首页 | 本学科首页   官方微博 | 高级检索  
     检索      


A comparative study of crystal structures and inclusion properties of fluorinated triazines
Authors:Katharina Reichenbaecher  Edwin Weber
Institution:a Department of Chemistry and Biochemistry, University of Berne, Freiestrasse 3, 3012 Berne, Switzerland
b Institute of Chemistry, University of Neuchâtel, Av. Bellevaux 51, CH-2007 Neuchâtel, Switzerland
c Institute of Organic Chemistry, TU Bergakademie Freiberg, Leipziger Str. 29, D-09596 Freiberg/Sachsen, Germany
Abstract:Three perfluorinated host compounds of the triazine type, namely 2,4,6-tris(pentafluorophenoxy)-1,3,5-triazine (1), 2,4,6-tris(pentafluorothiophenoxy)-1,3,5-triazine (2) and 2,4,6-tris(pentafluorophenamin)-1,3,5-triazine (3), were synthesized differing only in the linking heteroatom (O, S and NH) between the triazine core and the pentafluorophenyl groups. The crystal structures involving compounds 1, 2 and their inclusion compounds are dominated by a variety of fluorine interactions (phenyl-perfluorophenyl, C-H?F, F?F, C-F?πF). However, in the structure of 3, possessing additional hydrogen atoms of the linkage NH-groups, the formation of hydrogen bonds is favoured, whereas fluorine contacts are less apparent. Investigations by powder X-ray diffraction and thermogravimetric analysis revealed substantial differences in the host-guest interactions of the inclusion compounds.
Keywords:Fluorine compounds  Triazines  Inclusions  Host-guest compounds  Fluorine interactions
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号