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Cerium;platinum | 12014-80-1

中文名称
——
中文别名
——
英文名称
Cerium;platinum
英文别名
cerium;platinum
Cerium;platinum化学式
CAS
12014-80-1
化学式
CePt3
mdl
——
分子量
725.36
InChiKey
RGFDERCUHJLGRF-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:
    4
  • 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

  • 作为反应物:
    描述:
    Cerium--palladium (1/3)Cerium;platinum 以 neat (no solvent) 为溶剂, 生成
    参考文献:
    名称:
    Crystal structure and valence state of cerium in CePd3−xPtx alloys
    摘要:
    DOI:
    10.1016/0375-9601(82)90700-9
  • 作为产物:
    描述:
    氢化铈 (CeH3) 以 neat (no solvent) 为溶剂, 生成 Cerium;platinum
    参考文献:
    名称:
    Electronic structure of Ce and its intermetallic compounds
    摘要:
    DOI:
    10.1103/physrevb.27.7330
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文献信息

  • Electronic structure of Ce and its intermetallic compounds
    作者:J. C. Fuggle、F. U. Hillebrecht、Z. Zołnierek、R. Lässer、Ch. Freiburg、O. Gunnarsson、K. Schönhammer
    DOI:10.1103/physrevb.27.7330
    日期:——
  • Transition to nonmagnetic<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline"><mml:mi>f</mml:mi></mml:math>states in Ce intermetallic compounds studied by bremsstrahlung isochromat spectroscopy
    作者:F. U. Hillebrecht、J. C. Fuggle、G. A. Sawatzky、M. Campagna、O. Gunnarsson、K. Schönhammer
    DOI:10.1103/physrevb.30.1777
    日期:——
  • Structure and magnetism in<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline"><mml:mrow><mml:msub><mml:mrow><mml:mi mathvariant="normal">CePt</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn><mml:mo>+</mml:mo><mml:mi>x</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math>
    作者:J. M. Lawrence、Y.-C. Chen、G. H. Kwei、M. F. Hundley、J. D. Thompson
    DOI:10.1103/physrevb.56.5
    日期:——
    Neutron diffraction results for CePt2+x alloys with 0 less than or equal to x less than or equal to 1, combined with low resolution room temperature x-ray diffraction and electron microscopy, confirm that the alloys are single phase. The data dan be fit for all x with nearly equal agreement factors by structural refinements in either the C15 (MgCu2) phase br the C15b (AuBe5) structure. Observation of small peaks in the diffraction pattern for CePt, that are forbidden in C15 suggest that C15b is the correct structure for this composition (and possibly for the other alloy compositions); and application of Hamilton's test indicates that the C15b structure is preferred over the C15 to the 95% confidence level. Magnetic susceptibility and specific heat measurements indicate that the cerium is essentially localized and trivalent for all x. The antiferromagnetism observed for CePt, may be absent in the alloys, which behave as typical nonmagnetic cerium heavy fermion compounds with Kondo temperature T-K approximate to 2 K.
  • Disorder effects on Kondo behavior in CePt2+x
    作者:Y.Y. Chen、P.H. Huang、C.H. Booth、J.M. Lawrence
    DOI:10.1016/j.physb.2006.01.479
    日期:2006.5
    CePt2 is an antiferromagnetic (AF) Kondo-lattice compound with T-N similar to 1.7K and T-K similar to 4.6K. The evolution of AF and Kondo interactions in CePt2+x with x = 0,0.5 and 1 is observed by analysis of the temperature-dependent specific heat. This analysis shows that similar to 56% of the Ce in CePt2 is involved in Kondo interactions, with the rest involved in magnetic correlations. While 100% of the expected entropy (R ln2) is recovered by 15 K in CePt2, only 95% and 93% is recovered for x = 0.5 and 1.0, respectively. Meanwhile a larger Kondo fraction (80-90%) and a smaller AF fraction (15-3%) is observed, while T-K decreases from 4.6 K to 2.8 K as x increases from 0 to 1. This trend in T-K is opposite that expected from the measured lattice contraction. We conjecture that lattice disorder induced by Pt alloying is responsible for these results. (c) 2006 Elsevier B.V.. All rights reserved.
  • Crystal structure and valence state of cerium in CePd3−xPtx alloys
    作者:D. Rambabu、S.K. Dhar、S.K. Malik、R. Vijayaraghavan
    DOI:10.1016/0375-9601(82)90700-9
    日期:1982.1
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