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[2,7,12,17-tetrakis(dimethylamino)-3,8,13,18-tetrakis(2,5-dimethyl-1H-pyrrol-1-yl)porphyrazinato]manganese(III) chloride | 1365692-68-7

中文名称
——
中文别名
——
英文名称
[2,7,12,17-tetrakis(dimethylamino)-3,8,13,18-tetrakis(2,5-dimethyl-1H-pyrrol-1-yl)porphyrazinato]manganese(III) chloride
英文别名
——
[2,7,12,17-tetrakis(dimethylamino)-3,8,13,18-tetrakis(2,5-dimethyl-1H-pyrrol-1-yl)porphyrazinato]manganese(III) chloride化学式
CAS
1365692-68-7
化学式
C48H56ClMnN16
mdl
——
分子量
947.471
InChiKey
DFDFSXIDCJQEFQ-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

反应信息

  • 作为产物:
    描述:
    2-dimethylamino-3-(2,5-dimethyl-1H-pyrrol-1-yl)-(2Z)-butene-1,4-dinitrile 在 manganese(II) chloride tetrahydrate 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 戊醇 为溶剂, 反应 24.0h, 以61%的产率得到[2,7,12,17-tetrakis(dimethylamino)-3,8,13,18-tetrakis(2,5-dimethyl-1H-pyrrol-1-yl)porphyrazinato]manganese(III) chloride
    参考文献:
    名称:
    Synthesis, characteristics and photochemical studies of novel porphyrazines possessing peripheral 2,5-dimethylpyrrol-1-yl and dimethylamino groups
    摘要:
    The synthesis and physicochemical properties of novel porphyrazines possessing an alternate system of two peripheral substituents, 2,5-dimethylpyrrol-1-yl and dimethylamino, are presented. All the macrocycles were subjected to HPLC purity studies. Spectroscopic studies of magnesium(II) porphyrazine encompassed steady state absorption, emission measurements, including fluorescence decays, transient absorption spectra, and thermoluminescence. Additionally, magnesium(II) porphyrazine was found to be a moderate photosensitizer with singlet oxygen generation values of 0.12 and 0.14 in DMF and DMSO, respectively. Comparison of the quantum yields of singlet oxygen generation before and after deoxygenation showed that the photodynamic effect of magnesium(II) porphyrazine is governed by the photosensitization mechanism II. Magnesium(II) and manganese(III) porphyrazines were characterized using X-ray crystallography. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.02.010
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