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Spectral and DFT studies of anion bound organic receptors: Time dependent studies and logic gate applications

机译:阴离子结合的有机受体的光谱和DFT研究:时间依赖性研究和逻辑门应用

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New colorimetric receptors R1 and R2 with varied positional substitution of a cyano and nitro signaling unit having a hydroxy functionality as the hydrogen bond donor site have been designed, synthesized and characterized by FTIR, 1H NMR spectroscopy and mass spectrometry. The receptors R1 and R2 exhibit prominent visual response for F? and AcO– ions allowing the real time analysis of these ions in aqueous media. The formation of the receptor–anion complexes has been supported by UV–vis titration studies and confirmed through binding constant calculations. The anion binding process follows a first order rate equation and the calculated rate constants reveal a higher order of reactivity for AcO? ions. The 1H NMR titration and TDDFT studies provide full support of the binding mechanism. The Hg2+ and F? ion sensing property of receptor R1 has been utilized to arrive at “AND” and “INHIBIT” molecular logic gate applications.
机译:通过FTIR, 1 H NMR光谱和质谱设计,合成和表征了新的比色受体R1和R2,它们在位置上被具有羟基官能团的氰基和硝基信号单元进行了不同的取代,并具有氢键供体位点光谱法。 R1和R2受体对F ?和AcO – 离子表现出明显的视觉响应,从而可以实时分析这些离子在水性介质中的作用。 UV-vis滴定研究支持了受体-阴离子络合物的形成,并通过结合常数计算得到了证实。阴离子结合过程遵循一阶速率方程,计算出的速率常数显示出对AcO α离子具有更高的反应活性。 1 H NMR滴定和TDDFT研究为结合机理提供了充分的支持。受体R1的Hg 2 + 和F ?离子感测特性已被用于“ AND”和“ INHIBIT”分子逻辑门的应用。

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