Crystal structures and isometricity comparison of methylated bisphenol F derivatives

Gruber, T. and Nestler, R. and Seichter, W. and Bombicz, Petra (2014) Crystal structures and isometricity comparison of methylated bisphenol F derivatives. JOURNAL OF MOLECULAR STRUCTURE, 1056-1 (1). pp. 319-325. ISSN 0022-2860


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The syntheses and X-ray structures of three methylated bisphenol F derivatives and one respective analogue are reported. A special emphasis lies on the influence of methyl groups on the conformation of the common diphenylmethane scaffold. The introduction of four methyl groups to bisphenol F was found not to disturb its typical strong hydrogen bond network, and yet, to change the pattern of the aromatic interactions in the overall packing. According to the isometricity comparison, the addition of methyl groups to the diphenylmethane core has a greater influence on the conformation of the individual molecules, than the presence or absence of hydrogen bonding donors or acceptors. © 2013 Elsevier B.V. All rights reserved.

Item Type: Article
Uncontrolled Keywords: Single crystal X-ray structure; Keywords; Isometricity comparison; Estrogenic activity; C-Hâ̄π-interaction; Bisphenol
Subjects: Q Science / természettudomány > QD Chemistry / kémia
Depositing User: MTMT SWORD
Date Deposited: 19 Feb 2015 13:50
Last Modified: 19 Feb 2017 00:15

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