Synthesis, characterisation, optical and nonlinear optical properties of thiazole and benzothiazole derivatives: a dual approach

References

• Papadopoulos MG , Sadlej AJ , Leszczynski J . Non-linear optical properties of matter. Berlin: Springer; 2006.10.1007/1-4020-4850-5
   Google Scholar
• Muhammad S , Nakano M . Computational strategies for nonlinear optical properties of carbon nano-systems. Nanosci Comput Chem Res Prog. 2013;309.
   Google Scholar
• Muhammad S , Xu H-L , Zhong R-L , et al. Quantum chemical design of nonlinear optical materials by sp 2-hybridized carbon nanomaterials: issues and opportunities. J Mater Chem. 2013;1:5439–5449.
   Web of Science ®Google Scholar
• Bosshard C , Hulliger J , Florsheimer M , et al . Organic nonlinear optical materials. Boca Raton (FL): CRC Press; 2001.
   Google Scholar
• Muhammad S , Janjua MRSA , Su Z . investigation of dibenzoboroles having π-electrons: toward a new type of two-dimensional NLO molecular switch? J Phys Chem C. 2009;113:12551–12557.10.1021/jp903075s
   Web of Science ®Google Scholar
• Muhammad S , Xu H , Janjua MRSA , et al . Quantum chemical study of benzimidazole derivatives to tune the second-order nonlinear optical molecular switching by proton abstraction. Phys Chem Chem Phys. 2010;12:4791–4799.10.1039/b924241d
   PubMed Web of Science ®Google Scholar
• Muhammad S , Al-Sehemi AG , Irfan A , et al . Tuning the push–pull configuration for efficient second-order nonlinear optical properties in some chalcone derivatives. J Mol Graph Model. 2016;68:95–105.10.1016/j.jmgm.2016.06.012
   PubMed Web of Science ®Google Scholar
• Muhammad S , Al-Sehemi AG , Irfan A , et al . The impact of position and number of methoxy group (s) to tune the nonlinear optical properties of chalcone derivatives: a dual substitution strategy. J Mol Model. 2016;22:1–9.
   PubMed Web of Science ®Google Scholar
• Muhammad S , Irfan A , Shkir M , et al . How does hybrid bridging core modification enhance the nonlinear optical properties in donor-π-acceptor configuration? A case study of dinitrophenol derivatives. J Comput Chem. 2015;36:118–128.10.1002/jcc.23777
   PubMed Web of Science ®Google Scholar
• Muhammad S , Nakano M , Al-Sehemi AG , et al . Role of a singlet diradical character in carbon nanomaterials: a novel hot spot for efficient nonlinear optical materials. Nanoscale. 2016;8:17998–18020.10.1039/C6NR06097H
   PubMed Web of Science ®Google Scholar
• Muhammad S . Second-order nonlinear optical properties of dithienophenazine and TTF derivatives: a butterfly effect of dimalononitrile substitutions. J Mol Graph Model. 2015;59:14–20.10.1016/j.jmgm.2015.03.003
   PubMed Web of Science ®Google Scholar
• Muhammad S , Fukuda K , Minami T , et al . Interplay between the diradical character and third-order nonlinear optical properties in fullerene systems. Chem Eur J. 2013;19:1677–1685.10.1002/chem.201203463
   PubMed Web of Science ®Google Scholar
• Hameed A , al-Rashida M , Uroos M , et al . Schiff bases in medicinal chemistry: a patent review (2010-2015). Expert Opin Ther Pat. 2017;27:63–79.10.1080/13543776.2017.1252752
   PubMed Web of Science ®Google Scholar
• Leela S , Deepa Rani TD , Subashini A , et al . Studies on growth and characterization of nonlinear optical material 4-chloro-4′ methoxy benzylideneaniline: a Schiff base organic material. Arabian J Chem. 2017;10:S3974–S3981.10.1016/j.arabjc.2014.06.008
   Web of Science ®Google Scholar
• Manjunatha K , Rajarao R , Umesh G , et al . All-optical switching and limiting properties of a Ru (II) Schiff-base complex for nonlinear optical applications. Laser Phys. 2017;27:085401.10.1088/1555-6611/aa7370
   Web of Science ®Google Scholar
• Oliveri IP , Di Bella S . Lewis basicity of relevant monoanions in a non-protogenic organic solvent using a zinc (ii) Schiff-base complex as a reference Lewis acid. Dalton Trans. 2017;46:11608–11614.10.1039/C7DT02821K
   PubMed Web of Science ®Google Scholar
• Gökce H , Öztürk N , Kazıcı M , et al. Structural, spectroscopic, electronic, nonlinear optical and thermodynamic properties of a synthesized Schiff base compound: a combined experimental and theoretical approach. J Mol Struct. 2017;1136:288–302.10.1016/j.molstruc.2017.01.089
   Web of Science ®Google Scholar
• Ozdemir M , Sonmez M , Sen F , et al . Synthesis of a new heterocyclic Schiff base ligand ‘(E)-5-benzoyl-4-phenyl-1-((pyridin-2-ylmethylene) amino) pyrimidin-2(1H)-one’: an experimental and computational modeling study. J Mol Struct. 2017;1127:626–635.10.1016/j.molstruc.2016.08.031
   Web of Science ®Google Scholar
