A Photoswitchable Chalcone-Carbohydrate Conjugate Obtained by CuAAC Click Reaction

Compounds Pub Date : 2022-03-29 DOI:10.3390/compounds2020008
Micael Paulino, M. M. Pereira, N. Basílio
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引用次数: 2

Abstract

Flavylium/Chalcone-based molecular switches comprise features such as pH-gated photochromism and fluorescence properties that make them attractive for many applications, ranging from stimuli-responsive materials to photopharmacology. However, in contrast to other common photoswitches, the application of flavylium compounds in these areas remains largely unexplored. Among other possible reasons, this may be due to the lack of general strategies to attach these molecules to substrates such as polymers, nanoparticles, biomolecules, or surfaces. In this work, we have shown that a copper (I) catalyzed azide-alkyne cycloaddition (CuAAC) can be employed to obtain a chalcone conjugate. We used an isosorbide carbohydrate to demonstrate this strategy and investigated the photochemical properties of the chalcone-isosorbide conjugate. The obtained results show that the photochemical properties of this new compound are similar to other equivalent flavylium/chalcone photoswitches, confirming the feasibility of the conjugation strategy.
一种可光切换的查尔酮-碳水化合物缀合物
基于黄酮/查尔酮的分子开关包括ph门控光致变色和荧光特性等特征,使其在许多应用中具有吸引力,从刺激响应材料到光药理学。然而,与其他常见的光开关相比,黄酮类化合物在这些领域的应用在很大程度上仍未开发。在其他可能的原因中,这可能是由于缺乏将这些分子附着在聚合物、纳米颗粒、生物分子或表面等底物上的通用策略。在这项工作中,我们已经证明了铜(I)催化叠氮-炔环加成(CuAAC)可以得到查尔酮缀合物。我们用一个异山梨酯碳水化合物来证明这一策略,并研究了查尔酮-异山梨酯缀合物的光化学性质。结果表明,该化合物的光化学性质与其他等效的黄/查尔酮光开关相似,证实了该偶联策略的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.30
自引率
0.00%
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