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Merck
CN

Hydration energies of protonated and sodiated thiouracils.

Journal of the American Society for Mass Spectrometry (2014-10-02)
Henryk Wincel
ABSTRACT

Hydration reactions of protonated and sodiated thiouracils (2-thiouracil, 6-methyl-2-thiouracil, and 4-thiouracil) generated by electrospray ionization have been studied in a gas phase at 10 mbar using a pulsed ion-beam high-pressure mass spectrometer. The thermochemical data, ΔH(o)n, ΔS(o)n, and ΔG(o)n, for the hydrated systems were obtained by equilibrium measurements. The water binding energies of protonated thiouracils, [2SU]H(+) and [6Me2SU]H(+), were found to be of the order of 51 kJ/mol for the first, and 46 kJ/mol for the second water molecule. For [4SU]H(+), these values are 3-4 kJ/mol lower. For sodiated complexes, these energies are similar for all studied systems, and varied between 62 and 68 kJ/mol for the first and between 48 and 51 kJ/mol for the second water molecule. The structural aspects of the precursors for hydrated complexes are discussed in conjunction with available literature data.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
2-Thiouracil, ≥99%
Sigma-Aldrich
6-Methyl-2-thiouracil, purum, ≥98.0% S basis (elemental analysis)
Supelco
6-Methyl-2-thiouracil, VETRANAL®, analytical standard
Sigma-Aldrich
2-Thiouracil, Vetec, reagent grade, 99%
Sigma-Aldrich
4-Thiouracil, 97%