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Multidimensional X-Ray Spectroscopy of Valence and Core Excitations in Cysteine

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TLDR
The coupling between valence- and core-excited states can be visualized in three-dimensional plots, revealing the origin of the polarizability that controls the simpler pump-probe SXRS signals.
Abstract
Several nonlinear spectroscopy experiments which employ broadband x-ray pulses to probe the coupling between localized core and delocalized valence excitation are simulated for the amino acid cysteine at the K-edges of oxygen and nitrogen and the K and L-edges of sulfur. We focus on two dimensional (2D) and 3D signals generated by two- and three-pulse stimulated x-ray Raman spectroscopy (SXRS) with frequency-dispersed probe. We show how the four-pulse x-ray signals $\boldsymbol{k}_\mathrm{I}=-\boldsymbol{k}_1+\boldsymbol{k}_2+\boldsymbol{k}_3$ and $\boldsymbol{k}_\mathrm{II}=\boldsymbol{k}_1-\boldsymbol{k}_2+\boldsymbol{k}_3$ can give new 3D insight into the SXRS signals. The coupling between valence- and core-excited states can be visualized in three dimensional plots, revealing the origin of the polarizability that controls the simpler pump-probe SXRS signals.

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Ab initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields

TL;DR: In this paper, the unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio using DFT, MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set.
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Recent experimental and theoretical developments in time-resolved X-ray spectroscopies

TL;DR: In this paper, the authors discuss recent experimental and theoretical developments in ultrafast X-ray absorption spectroscopies (XAS) and explore the new opportunities they offer, as well as the driving force for new theoretical methods permitting a detailed interpretation of the spectra in terms of the geometrical and electronic properties of the system.
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Photochemical Processes Revealed by X-ray Transient Absorption Spectroscopy

TL;DR: In this paper, the authors reviewed current achievements and capabilities in chemical dynamics from XTA spectroscopy based mainly on studies by the authors, collaborators, and cousers of the same facility and then outlined some future challenges and impacts in chemical sciences using pulsed X-rays from the third-generation synchrotron and the fourth-generation X-ray free-electron light sources.
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Watching energy transfer in metalloporphyrin heterodimers using stimulated X-ray Raman spectroscopy

TL;DR: This work shows how ultrafast hard X-ray pulses may be used to create localized electronic wavepackets in a metalloporphyrin dimer by combining the broad bandwidth of attosecond pulses with the localized nature of core orbitals results in a much higher degree of localization and temporal resolution than is possible with optical pulses.
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Multidimensional resonant nonlinear spectroscopy with coherent broadband x-ray pulses

TL;DR: Bennett et al. as mentioned in this paper survey various possible types of multidimensional x-ray spectroscopy techniques and demonstrate the novel information they can provide about molecules, such as core-electronic structure and couplings, real-time tracking of impulsively created valence-electronics wavepackets and electronic coherences, and monitoring ultrafast processes such as nonadiabatic electron-nuclear dynamics near conical-intersection crossings.
References
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Book

Principles of Nonlinear Optical Spectroscopy

Shaul Mukamel
TL;DR: In this article, the authors present a simulation of the optical response functions of a multilevel system with relaxation in a multimode Brownian Oscillator Model and a wavepacket analysis of nonimpulsive measurements.
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Time-dependent density functional theory within the Tamm–Dancoff approximation

TL;DR: In this article, the Tamm-Dancoff approximation to time-dependent density functional theory is proposed and implemented for molecular excited states, which yields excitation energies for several closed-and open-shell molecules that are essentially of the same quality as those obtained from time dependent density functional theories itself, when the same exchange correlation functional is used.
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Coherently wired light-harvesting in photosynthetic marine algae at ambient temperature

TL;DR: Observations provide compelling evidence for quantum-coherent sharing of electronic excitation across the 5-nm-wide proteins under biologically relevant conditions, suggesting that distant molecules within the photosynthetic proteins are ‘wired’ together by quantum coherence for more efficient light-harvesting in cryptophyte marine algae.
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Structure of the amide i band of peptides measured by femtosecond nonlinear-infrared spectroscopy

TL;DR: In this paper, a femtosecond pump probe and dynamic hole burning experiments were used to examine the ultrafast response of the modes in the 1600−1700 cm-1 region (the so-called amide I modes) of N-methylacetamide (NMA) and three small globular peptides, apamin, scyllatoxin, and bovine pancreatic trypsin inhibitor (BPTI).
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