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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >The effects of altering reaction conditions in synthesis of a novel lead(II) 2D coordination polymer as well as in achieving the same morphologies of lead(II)oxide micro-nano structures via solid-state process
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The effects of altering reaction conditions in synthesis of a novel lead(II) 2D coordination polymer as well as in achieving the same morphologies of lead(II)oxide micro-nano structures via solid-state process

机译:改变反应条件在新型铅(II)2D配位聚合物的合成中的影响以及通过固态过程实现铅(II)氧化物微纳米结构的相同形态

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摘要

One lead(II) coordination polymer compound (CPC) [Pb(L)(NCS)](n) (1) (2D layer), in which L stands for C5H4NCOO {pyridine-3-carboxylate(-) anion), has been synthesized following two different experimental approaches; branched tube and sonochemical irradiation methods. Independently of the methodology used, the same crystalline phase is obtained for complex. Single crystal X-ray analyses of compound 1 showed that Pb2+ ions are 5-coordinated, and Hirschfeld surface analyses were studied for 1, showing the role of sonochemistry to modulate both morphology and dimensions of the resulting crystalline material. In order to study the effects of the solvent and time of reaction on the formation of [Pb(L)(NCS)](n) (1) CPC, some experiments were designed, and four samples of 1 were synthesized by sonochemical process. Less time of reaction resulted in the formation of compound 1 mainly like micro-nano rods. With more time of reaction, various morphologies, mainly microhexagonal of 1, were obtained. These four samples have been used as new precursors for the preparation of lead(II)oxide micro-nano structures via solid-state thermal decomposition process. Mix morphology, mainly like sphere micro-nano structures of lead(II)oxide could be prepared from 1. These micro-nano structures were characterized by IR spectroscopy, X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). (C) 2018 Published by Elsevier Ltd.
机译:一种引线(II)配位聚合物化合物(CPC)[PB(1)(NCS)](N)(N)(1)(2D层),其中L代表C5H4NCOO(吡啶-3-羧酸盐( - )阴离子),具有在两种不同的实验方法后被合成;分枝管和儿子化学辐照方法。独立于所用方法,得到相同的结晶相对于复合物。化合物1的单晶X射线分析表明,PB2 +离子是5-协调的,并且研​​究了Hirschfeld表面分析1,显示了Sonochemisty调节所得晶体材料的形态和尺寸的作用。为了研究溶剂和反应时间对[Pb(1)(NCS)](n)(n)(n)(1)的CPC的影响,设计了一些实验,并通过多言化方法合成了四个1样品。反应时间越少导致化合物1的形成主要像微纳米棒一样。通过更多的反应时间,获得各种形态,主要是1的微曲面。这四个样品已被用作通过固态热分解过程制备铅(II)氧化物微纳米结构的新前体。混合形态,主要类似于球形微纳米结构的铅(II)氧化物可以由1.通过IR光谱,X射线粉末衍射(XRD)和扫描电子显微镜(SEM)表征这些微纳米结构。 (c)2018年由elestvier有限公司发布

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