کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1312800 | 975497 | 2007 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Supramolecular rods via halogen bonding-based self-assembly of fluorinated phosphazene nanopillars Supramolecular rods via halogen bonding-based self-assembly of fluorinated phosphazene nanopillars](/preview/png/1312800.png)
A cyclotriphosphazene derivative bearing six 4-iodotetrafluorophenyl-substituted arms self-assembles with dipyridyl derivatives under the control of N⋯I halogen bonding to give rise to complexes where the starting modules are present in a 1:3 stoichiometric ratio, respectively. The directionality of the N⋯I halogen bonding translates the pillar-like arrangement adopted by the cyclotriphosphazene module into the rod-shaped supramolecular structure of the formed infinite chains. The invariance of N⋯I interactions translates the different size of the used dipyridyl modules into different pitches along the self-assembled rods. The obtained supramolecular architectures show a remarkable structural similarity confirming the reliability of halogen bonding in the design of complex supramolecular networks.
A cyclotriphosphazene derivative bearing six 4-iodotetrafluorophenyl-substituted arms self-assembles with dipyridyl derivatives under the control of N⋯I halogen bonding to give rise to complexes where the starting modules are present in a 1:3 stoichiometric ratio, respectively. The directionality of the N⋯I halogen bonding translates the pillar-like arrangement adopted by the cyclotriphosphazene module into the rod-shaped supramolecular structure of the formed infinite chains.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 360, Issue 3, 15 February 2007, Pages 1191–1199