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Crystal and molecular structure of 5-trifluorothymine, a metabolite from human urine: Role of fluorine in stacking and hydrogen bonded interactions

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JOURNAL OF FLUORINE CHEMISTRY
卷 129, 期 6, 页码 493-497

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2008.03.003

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polyflourinated thymines; stacking of fluorinated bases; dimeric hydrogen bonding of nucleic acid bases

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The crystal structure of the metabolite from urine, 5-trifluorothymine [5F(3)T] has been determined by single crystal X-ray diffractometric methods. Crystals of 5F(3)T are monoclinic, space group P2(1)/c with cell dimensions a = 6.7468(2), b = 15.0740(6), c = 13.4405(6), beta = 90.412(2), V = 1366.88(8), Z = 8 (two molecules per asymmetric unit). Crystal structure of 5F3T was determined with 3039 independent data and refined by full-matrix least squares methods to a final reliability factor of 0.047. Molecules of 5F(3)T are connected by dimeric type of N-H center dot center dot center dot O hydrogen bonding linking molecules related by a center of inversion into an extensive layer of dimeric molecules. These layers are stacked on top of each other at a stacking distance of 3.280 angstrom with a head-to-head stacking of the fluorine atoms on top of each other with no hydrogen bonding involving the fluorine atoms. (C) 2008 Elsevier B.V. All rights reserved.

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