Molecular dynamics and metadynamics simulations of [2+2] photocycloaddition

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F18%3A43916686" target="_blank" >RIV/60461373:22310/18:43916686 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/60461373:22340/18:43916686

Výsledek na webu

<a href="https://onlinelibrary.wiley.com/doi/epdf/10.1002/qua.25534" target="_blank" >https://onlinelibrary.wiley.com/doi/epdf/10.1002/qua.25534</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/qua.25534" target="_blank" >10.1002/qua.25534</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Molecular dynamics and metadynamics simulations of [2+2] photocycloaddition

Popis výsledku v původním jazyce

Triplet state mechanism of [2+2] photocycloaddition forming a cyclobutane ring from two ethylenes is investigated in the context of photocatalysis. High-level ab initio calculations are combined with ab initio adiabatic molecular dynamics and ab initio metadynamics for rare events modeling. In a photocatalytic scheme, a reactant reaches the triplet state either via intersystem crossing (ISC) or triplet sensitization. The model system adopts a biradical structure, which represents energy intersection with the ground state. The system either completes cyclization or undergoes fragmentation into two olefinic units. The potential and free energy surfaces of the cyclobutane/ethylenes system are mapped with multireference approaches describing possible reaction pathways. To obtain a full picture of a double bond photoreactivity, ab initio adiabatic dynamical calculations were used to estimate reaction yields and to model the effects of excess energy. The potential use of density functional theory based approaches for [2+2] photocycloaddition was investigated for future simulations and design of realistic photocatalytic systems. Dynamical aspects of [2+2] photocycloaddition via a triplet state manifold are investigated by combining ab initio multireference methods and ab initio molecular dynamics and metadynamics. The reaction pathways are studied for a model system of two ethylenes forming a cyclobutane ring to provide a basis for further studies on design of photocatalytic systems.

Název v anglickém jazyce

Molecular dynamics and metadynamics simulations of [2+2] photocycloaddition

Popis výsledku anglicky

Triplet state mechanism of [2+2] photocycloaddition forming a cyclobutane ring from two ethylenes is investigated in the context of photocatalysis. High-level ab initio calculations are combined with ab initio adiabatic molecular dynamics and ab initio metadynamics for rare events modeling. In a photocatalytic scheme, a reactant reaches the triplet state either via intersystem crossing (ISC) or triplet sensitization. The model system adopts a biradical structure, which represents energy intersection with the ground state. The system either completes cyclization or undergoes fragmentation into two olefinic units. The potential and free energy surfaces of the cyclobutane/ethylenes system are mapped with multireference approaches describing possible reaction pathways. To obtain a full picture of a double bond photoreactivity, ab initio adiabatic dynamical calculations were used to estimate reaction yields and to model the effects of excess energy. The potential use of density functional theory based approaches for [2+2] photocycloaddition was investigated for future simulations and design of realistic photocatalytic systems. Dynamical aspects of [2+2] photocycloaddition via a triplet state manifold are investigated by combining ab initio multireference methods and ab initio molecular dynamics and metadynamics. The reaction pathways are studied for a model system of two ethylenes forming a cyclobutane ring to provide a basis for further studies on design of photocatalytic systems.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

International Journal of Quantum Chemistry

ISSN

1097-461X

e-ISSN

—

Svazek periodika

118

Číslo periodika v rámci svazku

10

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

11

Strana od-do

—

Kód UT WoS článku

000429003500004

EID výsledku v databázi Scopus

2-s2.0-85044826356