Constitutional isomers of brominated-functionalized copillar[5]arenes: synthesis, characterization, and crystal structures
Author:
Affiliation:
1. Chemistry Department
2. Kuwait University
3. Kuwait
Abstract
Constitutional isomers of brominated-functionalized pillar[5]arenes were synthesized using a co-cyclization strategy.
Funder
Kuwait Foundation for the Advancement of Sciences
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/RA/C9RA02313E
Reference29 articles.
1. para-Bridged Symmetrical Pillar[5]arenes: Their Lewis Acid Catalyzed Synthesis and Host–Guest Property
2. Formation of Linear Supramolecular Polymers That Is Driven by CH⋅⋅⋅π Interactions in Solution and in the Solid State
3. DIBPillar[n]arenes (n = 5, 6): Syntheses, X-ray Crystal Structures, and Complexation with n-Octyltriethyl Ammonium Hexafluorophosphate
4. A Facile and Efficient Preparation of Pillararenes and a Pillarquinone
5. Efficient synthesis of copillar[5]arenes and their host–guest properties with dibromoalkanes
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2. Crystal structure and supramolecular features of a bis-urea-functionalized pillar[5]arene;Acta Crystallographica Section E Crystallographic Communications;2023-10-19
3. Spatially Designed Supramolecular Anion Receptors Based on Pillar[5]arene Scaffolds: Synthesis and Halide Anion Binding Properties;ACS Omega;2022-12-27
4. “Rim‐Differentiated” Pillar[6]arenes;Angewandte Chemie International Edition;2022-05-03
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