Adhesion to wet and dynamic surfaces is vital for many biomedical applications. However, the development of effective tissue adhesives has been challenged by the required combination of properties, which includes mechanical similarity to the native tissue, high adhesion to wet surfaces, hemostatic properties, biodegradability, high biocompatibility, and ease of use. In this study, we report a novel bioinspired design with bioionic liquid (BIL) conjugated polymers to engineer multifunctional highly sticky, biodegradable, biocompatible, and hemostatic adhesives. Choline-based BIL is a structural precursor of the phospholipid bilayer in the cell membrane. We show that the conjugation of choline molecules to naturally derived polymers (i.e., gelatin) and synthetic polymers (i.e., polyethylene glycol) significantly increases their adhesive strength and hemostatic properties. Synthetic or natural polymers and BILs were mixed at room temperature and cross-linked via visible light photopolymerization to make hydrogels with tunable mechanical, physical, adhesive, and hemostatic properties. The hydrogel adhesive exhibits a close to 50% decrease in the total blood volume loss in tail cut and liver laceration rat animal models compared to the control. This technology platform for adhesives is expected to have further reaching application vistas from tissue repair to wound dressings and the attachment of flexible electronics.

Planar bismuth compounds exhibit tunable Lewis acidity and high catalytic activity for lactone polymerization.

No abstract

Geometric deformation in main group compounds can be used to elicit unique properties including strong Lewis acidity. Here we report on a family of planar bismuth (III) complexes (c.f. typically pyramidal structure for such compounds), which show a geometric Lewis acidity that can be further tuned by varying the steric and electronic features of the triamide ligand employed. The structural dynamism of the planar bismuth complexes was probed in both the solid and solution phase, revealing at least three distinct modes of intermolecular association. A modified Gutmann-Beckett method was used to assess their electrophilicity by employing trimethylphosphine sulfide in addition to triethylphosphine oxide as probes, providing insights into the preference for binding hard or soft substrates. Experimental binding studies were complemented by a computational assessment of the affinities and dissection of the latter into their intrinsic bond strength and deformation energy components. The results show comparable Lewis acidity to triarylboranes, with the added ability to bind two bases simultaneously and reduced discrimination against soft substrates. We also study the catalytic efficacy of these complexes in the ring opening polymerization of cyclic esters ε-caprolactone and rac-lactide. The polymers obtained are in the ultra-high molecular weight regime and show excellent dispersity values. The complexes retain their performance under industrially relevant conditions suggesting they may be useful as less toxic alternatives to tin catalysts in the production of medical grade materials. Collectively, these results establish planar bismuth complexes as not only a novel neutral platform for main group Lewis acidity, but also a potentially valuable one for catalysis.

Geometric deformation in main group compounds can be used to elicit unique properties including strong Lewis acidity. Here we report on a family of planar bismuth (III) complexes (c.f. typically pyramidal structure for such compounds), which show a geometric Lewis acidity that can be further tuned by varying the steric and electronic features of the triamide ligand employed. The structural dynamism of the planar bismuth complexes was probed in both the solid and solution phase, revealing at least three distinct modes of intermolecular association. A modified Gutmann-Beckett method was used to assess their electrophilicity by employing trimethylphosphine sulfide in addition to triethylphosphine oxide as probes, providing insights into the preference for binding hard or soft substrates. Experimental binding studies were complemented by a computational assessment of the affinities and dissection of the latter into their intrinsic bond strength and deformation energy components. The results show comparable Lewis acidity to triarylboranes, with the added ability to bind two bases simultaneously and reduced discrimination against soft substrates. We also study the catalytic efficacy of these complexes in the ring opening polymerization of cyclic esters ε-caprolactone and rac-lactide. The polymers obtained are in the ultra-high molecular weight regime and show excellent dispersity values. The complexes retain their performance under industrially relevant conditions suggesting they may be useful as less toxic alternatives to tin catalysts in the production of medical grade materials. Collectively, these results establish planar bismuth complexes as not only a novel neutral platform for main group Lewis acidity, but also a potentially valuable one for catalysis.