首页> 外文期刊>Inorganica Chimica Acta >The effects of modifying reaction conditions in green sonochemical synthesis of a copper(II) coordination polymer as well as in achieving to different morphologies of copper(II) oxide micro crystals via solid-state process
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The effects of modifying reaction conditions in green sonochemical synthesis of a copper(II) coordination polymer as well as in achieving to different morphologies of copper(II) oxide micro crystals via solid-state process

机译:通过固态工艺实现改变反应条件在铜(II)配位聚合物的绿色化学合成中的反应条件的影响,以及通过固态工艺实现铜(II)氧化铜微晶的不同形态

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摘要

One copper(II) coordination polymer (CP) [Cu(L)(LSUP//SUP(center dot HINF2/INFO]INFn/INFcenter dot(NOINF3/INF )(2HINF2/INFO) (1) (1D zig-zag chain) (where L stands for CINF6/INFHINF5/INFNOINF2/INF (isonicotinic acid) and LSUP//SUP is CINF12/INFHINF8/INFNINF2/INFcenter dotINF/INFHINF2/INFO (1,10-phenanthroline) has been synthesized following two different experimental approaches, the hydrothermal and sonochemical irradiation methods. Independently of the methodology used, the same crystalline phase is obtained for the complex. Single crystal X-ray analyses on compound 1 illustrated that CuSUP2+/SUP ions are 5-coordinatedshowing the role of sonochemistry to modulate both morphology and dimensions of the resulting crystalline material. In order to study the effects of solvent and time of reaction on the formation of [Cu(L)(LSUP//SUP(center dot HINF2/INFO]INFn/INFcenter dot(NOINF3/INF )(2HINF2/INFO) (1) coordination polymer, 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 microrods. 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 copper(II) oxide micro crystals via solid-state thermal decomposition process. Flower and rod micro crystals of copper(II) oxide could be prepared from 1. These micro crystals were characterized by IR spectroscopy, X-ray powder diffraction (XRD) and Scanning Electron Microscopy (SEM).
机译:一种铜(II)配位聚合物(CP)[铜(L)(L< SUP> /< / SUP>(中心点H< INF→2< / INF> O]< INF将N< / INF>中心点(第3&& / inf&)(2h& inf& 2 o)(1)(1)(1d Zig-Zag链)(其中L代表C& inf& h& inf& 5& / inf& 2& inf&(异种烟酸)和l / st; / st;& / sup& h& inf&gt. n& inf& 2& inf&中心点& inf& h& inf& h& inf& 2& inf& o(1,10-菲咯啉),在两种不同的实验方法,水热和多个化学辐照后已经合成方法。用于所用方法,为复合物获得相同的结晶相。化合物1上的单晶X射线分析说明的化合物1表示Cu& 2 +& / sup&离子是Sonochemisty的作用。调节所得晶体材料的形态和尺寸。为了研究溶剂和反应时间对[Cu(1)(L& / sup& / sup.2& inf& o]& inf& n& / inf& n 3 ;中心点(第3&L; 3& / inf& )(2H& inf& 2& / inf& o)(1)配位聚合物,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微立体的形成。随着更多的反应时间,获得了各种形态,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铜(II)氧化铜微晶的新前体。铜(II)氧化物的花和杆状微晶可由1中制备。通过IR光谱,X射线粉末衍射(XRD)和扫描电子显微镜(SEM)表征这些微晶体。

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