Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues

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Standard

Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues. / Faisal, Ayman G.; Hassan, Qusay M. A.; Alsalim, Tahseen A.; Sultan, H. A.; Kamounah, Fadhil S.; Emshary, C. A.

I: Journal of Physical Organic Chemistry, Bind 35, Nr. 10, 4401, 2022.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Faisal, AG, Hassan, QMA, Alsalim, TA, Sultan, HA, Kamounah, FS & Emshary, CA 2022, 'Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues', Journal of Physical Organic Chemistry, bind 35, nr. 10, 4401. https://doi.org/10.1002/poc.4401

APA

Faisal, A. G., Hassan, Q. M. A., Alsalim, T. A., Sultan, H. A., Kamounah, F. S., & Emshary, C. A. (2022). Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues. Journal of Physical Organic Chemistry, 35(10), [4401]. https://doi.org/10.1002/poc.4401

Vancouver

Faisal AG, Hassan QMA, Alsalim TA, Sultan HA, Kamounah FS, Emshary CA. Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues. Journal of Physical Organic Chemistry. 2022;35(10). 4401. https://doi.org/10.1002/poc.4401

Author

Faisal, Ayman G. ; Hassan, Qusay M. A. ; Alsalim, Tahseen A. ; Sultan, H. A. ; Kamounah, Fadhil S. ; Emshary, C. A. / Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues. I: Journal of Physical Organic Chemistry. 2022 ; Bind 35, Nr. 10.

Bibtex

@article{ac35cc29508747fb9be5338c7e57212a,
title = "Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues",
abstract = "The curcumin analogues (Cur-MeS and Cur-MeO) are synthesized using the 3-chloroacetyl acetone and aromatic aldehydes reaction. Both compounds are characterized using FTIR, LC-MS, H-1 NMR, and C-13 NMR spectroscopies. The geometric optimization and thermodynamic properties of the two compounds are carried out theoretically using DFT. The highest HOMO, lowest LUMO, and Mullikan atom charges of the two compounds are calculated using the B3LYP and CAM-B3LYP methods which are hybrid functionals with a 6-311+G(2d,p) as the basis set. The nonlinear optical (NLO) properties of both compounds are studied using the spatial self-phase modulation (SSPM) through the diffraction ring patterns (DRPs) and the Z-scan techniques, using a continuous wave (cw) low power 473 nm laser beam. The index of nonlinear refraction (INR) of both compounds is calculated by the two techniques. The all-optical switching property of both samples is tested using two visible cw laser beams.",
keywords = "all-optical switching, curcumin analogues, DFT, Z-scan, LIMITING PROPERTIES, CRYSTAL-STRUCTURE, MOLECULAR-STRUCTURE, DERIVATIVES, ANTIOXIDANT, MODULATION, COMPLEXES, MECHANISM, PATTERNS",
author = "Faisal, {Ayman G.} and Hassan, {Qusay M. A.} and Alsalim, {Tahseen A.} and Sultan, {H. A.} and Kamounah, {Fadhil S.} and Emshary, {C. A.}",
year = "2022",
doi = "10.1002/poc.4401",
language = "English",
volume = "35",
journal = "Journal of Physical Organic Chemistry",
issn = "0894-3230",
publisher = "JohnWiley & Sons Ltd",
number = "10",

}

RIS

TY - JOUR

T1 - Synthesis, optical nonlinear properties, and all-optical switching of curcumin analogues

AU - Faisal, Ayman G.

AU - Hassan, Qusay M. A.

AU - Alsalim, Tahseen A.

AU - Sultan, H. A.

AU - Kamounah, Fadhil S.

AU - Emshary, C. A.

PY - 2022

Y1 - 2022

N2 - The curcumin analogues (Cur-MeS and Cur-MeO) are synthesized using the 3-chloroacetyl acetone and aromatic aldehydes reaction. Both compounds are characterized using FTIR, LC-MS, H-1 NMR, and C-13 NMR spectroscopies. The geometric optimization and thermodynamic properties of the two compounds are carried out theoretically using DFT. The highest HOMO, lowest LUMO, and Mullikan atom charges of the two compounds are calculated using the B3LYP and CAM-B3LYP methods which are hybrid functionals with a 6-311+G(2d,p) as the basis set. The nonlinear optical (NLO) properties of both compounds are studied using the spatial self-phase modulation (SSPM) through the diffraction ring patterns (DRPs) and the Z-scan techniques, using a continuous wave (cw) low power 473 nm laser beam. The index of nonlinear refraction (INR) of both compounds is calculated by the two techniques. The all-optical switching property of both samples is tested using two visible cw laser beams.

AB - The curcumin analogues (Cur-MeS and Cur-MeO) are synthesized using the 3-chloroacetyl acetone and aromatic aldehydes reaction. Both compounds are characterized using FTIR, LC-MS, H-1 NMR, and C-13 NMR spectroscopies. The geometric optimization and thermodynamic properties of the two compounds are carried out theoretically using DFT. The highest HOMO, lowest LUMO, and Mullikan atom charges of the two compounds are calculated using the B3LYP and CAM-B3LYP methods which are hybrid functionals with a 6-311+G(2d,p) as the basis set. The nonlinear optical (NLO) properties of both compounds are studied using the spatial self-phase modulation (SSPM) through the diffraction ring patterns (DRPs) and the Z-scan techniques, using a continuous wave (cw) low power 473 nm laser beam. The index of nonlinear refraction (INR) of both compounds is calculated by the two techniques. The all-optical switching property of both samples is tested using two visible cw laser beams.

KW - all-optical switching

KW - curcumin analogues

KW - DFT

KW - Z-scan

KW - LIMITING PROPERTIES

KW - CRYSTAL-STRUCTURE

KW - MOLECULAR-STRUCTURE

KW - DERIVATIVES

KW - ANTIOXIDANT

KW - MODULATION

KW - COMPLEXES

KW - MECHANISM

KW - PATTERNS

U2 - 10.1002/poc.4401

DO - 10.1002/poc.4401

M3 - Journal article

VL - 35

JO - Journal of Physical Organic Chemistry

JF - Journal of Physical Organic Chemistry

SN - 0894-3230

IS - 10

M1 - 4401

ER -

ID: 317720865