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高价碘化合物中的卤键

Halogen Bonding in Hypervalent Iodine Compounds.

作者信息

Catalano Luca, Cavallo Gabriella, Metrangolo Pierangelo, Resnati Giuseppe, Terraneo Giancarlo

机构信息

Laboratory of Nanostructured Fluorinated Materials (NFMLab), Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Via L. Mancinelli 7, 20131, Milan, Italy.

出版信息

Top Curr Chem. 2016;373:289-309. doi: 10.1007/128_2015_666.

Abstract

Halogen bonds occur when electrophilic halogens (Lewis acids) attractively interact with donors of electron density (Lewis bases). This term is commonly used for interactions undertaken by monovalent halogen derivatives. The aim of this chapter is to show that the geometric features of the bonding pattern around iodine in its hypervalent derivatives justify the understanding of some of the longer bonds as halogen bonds. We suggest that interactions directionality in ionic and neutral λ(3)-iodane derivatives is evidence that the electron density distribution around iodine atoms is anisotropic, a region of most positive electrostatic potential exists on the extensions of the covalent bonds formed by iodine, and these positive caps affect, or even determine, the crystal packing of these derivatives. For instance, the short cation-anion contacts in ionic λ(3)-iodane and λ(5)-iodane derivatives fully match the halogen bond definition and geometrical prerequisites. The same holds for the short contacts the cation of ionic λ(3)-iodanes forms with lone-pair donors or the short contacts given by neutral λ(3)-iodanes with incoming nucleophiles. The longer and weaker bonds formed by iodine in hypervalent compounds are usually called secondary bondings and we propose that the term halogen bond can also be used. Compared to the term secondary bond, halogen bond may possibly be more descriptive of some bonding features, e.g., its directionality and the relationships between structure of interacting groups and interaction strength.

摘要

当亲电卤素(路易斯酸)与电子密度供体(路易斯碱)发生吸引性相互作用时,就会形成卤键。该术语通常用于描述单价卤素衍生物的相互作用。本章的目的是表明,高价碘衍生物中碘周围键合模式的几何特征证明了将一些较长的键理解为卤键是合理的。我们认为,离子型和中性λ(3)-碘烷衍生物中的相互作用方向性表明,碘原子周围的电子密度分布是各向异性的,在由碘形成的共价键的延长线上存在一个静电势最正的区域,并且这些正电端会影响甚至决定这些衍生物的晶体堆积。例如,离子型λ(3)-碘烷和λ(5)-碘烷衍生物中短的阳离子-阴离子接触完全符合卤键的定义和几何先决条件。离子型λ(3)-碘烷的阳离子与孤对供体形成的短接触以及中性λ(3)-碘烷与亲核试剂形成的短接触也是如此。高价化合物中由碘形成的较长且较弱的键通常被称为次级键合,我们建议也可以使用卤键这一术语。与次级键这一术语相比,卤键可能更能描述某些键合特征,例如其方向性以及相互作用基团的结构与相互作用强度之间的关系。

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