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Topologically Controlled Synthesis of Reversible Macrocyclic Compounds in Microemulsions

机译:微型乳液中拓扑控制合成可逆式大环化合物

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摘要

A novel and simple approach was used to synthesize a reversible macrocyclic compound. This approach is based on capturing molecules with a photodynamic covalent bond inside microemulsions as nanoreactors and exposing them to UV radiation to facilitate a stereoselective reaction to form cyclic compounds quantitatively and selectively. The size of the microemulsion droplets used played a crucial role in synthesizing the reversible macrocyclic compounds. The formed macrocyclic compound was able to revert to monomers under UV irradiation of a shorter wavelength.
机译:使用一种新颖而简单的方法来合成可逆的大环化合物。 该方法基于捕获具有光动力学共价键的分子作为纳米反应器,并将其暴露于UV辐射,以促进定量选择性和选择性地形成环状化合物。 使用的微乳液液滴的尺寸在合成可逆大环化合物中起着至关重要的作用。 形成的大环化合物能够在较短波长的UV照射下恢复单体。

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