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[IPrMe]Br | 1610591-51-9

中文名称
——
中文别名
——
英文名称
[IPrMe]Br
英文别名
[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene(Me)]Br
[IPrMe]Br化学式
CAS
1610591-51-9
化学式
Br*C28H39N2
mdl
——
分子量
483.535
InChiKey
RNNYVZOEUPGGKM-UHFFFAOYSA-M
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):
    4.56
  • 重原子数:
    31.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    8.81
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为产物:
    描述:
    1,3-bis-(2,6-diisopropylphenyl)-imidazol-2-methylidene氢溴酸 作用下, 以 甲苯 为溶剂, 反应 0.01h, 以96%的产率得到[IPrMe]Br
    参考文献:
    名称:
    Synthesis and Luminescent Properties of Lewis Base-Appended Borafluorenes
    摘要:
    A series of Lewis base adducts of 9-bromo-9-borafluorene (BrBFl-LB, LB = IPr, IPrCH2, PPh3, and PCy3), parent borafluorenes (HBFl-IPr and HBFl-IPrCH2), and the bisadduct [(DMAP)(2)BFl]Br were prepared and structurally characterized (IPr = [(HCNDipp)(2)C:], IPrCH2 = [(HCNDipp)(2)C=CH2], Dipp = 2,6-i-Pr2C6H3, and DMAP = N,N-dimethylaminopyridine). The adducts BrBFl-IPr, BrEFl-PPh3, BrBFl-PCy3, [(DMAP)(2)BFI]Br, BrBFl-IPrCH2, and HBFl-IPrCH2 were found to exhibit bright blue luminescence with low to moderately high quantum efficiencies (19 to 63%). Selective irradiation at different excitation wavelengths revealed the presence of two distinct emission processes in the adducts BrBFl-LB, leading to a ligand-independent, presumably borafluorene-based, blue light emission at 435 nm and another less intense emission band in the ultraviolet region (315-324 nm); [(DMAP)(2)BFl]Br exhibits an emission profile that tails into the visible region. Time-dependent density functional theory studies are also included for representative borafluorene adducts. With a judicious choice of functional groups at boron, one can envisage the future generation of a whole library of 4-coordinate borafluorene-based luminogens that complement the efficient light-emitting behavior known for the widely studied boron-dipyrromethene analogues.
    DOI:
    10.1021/ic402408t
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