Screening of π-Basic Naphthalene and Anthracene Amplifiers for π-Acidic Synthetic Pore Sensors
摘要:
Synthetic ion channels and pores attract current attention as multicomponent sensors in complex matrixes. This application requires the availability of reactive signal amplifiers that covalently capture analytes and drag them into the pore. pi-Basic 1,5-dialkoxynaphthalenes (1,5-DAN) are attractive amplifiers because aromatic electron donor-acceptor (AEDA) interactions account for their recognition within pi-acidic naphthalenediimide (NDI) rich synthetic pores. Focusing on amplifier design, we report here the synthesis of a complete collection of DAN and dialkoxyanthracene amplifiers, determine their oxidation potentials by cyclic voltammetry, and calculate their quadrupole moments. Blockage experiments reveal that subtle structural changes in regioisomeric DAN amplifiers can be registered within NDI pores. Frontier orbital overlap in AEDA complexes, oxidation potentials, and, to a lesser extent, quadrupole moments are shown to contribute to isomer recognition by synthetic pores. Particularly important with regard to practical applications of synthetic pores as multianalyte sensors, we further demonstrate that application of the lessons learned with DAN regioisomers to the expansion to dialkoxyanthracenes provides access to privileged amplifiers with submicromolar activity.
Microwave-assisted synthesis and evaluation of antibacterial activity of 2,2'-(naph- thalene-2,7-diylbis(oxy))bis(N'-substituted acetohydrazide) derivatives
Ultrasound-assisted synthesis of 2,5-dimethyl-N-substituted pyrroles catalyzed by uranyl nitrate hexahydrate
作者:V.S.V. Satyanarayana、A. Sivakumar
DOI:10.1016/j.ultsonch.2011.02.007
日期:2011.9
An efficient synthesis of different novel 2,5-dimethyl-N-substituted pyrrole derivatives by the Paal-Knorr condensation has been accomplished using uranylnitratehexahydrate as catalyst under soft conditions and ultrasonic irradiation. The synthesized compounds were confirmed through spectral characterization using IR, (1)H NMR, (13)C NMR and mass spectra.
Ultrasonic Assisted Synthesis of Naphthalene Substituted Schiff Base Derivatives and Their Antioxidant Activity Studies
作者:K. Venkatesan、V. S. V. Satyanarayana、A. Sivakumar
DOI:10.1002/jccs.201190091
日期:2011.9
aryl/hetero aromatic aldehydes with 2,2′‐ [naphthalene‐2,7‐diylbis(oxy)]diacetohydrazide (3) under reflux temperature and ultrasonic irradiation. These Schiff base derivatives were confirmed through spectralcharacterization using IR, 1H NMR, 13C NMR and mass spectra. All the synthesized compounds were screened for their antioxidant activity using DPPH free radical scavenging method.
通过芳基/杂芳族醛与2的酸催化缩合反应合成了新的席夫碱衍生物2,2'-[萘-2,7-二基双(氧基)]双[N'-取代的乙酰肼](4a-m)回流温度和超声辐射下,2'-[萘-2,7-二基双(氧基)]二乙酰肼(3)。这些席夫碱衍生物通过使用IR,1 H NMR,13 C NMR和质谱的光谱表征来确认。使用DPPH自由基清除方法筛选所有合成的化合物的抗氧化活性。