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Shivani, , Mishra, Akriti, Kaur, Paramjit, Singh, Kamaljit (2023) Perpetual Extension of Conjugation of Fluorene-Based Donor–Acceptor Dyads Yield Diminished Nonlinear Optical Response. The Journal of Physical Chemistry C, 127 (2) 1260-1272 doi:10.1021/acs.jpcc.2c07825

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Reference TypeJournal (article/letter/editorial)
TitlePerpetual Extension of Conjugation of Fluorene-Based Donor–Acceptor Dyads Yield Diminished Nonlinear Optical Response
JournalThe Journal of Physical Chemistry C
AuthorsShivani, Author
Mishra, AkritiAuthor
Kaur, ParamjitAuthor
Singh, KamaljitAuthor
Year2023 (January 19)Volume127
Issue2
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/acs.jpcc.2c07825Search in ResearchGate
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Mindat Ref. ID15679002Long-form Identifiermindat:1:5:15679002:6
GUID0
Full ReferenceShivani, , Mishra, Akriti, Kaur, Paramjit, Singh, Kamaljit (2023) Perpetual Extension of Conjugation of Fluorene-Based Donor–Acceptor Dyads Yield Diminished Nonlinear Optical Response. The Journal of Physical Chemistry C, 127 (2) 1260-1272 doi:10.1021/acs.jpcc.2c07825
Plain TextShivani, , Mishra, Akriti, Kaur, Paramjit, Singh, Kamaljit (2023) Perpetual Extension of Conjugation of Fluorene-Based Donor–Acceptor Dyads Yield Diminished Nonlinear Optical Response. The Journal of Physical Chemistry C, 127 (2) 1260-1272 doi:10.1021/acs.jpcc.2c07825
In(2023, January) The Journal of Physical Chemistry C Vol. 127 (2) American Chemical Society (ACS)

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Shivani, , Mishra, Akriti, Kaur, Paramjit, Singh, Kamaljit (2023) Correction to “Perpetual Extension of Conjugation of Fluorene-Based Donor–Acceptor Dyads Yield Diminished Nonlinear Optical Response”. The Journal of Physical Chemistry C, 127 (7) 3910-3911 doi:10.1021/acs.jpcc.3c00440
Kaur, Khushdeep, de Coene, Yovan, Clays, Koen, Kaur, Paramjit, Singh, Kamaljit (2024) Nonlinear optical response of 1H-indene-based donor-acceptor chromophores. Influence of the higher-lying states on the first hyperpolarizability. Journal of Molecular Structure, 1310. 138272 doi:10.1016/j.molstruc.2024.138272
Kumar, Pawan, de Coene, Yovan, Clays, Koen, Kaur, Paramjit, Singh, Kamaljit (2023) Size economy and first hyperpolarizability: synthesis and nonlinear optical behavior of ferrocene-based donor–acceptor chromophores lacking π-linkers. Dalton Transactions, 52 (34) 12130-12142 doi:10.1039/d3dt01897k
Kaur, Sarbjeet, Dhoun, Sugandha, Depotter, Griet, Kaur, Paramjit, Clays, Koen, Singh, Kamaljit (2015) Synthesis, linear and nonlinear optical properties of thermally stable ferrocene-diketopyrrolopyrrole dyads. RSC Advances, 5 (103). 84643-84656 doi:10.1039/c5ra17977g
Kaur, Navdeep, Van Steerteghem, Nick, Singla, Priya, Kaur, Paramjit, Clays, Koen, Singh, Kamaljit (2017) Second-order nonlinear polarizability of ferrocene–BODIPY donor–acceptor adducts. Quantifying charge redistribution in the excited state. Dalton Transactions, 46 (4). 1124-1133 doi:10.1039/c6dt04455g
Kumar, Virendra, Sony, Simran, Kaur, Navpreet, Mobin, Shaikh M., Kaur, Paramjit, Singh, Kamaljit (2022) Thiazolothiazole based donor-π-acceptor fluorophore: Protonation/deprotonation triggered molecular switch, sensing and bio-imaging applications. Analytica Chimica Acta, 1206. 339776pp. doi:10.1016/j.aca.2022.339776
Kaur, Paramjit, Kaur, Mandeep, Singh, Kamaljit (2011) Ferrocene based chemosensor for Cu2+—A dual channel signaling system. Talanta, 85 (2). 1050-1055 doi:10.1016/j.talanta.2011.05.026
Kaur, Paramjit, Kaur, Hardeep, Singh, Kamaljit (2013) A ‘turn-off’ emission based chemosensor for HSO4−– formation of a hydrogen-bonded complex. The Analyst, 138 (2). 425-428 doi:10.1039/c2an36100k
Singh, Anuja, Pati, Avik Kumar, Mishra, Ashok Kumar (2019) Photophysical Impact of Diacetylenic Conjugation on Classical Donor–Acceptor Electronic Energy Pair. The Journal of Physical Chemistry A, 123 (2). 443-453 doi:10.1021/acs.jpca.8b09689
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Dhoun, Sugandha, Depotter, Griet, Kaur, Sarbjeet, Kaur, Paramjit, Clays, Koen, Singh, Kamaljit (2016) Thermally stable ferrocene-α-cyanostilbenes as efficient materials for second order nonlinear optical polarizability. RSC Advances, 6 (56). 50688-50696 doi:10.1039/c6ra10084h
 
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