...
首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Novel redox receptors for ion-pair and α-amino acid: synthesis and complexation properties of calix[4]arene derivatives bearing large conjugated ferrocene groups
【24h】

Novel redox receptors for ion-pair and α-amino acid: synthesis and complexation properties of calix[4]arene derivatives bearing large conjugated ferrocene groups

机译:用于离子对和α-氨基酸的新型氧化还原受体:带有大共轭二茂铁基团的杯[4]芳烃衍生物的合成和络合特性

获取原文
获取原文并翻译 | 示例

摘要

By reacting calix[4]arene 1,3-bi-hydrazide derivative (2) with formacylferrocene in “1 + 2” condensation mode, novel calix[4]arene derivative bearing two conjugated ferrocene groups (3) was obtained in yield of 88%. By reacting 1,3-bi-substituted [2-(p-formylphenyloxy)ethyloxy]-p-tert-butylcalix[4]arene (5) with 1,1′-diacetylferrocene hydrazone (4) in “1 + 1” condensation mode, novel calix[4]arene derivative with 1,3-substituted large conjugated ferrocene bridge (6) was synthesized in yield of 83%. The structures and conformations of new compounds were confirmed by elemental analyses, IR spectra, ESI-MS, 1H NMR, etc. The electrochemical cyclic voltammetry experiments revealed that compounds 3 and 6 possessed excellent reversible electrochemical properties. The 1H NMR titration study showed that compound 6 possessed excellent complexation abilities for NaH2PO4 and glycine in 1:1 host–guest complex with the association constants of 3,850 and 2,460 M−1, respectively.
机译:将杯[4]芳烃1,3-二酰肼衍生物(2)与甲酰基二茂铁以“ 1 + 2”缩合反应,得到带有两个共轭二茂铁基团(3)的新型杯[4]芳烃衍生物,收率为88。 %。在“ 1 +1”缩合反应中,使1,3-双取代的[2-(对甲酰基苯氧基)乙氧基]-对叔丁基杯[4]芳烃与1,1'-二乙酰基二茂铁(4)反应模式下,合成了具有1,3-取代的大共轭二茂铁桥(6)的杯新杯[4]芳烃衍生物,产率为83%。通过元素分析,红外光谱,ESI-MS, 1 1 H NMR等方法证实了新化合物的结构和构象。电化学循环伏安实验表明,化合物3和6具有优异的可逆电化学性能。 1 H NMR滴定研究表明,化合物6对1:1宿主-客体复合物中的NaH 2 PO 4 和甘氨酸具有出色的络合能力。分别具有3,850和2,460 M -1 的缔合常数。

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