We present the basic principles of dynamic rotational spectroscopy for the highly vibrationally excited symmetric top molecule trifluoropropyne (TFP,CF3CCH). Single molecular eigenstate rotational spectra of TFP were recorded in the region of the first overtone of the nu(1) acetylenic stretching mode at 6550 cm(-1) by infrared-pulsed microwave-Fourier transform microwave triple resonance spectroscopy. The average rotational constant (B) of the highly vibrationally mixed quantum states at 6550 cm(-1) is 2909.33 MHz, a value that is 40 MHz larger than the rotational constant expected for the unperturbed C-H stretch overtone (2869.39 MHz). The average rotational constant and rotational line shape of the molecular eigenstate rotational spectra are compared to the distribution of rotational constants expected for the ensemble of normal-mode vibrational states at 6550 cm(-1) that can interact by intramolecular vibrational energy redistribution (IVR). The normal-mode population distribution at 6550 cm(-1) can be described using a Boltzmann distribution with a microcanonical temperature of 1200 K. At this energy the rotational constant distribution in the normal-mode basis set is peaked at about 2910 MHz with a width of about 230 MHz. The distribution is slightly asymmetric with a tail to the high end. The experimentally measured dynamic rotational spectra are centered at the normal-mode distribution peak; however, the spectral width is significantly narrower (40 MHz) than normal-mode ensemble width (230 MHz). This reduction of the width, along with the Lorentzian shape of the eigenstate rotational spectra when compared to the Gaussian shape of the calculated ensemble distribution, illustrates the narrowing of the spectrum due to IVR exchange. The IVR exchange rate was determined to be 120 ps, about ten times faster than the rate at which energy is redistributed from the v=2 level of the acetylenic stretch.

Download full-text PDF

Source
http://dx.doi.org/10.1063/1.1780164DOI Listing

Publication Analysis

Top Keywords

6550 cm-1
20
rotational spectra
16
rotational constant
16
rotational
12
eigenstate rotational
12
intramolecular vibrational
8
vibrational energy
8
energy redistribution
8
dynamic rotational
8
highly vibrationally
8

Similar Publications

Regulating the Solvation Shell Structure of Lithium Ions for Smooth Li Metal Deposition in Quasi-Solid-State Batteries.

ChemSusChem

April 2023

MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, 150001, Harbin, P. R. China.

Gel polymer electrolytes (GPE) are promising next-generation electrolytes for high-energy batteries, combining the multiple advantages of liquid and all-solid-state electrolytes. Herein, we a synthesized GPE using poly(ethylene glycol)acrylate (PEGDA) in order to understand how the GPE efficiently inhibits lithium dendrite formation and growth. The effects of PEGDA on the solvation shell structure of the lithium ion are investigated using density functional theory (DFT) and ab initio molecular dynamics (AIMD) simulations, which are also supported by Raman spectroscopy.

View Article and Find Full Text PDF

A Study of NbMo and NbMo by Anion Photoelectron Spectroscopy.

J Phys Chem A

November 2021

Chemistry Department, University of Minnesota, 207 Pleasant Street S.E., Minneapolis, Minnesota55455, United States.

Photoelectron spectra of the niobium-molybdenum diatomic anion, obtained at 488 and 514 nm, display vibrationally resolved transitions from the ground state and one excited electronic state of the anion to the ground state and one excited electronic state of the neutral molecule. The electron affinity of NbMo is measured to be 1.130 ± 0.

View Article and Find Full Text PDF

Two-dimensional semiconductors such as MoS are promising for future electrical devices. The interface to metals is a crucial and critical aspect for these devices because undesirably high resistances due to Fermi level pinning are present, resulting in unwanted energy losses. To date, experimental information on such junctions has been obtained mainly indirectly by evaluating transistor characteristics.

View Article and Find Full Text PDF

In Vitro Cytocompatibility Assessment of Ti-Modified, Silicon-oxycarbide-Based, Polymer-Derived, Ceramic-Implantable Electrodes under Pacing Conditions.

ACS Appl Mater Interfaces

April 2020

Laboratory for High Performance Ceramics, Empa, Swiss Federal Laboratories for Material Science and Technology, Duebendorf 8600, Switzerland.

Polymer-derived ceramics (PDC) have recently gained increased interest in the field of bioceramics. Among PDC's, carbon-rich silicon oxycarbide ceramics (SiOC) possess good combined electrical and mechanical properties. Their durability in aggressive environments and proposed cytocompatibility makes them an attractive material for fabrication of bio-MEMS devices such as pacemaker electrodes.

View Article and Find Full Text PDF

We report the synthesis of a semiquinoid-bridged single-chain magnet, as generated through a thermally induced metal-ligand electron transfer. Reaction of FeCl with 2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone (LH) in the presence of (NMe)Cl gave the compound (NMe)[LFeCl]. Together, variable-temperature X-ray diffraction, Mössbauer spectra, Raman spectra, and dc magnetic susceptibility reveal a transition from a chain containing (L)Fe units to one with (L)Fe upon decreasing temperature, with a transition temperature of T = 213 K.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!