Related Experiment Video
Updated: Jan 7, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Study of Vibronic and Cationic Features of m-Diethoxybenzene via REMPI, Hole-Burning, and MATI Spectroscopy
Xiateng Qin1, Chunyang Duan1, Yan Zhao2
1State Key Laboratory of Quantum Optics Technologies and Devices, Institute of Laser Spectroscopy, Shanxi University, Taiyuan 030006, China.
Abstract:
Phenetole derivatives are widely used in various fields, and the presence of the ethoxy group, with its longer alkyl chain, suggests the possibility of multiple rotamers. In particular, diethoxybenzene derivatives, containing two ethoxy groups, exhibit an even greater number of rotameric forms. In this study, we report the first investigation of the stable structures, vibronic spectra, and cationic spectra of different rotamers of m-diethoxybenzene (MDEB). Resonance-enhanced multiphoton ionization (REMPI) spectra of the rotamers were identified via hole-burning (HB) experiments, while mass-analyzed threshold ionization (MATI) spectra provided precise adiabatic ionization energies (IEs) of the observed rotamers, as well as the active vibrations of their corresponding cations. Density functional theory (DFT) calculations predicted thirteen rotamers of MDEB, but only two rotamers were observed in the supersonic molecular beam. The band origins of the S1 ← S0 transition and the adiabatic IEs of the down-up and down-down rotamers of MDEB were determined to be 36,091 ± 2 cm-1 and 36,165 ± 2 cm-1 and 62,419 ± 5 cm-1 and 63,378 ± 5 cm-1, respectively. Franck-Condon spectral simulations for the S1 ← S0 and D0 ← S1 transitions were performed based on DFT calculations, and the theoretical results showed good agreement with the experimental data. Vibrational features observed in the S1 and D0 states were assigned by comparing the experimentally measured spectra with the simulated spectra as well as the previously reported vibrational spectra of structurally similar molecules. Finally, several key findings and molecular characteristics are discussed in detail.
More Related Videos
08:54Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
Published on: January 25, 2020
12:19Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
Related Concept Videos
NMR Spectroscopy of Benzene Derivatives
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals
Chemical Ionization (CI) Mass Spectrometry
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
¹H NMR: Complex Splitting
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied...