Thermodynamic Properties of Gaseous Selenium Species of Atmospheric Interest

Selenium (Se) is an essential element for fauna, flora, and human health. Up to a third of Se can cycle through the atmosphere. The volatile organic Se species include dimethyl selenide (CH<sub>3</sub>SeCH<sub>3</sub>), dimethyl diselenide (CH<sub>3</sub>SeSeCH<sub>3</sub>), and methaneselenol (CH<sub>3</sub>SeH), and will undergo rapid atmospheric oxidation. To better constrain the fate of atmospheric Se compounds, high-level <i>ab initio</i> electronic structure calculations were performed to estimate the thermodynamic properties of 11 gaseous Se species (HSe<sup>•</sup>, H<sub>2</sub>Se, CH<sub>2</sub>Se, CH<sub>3</sub>SeH, <sup>•</sup>CH<sub>2</sub>SeH, CH<sub>3</sub>Se<sup>•</sup>, CH<sub>3</sub>SeSe<sup>•</sup>, CH<sub>3</sub>SeCH<sub>3</sub>, CH<sub>3</sub>Se<sup>•</sup>CH<sub>2</sub>, CH<sub>3</sub>SeSeCH<sub>3</sub>, and CH<sub>3</sub>SeSe<sup>•</sup>CH<sub>2</sub>) using their atomization reactions. Several corrections were applied to provide highly accurate calculated standard enthalpies of formation at 298 K, Δ<sub><i>f</i></sub><i>H°</i><sub>298 K</sub>. Standard molar entropy at 298 K, <i>S</i>°<sub>298 K</sub>, and heat capacity, <i>C</i><sub>p</sub>(<i>T</i>) over the temperature range 300-1500 K, from vibrational, translational, and external rotation contributions were computed using statistical thermodynamics based on the vibrational frequencies and structures obtained at the CCSD(T)/aVTZ level of theory. Hindered rotational contributions to <i>S</i>°<sub>298 K</sub> and <i>C</i><sub>p</sub>(T) were calculated from the energy levels, where the internal rotation potential was calculated at the MP2/aVTZ level of theory. The bond dissociation energies at 298 K for H-Se, Se-Se, and C-Se bonds in the Se molecules were derived from their calculated Δ<sub><i>f</i></sub><i>H°</i><sub>298 K</sub> values. The same protocol was applied to O and S species for comparison with Se. Their Δ<sub><i>f</i></sub><i>H°</i><sub>298 K</sub>, <i>S</i>°<sub>298 K</sub>, and <i>C</i><sub>p</sub>(T) values were in good agreement with the corresponding available literature data. This work provided the first thermodynamic properties for the organic Se species. The data obtained in this work could be used in chemical-transport models to assess the fate of atmospheric Se and its speciation unravelling the Se biogeochemical cycles.

Authors

Institutions

Publication Details

Journal
The Journal of Physical Chemistry A
Published
2025-12-08
DOI
https://doi.org/10.1021/acs.jpca.5c03608
Primary Topic
Chemical Thermodynamics and Molecular Structure
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Thermodynamic Properties of Gaseous Selenium Species of Atmospheric Interest

Luna Cartayrade, Oscar N. Ventura, Alejandro L. Cardona, Florent Louis et al.
The Journal of Physical Chemistry A
Chemical Thermodynamics and Molecular Structure
article

Thermodynamic Properties of Gaseous Selenium Species of Atmospheric Interest

Luna Cartayrade, Oscar N. Ventura, Alejandro L. Cardona, Florent Louis, Sonia Taamalli, Nadine Borduas‐Dedekind, Marc E. Segovia, Maurício Vega-Teijido, A. Ortiz Martínez
article en

Abstract

Selenium (Se) is an essential element for fauna, flora, and human health. Up to a third of Se can cycle through the atmosphere. The volatile organic Se species include dimethyl selenide (CH<sub>3</sub>SeCH<sub>3</sub>), dimethyl diselenide (CH<sub>3</sub>SeSeCH<sub>3</sub>), and methaneselenol (CH<sub>3</sub>SeH), and will undergo rapid atmospheric oxidation. To better constrain the fate of atmospheric Se compounds, high-level <i>ab initio</i> electronic structure calculations were performed to estimate the thermodynamic properties of 11 gaseous Se species (HSe<sup>•</sup>, H<sub>2</sub>Se, CH<sub>2</sub>Se, CH<sub>3</sub>SeH, <sup>•</sup>CH<sub>2</sub>SeH, CH<sub>3</sub>Se<sup>•</sup>, CH<sub>3</sub>SeSe<sup>•</sup>, CH<sub>3</sub>SeCH<sub>3</sub>, CH<sub>3</sub>Se<sup>•</sup>CH<sub>2</sub>, CH<sub>3</sub>SeSeCH<sub>3</sub>, and CH<sub>3</sub>SeSe<sup>•</sup>CH<sub>2</sub>) using their atomization reactions. Several corrections were applied to provide highly accurate calculated standard enthalpies of formation at 298 K, Δ<sub><i>f</i></sub><i>H°</i><sub>298 K</sub>. Standard molar entropy at 298 K, <i>S</i>°<sub>298 K</sub>, and heat capacity, <i>C</i><sub>p</sub>(<i>T</i>) over the temperature range 300-1500 K, from vibrational, translational, and external rotation contributions were computed using statistical thermodynamics based on the vibrational frequencies and structures obtained at the CCSD(T)/aVTZ level of theory. Hindered rotational contributions to <i>S</i>°<sub>298 K</sub> and <i>C</i><sub>p</sub>(T) were calculated from the energy levels, where the internal rotation potential was calculated at the MP2/aVTZ level of theory. The bond dissociation energies at 298 K for H-Se, Se-Se, and C-Se bonds in the Se molecules were derived from their calculated Δ<sub><i>f</i></sub><i>H°</i><sub>298 K</sub> values. The same protocol was applied to O and S species for comparison with Se. Their Δ<sub><i>f</i></sub><i>H°</i><sub>298 K</sub>, <i>S</i>°<sub>298 K</sub>, and <i>C</i><sub>p</sub>(T) values were in good agreement with the corresponding available literature data. This work provided the first thermodynamic properties for the organic Se species. The data obtained in this work could be used in chemical-transport models to assess the fate of atmospheric Se and its speciation unravelling the Se biogeochemical cycles.

The Journal of Physical Chemistry AVol. 129(50)
University of British Columbia (CA), Universidad de la República de Uruguay (UY), PhysicoChimie des Processus de Combustion et de l'Atmosphère (FR)
Openalex Percentile: Top 71%
Chemical Thermodynamics and Molecular Structure
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.