DFT calculations, Hirshfeld surface analysis and docking studies of 3-anisaldehyde thiosemicarbazone

Author:

Guin MridulaORCID,Khanna Sonia,Elavarasi S Begam,Sarkar Paratpar

Funder

Science and Engineering Research Board

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Reference31 articles.

1. Lobana T S, Sharma R, Bawa G and Khanna S 2009 Bonding and structure trends of thiosemicarbazone derivatives of metals—an overview Coord. Chem. Rev. 253 977

2. Lobana T S, Indoria S, Jassal A K, Kaur H, Arora D S and Jasinski J P 2014 Synthesis, structures, spectroscopy and antimicrobial properties of complexes of copper(II) with salicylaldehyde N- substituted thiosemicarbazones and 2,2’-bipyridine or 1,10-phenanthroline Eur. J. Med. Chem. 76 154

3. West D X, Liberta A E, Padhye S B, Chikate R C, Sonawane P B, Kumbhar A S and Yerande R G 1993 Thiosemicarbazone complexes of copper(II): structural and biological studies Coord. Chem. Rev. 123 49

4. Mahajan R K, Kaur I and Lobana T S 2003 A mercury (II) ion-selective electrode based on neutral salicylaldehyde thiosemicarbazone Talanta 59 101

5. Ali M A, Khalifa M E, Ghazy S E and Hassanien M M 2002 Selective flotation-separation and spectrophotometric determination of cadmium using phenanthraquinone monophenythiosemicarbazone Anal. Sci. 18 1235

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