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(2-(2,5-di-tert-butylphenyl)-1,3-dioxo-2,3-dihydro-1H-benzo[10,5]anthra[2,1,9-def]isoquinolin-8-yl)(nitrooxy)bis(triethyl-l5-phosphaneyl)platinum | 1250889-96-3

中文名称
——
中文别名
——
英文名称
(2-(2,5-di-tert-butylphenyl)-1,3-dioxo-2,3-dihydro-1H-benzo[10,5]anthra[2,1,9-def]isoquinolin-8-yl)(nitrooxy)bis(triethyl-l5-phosphaneyl)platinum
英文别名
——
(2-(2,5-di-tert-butylphenyl)-1,3-dioxo-2,3-dihydro-1H-benzo[10,5]anthra[2,1,9-def]isoquinolin-8-yl)(nitrooxy)bis(triethyl-l5-phosphaneyl)platinum化学式
CAS
1250889-96-3
化学式
C48H60N2O5P2Pt
mdl
——
分子量
1002.04
InChiKey
FYKUXHGESMJZIQ-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

  • 作为反应物:
    参考文献:
    名称:
    Highly Fluorescent Platinum(II) Organometallic Complexes of Perylene and Perylene Monoimide, with Pt σ-Bonded Directly to the Perylene Core
    摘要:
    3-Bromoperylene (BrPer) or N-(2,5-di-tert-butylphenyl)-9-bromo-perylene-3,4-dicarboximide (BrPMI) react with [Pt(PEt3)(4)] to yield trans-[PtR(PEt3)(2)Br] (R = Per, la; R = PMI, lb). Neutral and cationic perylenyl complexes containing a Pt(PEt3)X group have been prepared from la,b by substitution of the Br ligand by a variety of other ligands (NCS, ON, NO3, (CNBu)-Bu-t, PyMe). The X-ray structures of trans-[PtR(PEt3)(2)X] (R = Per, X = NCS (2a); R = PMI, X = NO3 (4b); R = Per, X = (CNBu)-Bu-t (5a)) show that the perylenyl fragment remains nearly planar and is arranged almost orthogonal to the coordination plane: The three molecules appear as individual entities in the solid state, with no pi-pi stacking of perylenyl rings. Each platinum complex exhibits fluorescence associated to the perylene or PMI fragments with emission quantum yields, in solution at room temperature, in the range 0.30-0.80 and emission lifetimes similar to 4 ns, but with significantly different emission maxima, by influence of the X ligands on Pt. The similarity of the overall luminescence spectra of these metalated complexes with the perylene or PMI strongly suggests a perylene-dominated intraligand pi-pi(star) emissive state, metal-perturbed by interaction of the platinum fragment mostly via polarization of the Ar-Pt bond.
    DOI:
    10.1021/ic1003319
  • 作为产物:
    描述:
    silver nitrate丙酮 为溶剂, 以86%的产率得到(2-(2,5-di-tert-butylphenyl)-1,3-dioxo-2,3-dihydro-1H-benzo[10,5]anthra[2,1,9-def]isoquinolin-8-yl)(nitrooxy)bis(triethyl-l5-phosphaneyl)platinum
    参考文献:
    名称:
    Highly Fluorescent Platinum(II) Organometallic Complexes of Perylene and Perylene Monoimide, with Pt σ-Bonded Directly to the Perylene Core
    摘要:
    3-Bromoperylene (BrPer) or N-(2,5-di-tert-butylphenyl)-9-bromo-perylene-3,4-dicarboximide (BrPMI) react with [Pt(PEt3)(4)] to yield trans-[PtR(PEt3)(2)Br] (R = Per, la; R = PMI, lb). Neutral and cationic perylenyl complexes containing a Pt(PEt3)X group have been prepared from la,b by substitution of the Br ligand by a variety of other ligands (NCS, ON, NO3, (CNBu)-Bu-t, PyMe). The X-ray structures of trans-[PtR(PEt3)(2)X] (R = Per, X = NCS (2a); R = PMI, X = NO3 (4b); R = Per, X = (CNBu)-Bu-t (5a)) show that the perylenyl fragment remains nearly planar and is arranged almost orthogonal to the coordination plane: The three molecules appear as individual entities in the solid state, with no pi-pi stacking of perylenyl rings. Each platinum complex exhibits fluorescence associated to the perylene or PMI fragments with emission quantum yields, in solution at room temperature, in the range 0.30-0.80 and emission lifetimes similar to 4 ns, but with significantly different emission maxima, by influence of the X ligands on Pt. The similarity of the overall luminescence spectra of these metalated complexes with the perylene or PMI strongly suggests a perylene-dominated intraligand pi-pi(star) emissive state, metal-perturbed by interaction of the platinum fragment mostly via polarization of the Ar-Pt bond.
    DOI:
    10.1021/ic1003319
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