Identification of unusual C–Cl⋯π contacts in 2-(alkylamino)-3-chloro-1,4-naphthoquinones: effect of N-substituents on crystal packing, fluorescence, redox and anti-microbial properties
Author:
Affiliation:
1. Department of Chemistry
2. Faculty of Science
3. The M. S. University of Baroda
4. Vadodara-390 002
5. India
6. National Single Crystal X-ray Diffraction Facility
7. IIT Bombay
8. Mumbai 400 076
Abstract
XRD study demonstrates the opening of unusual C–Cl⋯π synthon in 2-(alkylamino)-3-chloro-1,4-naphthoquinone. Notably, compound holding N-pyridylmethyl exhibits enhanced activity against S. aureus and proved to be more potent than ciprofloxacin.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA02295A
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