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[Pt(2,2':6',2''-terpyridine)(CCPh)][SbF6] | 935880-76-5

中文名称
——
中文别名
——
英文名称
[Pt(2,2':6',2''-terpyridine)(CCPh)][SbF6]
英文别名
[Pt(trpy)(CCPh)][SbF6]
[Pt(2,2':6',2''-terpyridine)(CCPh)][SbF6]化学式
CAS
935880-76-5
化学式
C23H16N3Pt*F6Sb
mdl
——
分子量
765.221
InChiKey
JBERWYMBWPMXQI-UHFFFAOYSA-H
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    [Pt(2,2':6',2''-terpyridine)Cl]SbF6苯基乙炔三丁基锡乙腈 为溶剂, 以70%的产率得到[Pt(2,2':6',2''-terpyridine)(CCPh)][SbF6]
    参考文献:
    名称:
    Synthesis, crystal structure and solid state photoluminescence of [Pt(trpy)(CCPh)]SbF6 (trpy=2,2′:6′,2″-terpyridine)
    摘要:
    The synthesis a and characterisation of an orange polymorph of [Pt(trpy)(C CPh)]SbF6 is described where trpy = 2,2':6',2 ''-terpyridine. An X-ray crystal structure determination at 293 K reveals that the cations are planar and stacked head-to-tail with alternating Pt center dot center dot center dot Pt distances of 3.604(l) and 4.412(l) angstrom. The perpendicular distances between successive cation planes are constant along the stack at a value of 3.33 angstrom. Crystal structure determinations at 240 and 200 K show that reducing the temperature to 200 K has no significant effect on the cation arrangement, However, below 200 K there is a phase change that we have not been able to characterise, but which has an effect on the solid state photoluminescence exhibited by [Pt(trpy)(C CPh)]SbF6. Thus, whereas at temperatures of >= 200 K, a broad peak with two components at ca. 566 and 597 nm is observed, below 200 K a longer wavelength peak develops that red-shifts as the temperature is lowered [lambda(em)(max) = 637 nm at 80 K]. We assign the >= 200 K emission as (MLLCT)-M-3 in origin, since the X-ray data show that ligand-ligand (LL) and not metal metal (MM) interactions are important at T >= 200 K. On the other hand, the long wavelength emission observed below 200 K is typical of (MMLCT)-M-3 emission, suggesting that the phase change leads to d(z2) (Pt)-d(z2) (Pt) orbital interactions. Of particular interest is that the cation exhibits (MLCT)-M-3 emission in dichloromethane that maximizes at 619 nm, i.e., the high temperature solid state emission occurs at a shorter wavelength, an unexpected result since intermolecular interactions in the solid usually cause the emission to occur at longer wavelengths. A possible explanation for this unexpected result is given. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2006.08.061
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