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Issue 17, 1996
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Metastable intermediates from glassy solutions. Part 3.—FTIR spectra of α-carbonic acid and its 2H and 13C isotopic forms, isolated from methanolic solution

Abstract

Layers of glassy solutions of KH12CO3(KD12CO3, K213CO3) and of excess HCl (DCl) dissolved in CH3OH (CH3OD) and in 70 wt.% glycerol–water have been deposited sequentially at 78 K in the form of droplets, and their reaction in the temperature range 78–300 K studied by FTIR spectroscopy (from 4000 to 400 cm–1). At ca. 20 K above the glass-transition temperature (Tg) of the solvent, a decrease in viscosity initiated coalescence of the droplets. At ca. 40 K above Tg, protonation of the hydrogen carbonate (carbonate) and formation of H2CO3 occurred in the liquid state. After pumping off the solvent, residual ice and excess HCl, amorphous H212CO3(D212CO3, H213CO3) was isolated, crystallizing at ca. 190–200 K to α-carbonic acid. Assignments for the spectral features of α-H2CO3 and its isotopic forms are given. Base pressure, water content and heating rate lead to varying degrees of disorder in the crystalline phase. The cryogenic method for formation of metastable short-lived intermediates from reaction of non-volatile reactants is discussed. The intermediates can be studied in solution or as amorphous or crystalline solids.

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Article type: Paper
DOI: 10.1039/FT9969203183
J. Chem. Soc., Faraday Trans., 1996,92, 3183-3195

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    Metastable intermediates from glassy solutions. Part 3.—FTIR spectra of α-carbonic acid and its 2H and 13C isotopic forms, isolated from methanolic solution

    W. Hage, A. Hallbrucker and E. Mayer, J. Chem. Soc., Faraday Trans., 1996, 92, 3183
    DOI: 10.1039/FT9969203183

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