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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Misra, Rajneesh | en_US |
| dc.date.accessioned | 2022-03-17T01:00:00Z | - |
| dc.date.accessioned | 2022-03-21T11:31:02Z | - |
| dc.date.available | 2022-03-17T01:00:00Z | - |
| dc.date.available | 2022-03-21T11:31:02Z | - |
| dc.date.issued | 2017 | - |
| dc.identifier.citation | Maragani, R., Sharma, R., & Misra, R. (2017). Donor-acceptor triphenylvinyl and tetraphenyl conjugates: Synthesis, aggregation and computational studies. ChemistrySelect, 2(31), 10033-10037. doi:10.1002/slct.201701373 | en_US |
| dc.identifier.issn | 2365-6549 | - |
| dc.identifier.other | EID(2-s2.0-85041951572) | - |
| dc.identifier.uri | https://doi.org/10.1002/slct.201701373 | - |
| dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9095 | - |
| dc.description.abstract | Triphenylvinyl (TPV) substituted bisthiazole 4 and tetraphenylethylene (TPE) substituted triphenylamine functionalized oxazole 5 were designed and synthesized by the Pd-catalyzed Suzuki cross-coupling reaction. The TPV 4 shows Aggregation-induced emission (AIE) behavior and TPE 5 shows aggregation-caused quenching (ACQ) in THF/water mixture due to π-π stacking. The TGA analysis reveals that the TPE 5 show better thermal stability as compared to TPV 4. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley-Blackwell | en_US |
| dc.source | ChemistrySelect | en_US |
| dc.title | Donor-Acceptor Triphenylvinyl and Tetraphenyl Conjugates: Synthesis, Aggregation and Computational Studies | en_US |
| dc.type | Journal Article | en_US |
| Appears in Collections: | Department of Chemistry | |
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