Structure–Reactivity–Property Relationships in Covalent Adaptable Networks

Polymer networks built out of dynamic covalent bonds offer the potential to translate the control and tunability of chemical reactions to macroscopic physical properties. Under conditions at which these reactions occur, the topology of covalent adaptable networks (CANs) can rearrange, meaning that they can flow, self-heal, be remolded, and respond to stimuli. Materials with these properties are necessary to fields ranging from sustainability to tissue engineering; thus the conditions and time scale of network rearrangement must be compatible with the intended use. The mechanical properties of CANs are based on the thermodynamics and kinetics of their constituent bonds. Therefore, strategies are needed that connect the molecular and macroscopic worlds. In this Perspective, we analyze structure–reactivity–property relationships for several classes of CANs, illustrating both general design principles and the predictive potential of linear free energy relationships (LFERs) applied to CANs. We discuss opportunities in the field to develop quantitative structure–reactivity–property relationships and open challenges

Porphyrin–Peptoid Conjugates: Face-to-Face Display of Porphyrins on Peptoid Helices

Distance, orientation, and number controlled porphyrin–peptoid conjugates (PPCs) were efficiently synthesized. Cofacial (<b>1</b>, <b>2</b>, and <b>4</b>), slipped-cofacial (<b>3</b>), and unstructured (<b>5</b>) arrangements of porphyrins provided distinct optical and electronic properties characterized by UV–vis and circular dichroism spectroscopy. In addition, ECCD spectra confirmed the handedness of peptoid helices