首页> 外文期刊>Journal of Organometallic Chemistry >Solid-state conversion of thallium(I) coordination polymer nanoparticles with cubic cage units to an organometallic silver(I) coordination polymer
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Solid-state conversion of thallium(I) coordination polymer nanoparticles with cubic cage units to an organometallic silver(I) coordination polymer

机译:用立方笼单元与有机金属银(I)配位聚合物的固态转化铊(I)配位聚合物纳米颗粒

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摘要

Solid-state structural transformation of three-dimensional Tl(I) coordination polymer nanoparticles with cubic cage Tl4O4unit, prepared by sonochemical procedure, to three-dimensional organometallic Ag(I) coordination polymer nanostructures has been observed upon mechanochemical reaction of compound [Tl4(μ8-B-4-hps)2]n(1), [H2B-4-hps?=?bis(4-hydroxyphenyl) sulfone] with AgNO3. During this conversion, compound2with higher symmetry in its unit cell is formed. Although B-4-hps2-in both compounds hasμ8coordination modes but these two modes are different from each other. These nanostructures were characterized by Scanning Electron Microscopy (SEM). IR spectroscopy, X-ray powder diffraction (XRD) and thermo gravimetry and differential thermal analyses (TG-DTA), indicated that this conversion is irreversible. The irreversibility of this transformation is due to the formation of stronger Ag-O and Ag-C bonds (in2) in comparison with initial Tl-O bonds in1.
机译:通过多次化学手术制备的三维T1(I)配位聚合物纳米颗粒的固态结构转化,通过多次组织化学方法制备三维有机金属Ag(I)配位聚合物纳米结构[TL4(μ8]的机械化学反应时,已经观察到三维有机金属Ag(I)配位聚合物纳米结构。(μ8 -B-4-HPS)2] N(1),[H2B-4-HPS =α砜]用AgNO3砜]。 在该转化过程中,形成其单位电池中的较高对称性的化合物2。 虽然B-4-HPS2-在两种化合物中有μ6煎作动,但这两种模式彼此不同。 通过扫描电子显微镜(SEM)表征这些纳米结构。 IR光谱,X射线粉末衍射(XRD)和热重量法和差分热分析(TG-DTA),表明该转化是不可逆转的。 与初始TL-O键合相比,该转化的不可逆转性是由于形成更强的Ag-O和Ag-C键(In2)。

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