B–O bonds are effective for constructing self-healing polymers, because of their unique combination of high thermodynamic stability and kinetic tunability. However, it is still challenging to develop boron-containing polymers that show simultaneously high mechanical strength, good hydrolytic stability, and autonomous self-healing ability. Herein, we designed and synthesized a phenol compound with three hydroxyls, two of which form boronic ester with boronic acid while the other one can promote the dynamic exchange of B–O bonds. Taking advantage of the new boronic esters as the cross-linking sites, a series of strong and tough elastomers with outstanding self-healing capacities at room temperature were successfully fabricated. The new design...
Covalent cross-linking of rubbers is essential for obtaining high resilience and environmental resis...
Multifunctional and multiresponsive hydrogels have presented a promising platform to design and fabr...
The pursuit of dynamic molecular interactions to control macroscopic properties of polymers represen...
Despite numerous strategies involving dynamic covalent bond exchange for dynamic and self-healing ma...
The dynamic covalent characteristics of oxime and boronate ester bonds have been explored. A small e...
Covalently cross-linked rubbers are renowned for their high elasticity that play an indispensable ro...
Dynamic interaction can impart useful functionality to the polymer. Boronic esters are known to form...
Self-healable hydrogels based on the dynamically reversible boronate ester or borate ester bonds are...
The fabrication of mechanically robust polymeric materials capable of self-healing and recycling rem...
Boronic esters prepared by condensation of boronic acids and diols have been widely used as dynamic ...
This report describes the synthesis and characterization of boronate ester-cross-linked hydrogels ca...
Drawing on inspiration from nature, transient, dynamic interactions can encode function into synthet...
It has been a long-standing goal to develop self-healable polyurethane elastomers with desirable mec...
Dynamic materials including self-healing polymers and vitrimers have huge potential for improving cu...
All polymeric materials are subject to thermal, mechanical as well as chemical degradation and destr...
Covalent cross-linking of rubbers is essential for obtaining high resilience and environmental resis...
Multifunctional and multiresponsive hydrogels have presented a promising platform to design and fabr...
The pursuit of dynamic molecular interactions to control macroscopic properties of polymers represen...
Despite numerous strategies involving dynamic covalent bond exchange for dynamic and self-healing ma...
The dynamic covalent characteristics of oxime and boronate ester bonds have been explored. A small e...
Covalently cross-linked rubbers are renowned for their high elasticity that play an indispensable ro...
Dynamic interaction can impart useful functionality to the polymer. Boronic esters are known to form...
Self-healable hydrogels based on the dynamically reversible boronate ester or borate ester bonds are...
The fabrication of mechanically robust polymeric materials capable of self-healing and recycling rem...
Boronic esters prepared by condensation of boronic acids and diols have been widely used as dynamic ...
This report describes the synthesis and characterization of boronate ester-cross-linked hydrogels ca...
Drawing on inspiration from nature, transient, dynamic interactions can encode function into synthet...
It has been a long-standing goal to develop self-healable polyurethane elastomers with desirable mec...
Dynamic materials including self-healing polymers and vitrimers have huge potential for improving cu...
All polymeric materials are subject to thermal, mechanical as well as chemical degradation and destr...
Covalent cross-linking of rubbers is essential for obtaining high resilience and environmental resis...
Multifunctional and multiresponsive hydrogels have presented a promising platform to design and fabr...
The pursuit of dynamic molecular interactions to control macroscopic properties of polymers represen...