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((bpyz-B(C6F5)3))Pt(4-CF3-Ph)2 | 1444004-59-4

中文名称
——
中文别名
——
英文名称
((bpyz-B(C6F5)3))Pt(4-CF3-Ph)2
英文别名
((2,2'-bipyrazine-B(C6F5)3))Pt(4-CF3-Ph)2
((bpyz-B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>))Pt(4-CF<sub>3</sub>-Ph)<sub>2</sub>化学式
CAS
1444004-59-4
化学式
C40H14BF21N4Pt
mdl
——
分子量
1155.44
InChiKey
BIOUFDLUWAVZRX-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):
    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:
    参考文献:
    名称:
    Postsynthetic Systematic Electronic Tuning of Organoplatinum Photosensitizers via Secondary Coordination Sphere Interactions
    摘要:
    In this work we show that postsynthetic addition of borane Lewis acids to Lewis base decorated organoplatinum photosensitizers induces significant changes in the optical and electrochemical properties. In particular, the charge transfer (CT) energies of these chromophores are significantly modified by these outer-sphere interactions. The direction of the CT shift depends on the site of Lewis acid binding, which occurs either at the diimine ligand in bipyrazine-linked molecules or at an ancillary acetylide ligand in pyridyl-substituted bis(acetylide) molecules. The magnitude of the shift depends on the Lewis acidity of the borane and the number of equivalents added and is comparable to the perturbation brought on by covalent substituent modification of supporting ligands in related complexes. This approach offers a new means of tuning the properties of organometallic phosphors that complements the traditional approach of covalent modification and other postsynthetic modification strategies.
    DOI:
    10.1021/acs.organomet.6b00332
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文献信息

  • A Remote Lewis Acid Trigger Dramatically Accelerates Biaryl Reductive Elimination from a Platinum Complex
    作者:Allegra L. Liberman-Martin、Robert G. Bergman、T. Don Tilley
    DOI:10.1021/ja404339u
    日期:2013.7.3
    A strategy for the control of electron density at a metal center is reported, which uses a remote chemical switch involving second-sphere Lewis acid binding that modulates electron density in the first coordination sphere. Binding of the Lewis acid B(C6F5)(3) at remote nitrogen positions of a bipyrazine-diarylplatinum(II) complex accelerates biaryl reductive elimination by a factor of 64,000.
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