Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/7818
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dc.contributor.authorSubashinia, A.-
dc.contributor.authorVeeramani, V.-
dc.contributor.authorThamaraiselvi, K.-
dc.contributor.authorCrochet, Aurelien-
dc.contributor.authorRose, Priya-
dc.contributor.authorPhilip, Reji-
dc.contributor.authorRamesh Babu, R.-
dc.contributor.authorK., Ramamurthi-
dc.date.accessioned2021-09-07T08:14:26Z-
dc.date.available2021-09-07T08:14:26Z-
dc.date.issued2021-07-
dc.identifier.citationOptical Materials, 2021, Vol.117, p111081en_US
dc.identifier.issn0925-3467-
dc.identifier.urihttp://hdl.handle.net/2289/7818-
dc.descriptionRestricted Access.en_US
dc.description.abstractBenzylideneaniline compounds of N-(4-bromobenzylidene)-4-fluoroaniline (BBFA) and N-(4-bromobenzylidene)-4-methoxyaniline (BBMOA) have been synthesized by the condensation reaction process, and single crystals of these compounds are grown at room temperature by the slow evaporation solution growth technique. The compounds BBFA and BBMOA crystallize in the orthorhombic crystal system with different space groups. Placement of hydrogen atoms in BBFA and BBMOA compounds is confirmed from 1H NMR spectral studies. Fourier transform infrared and Raman spectral analyses are employed to study the presence of functional groups in the compounds. Single stage weight loss and melting point of these compounds are determined from thermogravimetric and differential thermal analyses respectively. Nonlinear optical properties are measured using powder second harmonic generation study and open aperture Z-scan technique. Biological activities are studied using the minimum inhibitory concentration method.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.urihttps://doi.org/10.1016/j.optmat.2021.111081en_US
dc.rights2021 Elsevier B.V.en_US
dc.subjectX-ray diffractionen_US
dc.subjectBenzylideneanilineen_US
dc.subjectCrystal structureen_US
dc.subjectOrthorhombicen_US
dc.subjectTwo photon absorptionen_US
dc.titleSynthesis, growth and characterization of benzylideneaniline compounds: N-(4-bromobenzylidene)-4-fluoroaniline and N-(4-bromobenzylidene)-4-methoxyanilineen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (LAMP)

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