Decades of theoretical and experimental work on excited-state intramolecular proton transfer systems indicate that electronic-vibrational (vibronic) coupling plays a significant role in ultrafast proton transfer reactions. However, the participating atomic motions of this chemical reaction have yet to be directly observed. The challenge in observing these rapid proton transfer processes lies in simultaneously probing both the electronic and vibrational degrees of freedom. Addressing these challenges requires advanced spectroscopic techniques that provide multidimensional (electronic and vibrational) structural information with femtosecond time resolution. Here, we use multidimensional electronic-vibrational spectroscopy to directly observe the vibronic motions driving the non-adiabatic excited-state proton transfer process in 10-hydroxybenzo[h]quinoline. We measure the interplay between high and low-frequency vibrations, mapping the proton transfer trajectory on two vibronically coupled electronic states. Our study enables the observation of vibronic coherence transfer, structural rearrangements, and intramolecular vibrational redistribution during and following proton transfer.

The coupled structural and electronic parameters of intramolecular hydrogen bonding play an important role in ultrafast chemical reactions, such as proton transfer processes. We perform one- and two-dimensional vibrational-electronic (1D and 2D VE) spectroscopy experiments to understand the couplings between vibrational and electronic coordinates in 10-Hydroxybenzo[h]quinoline, an ultrafast proton transfer system. The experiments reveal that the OH stretch (nu(OH)) is strongly coupled to the electronic excitation, and Fourier analysis of the 1D data shows coherent oscillations from the low frequency backbone vibrational modes coupled to the nu OH mode, resulting in an electronically detected vibronic signal. In-plane low-frequency vibrations at 242 and 386 cm(-1) change the hydrogen bond distance and modulate the observed electronic signal in the polarization-selective 1D VE experiment through orientation-dependent coupling with the nu OH mode. Resolution of the excitation frequency axis with 2D VE experiments reveals that excitation frequency, detection frequency, and experimental delay affect the frequency and strength of the vibronic transitions observed. Our results demonstrate evidence of direct coupling of the high frequency nu OH mode with the S-1 <- S(0 )electronic transition in 10-Hydroxybenzo[h]quinoline (HBQ), and orientation-dependent couplings of the low-frequency 242 and 386 cm(-1) modes to the nu OH mode and the electronic transition. This demonstration of multidimensional VE spectroscopy on HBQ reveals the potential of using 1D and 2D VE spectroscopy to develop a quantitative understanding of the role of vibronic coupling in hydrogen bonding and ultrafast proton transfer for complex systems.

AbstractFemtosecond pump-probe spectroscopy using ultrafast optical and infrared pulses has become an essential tool to discover and understand complex electronic and structural dynamics in solvated molecular, biological, and material systems. Here we report the experimental realization of an ultrafast two-color X-ray pump X-ray probe transient absorption experiment performed in solution. A 10 fs X-ray pump pulse creates a localized excitation by removing a 1s electron from an Fe atom in solvated ferro- and ferricyanide complexes. Following the ensuing Auger–Meitner cascade, the second X-ray pulse probes the Fe 1s → 3p transitions in resultant novel core-excited electronic states. Careful comparison of the experimental spectra with theory, extracts +2 eV shifts in transition energies per valence hole, providing insight into correlated interactions of valence 3d with 3p and deeper-lying electrons. Such information is essential for accurate modeling and predictive synthesis of transition metal complexes relevant for applications ranging from catalysis to information storage technology. This study demonstrates the experimental realization of the scientific opportunities possible with the continued development of multicolor multi-pulse X-ray spectroscopy to study electronic correlations in complex condensed phase systems.