• George M , John NL , Saravana Kumar M , et al . Physico-chemical studies of the experimental and theoretical properties of organic nonlinear optical material 4-chloro-4′methoxy benzylideneaniline. J Mol Struct. 2017;1128:754–768.10.1016/j.molstruc.2016.09.034
   Web of Science ®Google Scholar
• Kumar S , Kumari M , Dutta P , et al . Chitosan biopolymer Schiff base: preparation, characterization, optical, and antibacterial activity. Int J Polym Mater Polym Biomate. 2014;63:173–177.10.1080/00914037.2013.812088
   Web of Science ®Google Scholar
• Kumar S , Dutta J , Dutta P . Preparation and characterization of N-heterocyclic chitosan derivative based gels for biomedical applications. Int J Biol Macromol. 2009;45:330–337.10.1016/j.ijbiomac.2009.08.002
   PubMed Web of Science ®Google Scholar
• Kumar S , Koh J . Physiochemical and optical study of chitosan–terephthaldehyde derivative for biomedical applications. Int J Biol Macromol. 2012;51:1167–1172.10.1016/j.ijbiomac.2012.09.001
   PubMed Web of Science ®Google Scholar
• Kumar S , Dutta PK , Koh J . A physico-chemical and biological study of novel chitosan–chloroquinoline derivative for biomedical applications. Int J Biol Macromol. 2011;49:356–361.10.1016/j.ijbiomac.2011.05.017
   PubMed Web of Science ®Google Scholar
• Zhang Y , Zhu W , Wang W , et al . Synthesis and nonlinear optical properties of rod-like luminescent materials containing Schiff-base and naphthalimide units. J Mater Chem. 2002;12:1294–1300.10.1039/b109384n
   Web of Science ®Google Scholar
• Wang H-Q , Wang L , Xia Y-Y , et al . Multinuclear ‘staircase’ oligomers based on the (Et2C2B4H4) Fe (η6-C6H6) sandwich unit: quantitative tailorable and redox switchable nonlinear optics. J Phys Chem C. 2017;121:16470–16480.10.1021/acs.jpcc.7b03834
   Web of Science ®Google Scholar
• Wang H-Q , Wang L , Ye J-T , et al . Planar octagonal tetranuclear cobaltacarborane macrocycle [(η5-C5Me5) Co (2,3-Et2C2B4H3-5-C≡C-7-C≡C)]4 for 2D nonlinear optics: ultra-high-response and multistate controlled cubic NLO switch. J Phys Chem C. 2017;121:28462–28474.10.1021/acs.jpcc.7b10144
   Web of Science ®Google Scholar
• Suponitsky KY , Liao Y , Masunov AE . Electronic hyperpolarizabilities for donor–acceptor molecules with long conjugated bridges: calculations versus experiment. J Phys Chem A. 2009;113:10994–11001.10.1021/jp902293q
   PubMed Web of Science ®Google Scholar
• Frisch MJ , Trucks GW , Schlegel HB , et al . Gaussian 09. Wallingford (CT): Gaussian, Inc.; 2009. There is no corresponding record for this reference.
   Google Scholar
• Boyle A . Tenderholt and KM Langner. J Comput Chem. 2008;29:839.10.1002/(ISSN)1096-987X
   PubMed Web of Science ®Google Scholar
• Castro AN , Almeida LR , Anjos MM , et al . Theoretical study on the third-order nonlinear optical properties and structural characterization of 3-acetyl-6-bromocoumarin. Chem Phys Lett. 2016;653:122–130.10.1016/j.cplett.2016.04.070
   Web of Science ®Google Scholar
• Silva PSP , El Ouazzani H , Pranaitis M , et al . Experimental and theoretical studies of the second-and third-order NLO properties of a semi-organic compound: 6-aminoquinolinium iodide monohydrate. Chem Phys. 2014;428:67–74.10.1016/j.chemphys.2013.11.001
   Web of Science ®Google Scholar
• Hatua K , Nandi PK . Theoretical study of electronic structure and third-order optical properties of beryllium–hydrocarbon complexes. Comput Theor Chem. 2012;996:82–90.10.1016/j.comptc.2012.07.018
   Web of Science ®Google Scholar
• Karakas A , Migalska-Zalas A , El Kouari Y , et al . Quantum chemical calculations and experimental studies of third-order nonlinear optical properties of conjugated TTF–quinones. Opt Mater. 2013;36:22–26.10.1016/j.optmat.2013.07.005
   Web of Science ®Google Scholar
• Nakano M , Okumura M , Yamaguchi K , et al . CNDO/S‒CI calculations of hyperpolarizabilities. III. regular polyenes, charged polyenes, di-substituted polyenes, polydiacetylene and related species. Mol Cryst Liq Cryst. 1990;182:1–15.
   Web of Science ®Google Scholar
• Li Z-J , Wang F-F , Li Z-R , et al . Large static first and second hyperpolarizabilities dominated by excess electron transition for radical ion pair salts M2 +TCNQ− (M = Li, Na, K). Phys Chem Chem Phys. 2009;11:402–408.10.1039/B809161G
   PubMed Web of Science ®Google Scholar
• Muhammad S , Al-Sehemi AG , Su Z , et al . First principles study for the key electronic, optical and nonlinear optical properties of novel donor-acceptor chalcones. J Mol Graph Model. 2017;72:58–69.10.1016/j.jmgm.2016.12.009
   PubMed Web of Science ®Google Scholar