首页> 外文期刊>Tetrahedron >Synthesis and intramolecular charge transfer of bipyridinium-crown ether conjugates in response to alkali metal ions
【24h】

Synthesis and intramolecular charge transfer of bipyridinium-crown ether conjugates in response to alkali metal ions

机译:联吡啶鎓-冠醚共轭物的合成和分子内电荷转移对碱金属离子的响应

获取原文
获取原文并翻译 | 示例
           

摘要

Two types of hosts, 1 and 2, in which benzocrown ether units were conjugated to monocationic pyridinium and dicationic bipyridinium units, respectively, have been prepared. 1 and 2 exhibited color-to-colorless changes induced by alkali metal ion, associated with blue shift of their intramolecular charge transfer (ICT) absorptions due to the formation of a 1:1 host-guest inclusion complex. 3 and 4 being the noncrown ether analogues of 1 and 2 also exhibited ICT absorptions, but did not shift upon addition of the guest because of no guest-binding abilities. The monocationic 1 and 3 showed red shift in their ICT bands upon addition of organic acid, such as p-toluenesulfonic acid due to their acceptor character changes by protonation on the terminal pyridine ring. Such guest-induced absorption variations of 1 and 2 were used for alkali metal ion sensing. The sensing abilities are roughly parallel to their binding constants.
机译:制备了两种类型的宿主,分别为1和2,其中苯并冠醚单元分别与单阳离子吡啶鎓和双联吡啶鎓单元共轭。图1和图2显示了由碱金属离子引起的颜色到无色的变化,与它们的分子内电荷转移(ICT)吸收的蓝移有关,这归因于1:1主体-客体包合物的形成。作为1和2的非冠醚类似物的3和4也表现出ICT吸收,但是由于没有客体结合能力而在加入客体时不发生变化。一价阳离子1和3在加入有机酸(例如对甲苯磺酸)后显示出其ICT带中的红移,这是由于它们的受体特性由于末端吡啶环上的质子化而改变。这种由客体引起的1和2的吸收变化用于碱金属离子感测。感测能力与它们的结合常数大致平行。

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