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Flavylium 离子与磺化杯[4]芳烃的结合及其在水相生物相关客体光释放中的意义。

Binding of Flavylium Ions to Sulfonatocalix[4]arene and Implication in the Photorelease of Biologically Relevant Guests in Water.

机构信息

CIQSO-Center for Research in Sustainable Chemistry and Department of Chemistry , University of Huelva , Campus de El Carmen s/n , E-21071 Huelva , Spain.

Laboratório Associado para a Química Verde (LAQV), Rede de Química e Tecnologia (REQUIMTE), Departamento de Química, Faculdade de Ciências e Tecnologia , Universidade NOVA de Lisboa , 2829-516 Caparica , Portugal.

出版信息

J Org Chem. 2019 Sep 6;84(17):10852-10859. doi: 10.1021/acs.joc.9b01420. Epub 2019 Aug 14.

Abstract

The formation of host-guest complexes between seven flavylium cations and water-soluble -sulfonatocalix[4]arene (SC4) was investigated by UV/vis absorption, fluorescence, and NMR spectroscopies. The results show the cationic guests form complexes with affinities in the submillimolar range. A representative chalcone/flavylium photoswitch was investigated in more detail regarding its pH- and light-triggered interconversion between the two forms. The dramatic affinity differentiation of the SC4 binding of the two switchable species (40 M for the -chalcone versus 3.5 × 10 M for the flavylium cation) enables the pH-gated photocontrol of the complexation process. These responsive properties were explored to demonstrate the competitive and selective release of biologically relevant guests from their supramolecular complexes with -sulfonatocalix[4]arene (SC4), following the principle of AND logic. The guest release can be reverted by the thermally activated reaction of the flavylium ion back to the -chalcone.

摘要

七种花菁阳离子与水溶性 - 磺化杯[4]芳烃(SC4)之间形成主客体配合物的研究采用紫外/可见吸收光谱、荧光光谱和 NMR 光谱法进行。结果表明,阳离子客体以亚毫摩尔范围的亲和力形成配合物。更详细地研究了一种代表性的查尔酮/花菁光致开关,以研究其在两种形式之间的 pH 和光触发的互变异构。两种可切换物种(- 查尔酮为 40 μM,花菁阳离子为 3.5×10 M)与 SC4 结合的亲和力差异显著,使配合物形成过程的 pH 门控光控成为可能。这些响应特性被探索用于证明生物相关客体从与 - 磺化杯[4]芳烃(SC4)的超分子配合物中进行竞争性和选择性释放,遵循“与”逻辑的原理。客体的释放可以通过花菁离子热激活反应回收到 - 查尔酮来逆转。

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