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Acid/Base Switching of the Tautomerism and Conformation of a Dioxoporphyrin for Integrated Binary Subtraction

机译:酸/碱转换的互变异构和构二聚卟啉的二元减法。

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摘要

Compared with most of the reported logic devices based on the supramolecular approach, systems based on individual molecules can avoid challenging construction requirements. Herein, a novel dioxoporphyrin DPH_(22) was synthesized and two of its tautomers were characterized by single-crystal X-ray diffraction studies. Compound DPH_(22) exhibits multichannel controllable stepwise tautomerization, protonation, and deprotonation processes through interactions with H~+ and F~- ions. By using the addition of H~+ and F~- ions as inputs and UV/Vis absorption values at λ=412, 510, 562, and 603 nm as outputs, the controlled tautomerism of DPH_(22) has been successfully used for the construction of an integrated molecular level half-subtractor and comparator. In addition, this acid/base-switched tautomerism is reversible, thus endowing the system with ease of reset and recycling; consequently, there is no need to modulate complicated intermolecular interactions and electron-/chargetransfer processes.
机译:与大多数报告的基于超分子方法的逻辑器件相比,基于单个分子的系统可以避免具有挑战性的构造要求。本文合成了一种新型的二氧卟啉DPH_(22),并通过单晶X射线衍射研究对其两个互变异构体进行了表征。化合物DPH_(22)通过与H〜+和F〜-离子的相互作用,表现出多通道可控的逐步互变异构,质子化和去质子化过程。通过添加H〜+和F〜-离子作为输入,并使用λ= 412、510、562和603 nm的UV / Vis吸收值作为输出,DPH_(22)的受控互变异构已成功用于集成的分子水平半减法器和比较器的构建。此外,这种酸/碱转换的互变异构是可逆的,因此使系统易于重置和回收。因此,不需要调节复杂的分子间相互作用和电子/电荷转移过程。

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