首页> 外文期刊>Synthetic Metals >Synthesis and photophysics of new metallo phthalocyanine complexes with thiazole groups and their fluorescence quenching studies with benzoquinone
【24h】

Synthesis and photophysics of new metallo phthalocyanine complexes with thiazole groups and their fluorescence quenching studies with benzoquinone

机译:新型带噻唑基金属酞菁配合物的合成,光物理性质及对苯醌的荧光猝灭研究

获取原文
获取原文并翻译 | 示例
           

摘要

The synthesis of novel, symmetrical, tetra substituted metallo-phthalocyanines (cobalt, zinc and copper) bearing four 2-(4-methyl-l,3-thiazol-5-yl)ethoxy units was reported. The reaction of 2-(4-methyl-l,3-thiazol-5-yl)ethanol with 4-nitrophthalonitrile in the presence of K2CO3 led to formation of 4-[2-(4-methyl-l,3-thiazol-5-yl)ethoxy]phthalonitrile. Co and Zn phthalocyanines were synthesized using microwave irradiation from the corresponding phthalonitrile compound and metal salts (CoCl_2 and Zn(CH_3COO)_2) in hexanol in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Cu phthalocyanine was obtained by heating the phthalonitrile derivative and copper (II) chloride at 160 C in n-hexanol in the presence of DBU. The resulting products were purified by column chromatography and characterized by several chemical and spectroscopic analysis methods. Photophysical properties with zinc (II) phthalocyanine were found, including electronic absorption and fluorescence quantum yield. The fluorescence of the complexes was investigated in DMF and it was found that benzoquinone (BQ) was an effective quencher.
机译:报道了带有四个2-(4-甲基-1,3-噻唑-5-基)乙氧基单元的新型对称的四取代金属酞菁(钴,锌和铜)的合成。在K2CO3存在下2-(4-甲基-1,3-噻唑-5-基)乙醇与4-硝基苯甲腈的反应导致形成4- [2-(4-甲基-1,3-噻唑- 5-基)乙氧基]邻苯二甲腈。在1,8-二氮杂双环[5.4.0]十一碳-7-烯(DBU)存在下,用相应的邻苯二甲腈化合物和金属盐(CoCl_2和Zn(CH_3COO)_2)在己醇中进行微波辐射合成Co和Zn酞菁。 。在DBU存在下,在正己醇中于160°C加热邻苯二甲腈衍生物和氯化铜(II),即可得到酞菁铜。所得产物通过柱色谱纯化,并通过几种化学和光谱分析方法表征。发现具有锌(II)酞菁的光物理性质,包括电子吸收和荧光量子产率。在DMF中研究了配合物的荧光,发现苯醌(BQ)是有效的淬灭剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号