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2,2,5,5-tetramethyl-3-[3-(4-dimethylaminostyryl)-4,4-difluoro-1,5,7-trimethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacen-8-yl]-2,5-dihydro-1H-pyrrole | 1236042-41-3

中文名称
——
中文别名
——
英文名称
2,2,5,5-tetramethyl-3-[3-(4-dimethylaminostyryl)-4,4-difluoro-1,5,7-trimethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacen-8-yl]-2,5-dihydro-1H-pyrrole
英文别名
——
2,2,5,5-tetramethyl-3-[3-(4-dimethylaminostyryl)-4,4-difluoro-1,5,7-trimethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacen-8-yl]-2,5-dihydro-1H-pyrrole化学式
CAS
1236042-41-3
化学式
C34H45BF2N4
mdl
——
分子量
558.566
InChiKey
QLFNXLVKBYTHQB-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:
    1-oxyl-2,2,5,5-tetramethyl-3-[4,4-difluoro-1,3,5,7-tetramethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacen-8-yl]-2,5-dihydro-1H-pyrrole对二甲氨基苯甲醛哌啶溶剂黄146 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以15%的产率得到2,2,5,5-tetramethyl-3-[3-(4-dimethylaminostyryl)-4,4-difluoro-1,5,7-trimethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacen-8-yl]-2,5-dihydro-1H-pyrrole
    参考文献:
    名称:
    Synthesis of redox sensitive dyes based on a combination of long wavelength emitting fluorophores and nitroxides
    摘要:
    New, nitroxide-fluorophore acceptor-donor compounds were synthesized based on long wavelength (570-790 nm) emitting 9-diethylamino-5H-benzo[a]phenoxazin-5-one, 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene and metal-ligand complex fluorophores. The fluorophores and nitroxides were linked via a robust C=C bond. The steady-state spectral properties of the new donor-acceptor compounds and their diamagnetic (sterically hindered amine) derivatives were studied. Titration of nitroxides with ascorbic acid sodium salt to diamagnetic N-hydroxy compounds resulted in fluorescence enhancement The Ru-complex modified with nitroxide exhibited fluorescence increase and electron paramagnetic resonance band broadening upon B-deoxyribonucleic acid addition providing evidence of binding with B-deoxyribonucleic acid. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.dyepig.2010.03.030
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