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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Syntheses, crystal structures, luminescent and magnetic properties of two molecular solids containing naphthylmethylene triphenylphosphinium cations and tetra(isothiocyanate)cobalt(II) dianion
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Syntheses, crystal structures, luminescent and magnetic properties of two molecular solids containing naphthylmethylene triphenylphosphinium cations and tetra(isothiocyanate)cobalt(II) dianion

机译:含有萘基亚甲基三苯基phosph阳离子和四(异硫氰酸酯)钴(II)二价阴离子的两种分子固体的合成,晶体结构,发光和磁性

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The reaction of CoCl2 with the naphthalene methylated triphenylphosphinium bromide [n-NAPMeTPP]Br (n = 1, 2) and KSCN, in a methanolic medium at ambient temperature, leads to the self-assembly formation of hybrid 2:1 organic-inorganic molecular solids, [1-NAPMeTPP](2)[Co(NCS)(4)](1) and [2-NAPMeTPP](2)[Co(NCS)(4)](2) ([NAPMeTPP](+) = (naphthylmethylene)(triphenyl)phosphinium), which have been characterized by elemental analyses, IR spectroscopy, UV-Vis spectra, ESI-MS, molar conductivity and single-crystal X-ray diffraction structural analyses. Compound 1 crystallizes in the orthorhombic space group Pna2(1), while 2 does in the monoclinic space group C2/c. The cations form a dimer through the weak intermolecular C-H...pi it interactions in 1 and it pi...pi interaction in 2, while the anion and cation are linked by the C-H...S hydrogen bond in 1. Two molecular solids show dual functionalities: (1) the broad fluorescence emission around 400 nm in the solid state at room temperature; (2) the weak antiferromagnetic coupling behavior. (C) 2015 Elsevier B.V. All rights reserved.
机译:CoCl2与萘甲基化三苯基溴化膦[n-NAPMeTPP] Br(n = 1,2)和KSCN在环境温度下的甲醇介质中的反应导致杂化2:1有机-无机分子的自组装形成固体,[1-NAPMeTPP](2)[Co(NCS)(4)](1)和[2-NAPMeTPP](2)[Co(NCS(4)](2)([NAPMeTPP](+) =(萘基亚甲基)(三苯基)phosph),其通过元素分析,IR光谱,UV-Vis光谱,ESI-MS,摩尔电导率和单晶X射线衍射结构分析来表征。化合物1在正交空间群Pna2(1)中结晶,而化合物2在单斜空间群C2 / c中结晶。阳离子通过弱分子间CH ... pi相互作用而形成二聚体,它在1中相互作用,而pi ... pi相互作用在2中,而阴离子和阳离子则通过CH ... S氢键在1中相互作用。两个分子固体具有双重功能:(1)室温下在固态下约400 nm处有宽广的荧光发射; (2)弱的反铁磁耦合行为。 (C)2015 Elsevier B.V.保留所有权利。

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