ChemInform Abstract: Direct Chemical Dynamics Simulations: Coupling of Classical and Quasiclassical Trajectories with Electronic Structure Theory

ChemInform ◽  
2013 ◽  
Vol 44 (48) ◽  
pp. no-no
Author(s):  
Manikandan Paranjothy ◽  
Rui Sun ◽  
Yu Zhuang ◽  
William L. Hase
Keyword(s):  
Electronic Structure ◽  
Electronic Structure Theory ◽  
Structure Theory ◽  
Chemical Dynamics ◽  
Quasiclassical Trajectories ◽  
Dynamics Simulations

The VENUS/NWChem software package. Tight coupling between chemical dynamics simulations and electronic structure theory

2014 ◽  
Vol 185 (3) ◽  
pp. 1074-1080 ◽  
Author(s):  
Upakarasamy Lourderaj ◽  
Rui Sun ◽  
Swapnil C. Kohale ◽  
George L. Barnes ◽  
Wibe A. de Jong ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Software Package ◽  
Electronic Structure Theory ◽  
Structure Theory ◽  
Chemical Dynamics ◽  
Tight Coupling ◽  
Dynamics Simulations

Theoretical Studies of Unimolecular Decomposition of Thiophene at High Temperatures

2021 ◽  
Author(s):  
Erum Gull Naz ◽  
Manikandan Paranjothy
Keyword(s):  
Thermal Decomposition ◽  
Electronic Structure ◽  
Density Functional ◽  
Fossil Fuels ◽  
Experimental Studies ◽  
Intramolecular Proton Transfer ◽  
Electronic Structure Theory ◽  
Structure Theory ◽  
Unimolecular Decomposition ◽  
Dynamics Simulations

Abstract Thiophene is an organo-sulfur aromatic molecule present in fossil fuels and alternate fuels such as shale oils and contributes to air pollution via fuel burning. Hence, it is essential to remove thiophene and its derivatives during the refining process. In this regard, experimental and electronic structure theory studies investigating the thermal decomposition of thiophene have been reported in the literature. In the present work, high temperature thermal decomposition of thiophene was investigated using Born-Oppenheimer direct dynamics simulations. The trajectory integrations were performed on-the-fly at the density functional B3LYP/6-31+G* level of electronic structure theory to investigate the atomic level decomposition mechanisms. Simulation results show that C-S cleavage accompanied by an intramolecular proton transfer to C is the dominant initial dissociation step. Acetylene was observed as primary decomposition product and the results are in agreement with previous experimental studies.

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