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Synthesis, characterization, crystal structure and solution studies of a novel proton transfer (charge transfer) complex of 2,2′-dipyridylamine with 2,6-pyridine dicarboxylic acid

机译:2,2'-二吡啶胺与2,6-吡啶二羧酸的新型质子转移(电荷转移)配合物的合成,表征,晶体结构和溶液研究

摘要

Reaction between 2,2′-dipyridylamine (DPA) and 2,6-pyridine dicarboxylic acid (dipicolinic acid, dipicH2), in water results in the formation of a proton transfer or charge transfer (CT) complex, (DPAH)+(dipicH)−·H2O, 1. The characterization was performed using 1H NMR and FTIR spectroscopy, elemental analysis and X-ray crystallography. The crystal system is triclinic with space group P1. The structural investigations exhibit that the hydrogen bonds and π–π stacking interactions stabilize the crystal structure of proton transfer complex. The protonation constants of 2,6-pyridine dicarboxylic acid, 2,2′-dipyridylamine and the equilibrium constants for dipic–DPA (1:1) proton transfer system were calculated by potentiometric pH titration method using Hyperquad2008 program. The stoichiometries of the proton transfer species in solution was in agreement with the solid state result.
机译:水中的2,2'-联吡啶胺(DPA)与2,6-吡啶二甲酸(dipicolinic acid,dipicH2)之间的反应导致质子转移或电荷转移(CT)络合物(DPAH)+(dipicH )-·H 2 O,1.使用1H NMR和FTIR光谱,元素分析和X射线晶体学进行表征。晶体系统是三斜晶系,具有空间群P1。结构研究表明,氢键和π-π堆积相互作用可稳定质子转移配合物的晶体结构。使用Hyperquad2008程序通过电位pH滴定法计算了2,6-吡啶二甲酸,2,2'-联吡啶胺的质子化常数和二ic基-DPA(1:1)质子转移系统的平衡常数。溶液中质子转移物质的化学计量与固态结果一致。

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