Please use this identifier to cite or link to this item: https://gnanaganga.inflibnet.ac.in:8443/jspui/handle/123456789/2215
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dc.contributor.authorRamanand, Vinutha Pudiyaneravana-
dc.contributor.authorArasalike, Jayarama-
dc.contributor.authorC S, Kaliprasad-
dc.contributor.authorYerol, Narayana-
dc.contributor.authorKullaiah, Byrappa-
dc.contributor.authorKumar, Madan S-
dc.contributor.authorM R, Suresh Kumar-
dc.date.accessioned2023-12-08T10:20:20Z-
dc.date.available2023-12-08T10:20:20Z-
dc.date.issued2017-08-
dc.identifier.citationVol. 9-10; pp. 208-219en_US
dc.identifier.issn2405-8300-
dc.identifier.urihttps://doi.org/10.1016/j.cdc.2017.06.007-
dc.identifier.urihttp://gnanaganga.inflibnet.ac.in:8080/jspui/handle/123456789/2215-
dc.description.abstractThe title compound, (2E)-1-(4′-bromobiphenyl-4-yl)-3-(3,4-dichlorophenyl)-3-hydroxypropan-1-one (BDCP) was synthesized, spectrally characterized (IR, UV, FT-IR, 1H NMR, and FT-Raman), and its three- dimensional structure was confirmed by single crystal diffraction studies. In addition, Second Harmonic Generation (SHG) efficiency of the crystal, thermogravimetric analysis (TGA), and powder XRD were performed. The bromo phenyl ring makes a dihedral angle of 50.8 (2)0 and 34.5 (2)° with the methoxy phenyl ring and central phenyl moiety. The dihedral angle between the methoxy phenyl ring and the central phenyl moiety is 17.1(2)0. The short contacts C9—O1…Cg1 and C3—H3…Cg3 are involved in crystal structure stabilization. The SHG conversion of the BDCP is found to be 1.33 times that of Urea. Grapen_US
dc.language.isoenen_US
dc.publisherChemical Data Collectionsen_US
dc.subjectSingle crystal structureen_US
dc.subjectSpectroscopicen_US
dc.subjectThermogravimetric analysis (TGA)en_US
dc.subjectSecond Harmonic Generation (SHG)en_US
dc.titleSynthesis, Single Crystal Structure and Spectroscopic Aspects of Chalcone 2(2E)-1-(4′-Bromobiphenyl-4-Yl)-3-(2, 3-Dimethoxybenzaldhyde) Prop-2-Ene-1-Oneen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles

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