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| {{short description|Method in quantum chemistry}} | |||
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| ⚫ | The '''ab initio multiple spawning''', or '''AIMS''', method is a time-dependent ] of ]. | ||
| ⚫ | In AIMS, nuclear dynamics and electronic structure problems are solved ]. ] in the nuclear dynamics are included, especially the ] which are crucial in modeling dynamics on multiple electronic states. | ||
| {{linkless-date|September 2006}} | |||
| ⚫ | The AIMS method makes it possible to describe ] from first principles molecular dynamics, with no empirical parameters. The method has been applied to two molecules of interest in organic photochemistry - ] and ]. | ||
| ⚫ | The '''ab initio multiple spawning''', or '''AIMS''' method is a time-dependent formulation of ]. | ||
| ⚫ | The photodynamics of ] involves both ] and ]ic electronic excited states and the return to the ground state proceeds through a pyramidalized geometry. For the photoinduced ring opening of cyclobutene, is it shown that the disrotatory motion predicted by the ] is established within the first 50 fs after optical excitation. | ||
| ⚫ | In AIMS, nuclear dynamics and electronic structure problems are solved simultaneously. Quantum mechanical effects in the nuclear dynamics are included, especially the ] which are crucial in modeling dynamics on multiple electronic states. | ||
| ⚫ | The method was developed by chemistry professor ]. | ||
| ⚫ | The AIMS method makes it possible to describe ] from first principles molecular dynamics, with no empirical parameters. The method has been applied to two molecules of interest in organic photochemistry-] and ]. | ||
| ==References== | |||
| ⚫ | The photodynamics of ethylene involves both ] and ] electronic excited states and the return to the ground state proceeds through a pyramidalized geometry. For the photoinduced ring opening of cyclobutene, is it shown that the disrotatory motion predicted by the ] is established within the first 50 fs after optical excitation. | ||
| * Ab Initio Multiple Spawning: Photochemistry from First Principles Quantum Molecular Dynamics, M. Ben-Nun, Jason Quenneville, and Todd J. Martínez, ''J. Phys. Chem. A'' '''104''' (2000), #22, pp. 5161–5175. DOI . | |||
| * Nonadiabatic molecular dynamics: Validation of the multiple spawning method for a multidimensional problem, M. Ben-Nun and Todd J. Martínez, ''Journal of Chemical Physics'' '''108''', #17 (May 1, 1998), pp. 7244–7257. DOI . | |||
| ⚫ | The method was developed by ]. | ||
| ⚫ | {{chemistry-stub}} | ||
| {{DEFAULTSORT:Ab Initio Multiple Spawning}} | |||
| ] | ] | ||
| ] | ] | ||
| ⚫ | {{quantum-chemistry-stub}} | ||
Latest revision as of 21:47, 15 July 2022
Method in quantum chemistryThe ab initio multiple spawning, or AIMS, method is a time-dependent formulation of quantum chemistry.
In AIMS, nuclear dynamics and electronic structure problems are solved simultaneously. Quantum mechanical effects in the nuclear dynamics are included, especially the nonadiabatic effects which are crucial in modeling dynamics on multiple electronic states.
The AIMS method makes it possible to describe photochemistry from first principles molecular dynamics, with no empirical parameters. The method has been applied to two molecules of interest in organic photochemistry - ethylene and cyclobutene.
The photodynamics of ethylene involves both covalent and ionic electronic excited states and the return to the ground state proceeds through a pyramidalized geometry. For the photoinduced ring opening of cyclobutene, is it shown that the disrotatory motion predicted by the Woodward–Hoffmann rules is established within the first 50 fs after optical excitation.
The method was developed by chemistry professor Todd Martinez.
References
- Ab Initio Multiple Spawning: Photochemistry from First Principles Quantum Molecular Dynamics, M. Ben-Nun, Jason Quenneville, and Todd J. Martínez, J. Phys. Chem. A 104 (2000), #22, pp. 5161–5175. DOI 10.1021/jp994174i.
- Nonadiabatic molecular dynamics: Validation of the multiple spawning method for a multidimensional problem, M. Ben-Nun and Todd J. Martínez, Journal of Chemical Physics 108, #17 (May 1, 1998), pp. 7244–7257. DOI 10.1063/1.476142.
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