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Synthesis, structure, and properties of ternary transition metal sulfides, chloridesulfides, and nitrides.

机译:三元过渡金属硫化物,氯化物硫化物和氮化物的合成,结构和性质。

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摘要

Several new compounds have been prepared, each yielding interesting structural aspects that are unique to sulfide literature. The correct compositions and structural characteristics of the rare-earth chromium sulfide and chloridesulfide phases have now been determined. Single-phase La15.9(2)Cr 5.4(2)S32 was synthesized and extensively analyzed, proving to be an excellent model for the determination of the chloride incorporated analogues. By exchanging the rare-earth metal in La15.9(2)Cr 5.4(2)S32 and adding a source of chloride to the reaction mixture, the compounds Ce15.8(2)Cr5.6(2)S32-x Clx, Pr15.8(2)Cr5.6(2)S32-x Clx, and Nd15.8(2)Cr5.6(2)S32-x Clx can be prepared in single-crystal form. An extremely strict and unforgiving synthesis is used to obtain these products as single-phase materials. Upon heating, the metastable chloride incorporated phases reported in the literature. The title phases all contain Cr2S9 12- face-shared bioctahedra that are connected to one another by cubic clusters of rare-earth and transition metal atoms. In La15.9(2) Cr5.4(2)S32, the Cr2S9 12- bioctahedral units are observed to be antiferromagnetically coupled, resulting in an overall spin state of almost zero at low temperatures.;The ternary yttrium chromium sulfide family of compounds was revisited to find new phases existing between known stoichiometric end-member phases. The isolation and analyses of previously reported compounds yielded important crystallographic and magnetic data aiding in such investigations. In the course of study, a new phase having the formula Y6Cr2S 11 was produced. This compound proves to be isostructural with the erbium analogue. It has been previously determined that known compounds in the erbium series are isostructural to the corresponding yttrium analogues.;Anion metathesis reactions involving ZrNCl were performed resulting in the production of two unique compounds, ZrN(CN) and Zr2N2 S. These compounds have been isolated as single-phase material and were characterized by a multitude of different analytical techniques confirming the compositions. Single-crystals were synthetically unobtainable for both compounds; however, significant analyses were performed on the isolated polycrystalline powders revealing structure and composition.
机译:已经制备了几种新的化合物,每种化合物都有有趣的结构方面,这是硫化物文献所独有的。现在已经确定了稀土铬硫化物和氯硫化物相的正确组成和结构特征。合成并广泛分析了单相La15.9(2)Cr 5.4(2)S32,被证明是测定结合了氯化物的类似物的出色模型。通过交换La15.9(2)Cr 5.4(2)S32中的稀土金属并向反应混合物中添加氯化物源,化合物Ce15.8(2)Cr5.6(2)S32-x Clx, Pr15.8(2)Cr5.6(2)S32-x Clx和Nd15.8(2)Cr5.6(2)S32-x Clx可以单晶形式制备。极其严格且无情的合成用于获得单相材料的这些产品。加热后,文献报道了亚稳的氯化物结合相。标题相均包含Cr2S9 12面共享的生物二十面体,它们通过稀土和过渡金属原子的立方簇相互连接。在La15.9(2)Cr5.4(2)S32中,观察到Cr2S9 12-生物八面体单元是反铁磁耦合的,导致低温下的整体自旋状态几乎为零。再次审查发现在已知化学计量末端成员相之间存在的新相。先前报道的化合物的分离和分析产生了重要的晶体学和磁性数据,有助于进行此类研究。在研究过程中,产生了具有式Y6Cr2S 11的新相。该化合物证明与with类似物是同构的。先前已确定that系列中的已知化合物与相应的钇类似物是同构的;进行了涉及ZrNCl的阴离子复分解反应,从而产生了两种独特的化合物ZrN(CN)和Zr2N2 S.作为单相材料,通过多种不同的分析技术对其成分进行了确认。两种化合物合成都无法获得单晶。然而,对分离出的多晶粉末进行了显着分析,揭示了其结构和组成。

著录项

  • 作者

    Sirchio, Scott Andrew.;

  • 作者单位

    University of Maryland, College Park.;

  • 授予单位 University of Maryland, College Park.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 162 p.
  • 总页数 162
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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