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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 | 2022-03-21T11:30:57Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:30:57Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Sharma, R., Maragani, R., & Misra, R. (2018). C 3-symmetric star shaped donor-acceptor truxenes: Synthesis and photophysical, electrochemical and computational studies. New Journal of Chemistry, 42(2), 882-890. doi:10.1039/c7nj03934d | en_US |
dc.identifier.issn | 1144-0546 | - |
dc.identifier.other | EID(2-s2.0-85040864688) | - |
dc.identifier.uri | https://doi.org/10.1039/c7nj03934d | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9079 | - |
dc.description.abstract | This manuscript reports the design and synthesis of C3-symmetric star shaped donor and acceptor substituted truxenes 6, 7, 10 and 11 using Pd-catalyzed Sonogashira cross-coupling and [2+2] cycloaddition-retroelectrocyclization reactions. Their photophysical, electrochemical and computational studies were explored, which indicate strong donor-acceptor interactions and effective tuning of the HOMO-LUMO gap. The computational studies reveal that the TCNE and TCNQ substituted truxenes 10 and 11 exhibit lower HOMO-LUMO gaps compared to truxenes 6 and 7. The reaction pathway of [2+2] cycloaddition-retroelectrocyclization was studied using computational calculations, which reveal that the donor substituted truxene 7 is favourable for cycloaddition-retroelectrocyclization reactions, whereas acceptor substituted truxene 6 is not favourable. © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.source | New Journal of Chemistry | en_US |
dc.subject | acetic acid | en_US |
dc.subject | dichloromethane | en_US |
dc.subject | hexane | en_US |
dc.subject | hydrochloric acid | en_US |
dc.subject | palladium | en_US |
dc.subject | polycyclic aromatic hydrocarbon | en_US |
dc.subject | tetrabutylammonium | en_US |
dc.subject | tetracyanoethylene | en_US |
dc.subject | truxene | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | alkylation | en_US |
dc.subject | Article | en_US |
dc.subject | carbon nuclear magnetic resonance | en_US |
dc.subject | catalysis | en_US |
dc.subject | chemical phenomena | en_US |
dc.subject | conformation | en_US |
dc.subject | cyclic potentiometry | en_US |
dc.subject | cyclization | en_US |
dc.subject | cycloaddition | en_US |
dc.subject | density | en_US |
dc.subject | donor acceptor system | en_US |
dc.subject | electrochemistry | en_US |
dc.subject | fluorescence | en_US |
dc.subject | mass spectrometry | en_US |
dc.subject | oxidation | en_US |
dc.subject | oxidation reduction potential | en_US |
dc.subject | priority journal | en_US |
dc.subject | proton nuclear magnetic resonance | en_US |
dc.subject | retroelectrocyclization | en_US |
dc.subject | solubility | en_US |
dc.subject | Sonogashira reaction | en_US |
dc.subject | synthesis | en_US |
dc.subject | thermogravimetry | en_US |
dc.subject | thermostability | en_US |
dc.subject | ultraviolet spectrophotometry | en_US |
dc.title | C 3-Symmetric star shaped donor-acceptor truxenes: Synthesis and photophysical, electrochemical and computational studies | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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