Title of article :
Crystal structures and isometricity comparison of methylated bisphenol F derivatives
Author/Authors :
Gruber، نويسنده , , Tobias and Nestler، نويسنده , , Robert and Seichter، نويسنده , , Wilhelm and Bombicz، نويسنده , , Petra، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
7
From page :
319
To page :
325
Abstract :
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.
Keywords :
Estrogenic Activity , Bisphenol , Isometricity comparison , C–H??-interaction , Single crystal X-ray structure
Journal title :
Journal of Molecular Structure
Serial Year :
2014
Journal title :
Journal of Molecular Structure
Record number :
1975230
Link To Document :
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