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Tb(cobalt)5 | 12017-69-5

中文名称
——
中文别名
——
英文名称
Tb(cobalt)5
英文别名
Cobalt;terbium;cobalt;terbium
Tb(cobalt)5化学式
CAS
12017-69-5
化学式
Co5Tb
mdl
——
分子量
453.891
InChiKey
QZUXOPCKXSLKFC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.01
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    氢化铽 以 neat (no solvent) 为溶剂, 生成 Tb(cobalt)5
    参考文献:
    名称:
    Rare-earth contributions to the x-ray magnetic circular dichroism at the CoKedge in rare-earth–cobalt compounds investigated by multiple-scattering calculations
    摘要:
    The x-ray magnetic circular dichroism (XMCD) has been measured at the Co K edge in hcp-Co and X-Co compounds (R = La,Tb,Dy). The structure of the experimental XMCD spectra in the near-edge region has been observed to be highly sensitive to the magnetic environment of the absorbing site. Calculations of the XMCD have been carried out at the Co K edge in Co metal, LaCo5, and TbCo5 within the multiple-scattering framework including the spin-orbit coupling. In the three systems, the XMCD spectra in the near-edge region are well reproduced. The possibility to separate the local effects from those due to the neighboring atoms in the XMCD cross section makes possible a more physical understanding of the spectra. The present results emphasize the major role played by the d states of the Tb ions in the XMCD spectrum at the Co K edge in the TbCo5 compound. [S0163-1829(98)04741-9].
    DOI:
    10.1103/physrevb.58.12271
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文献信息

  • Thermal expansion and spontaneous magnetostriction of RCo5 intermetallic compounds
    作者:A.V. Andreev、S.M. Zadvorkin
    DOI:10.1016/0921-4526(91)90011-3
    日期:1991.7
    Thermal expansion of RCo5 compounds (R = Pr, Nd, Sm, Gd, Tb, Dy, Ho) is investigated by X-ray diffractometry on single crystalline samples in the temperature range 5-1300 K. All compounds undergo large spontaneous magnetostrictive deformations, the volume effect reaches 3.2 x 10(-2) at 5 K in HoCo5.5. The contributions to the volume effect from Co-Co and R-Co exchange interactions are determined by comparison with YCo5, Y being the nonmagnetic analogue of R.
  • Exchange interactions and magnetocrystalline anisotcopy of rare-earth—cobalt compounds with CaCu5-type structure
    作者:A. S. Ermolenko
    DOI:10.1002/pssa.2210590144
    日期:1980.5.16
  • Magnetic properties of Tb1−xUxCo5 single crystals
    作者:A.V. Andreev
    DOI:10.1016/0925-8388(95)02155-8
    日期:1996.3
    U forms solid solutions in TbCo5 up to x = 0.6 with contraction of lattice in the basal plane and expansion along the c axis. The Curie temperature and the Co magnetic moment decrease with increasing U content. The interval of spin reorientation shifts to lower temperatures.
  • Rare-earth contributions to the x-ray magnetic circular dichroism at the Co<b><i>K</i></b>edge in rare-earth–cobalt compounds investigated by multiple-scattering calculations
    作者:J. P. Rueff、R. M. Galéra、Ch. Giorgetti、E. Dartyge、Ch. Brouder、M. Alouani
    DOI:10.1103/physrevb.58.12271
    日期:——
    The x-ray magnetic circular dichroism (XMCD) has been measured at the Co K edge in hcp-Co and X-Co compounds (R = La,Tb,Dy). The structure of the experimental XMCD spectra in the near-edge region has been observed to be highly sensitive to the magnetic environment of the absorbing site. Calculations of the XMCD have been carried out at the Co K edge in Co metal, LaCo5, and TbCo5 within the multiple-scattering framework including the spin-orbit coupling. In the three systems, the XMCD spectra in the near-edge region are well reproduced. The possibility to separate the local effects from those due to the neighboring atoms in the XMCD cross section makes possible a more physical understanding of the spectra. The present results emphasize the major role played by the d states of the Tb ions in the XMCD spectrum at the Co K edge in the TbCo5 compound. [S0163-1829(98)04741-9].
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