...
首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Effects of proton and metal cations on the fluorescence properties of anthracene bearing macrocyclic polyether and polyamine receptors
【24h】

Effects of proton and metal cations on the fluorescence properties of anthracene bearing macrocyclic polyether and polyamine receptors

机译:质子和金属阳离子对带有大环聚醚和多胺受体的蒽的荧光性质的影响

获取原文
获取原文并翻译 | 示例
           

摘要

An anthracene (AN) derivative bearing azacrown ether (1-aza-18-crown-6) and cyclen (1,4,7,10-tetraazacyclododecane) receptors (L1) has been synthesized. Effects of proton (H+) and metal cations (K+ and Zn2+) on the fluorescence properties of L1 have been studied in water and methanol. In water, H+ addition to L1 leads to a fluorescence intensity (IF) increase. Potentiometrical pH titration reveals that strong IF enhancement of L1 requires monoprotonation of both azacrown and cyclen moieties. Addition of Zn2+ and/or K+ is ineffective for IF enhancement because these cations do not coordinate with the azacrown moiety, leading to an electron transfer (ET) from the azacrown nitrogen to the photoexcited AN moiety. In methanol, the azacrown and cyclen moieties of L1 coordinate with K+ and Zn2+, respectively. Zn2+ or K+ addition to L1 shows very small or moderate IF enhancement because of ET from the uncoordinated azacrown or cyclen nitrogen to the excited AN. Addition of both K+ and Zn2+, however, still shows moderate IF enhancement, although both macrocycles coordinate with the respective metal cations. Ab initio calculation reveals that the azacrown-K+ coordination is weakened by an electrostatic repulsion between K+ and Zn2+ within the complex. This allows ET from the azacrown nitrogen to the excited AN, resulting in an insufficient IF enhancement. (C) 2007 Elsevier B.V. All rights reserved.
机译:合成了带有氮杂冠醚(1-aza-18-crown-6)和cycln(1,4,7,10-四氮杂环十二烷)受体(L1)的蒽(AN)衍生物。在水和甲醇中研究了质子(H +)和金属阳离子(K +和Zn2 +)对L1荧光性质的影响。在水中,向L1中添加H +会导致荧光强度(IF)增加。电位pH滴定表明,L1的强IF增强需要氮杂冠和周期部分的单质子化。 Zn 2+和/或K +的添加对IF的增强无效,因为这些阳离子不与氮杂冠部分配位,导致电子从氮杂冠氮转移到光激发的AN部分。在甲醇中,L1的氮杂冠和环素部分分别与K +和Zn2 +配合。 L1中添加的Zn2 +或K +显示出非常小的或中等的IF增强,这是因为从未配位的氮杂冠或循环氮到激发的AN的ET。然而,尽管两个大环均与各自的金属阳离子配位,但同时添加K +和Zn2 +仍显示出中等的IF增强。从头算计算表明,配合物中K +和Zn2 +之间的静电排斥削弱了氮杂皇冠K +配位。这允许从氮杂冠氮到被激发的AN的ET,导致IF增强不足。 (C)2007 Elsevier B.V.保留所有权利。

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