aniline (sp)-SO intermediate to a (sp)-SO rearranged product, we investigated tributylsulfoammonium betaine (TBSAB) as a milder -sulfamation to -sulfonate relay reagent. Initial investigations of a stepwise route involving TBSAB on selected anilines at room temperature enabled the isolation of (sp)-sulfamate.
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