Maxson Tristan, Jalilov Almaz S, Zeller Matthias, Rosokha Sergiy V
Department of Chemistry, Ball State University, Muncie, IN, 47306, USA.
Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran, 31261, Saudi Arabia.
Angew Chem Int Ed Engl. 2020 Sep 21;59(39):17197-17201. doi: 10.1002/anie.202004384. Epub 2020 Aug 7.
Halogen bonding between two negatively charged species, tetraiodo-p-benzoquinone anion radicals (I Q ) and iodide anions, was observed and characterized for the first time. X-ray structural and EPR/UV-Vis spectral studies revealed that the anion-anion bonding led to the formation of crystals comprising 2D layers of I Q anion radicals linked by iodides and separated by Et N counter-ions. Computational analysis suggested that the seemingly antielectrostatic halogen bonds in these systems were formed via a combination of several factors. First, an attenuation of the interionic repulsion by the solvent facilitated close approach of the anions leading to their mutual polarization. This resulted in the appearance of positively charged areas (σ-holes) on the surface of the iodine substituents in I Q responsible for the attractive interaction. Finally, the solid-state associations were also stabilized by multicenter (4:4) halogen bonding between I Q and iodide.
首次观察并表征了两个带负电荷的物种——四碘对苯醌阴离子自由基((I_Q))和碘离子之间的卤键。X射线结构分析以及电子顺磁共振/紫外-可见光谱研究表明,阴离子-阴离子键合导致形成了晶体,该晶体由通过碘离子连接并被乙基铵抗衡离子隔开的二维(I_Q)阴离子自由基层组成。计算分析表明,这些体系中看似反静电的卤键是由多种因素共同作用形成的。首先,溶剂使离子间排斥作用减弱,促进了阴离子的紧密靠近,导致它们相互极化。这使得(I_Q)中碘取代基表面出现带正电的区域(σ-空穴),从而产生吸引相互作用。最后,(I_Q)与碘离子之间的多中心(4:4)卤键也使固态缔合更加稳定。