Preference of halogen bonds over hydrogen bonds within a discrete three-component co-crystal that undergo a [2+2] cycloaddition reaction†
Abstract
The formation of a series of isostructural three-component co-crystals between 1,2,4,5-tetrachloro-3-iodobenzene (C6HICl4) and each of three isosteric bipyridines is reported. Even though C6HICl4 is capable of forming both halogen and hydrogen bonds the donor is found to form co-crystals with only I⋯N halogen bonds when the initial ratio of the molecular components is 2 : 1. Molecules of C6HICl4 stack in a homogeneous and face-to-face configuration which aligns the bipyridine-based acceptor molecule in a similar π-stacked orientation. As a result, the co-crystal containing trans-1,2-bis(4-pyridyl)ethylene undergoes a nearly quantitative [2+2] cycloaddition reaction in the solid state.
![Graphical abstract: Preference of halogen bonds over hydrogen bonds within a discrete three-component co-crystal that undergo a [2+2] cycloaddition reaction](/en/Image/Get?imageInfo.ImageType=GA&imageInfo.ImageIdentifier.ManuscriptID=D3NJ02449K&imageInfo.ImageIdentifier.Year=2023)
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