Plasmon-Assisted Transfer Hydrogenation: Kinetic Control of Reaction Chemoselectivity through a Light Illumination Mode
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F21%3A43922577" target="_blank" >RIV/60461373:22310/21:43922577 - isvavai.cz</a>
Výsledek na webu
<a href="https://pubs-acs-org.ezproxy.vscht.cz/doi/10.1021/acs.jpcc.0c11535" target="_blank" >https://pubs-acs-org.ezproxy.vscht.cz/doi/10.1021/acs.jpcc.0c11535</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jpcc.0c11535" target="_blank" >10.1021/acs.jpcc.0c11535</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Plasmon-Assisted Transfer Hydrogenation: Kinetic Control of Reaction Chemoselectivity through a Light Illumination Mode
Popis výsledku v původním jazyce
Recently, the utilization of plasmon assistance was demonstrated to be a useful tool for promoting various chemical transformations. Plasmon triggering can enhance the reaction rate or change the reaction pathways, affecting in this way the selectivity of chemical transformation. The plasmon-assisted selectivity was previously achieved through variations in excitation wavelengths and plasmonic structures. The aim of this work was to prove that the optimal combination of light irradiation and the heterophase process could increase the reaction conversion and change the reaction chemoselectivity. We utilized various light illumination regimes (with different pulse frequencies and shapes) for the control of reaction conversion and selectivity in the plasmon-assisted transfer hydrogenation of two functional groups attached to the bimetallic (Au/Pt) grating surface: 4-ethynylphenylene and 4-nitrophenylene. It was demonstrated that the utilization of a suitable illumination regime allows us to increase the reaction rate and reach the kinetic control of plasmon-assisted transfer hydrogenation.
Název v anglickém jazyce
Plasmon-Assisted Transfer Hydrogenation: Kinetic Control of Reaction Chemoselectivity through a Light Illumination Mode
Popis výsledku anglicky
Recently, the utilization of plasmon assistance was demonstrated to be a useful tool for promoting various chemical transformations. Plasmon triggering can enhance the reaction rate or change the reaction pathways, affecting in this way the selectivity of chemical transformation. The plasmon-assisted selectivity was previously achieved through variations in excitation wavelengths and plasmonic structures. The aim of this work was to prove that the optimal combination of light irradiation and the heterophase process could increase the reaction conversion and change the reaction chemoselectivity. We utilized various light illumination regimes (with different pulse frequencies and shapes) for the control of reaction conversion and selectivity in the plasmon-assisted transfer hydrogenation of two functional groups attached to the bimetallic (Au/Pt) grating surface: 4-ethynylphenylene and 4-nitrophenylene. It was demonstrated that the utilization of a suitable illumination regime allows us to increase the reaction rate and reach the kinetic control of plasmon-assisted transfer hydrogenation.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
20501 - Materials engineering
Návaznosti výsledku
Projekt
<a href="/cs/project/GA20-19353S" target="_blank" >GA20-19353S: Příprava a charakterizace hybridních plazmonických nanostruktur se silnou chirální odezvou</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Physical Chemistry C
ISSN
1932-7447
e-ISSN
—
Svazek periodika
125
Číslo periodika v rámci svazku
19
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
8
Strana od-do
10318-10325
Kód UT WoS článku
000655640900014
EID výsledku v databázi Scopus
2-s2.0-85106380513