Experimental demonstrations of polarization-selection two-dimensional Vibrational-Electronic (2D VE) and 2D Electronic-Vibrational (2D EV) spectroscopies aim to map the magnitudes and spatial orientations of coupled electronic and vibrational coordinates in complex systems. The realization of that goal depends on our ability to connect spectroscopic observables with molecular structural parameters. In this paper, we use a model Hamiltonian consisting of two anharmonically coupled vibrational modes in electronic ground and excited states with linear and bilinear vibronic coupling terms to simulate polarization-selective 2D EV and 2D VE spectra. We discuss the relationships between the linear vibronic coupling and two-dimensional Huang-Rhys parameters and between the bilinear vibronic coupling term and Duschinsky mixing. We develop a description of the vibronic transition dipoles and explore how the Hamiltonian parameters and non-Condon effects impact their amplitudes and orientations. Using simulated polarization-selective 2D EV and 2D VE spectra, we show how 2D peak positions, amplitudes, and anisotropy can be used to measure parameters of the vibronic Hamiltonian and non-Condon effects. This paper, along with the first in the series, provides the reader with a detailed description of reading, simulating, and analyzing multimode, polarization-selective 2D EV and 2D VE spectra with an emphasis on extracting vibronic coupling parameters from complex spectra.

Femtosecond x-ray pump-x-ray probe experiments are currently possible at free electron lasers such as the linac coherent light source, which opens new opportunities for studying solvated transition metal complexes. In order to make the most effective use of these kinds of experiments, it is necessary to determine which chemical properties an x-ray probe pulse will measure. We have combined electron cascade calculations and excited-state time-dependent density functional theory calculations to predict the initial state prepared by an x-ray pump and the subsequent x-ray probe spectra at the Fe K-edge in the solvated model transition metal complex, K4FeII(CN)6. We find several key spectral features that report on the ligand-field splitting and the 3p and 3d electron interactions. We then show how these features could be measured in an experiment.

Two-dimensional Electronic-Vibrational (2D EV) spectroscopy and two-dimensional Vibrational-Electronic (2D VE) spectroscopy are among the newest additions to the coherent multidimensional spectroscopy toolbox, and they are directly sensitive to vibronic couplings. In this first of two papers, the complete orientational response functions are developed for a model system consisting of two coupled anharmonic oscillators and two electronic states in order to simulate polarization-selective 2D EV and 2D VE spectra with arbitrary combinations of linearly polarized electric fields. Here, we propose analytical methods to isolate desired signals within complicated spectra and to extract the relative orientation between vibrational and vibronic dipole moments of the model system using combinations of polarization-selective 2D EV and 2D VE spectral features. Time-dependent peak amplitudes of coherence peaks are also discussed as means for isolating desired signals within the time-domain. This paper serves as a field guide for using polarization-selective 2D EV and 2D VE spectroscopies to map coupled vibronic coordinates on the molecular frame.

Transient IR and X-Ray spectroscopies were used to investigate excited state delocalization of a mixed valence Ru based donor-bridge-acceptor complex on a femtosecond timescale revealing the role of the electron density on the Ru-CN-Ru fragment.

A model vibronic Hamiltonian composed of coupled anharmonic vibrational modes and two electronic states provides a quantitative framework for understanding how vibronic couplings and dipole orientations are encoded in two-dimensional vibronic spectroscopy.

Femtosecond Fourier transform two-dimensional vibrational-electronic (2D VE) spectroscopy is a recently developed third-order nonlinear spectroscopic technique to measure coupled electronic and vibrational motions in the condensed phase. The viability of femtosecond multidimensional spectroscopy as an analytical tool requires improvements in data collection and processing to enhance the signal-to-noise ratio and increase the amount of data collected in these experiments. Here a continuous fast scanning technique for the efficient collection of 2D VE spectroscopy is described. The resulting 2D VE spectroscopic method gains sensitivity by reducing the effect of laser drift, as well as decreasing the data collection time by a factor of 10 for acquiring spectra with a high signal-to-noise ratio within 3 dB of the more time intensive step scanning methods. This work opens the door to more comprehensive studies where 2D VE spectra can be collected as a function of external parameters such as temperature, pH, and polarization of the input electric fields.