Search

Modern development of flexible electronics has made use of bioelectronic materials as artificial tissue in vivo. As hydrogels are more similar to nerve tissue, functional hydrogels have become a promising candidate for bioelectronics. Meanwhile, interfacing functional hydrogels and living tissues is at the forefront of bioelectronics. The peripheral nerve injury often leads to paralysis, chronic pain, neurologic disorders, and even disability, because it has affected the bioelectrical signal transmission between the brain and the rest of body. Here, a kind of light-stimuli-responsive and stretchable conducting polymer hydrogel (CPH) is developed to explore artificial nerve. The conductivity of CPH can be enhanced when illuminated by near-infrared light, which can promote the conduction of the bioelectrical signal. When CPH is mechanically elongated, it still has high durability of conductivity and, thus, can accommodate unexpected strain of nerve tissues in motion. Thereby, CPH can better serve as an implant of the serious peripheral nerve injury in vivo, especially in the case that the length of the missing nerve exceeds 10 mm.

Phase structures and transitions of a series of biphenyl containing side-chain liquid crystalline polyacetylenes (SCLCPAs) with different length of spacer and alkyl tail, poly((m + 2)-{[(4′-alkyloxy-4-biphenylyl)carbonyl]oxy}-1-yne) [P-m,7 (m = 4, 5, 8), P-m,5 (m = 9), P-m,5L (m = 3, 9), m is the number of methylene units in the spacer], were studied by differential scanning calorimeter, polarized light microscopy, one- and two-dimensional wide-angle X-ray diffraction. It is revealed that phase structures of the samples are strongly dependent on the lengths of spacer and alkyl tail. The samples with short spacer (m ≤ 4) render the molecular shape of sheet-like due to the strong coupling between the backbone and the biphenyl groups on side-chains. They form highly ordered smectic phase with an additional ordering on the subnanometer scale (SmXo) at low temperatures. For m > 5, P-m,7 exhibits the low-temperature phase of smectic B (SmB), while P-9,5 and P-9,5L form smectic E (SmE). As the long spacers adopt...

Self-assembly behaviors of a series of hydrophobic side-chain liquid crystalline (LC) polyacetylenes, namely, poly(5-{((4'-alkoxy-4-biphenylyl)carbonyl)oxy}-1-pentyne)s (P-3,m (m ) 5, 7, 9)), were studied in dilute solutions. The assembly was induced by tuning the solvent property to be selective for the alkyl tails on the side chains, with the processes characterized by turbidity, dynamic light scattering, 1 H NMR, and excitation fluorescence anisotropy measurements. The morphology and structure of the P-3,m aggregates formed in the solutions were investigated using atomic force microscopy and wide-angle X-ray diffraction. The experimental results indicate that the P-3,m polymers can form monolayer lamellae in selective solvents. In the lamella, the P-3,m molecules are sheetlike and pack parallel to each other with their backbones located in the lamellar center and their alkyl tails covering the top and bottom lamellar surfaces. The lamellar thickness is largely determined by the width of the molecular sheet. When the solvent becomes selective for the tails, the P-3,m chains may undergo shape stiffening to become more sheetlike.