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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 |
Files in This Item:
File | Description | Size | Format | |
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TH_706_Pankaj_Kumar_Gupta_1901131001.pdf | 9.57 MB | Adobe PDF | View/Open |
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