Herein we report the use of a tetrazinenorbornene inverse electron demand Diets Alder conjugation applied to polymer end-functionalization and polymer polymer coupling. The reaction was found to be applicable to polymer polymer coupling, as judged by SEC, DOSY NMR, and LCxSEC analyses, giving diblock copolymers by merely mixing the constituent homopolymers together under ambient conditions, using no catalyst, additive, or external stimulus
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
atom transfer radical polymerization (ATRP); azide-alkyne cycloaddition; click chemistry; controlled...
Herein we report the use of a tetrazine-norbornene inverse electron demand Diels–Alder conjugation a...
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 applications of 1,2,4,5-Tetrazines in polymer post-functionalization and Diels Alder cycloadditi...
A series of well-defined functional polyethylene graft copolymers with high molecular weights have b...
Well-defined norbornene-functional poly(carbonate)s were prepared by ring-opening polymerization a...
A new and highly efficient polymer, postpolymerization, modification platform based on an inverse el...
Click reactions have provided access to an array of remarkably complex polymer architectures. Howeve...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
Reaction of 3,6-bis(3,5-dimethylpyrazolyl)-1,2,4,5-tetrazine with mono- and di-amines gives rise to ...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
atom transfer radical polymerization (ATRP); azide-alkyne cycloaddition; click chemistry; controlled...
Herein we report the use of a tetrazine-norbornene inverse electron demand Diels–Alder conjugation a...
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 applications of 1,2,4,5-Tetrazines in polymer post-functionalization and Diels Alder cycloadditi...
A series of well-defined functional polyethylene graft copolymers with high molecular weights have b...
Well-defined norbornene-functional poly(carbonate)s were prepared by ring-opening polymerization a...
A new and highly efficient polymer, postpolymerization, modification platform based on an inverse el...
Click reactions have provided access to an array of remarkably complex polymer architectures. Howeve...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
Reaction of 3,6-bis(3,5-dimethylpyrazolyl)-1,2,4,5-tetrazine with mono- and di-amines gives rise to ...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
The introduction of functional end-groups into well-defined polymer structures often requires post-p...
atom transfer radical polymerization (ATRP); azide-alkyne cycloaddition; click chemistry; controlled...