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二氯吡啶 - 氧化物卤素键合配合物

Dichlorine-pyridine -oxide halogen-bonded complexes.

作者信息

Limberg Niklas, Rautiainen J Mikko, Lundell Jan, Riedel Sebastian, Rissanen Kari, Puttreddy Rakesh

机构信息

Department of Chemistry and Biochemistry, Freie Universität Berlin Fabeckstr. 34/36 14195 Berlin Germany

Department of Chemistry, University of Jyvaskyla P.O. BOX 35 FI-40014 Jyväskylä Finland

出版信息

Chem Sci. 2024 Oct 21;15(45):18840-5. doi: 10.1039/d4sc06270a.

Abstract

A new Cl-Cl···O-N halogen-bonded paradigm has been demonstrated, using dichlorine as a halogen bond (XB) donor and -oxide as an XB acceptor. Their crystalline complexes were formed during the warm-up process from -196 °C to -80 °C for X-ray diffraction analysis. They exhibit high instability in the crystalline state, even at these low temperatures, leading to rapid decomposition and the formation of Cl⋯H-O-N hydrogen-bonded complexes. The normalized XB interaction ratio ( ) of Cl⋯O interactions in the solid-state demonstrates affinity comparable to traditional I⋯O interactions observed in I-I···O-N halogen-bonded systems. The Cl-Cl⋯O XB angles vary from 172° to 177°, manifesting the structure-guiding influence of the electronegative chlorine atom's σ-hole on these XB interactions.

摘要

一种新的Cl-Cl···O-N卤键模式已得到证实,使用二氯作为卤键(XB)供体,而环氧化物作为XB受体。它们的晶体配合物是在从-196°C升温至-80°C的过程中形成的,用于X射线衍射分析。即使在这些低温下,它们在晶体状态下也表现出高度不稳定性,导致快速分解并形成Cl⋯H-O-N氢键配合物。固态中Cl⋯O相互作用的归一化XB相互作用比( )表明其亲和力与在I-I···O-N卤键体系中观察到的传统I⋯O相互作用相当。Cl-Cl⋯O XB角在172°至177°之间变化,表明电负性氯原子的σ-空穴对这些XB相互作用具有结构导向作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4eb/11578259/7061531773ee/d4sc06270a-f1.jpg

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