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Ground-State Chemical Reactivity under Vibrational Coupling to the Vacuum Electromagnetic Field.


ABSTRACT: The ground-state deprotection of a simple alkynylsilane is studied under vibrational strong coupling to the zero-point fluctuations, or vacuum electromagnetic field, of a resonant IR microfluidic cavity. The reaction rate decreased by a factor of up to 5.5 when the Si-C vibrational stretching modes of the reactant were strongly coupled. The relative change in the reaction rate under strong coupling depends on the Rabi splitting energy. Product analysis by GC-MS confirmed the kinetic results. Temperature dependence shows that the activation enthalpy and entropy change significantly, suggesting that the transition state is modified from an associative to a dissociative type. These findings show that vibrational strong coupling provides a powerful approach for modifying and controlling chemical landscapes and for understanding reaction mechanisms.

SUBMITTER: Thomas A 

PROVIDER: S-EPMC5113700 | biostudies-other | 2016 Sep

REPOSITORIES: biostudies-other

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Ground-State Chemical Reactivity under Vibrational Coupling to the Vacuum Electromagnetic Field.

Thomas Anoop A   George Jino J   Shalabney Atef A   Dryzhakov Marian M   Varma Sreejith J SJ   Moran Joseph J   Chervy Thibault T   Zhong Xiaolan X   Devaux Eloïse E   Genet Cyriaque C   Hutchison James A JA   Ebbesen Thomas W TW  

Angewandte Chemie (International ed. in English) 20160816 38


The ground-state deprotection of a simple alkynylsilane is studied under vibrational strong coupling to the zero-point fluctuations, or vacuum electromagnetic field, of a resonant IR microfluidic cavity. The reaction rate decreased by a factor of up to 5.5 when the Si-C vibrational stretching modes of the reactant were strongly coupled. The relative change in the reaction rate under strong coupling depends on the Rabi splitting energy. Product analysis by GC-MS confirmed the kinetic results. Tem  ...[more]

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