作者: S. M. Arrivo , V. D. Kleiman , W. T. Grubbs , T. P. Dougherty , E. J. Heilweil
DOI: 10.1155/1999/80323
关键词:
摘要: Transient picosecond infrared (IR) spectra of the OH and NH-stretch (v=0–1) absorption bands several hydrogen-bonded complexes have been investigated. Solutions of 1:1 weak acids (methanol, triethylsilanol pyrrole, < 0.1 mol/dm3) and bases (acetonitrile, pyridine tetrahydrofuran, 2 in CCl4 at 295 K were interrogated with IR excitation broadband probing. Lorentzian-shaped are uniformly bleached while those near-Gaussian bandshapes produce transient spectral holes. These results indicate a base functionality hydrogen-bond strength dependence for determining broadening mechanisms these absorptions.