Abstract
The molecular recognition properties of a novel calix[4]arene receptor fixed in a 1,3-alternate conformation bearing two dipyridyl moieties towards organic molecules containing hydroxylic (phenolic or alcoholic) or amino functionalities have been investigated by 1H NMR spectroscopy in CDCl3. The novel receptor selectively recognizes by hydrogen bonding only molecules having two OH phenolic groups.
Keywords: Calixarenes, Molecular recognition, Hydrogen bonding, Diphenols
Related Books
2-Deoxy-D-Glucose: Chemistry and Biology
Chiral Ionic Liquids: Applications in Chemistry and Technology
Basics of Organic Chemistry: A Textbook for Undergraduate Students
Advances in Organic Synthesis
The Synthetic Methods, Structures, and Properties of the Ca-C σ Bond Organocalcium Containing Compounds
Advances in Organic Synthesis
Chemistry of Bipyrazoles: Synthesis and Applications
Advances in Organic Synthesis
Advanced Nanocatalysis for Organic Synthesis and Electroanalysis
Advances in Organic Synthesis
20