Issue 11, 2016

Pyrazine-based donor tectons: synthesis, self-assembly and characterization

Abstract

Two new supramolecular building blocks derived from pyrazine are introduced. These molecules, having pendant pyridine units covalently linked to central pyrazine ring, are structurally rigid with pre-defined bite angles. Therefore they can act as donor tectons in design of supramolecular hexagons using coordination driven self-assembly protocol. Multinuclear NMR (including 1H DOSY) and mass spectrometry have been utilized to confirm the purity and stoichiometry of these self assembled hexagonal ensembles. PM6 molecular modeling studies corroborate their hexagonal shape and nanoscalar dimensions.

Graphical abstract: Pyrazine-based donor tectons: synthesis, self-assembly and characterization

Supplementary files

Article information

Article type
Paper
Submitted
15 Oct 2015
Accepted
09 Jan 2016
First published
13 Jan 2016

RSC Adv., 2016,6, 8992-9001

Author version available

Pyrazine-based donor tectons: synthesis, self-assembly and characterization

S. Bhowmick, S. Chakraborty, S. R. Marri, J. N. Behera and N. Das, RSC Adv., 2016, 6, 8992 DOI: 10.1039/C5RA21484J

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