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Synthesis, crystal structure and properties of a new noncentrosymmetric tetraoxidomolybdate(VI)

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dc.contributor.author Srinivasan, B.R.
dc.contributor.author Morajkar, S.M.
dc.contributor.author Khandolkar, S.S.
dc.contributor.author Gobre, V.V.
dc.contributor.author Apreyan, R.A.
dc.date.accessioned 2019-12-05T04:53:50Z
dc.date.available 2019-12-05T04:53:50Z
dc.date.issued 2019
dc.identifier.citation Journal of Molecular Structure. 1204; 2020; ArticleID_127518. en_US
dc.identifier.uri https://doi.org/10.1016/j.molstruc.2019.127518
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/5905
dc.description.abstract An attempted exchange of ammonium cations in (NH sub(4)) sub(6)[M sub(o7)O sub(24)].6H sub(2)O by reaction with tris(hydroxymethyl)aminomethane (tris) resulted in the serendipitous formation of a mixed cationic tetraoxidomolybdate(VI) viz. (NH sub(4))(trisH)[MoO sub(4)] 1. The spectral and thermal characteristics, solution conductivity study and the single crystal structure of 1 are reported. The presence of the tetrahedral [MoO sub(4)] sup(2-) unit is confirmed by the characteristic Raman spectrum. Compound 1 crystallizes in the noncentrosymmetric trigonal space group P3c1 with both the unique cations and the [MoO sub(4)] sup(2-) dianion located on a three-fold axis. The cations and the anion are interlinked with the aid of O-H...O, N-H...O and C-H...O interactions. The strength and number of O...H contacts affect the Mo-O bond distances. Compound 1 exhibits a piezoelectric effect, which is comparable with that of alpha-quartz. Irradiation of 1 with 1064 nm laser light results in a second harmonic generation (SHG) output which is twice that of potassium dihydrogen phosphate (KDP). Thermal decomposition of 1 results in the formation of orthorhombic alpha-MoO sub(3). en_US
dc.publisher Elsevier en_US
dc.subject Chemistry en_US
dc.title Synthesis, crystal structure and properties of a new noncentrosymmetric tetraoxidomolybdate(VI) en_US
dc.type Journal article en_US
dc.identifier.impf y


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