Mechanochromism and Strain-Induced Crystallization in Thiol-yne-Derived Stereoelastomers.

Most elastomers undergo strain-induced crystallization (SIC) under tension; as individual chains are held rigidly in a fixed position by an applied strain, their alignment along the strain field results in a shift from strain-hardening (SH) to SIC. A similar degree of stretching is associated with the tension necessary to accelerate mechanically coupled, covalent chemical responses of mechanophores in overstretched chains, raising the possibility of an interplay between the macroscopic response of SIC and the molecular response of mechanophore activation. Here, thiol-yne-derived stereoelastomers doped covalently with a dipropiolate-derivatized spiropyran (SP) mechanophore (0.

Structure-property relationships in 3D-printed poly(l-lactide-co-ε-caprolactone) degradable polymer.

The recent growth of polymer 3D-printing has brought innovation to the medical implant field. Implants with complex porous structures can be fabricated by printing to tune mechanical behavior and enable diffusion, consequently improving integration with tissues in the human body. Poly(L-lactide-co-ε-caprolactone) (PLCL) is a 3D-printable polymer that possess a wide range of possible mechanical properties depending on its monomer composition.

Supramolecular Assemblies for Electronic Materials.

This work presents a synergy between organic electronics and supramolecular chemistry, in which a host-guest complex is designed to function as an efficacious electronic material. Specifically, the noncovalent recognition of a fullerene, phenyl-C -butyric acid methyl ester (PC BM), by an alternating perylene diimide (P)-bithiophene (B) conjugated macrocycle (PBPB) results in a greater than five-fold enhancement in electron mobility, relative to the macrocycle alone. Characterization and quantification of the binding of fullerenes by host PBPB is provided alongside evidence for intermolecular electronic communication within the host-guest complexes.

Influence of Molecular Conformation on Electron Transport in Giant, Conjugated Macrocycles.

We describe here the direct connection between the molecular conformation of a conjugated macrocycle and its macroscopic charge transport properties. We incorporate chiral, helical perylene diimide ribbons into the two separate macrocycles as the n-type, electron transporting material. As the macrocycles' films and electronic structures are analogous, the important finding is that the macrocycles' molecular structures and their associated dynamics determine device performance in organic field effect transistors.