Computational and optoelectronic quantification of semi-conducting, warm ruby red color emanating Eu complexes with hetro-cyclic ligands.

Six Eu complexes were synthesised with β-keto acid as main ligand and secondary ligands through liquid assisted grinding method. These complexes were characterised by various techniques such as spectroscopic technique, XRD, EDAX, SEM analysis, thermal technique, Urbach energy and optical band gap investigation. The luminous photophysical properties were studied by PL spectroscopy in solid as well as solution phase and some theoretical calculation was done to investigate the radiative (A) & non-radiative (A) transition rate, quantum efficiency (ɸ), Judd Ofelt parameters for D → F transitions in both states.

Study of Judd-Ofelt, Urbach energy and photosensitization process in luminescent Sm(III) complexes with heterocyclic ligands.

Six samarium (III) complexes were synthesised by employing the β-ketocarboxylic acid as main ligand and five N-donor systems as ancillary ligands through the environmentally safe liquid-assisted grinding method. Various characterisation techniques were employed to determine the structure of the complexes i.e.

Strategies in synthetic design and structure-activity relationship studies of novel heterocyclic scaffolds as aldose reductase-2 inhibitors.

Heterocyclic scaffolds of natural as well as synthetic origin provide almost all categories of drugs exhibiting a wide range of pharmacological activities, such as antibiotics, antidiabetic and anticancer agents, and so on. Under normal homeostasis, aldose reductase 2 (ALR2) regulates vital metabolic functions; however, in pathological conditions like diabetes, ALR2 is unable to function and leads to secondary diabetic complications. ALR2 inhibitors are a novel target for the treatment of retinopathy (cataract) influenced by diabetes.

Augmentation of photophysical features and Judd-Ofelt analysis of extensively green glowing terbium (III) complexes with nitrogen donor ancillary ligands.

Six green glowing terbium (III) complexes were fabricated via grinding method utilizing a prime organic ligand (L) and nitrogen donor ancillary ligands. Characterization of synthesized complexes was accomplished through various spectroscopic techniques. The significant thermal stability was determined by thermogravimetric analysis while the energy bandgap and Urbach energy were investigated through diffused reflectance spectra of these complexes.

Applicability of Reddish-Orange Light Emitting Samarium (III) Complexes for Biomedical and Multifunctional Optoelectronic Devices.

Six crimson samarium (III) complexes based on β-ketone carboxylic acid and ancillary ligands were synthesized by adopting the grinding technique. All synthesized complexes were investigated via elemental analysis, infrared, UV-Vis, NMR, TG/DTG and photoluminescence studies. Optical properties of these photostimulated samarium (III) complexes exhibit reddish-orange luminescence due to G → H electronic transition at 606 nm of samarium (III) ions.

Designing of emerald terbium (III) ions with β-ketocarboxylic acid and heterocyclic ancillary ligands for biological and optoelectronic applications.

A green and highly efficient grinding method was adopted to synthesize emerald terbium complexes with 1-cyclopropyl-6-fluro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid as the main organic ligand and 2,2'-bipyridyl, 1,10-phenanthroline, neocuproine, 5,6-dimethyl-1,10-phenanthroline and bathophenanthroline as ancillary ligands. Structural analysis of these complexes was executed via elemental, infrared and H-nuclear magnetic resonance analysis, which confirmed that the ligand coordinated to the metal ion through β-ketone and hydroxyl groups of carboxylic acid. Thermal stability of these complexes was investigated by study of thermogravimetric/derivative thermogravimetric analysis.