J
James R. Durig
Researcher at University of Missouri–Kansas City
Publications - 1067
Citations - 15374
James R. Durig is an academic researcher from University of Missouri–Kansas City. The author has contributed to research in topics: Raman spectroscopy & Conformational isomerism. The author has an hindex of 46, co-authored 1067 publications receiving 15066 citations. Previous affiliations of James R. Durig include Lander University & Sandia National Laboratories.
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Vibrational spectra of monothiocarbamates-II. IR and Raman spectra, vibrational assignment, conformational analysis and ab initio calculations of S-methyl-N, N-dimethylthiocarbamate
TL;DR: In this article, a vibrational assignment for the -d0 molecule is facilitated by the availability of spectral data for five different isotopomers, including S-methyl-N, N-dimefhylthiocarbamate, (CH3)2NC(O)SCH3, and its isotopomer, S-d3, n-d6 and N -d9, for the gas and liquid.
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Fourier transform raman spectroscopy of synthetic and biological calcium phosphates
TL;DR: FT-Raman spectra of nascent, nonmineralized matrix vesicles (MV) show a distinct absence of the phosphate, consistent with formation of an OCP-like precursor during MV mineral formation that subsequently hydrolyzes to form hydroxyapatite.
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Far infrared spectra of palladium compounds—I. The influence of ligands upon the palladium chloride stretching frequency
TL;DR: The infrared spectra of a number of cis and trans palladium (II) complexes of the type PdL 2 Cl 2 have been recorded from 600 to 250 cm −1 as discussed by the authors.
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Raman and Infrared Spectra, Conformational Stability, Normal Coordinate Analysis, Vibrational Assignment, and ab Initio Calculations of 3,3-Difluorobutene
TL;DR: The Raman spectra (3300−10 cm-1) of gaseous, liquid and solid 3,3-difluorobutene, CH2CHCF2CH3, and the infrared spectra of the gas, xenon solution, and solid have been recorded.
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Vibrational spectrum of hydrazine-d sub 4 and a Raman study of hydrogen bonding in hydrazine.
TL;DR: A complete vibrational analysis based on band type, position, and depolarization values is given which satisfies the product rule for both the a and b vibrational symmetry species and indicates that part of the intensity of the 3189‐cm−1 band arises from a vibrational mode of the hydrazine monomer.