Issue 24, 2019, Issue in Progress

Constitutional isomers of brominated-functionalized copillar[5]arenes: synthesis, characterization, and crystal structures

Abstract

We herein report the preparation of constitutional isomers of brominated-functionalized pillar[5]arenes via co-condensation of 1,4-bis(2-bromoethoxy)benzene and 1,4-dimethoxybenzene. The structures of the obtained isomers were then established using single crystal X-ray diffraction. We also found that the isomeric yield distribution of the different constitutional isomers was independent of the monomer's mole feed ratio, as revealed by HPLC analysis of the crude mixture. Finally, further characterization of the separated constitutional isomers indicated that they possess different melting points, NMR spectra, crystal structures, binding constants and stacking patterns in the solid state.

Graphical abstract: Constitutional isomers of brominated-functionalized copillar[5]arenes: synthesis, characterization, and crystal structures

Supplementary files

Article information

Article type
Paper
Submitted
26 Mar 2019
Accepted
30 Apr 2019
First published
03 May 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 13814-13819

Constitutional isomers of brominated-functionalized copillar[5]arenes: synthesis, characterization, and crystal structures

T. F. Al-Azemi, M. Vinodh, F. H. Alipour and A. A. Mohamod, RSC Adv., 2019, 9, 13814 DOI: 10.1039/C9RA02313E

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