Palladium-mediated C–O bond activation of benzopyrone in 4-oxo-4H-chromone-3-carbaldehyde-4(N)-substituted thiosemicarbazone: synthesis, structure, nucleic acid/albumin interaction, DNA cleavage, antioxidant and cytotoxic studies

Author:

Shanmugapriya A.1,Kalaiarasi G.1,Ravi M.2,Sparkes H. A.3ORCID,Kalaivani P.4,Prabhakaran R.1ORCID

Affiliation:

1. Department of Chemistry, Bharathiar University, Coimbatore 641 046, India

2. Department of Biochemistry, University of Madras, Guindy Campus, Chennai-25, India

3. University of Bristol, School of Chemistry, Cantock's Close, Bristol BS8 1TS, UK

4. Department of Chemistry, Nirmala College for Women, Bharathiar University, Coimbatore 641018, India

Abstract

Palladium ion-mediated C–O activation at the C2 carbon of the benzopyrone moiety of 3-formylchromone-4(N)-substituted thiosemicarbazone (HL1–4) has been observed in square-planar palladium(ii) complexes.

Funder

University Grants Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

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