Synthesis, crystal structure and remote allosteric binding properties of cone thiacalix[4]pseudocrown receptors bearing anthraquinone function and different arms. Issue 56 (17th July 2017)

• Record Type: Journal Article
• Authors: Lv, Xue-Xin; Wang, Qian; Zhang, Li-Jing; Liu, Ling-Ling; Zhao, Mei; Guo, Dian-Shun
• Is Part Of: RSC advances. Volume 7:Issue 56(2017)
• Page Start: 35528
• Page End: 35536
• Publication Date: 2017-07-17
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c7ra06083a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Herein, three novel cone thiacalix[4]pseudocrown receptors1–3, bearing anthraquinone and triazole functions as well as different side arms, were successfully synthesized via a double click reaction as the key step. Abstract : Herein, three novel cone thiacalix[4]pseudocrown receptors1–3, bearing anthraquinone and triazole functions as well as different side arms, were successfully synthesized via a double click reaction as the key step. Their recognition properties have been fully evaluated using optical, electrochemical, and theoretical methods. Receptor1 features high selectivity for Pb 2+, whereas receptor2 can optically recognize Zn 2+ in the presence of Cd 2+ . This difference of binding specificity to metal ions may be ascribed to the remote tuning effect from the side arms connected to the lower rim of thiacalix[4]arene that realizes the accommodation of binding specificity. Moreover, the plausible coordination modes have been presented.