Aakeröy Christer B, Spartz Christine L
Department of Chemistry, Kansas State University, Manhattan, KS, 66506, USA.
Top Curr Chem. 2015;358:155-82. doi: 10.1007/128_2014_567.
Supramolecular synthesis is typically limited to one-pot reactions because of the reversibility of non-covalent bonds, and to overcome this restriction we need to be able to rank the relative structural importance of such interactions and build synthetic methods to utilize synthons which can operate side-by-side without interference. Halogen bonds have characteristics (strength and directionality) which potentially make them prime candidates as critical components of effective, transferable, and versatile supramolecular synthetic strategies. In this chapter, several halogen-bond driven crystal engineering strategies for the assembly of specific architectures in molecular solids are described in detail, and the utility of halogen bonds for the synthesis of co-crystals are addressed. Finally, the structural compatibility or competition between of halogen- and hydrogen bonds in the context of supramolecular synthesis are examined.
由于非共价键的可逆性,超分子合成通常局限于一锅法反应。为了克服这一限制,我们需要能够对这类相互作用的相对结构重要性进行排序,并构建合成方法来利用可以并行操作而不相互干扰的合成子。卤键具有一些特性(强度和方向性),这使其有可能成为有效、可转移且通用的超分子合成策略的关键组成部分。在本章中,将详细描述几种用于在分子固体中组装特定结构的卤键驱动的晶体工程策略,并探讨卤键在共晶合成中的应用。最后,将研究超分子合成背景下卤键与氢键之间的结构兼容性或竞争性。