Institute of Physical and Theoretical Chemistry, University of Bonn, 53115 Bonn, Germany.
Institute of Inorganic Chemistry, University of Bonn, 53121 Bonn, Germany.
Molecules. 2018 Jul 18;23(7):1758. doi: 10.3390/molecules23071758.
This work explores the use of Kuhn verdazyl radicals as building blocks in multifunctional molecular materials in an exemplary study, focusing on the magnetic and the electron transfer (ET) characteristics, but also addressing the question whether chemical modification by cross-coupling is possible. The ET in solution is studied spectroscopically, whereas solid state measurements afford information about the magnetic susceptibility or the conductivity of the given samples. The observed results are rationalized based on the chemical structures of the molecules, which have been obtained by X-ray crystallography. The crystallographically observed molecular structures as well as the interpretation based on the spectroscopic and physical measurements are backed up by DFT calculations. The measurements indicate that only weak, antiferromagnetic (AF) coupling is observed in Kuhn verdazyls owed to the low tendency to form face-to-face stacks, but also that steric reasons alone are not sufficient to explain this behavior. Furthermore, it is also demonstrated that ET reactions proceed rapidly in verdazyl/verdazylium redox couples and that Kuhn verdazyls are suited as donor molecules in ET reactions.
这项工作探讨了 Kuhn verdazyl 自由基作为多功能分子材料构建块的用途,在一个典型的研究中,重点研究了其磁学和电子转移 (ET) 特性,但也解决了通过交叉偶联进行化学修饰是否可能的问题。溶液中的 ET 通过光谱学进行研究,而固态测量则提供有关给定样品的磁化率或电导率的信息。基于 X 射线晶体学获得的分子结构,对观察到的结果进行了合理化解释。基于光谱和物理测量的化学结构观察以及解释得到了 DFT 计算的支持。测量结果表明,由于形成面对面堆叠的趋势较低,Kuhn verdazyl 中仅观察到弱反铁磁 (AF) 耦合,但仅靠空间位阻原因不足以解释这种行为。此外,还证明 verdazyl/verdazylium 氧化还原偶联中的 ET 反应迅速进行,并且 Kuhn verdazyl 适合作为 ET 反应中的供体分子。