Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/15523
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Khungar, Bharti | - |
dc.contributor.author | Sakhuja, Rajeev | - |
dc.date.accessioned | 2024-09-11T04:48:15Z | - |
dc.date.available | 2024-09-11T04:48:15Z | - |
dc.date.issued | 2024-12 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0143720824004303 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15523 | - |
dc.description.abstract | A series of organic fluorophores based on novel [1,2,4]triazolo [4′,3':1,2]pyrido [3,4-b]pyrazine architecture were synthesized by a simple two-step protocol. Synthesized organic fluorophores exhibit blue-to-green fluorescence and their UV absorption and fluorescent emission properties were studied. The photophysical properties of synthesized derivatives were tuned by introducing functionalities of varying electronic nature on the core nucleus. The luminescence maxima of the synthesized compounds are found in the range from 427 nm to 503 nm, and the quantum yields ranging from 0.01 to 0.64 were calculated. Among various synthesized molecules, 3-(4-bromophenyl)-8,9-bis(4-methoxyphenyl)-[1,2,4]triazolo [4′,3':1,2]pyrido [3,4-b]pyrazine showed highest quantum yield (ΦF = 0.64), and was further explored for its solvatochromic, acidochromic, aggregation induced fluorescence studies along with theoretical HOMO-LUMO calculations | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pyrido[3,4-b]pyrazine | en_US |
dc.subject | Synthesis | en_US |
dc.subject | UV–Vis | en_US |
dc.subject | Fluorescence | en_US |
dc.subject | Solvatochromism | en_US |
dc.title | Luminescent triazolo-fused pyrido[3,4-b]pyrazines as novel fluorophores | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.