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BF2dbm(I)OC12H25 | 1220995-74-3

中文名称
——
中文别名
——
英文名称
BF2dbm(I)OC12H25
英文别名
——
BF2dbm(I)OC12H25化学式
CAS
1220995-74-3
化学式
C27H34BF2IO3
mdl
——
分子量
582.277
InChiKey
GYBPIXYWAUPXLF-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

反应信息

  • 作为产物:
    描述:
    三氟化硼乙醚 作用下, 以 二氯甲烷 为溶剂, 反应 6.0h, 以0.424 g的产率得到BF2dbm(I)OC12H25
    参考文献:
    名称:
    Mechanochromic Luminescence Quenching: Force-Enhanced Singlet-to-Triplet Intersystem Crossing for Iodide-Substituted Difluoroboron−Dibenzoylmethane−Dodecane in the Solid State
    摘要:
    A lipid derivative of difluoroboron-iododibenzoylmethane (BF2-dbm(I)OC12H25) was synthesized via Claisen condensation and boronation. Green photoluminescence is observed for the complex in the solid state. Unlike the previously reported difluoroboron-avobenzone (BF(2)AVB) complex, which exhibited significantly red-shifted fluorescence upon mechanical perturbation, the emission of a BF(2)dbm(I)OC12H25 solid film is quenched when the sample is smeared under air but becomes orange under nitrogen. Spectroscopic and lifetime studies suggest that smearing brings the singlet excited state closer to the triplet state, thus increasing the coupling between the two states. As a result, intersystem crossing from the singlet to the triplet excited state is facilitated, and the total luminescence intensity is quenched at room temperature.
    DOI:
    10.1021/ic902591s
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文献信息

  • Mechanochromic luminescence of halide-substituted difluoroboron β-diketonate dyes
    作者:William A. Morris、Tiandong Liu、Cassandra L. Fraser
    DOI:10.1039/c4tc02268h
    日期:——

    Halide-substituted difluoroboron β-diketonates were synthesized and display mechanochromic luminescence and quenching. Material structure is halide dependent and dynamic recovery properties for halide dyes are slower than for the hydrogen counterpart.

    卤代取代的二β-二酮酸盐被合成并显示机械致变发光和猝灭。材料结构取决于卤素,卤素染料的动态恢复性质比氢的对应物慢。
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