posted on 2018-11-14, 00:00authored byPeter
A. Eckert, Kevin J. Kubarych
We
report a spectroscopic investigation of the ultrafast dynamics
of the second-generation poly(aryl ether) dendritic hydrogenase model
using two-dimensional infrared (2D-IR) spectroscopy to probe the metal
carbonyl vibrations of the dendrimer and a reference small molecule,
[Fe(μ-S)(CO)3]2. We find that the structural
dynamics of the dendrimer are reflected in a slow phase of the spectral
diffusion, which is absent from [Fe(μ-S)(CO)3]2, and we relate the slow phase to the quality of the solvent
for poly(aryl ether) dendrimers. We observe a solvent-dependent modulation
of the initial phase of vibrational relaxation of the carbonyl groups,
which we attribute to an inhibition of solvent assistance in the intramolecular
vibrational redistribution process for the dendrimer. There is also
a clear solvent dependence of the vibrational frequencies of both
the dendrimer and [Fe(μ-S)(CO)3]2. Our
data represent the first 2D-IR study of a dendritic complex and provide
insight into the solvent dependence of molecular conformation in solution
and the ultrafast dynamics of moderately sized, conformationally mobile
compounds.