Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 21st October 2020 from 07:00 AM to 07:00 PM (BST).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 46, 2019
Previous Article Next Article

Site-selective-induced isomerization of formamide

Author affiliations

Abstract

The new capacity of X-ray free-electron laser (XFEL) facilities to produce multi-color X-ray femtosecond pulses paves the way to explore ultrafast phenomena in matter induced by X-ray photons. In the present study, we exploit the site-selectivity and the high temporal resolution of a two-color X-ray femtosecond pump–probe sequence to investigate the isomerization of formamide. The pump pulse excites a particular atomic site in the molecule, while the probe pulse captures changes in the chemical environment at a remote atomic site. The response of the system is found to strongly depend on the nature of the excited site, and the core excitation provides selective control over chemical bond breaking. In particular, we show that the N1s → π* transition can induce the isomerization reaction in formamide and demonstrate the possibility to observe in real time hydrogen migration by measuring the chemical shifts with the X-ray probe pulse. This work opens a unique prospect for X-ray-induced photochemistry at XFEL facilities.

Graphical abstract: Site-selective-induced isomerization of formamide

Back to tab navigation

Article information


Submitted
10 Aug 2019
Accepted
02 Nov 2019
First published
04 Nov 2019

Phys. Chem. Chem. Phys., 2019,21, 25626-25634
Article type
Paper

Site-selective-induced isomerization of formamide

S. Oberli, J. González-Vázquez, E. Rodríguez-Perelló, M. Sodupe, F. Martín and A. Picón, Phys. Chem. Chem. Phys., 2019, 21, 25626
DOI: 10.1039/C9CP04441H

Social activity

Search articles by author

Spotlight

Advertisements