Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/16438
Title: NIR absorbing TCBD and DCNQ functionalized phenothiazines
Authors: Gupta, Pankaj Kumar
Supervisors: Misra, Rajneesh
Keywords: Chemistry
Issue Date: 31-Jul-2024
Publisher: Department of Chemistry, IIT Indore
Series/Report no.: TH706;
Abstract: The 10H-Phenothiazine has a tricyclic structure consisting of two benzene rings fused to a central thiazine ring. Its chemical structure can be represented in Figure 1. The phenothiazine has a nonplanar shape, good photostability, and thermal stability. The colourless crystalline solid compound 10H-phenothiazine has an absorption maximum in dichloromethane at 316 nm. Phenothiazine can be functionalized by the nucleophilic substitution reaction at the nitrogen (N) position or electrophilic substitution reaction at positions 3 and 7. Phenothiazine derivatives exhibit high electron density and low reversible oxidation potential, making them suitable candidates for use in a variety of applications such as chemical sensors, photovoltaic devices, organic light-emitting diodes (OLEDs) and dye-sensitized solar cells (DSSCs).
URI: https://dspace.iiti.ac.in:8080/jspui/handle/123456789/16438
Type of Material: Thesis_Ph.D
Appears in Collections:Department of Chemistry_ETD

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