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Biological evaluation of a novel amino acid‐based macrocyclic Mn(III) and Fe(III) complexes
Author(s) -
Joel C.,
Biju Bennie R.,
Daniel Abraham S.,
Iyyam Pillai S.,
Theodore David S.
Publication year - 2018
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.4516
Subject(s) - chemistry , fluorescence , förster resonance energy transfer , metal , metal ions in aqueous solution , intercalation (chemistry) , quenching (fluorescence) , crystallography , proton nmr , stereochemistry , photochemistry , inorganic chemistry , organic chemistry , physics , quantum mechanics
A new tetradentate ligand 4‐benzylidine‐1,7‐bis(4‐hydroxy‐3‐methoxyphenyl)hepta‐1,6‐diene‐3,5‐bis(2‐imino‐3‐phenylpropanoic acid) of the type N 2 O 2 has been synthesized from curcumin derived non‐enolisable diketone and L‐phenylalanine and complexed with Mn(III) and Fe(III) metal ions. The non‐enolisable curcumin was obtained by Knoevenagel condensation. The synthesized ligand and complexes (MnL & FeL) were characterized by various spectral techniques. Using absorption and emission spectral techniques CT‐DNA and BSA binding studies has been carried out. The absorption and emission spectral tools reveal the intercalative mode of binding between the CT‐DNA and the metal complexes. The fluorescence of BSA was quenched around 340 nm by the metal complexes followed by static quenching mechanism. The emission spectra of BSA were recorded at three different temperatures. The binding sites, mode of binding, binding energy and the donor‐acceptor distance on the basis of Forster's resonance energy transfer (FRET) were calculated. The binding site of the metal complexes with CT‐DNA and BSA has been discussed by molecular docking studies in order to substantiate the experimental results.