Herein, we report the development of a scalable and synthetically robust building block based on norbornadiene (NBD) that can be broadly incorporated into a variety of macromolecular architectures using traditional living polymerization techniques. By taking advantage of a selective and rapid deprotection with tetrazine, highly reactive "masked" cyclopentadiene (Cp) functionalities can be introduced into synthetic polymers as chain-end groups in a quantitative and efficient manner. The orthogonality of this platform further enables a cascade "click" process where the "unmasked" Cp can rapidly react with dienophiles, such as maleimides, through a conventional Diels-Alder reaction. Coupling proceeds with quantitative conversions allowing high...
The development of new functional materials requires reliable conjugation chemistry for coupling mol...
The development of new functional materials requires reliable conjugation chemistry for coupling mol...
ABSTRACT: The high fidelity and efficiency of Click chemistry are exploited in the synthesis of a li...
Herein, we report the development of a scalable and synthetically robust building block based on nor...
Herein, we report the development of a scalable and synthetically robust building block based on nor...
A novel method for facile postpolymerization functionalization of synthetic polymers using terminal ...
A new Diels–Alder (DA)-based photopatterning platform is presented, which exploits the irreversible,...
Linear oligomers of dicyclopentadiene (DCPD) are reactive precursors for thermoplastic and thermoset...
Linear oligomers of dicyclopentadiene (DCPD) are reactive precursors for thermoplastic and thermoset...
Linear oligomers of dicyclopentadiene (DCPD) are reactive precursors for thermoplastic and thermoset...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
The potential use of conjugated polymers in device applications is often limited by their less than ...
The development of new functional materials requires reliable conjugation chemistry for coupling mol...
The development of new functional materials requires reliable conjugation chemistry for coupling mol...
ABSTRACT: The high fidelity and efficiency of Click chemistry are exploited in the synthesis of a li...
Herein, we report the development of a scalable and synthetically robust building block based on nor...
Herein, we report the development of a scalable and synthetically robust building block based on nor...
A novel method for facile postpolymerization functionalization of synthetic polymers using terminal ...
A new Diels–Alder (DA)-based photopatterning platform is presented, which exploits the irreversible,...
Linear oligomers of dicyclopentadiene (DCPD) are reactive precursors for thermoplastic and thermoset...
Linear oligomers of dicyclopentadiene (DCPD) are reactive precursors for thermoplastic and thermoset...
Linear oligomers of dicyclopentadiene (DCPD) are reactive precursors for thermoplastic and thermoset...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
Post-polymerization modification of polymers derived from sustainable resources using the click reac...
The potential use of conjugated polymers in device applications is often limited by their less than ...
The development of new functional materials requires reliable conjugation chemistry for coupling mol...
The development of new functional materials requires reliable conjugation chemistry for coupling mol...
ABSTRACT: The high fidelity and efficiency of Click chemistry are exploited in the synthesis of a li...