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Eu(thenoyltrifluoroacetone)3(2,4,6-tri(2-pyridyl)-1,3,5-triazine) | 937181-02-7

中文名称
——
中文别名
——
英文名称
Eu(thenoyltrifluoroacetone)3(2,4,6-tri(2-pyridyl)-1,3,5-triazine)
英文别名
Eu(TTA)3TPTZ
Eu(thenoyltrifluoroacetone)3(2,4,6-tri(2-pyridyl)-1,3,5-triazine)化学式
CAS
937181-02-7
化学式
C42H24EuF9N6O6S3
mdl
——
分子量
1127.83
InChiKey
XKXXEFZHFAAXJJ-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:
    描述:
    europium(III) chloride hexahydrate 、 2-噻吩甲酰三氟丙酮2,4,6-三(2-吡啶基)三嗪 在 t-BuOK 作用下, 以 乙醇 为溶剂, 以78%的产率得到Eu(thenoyltrifluoroacetone)3(2,4,6-tri(2-pyridyl)-1,3,5-triazine)
    参考文献:
    名称:
    Adducts of lanthanide β-diketonates with 2,4,6-tri(2-pyridyl)-1,3,5-triazine: Synthesis, structural characterization, and photoluminescence studies
    摘要:
    Adducts of lanthanide beta-diketonates of the general formula LnL(3)(TPTZ) were synthesized and structurally characterized by single crystal X-ray diffraction [Ln = Eu3+, Tb3+, Er3+; L is the conjugate base of dibenzoylmethane (DBM), 1-benzoylacetone (BA), thenoyltrifluoroacetone (TTA), or 4,4,4-trifluoro-1-phenyl-1,3-butanedione (BTFA); TPTZ = 2,4,6-tri(2-pyridyl)-1,3,5-triazine, a rigid Lewis base with a large pi system]. The lanthanide ion in each of these complexes is nonacoordinate with six beta-diketonate oxygen atoms and three TPTZ nitrogen atoms, forming a coordination polyhedron best describable as a monocapped square antiprism. Characteristic red, green, and near infrared luminescence was observed for the Eu3+, Tb3+, and Er3+ complexes, respectively. All complexes showed significantly enhanced luminescence quantum yields when compared with the corresponding aqua analogues, with one of the Eu3+ complexes displaying a quantum yield of 69.7% in chloroform. (C) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2006.10.049
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