Related Experiment Video
Updated: Jan 22, 2026

FM Dye Cycling at the Synapse: Comparing High Potassium Depolarization, Electrical and Channelrhodopsin Stimulation
Published on: May 24, 2018
UV protective heterocyclic disperse azo dyes: Spectral properties, dyeing, potent antibacterial activity on dyed
Virendra R Mishra1, Chaitannya W Ghanavatkar1, Nagaiyan Sekar1
1Department of Dyestuff Technology, Institute of Chemical Technology, Matunga (E), Mumbai 400 019, Maharashtra, India.
Abstract:
Disperse azo dyes are synthesized and characterized by 1H NMR, 13C NMR, LC-MS, Elemental analysis, UV-visible, and fluorescence spectroscopy methods. The azo dyes show absorption maxima in the range of 460-493 nm. Dye with benzothiazole moiety i.e. VM7a and VM8a show a bathochromic shift in absorption maxima of 90 and 26 nm respectively in a polar aprotic solvent (i.e. DMF, DMSO). The dyes show deep red emission in a polar aprotic solvent (i.e. DMF, DMSO) with a Stokes shift of 62 to 180 nm. The dyes are applied on polyester fabric and the dyed fabric exhibit excellent to a good wash and sublimation fastness property. They show a very good UPF rating and almost blocking 95 to 98% of harmful UV radiation. Antibacterial activity of dyed polyester fabric is assessed qualitatively and quantitatively by using AATCC 147 and 100 test method respectively. The dyed fabrics exhibit excellent antibacterial activities against S.aureus (Gram-positive) and K. pneumoniae (Gram-negative). DFT method was used to identify the stable conformer. HOMO-LUMO gap and global reactivity descriptors were calculated using DFT method and correlated with antibacterial activities and light fastness properties respectively.
More Related Videos
12:51A 'Plug and Play' Method to Create Water-dispersible Nanoassemblies Containing an Amphiphilic Polymer, Organic Dyes and Upconverting Nanoparticles
Published on: November 14, 2015
11:19Synthesis of Multi-walled Carbon Nanotubes Modified with Silver Nanoparticles and Evaluation of Their Antibacterial Activities and Cytotoxic Properties
Published on: May 10, 2018
Related Concept Videos
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Properties of Enantiomers and Optical Activity
Basicity of Heterocyclic Aromatic Amines
Imaging Studies III: Computed Tomography
Distribution and Dispersion
Nomenclature of Aryl and Heterocyclic Amines