Abstract
The cover image by Simon van Hurne depicts the formation of a dynamic covalent boronate‐TetraAzaADamantane bond, which could be integrated in a covalent adaptable network. As a result of the on‐going dynamic bond exchange reactions within this network, the material could undergo stress relaxation. At the same time, the more robust triple bonding motif allowed for stronger materials compared to their conventional boronate ester‐based counterparts. DOI: 10.1002/pol.20230446 image
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