Quantum Interference Effect in Saturated Systems: Effect of Anchoring Group Position on Conductance of Bipiperidines and their in-situ Derived Dithiocarbamates.

IF 16.9
Umar Rashid, Abdalghani H S Daaoub, P A Sreelakshmi, Sara Sangtarash, Hatef Sadeghi, Veerabhadrarao Kaliginedi
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Abstract

This study investigates quantum interference in σ-only molecular systems, focusing on the impact of anchoring group nature and its position. Using a combined approach of mechanically controlled break junction experiments and quantum transport calculations, we demonstrate that meta-connected σ-conducting bipiperidine-based molecular junctions exhibit higher conductance than para-connected ones. This trend is opposite to that of the trend typically observed in π-molecular systems, indicating the existence of distinctly different quantum interference phenomenon in σ-only molecular systems. Further, we show that anchoring group modifications achieved through in-situ dithiocarbamylation significantly alters the conductance and decay factors. We also elucidate the mechanism behind multiple conductance features observed in aliphatic bipiperidines with cyclic secondary amine and dithiocarbamate anchoring groups. This work demonstrates σ-quantum interference in bipiperidine-based molecular systems and highlights how changes in junction configuration, nature of the anchoring group and its position can be used to control conductance in σ-only molecular systems.

饱和体系中的量子干涉效应:锚定基团位置对双哌替啶及其原位衍生二硫代氨基甲酸酯电导的影响。
本文研究了σ-纯分子体系中的量子干涉,重点研究了锚定基团性质及其位置对量子干涉的影响。利用机械控制断结实验和量子输运计算相结合的方法,我们证明了元连接的σ导双哌啶分子结比准连接的分子结具有更高的电导率。这一趋势与π-分子体系中典型的量子干涉趋势相反,说明σ-纯分子体系中存在着明显不同的量子干涉现象。此外,我们发现通过原位二硫代氨基化实现的锚定基团修饰显着改变了电导和衰变因子。我们还阐明了在具有环仲胺和二硫代氨基甲酸酯锚定基的脂肪族双哌替啶中观察到的多重电导特征背后的机制。这项工作证明了双哌啶分子体系中的σ-量子干涉,并强调了如何通过改变结结构、锚定基团的性质及其位置来控制σ-纯分子体系中的电导。
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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