Thermochemistry of uranium sulfide cations: guided ion beam and theoretical studies of reactions of U+ and US+ with CS2 and collision-induced dissociation of US+

被引:3
|
作者
Rockow, Sara [1 ]
Bubas, Amanda R. [1 ]
Krauel, Steven Peter [1 ]
Stevenson, Brandon C. [1 ]
Armentrout, P. B. [1 ]
机构
[1] Univ Utah, Dept Chem, 315 S 1400 E Rm 2020, Salt Lake City, UT 84112 USA
关键词
Actinide; bond dissociation energy; chalcogenide; SEQUENTIAL BOND-ENERGIES; MOLECULE REACTIONS; SILANE; MO+; DEPENDENCE; ACTINIDES; METHANE; OXIDE; SC+; UO+;
D O I
10.1080/00268976.2023.2175595
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reactions of atomic uranium cations with carbon disulfide form US+ in an efficient exothermic reaction and UCS+ in an inefficient endothermic process. The subsequent reaction of US+ with CS2 forms US2+ in an endothermic process having a low energy threshold. At much higher energies, UCS2+ and UCS+ are also formed. Collision-induced dissociation of US+ with Xe yields U+ + S exclusively in an endothermic reaction. Analysis of the kinetic energy dependent cross sections of the endothermic processes yields the 0 K bond dissociation energies of 5.73 +/- 0.15 eV for U+ - S, 3.89 +/- 0.08 eV for SU+ - S, 1.69 +/- 0.17 eV for U+ - CS, 2.78 +/- 0.33 eV for U+ - CS2, 1.53 +/- 0.30 eV for SU+ - CS, and 5.65 +/- 0.39 eV for S - UCS+. Theory is used to explore the structures and electron configurations of US+, US2+, UCS+, and UCS2+. The thermochemistry measured in this study is further compared to analogous values previously determined for select group 3 metals, lanthanides, and actinides.
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页数:15
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