Related Experiment Video
Updated: Jun 16, 2026

Proton Transfer and Protein Conformation Dynamics in Photosensitive Proteins by Time-resolved Step-scan Fourier-transform Infrared Spectroscopy
Published on: June 27, 2014
Direct observation of proton transfer in ice Ih using femtosecond spectroscopy
R L A Timmer1, M J Cox, H J Bakker
1FOM-institute for Atomic and Molecular Physics, Science Park 104, 1098 SG Amsterdam, The Netherlands. r.timmer@amolf.nl
Abstract:
We studied proton transfer in ice samples containing the photoacid 8-hydroxypyrene-1,3,6-trisulfonic acid and the base sodium formate using femtosecond pump-probe spectroscopy. Pump pulses, centered at a wavelength of 400 nm, electronically excited the photoacid molecules which released their protons. These protons subsequently traveled from the photoacid through the ice lattice to the base and were observed as they arrived at the base using the transient absorption of an infrared probe pulse. Both the temperature and concentration dependence of the proton transfer dynamics were modeled using a discrete set of two intrinsic transfer rates, associated with short and long-range proton transfer, respectively. Proton transfer in configurations where the acid and base were separated by up to about two water molecules, was found to occur on a approximately 1 ps time scale for all temperatures (240-270 K). Long range direct proton transfer through water wires of about four water molecules in length was found to occur on a approximately 300 ps time scale at 270 K. This latter process was observed to slow down significantly with decreasing temperature, with an activation energy of approximately 80 kJ/mol.
Related Concept Videos
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
Phase Transitions: Melting and Freezing

