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Synthesis, structure, electrochemistry, and electrochemiluminescence of thienyltriazoles

机译:噻吩基三唑的合成,结构,电化学和电致发光

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Four blue-emitting thienyltriazoles with desired N and O coordination atoms were prepared in high yield via click chemistry for potential incorporation into metal complexes. Three of their crystal structures were determined by X-ray crystallography. The electrochemical properties, electronic structures of these thienyltriazoles, 1-4, and their correlations were studied using cyclic voltammetry and differential pulse voltammetry techniques along with density function theory (DFT) calculations. All of the compounds underwent irreversible redox reactions, leading to unstable electrogenerated radical cations and anions. Electrochemical gaps determined from the differences between first formal reduction and oxidation reactions were correlated to HOMO-LUMO energy gaps obtained from UV-vis spectroscopy and the DFT calculations as well as energies of excited states measured from photoluminescence spectroscopy. We observed weak electrochemiluminescence (ECL) from annihilation of these thienyltriazole radicals in acetonitrile containing 0.1 M tetra-n-butylammonium perchlorate as electrolyte. An enhancement in ECL efficiency ranging from 0.16 to 0.50% was observed upon addition of benzoyl peroxide as a coreactant in the above electrolyte solutions. The generation of excimers in solutions of 1-4 was observed as seen by the red-shift in ECL maxima relative to their corresponding photoluminescence peak wavelengths. Our work is of importance for the development of efficient blue-emitting fluorophores via click chemistry that could be potential luminophores in metal complexes.
机译:通过点击化学以高收率制备了具有所需N和O配位原子的四种发蓝光的噻吩基三唑,可潜在地掺入金属络合物中。通过X射线晶体学确定它们的三个晶体结构。使用循环伏安法和微分脉冲伏安法以及密度泛函理论(DFT)计算,研究了这些噻吩基三唑1-4的电化学性质,电子结构及其相关性。所有这些化合物都发生不可逆的氧化还原反应,导致不稳定的电产生的自由基阳离子和阴离子。由第一次正式还原反应和氧化反应之间的差异确定的电化学间隙与通过UV-可见光谱和DFT计算获得的HOMO-LUMO能隙以及通过光致发光光谱法测量的激发态能量相关。我们观察到这些噻吩三唑自由基在含有0.1 M高氯酸四正丁基铵的乙腈中的an灭,从而观察到弱的电化学发光(ECL)。在上述电解质溶液中加入过氧化苯甲酰作为共反应剂时,观察到ECL效率提高了0.16%至0.50%。通过在ECL最大值中相对于其相应的光致发光峰波长的红移观察到了在1-4溶液中准分子的产生。我们的工作对于通过点击化学开发有效的发蓝色光的荧光团至关重要,这可能是金属络合物中的潜在发光体。

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