首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Synthesis,Chraracrerization,and Structural and Theoretical Analysis of Gd_4B_3C_4:A Novel Rare Earth metal Borocarbide Containing Two Different Boron-Carbon Arrangements
【24h】

Synthesis,Chraracrerization,and Structural and Theoretical Analysis of Gd_4B_3C_4:A Novel Rare Earth metal Borocarbide Containing Two Different Boron-Carbon Arrangements

机译:Gd_4B_3C_4的合成,表征以及结构和理论分析:一种新型的含有两种不同硼碳排列的稀土金属硼碳化物

获取原文
获取原文并翻译 | 示例
           

摘要

The synthesis by arc-melting techniques, the single-crystal_X-ray structure, and the theoretical analysis of GcLB~C. are reported. It crystallizes in the triclinic space group P1 with a = 3.637(2) A, b = 3.674(2) A, c = 11 .8~ ~, A, a. = 93·34(5)0, ~3 = 96.77(5)0, y = 90.24(5)0, and Z = 1. In this structure, the boron and carbon atoms form two different types of nonmetal arrangements: l-D (BCX.~ branched chains and finite (0-D) linear CBC “moleculaiK’ units. Gd4B3C4 is the first characterized member of the rare earth metal borocarbide series in which both 1 -D and “molecular” 0-D nonmetal atom systems coexist. From the structural and theoretical analysis, the following formal charge distribution can be proposed within the ionic limit: (Gd3~)4(BCj)(BC3)2.e. Tight-binding calculations suggest that the excess electron in the ionic limit is mainly localized on the Gd atoms (at the bottom of the Sd band). while LAPW calculations favor its localization on the (BCX. chain. The bonding within this compound is fully analyzed and compared to other members
机译:电弧熔化法合成,单晶X射线结构和GcLB〜C的理论分析。被报道。它在三边形空间群P1中结晶,其a = 3.637(2)A,b = 3.674(2)A,c = 11 .8〜〜,A,a。 = 93·34(5)0,〜3 = 96.77(5)0,y = 90.24(5)0,Z =1。在这种结构中,硼和碳原子形成两种不同类型的非金属排列:lD( BCX。〜支链和有限(0-D)线性CBC“分子”单元。Gd4B3C4是稀土金属硼碳化物系列的第一个特征成员,其中一维和“分子” 0-D非金属原子系统共存。通过结构和理论分析,可以在离子极限范围内提出以下形式的电荷分布:(Gd3〜)4(BCj)(BC3)2.e。紧密结合计算表明,离子极限范围内的过量电子主要是定位在Gd原子上(在Sd谱带的底部),而LAPW计算则倾向于将其定位在(BCX。)链上。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号