Hyperbranched polymers by thiol− yne chemistry: from small molecules to functional polymers
D Konkolewicz, A Gray-Weale… - Journal of the American …, 2009 - ACS Publications
Journal of the American Chemical Society, 2009•ACS Publications
A new synthesis of hyperbranched polymers is outlined. This paper presents the synthesis of
hyperbranched polymers by the recently highlighted thiol− yne reaction. In the thiol− yne
reaction, a catalytic amount of photoinitiator and UV radiation are used to add two thiols
across one alkyne bond at room temperature. This work demonstrates how the thiol− yne
reaction can be used to form hyperbranched polymers from both small organic molecules
and polymeric chains bearing an alkyne and a thiol. The UV-catalyzed reaction is fast …
hyperbranched polymers by the recently highlighted thiol− yne reaction. In the thiol− yne
reaction, a catalytic amount of photoinitiator and UV radiation are used to add two thiols
across one alkyne bond at room temperature. This work demonstrates how the thiol− yne
reaction can be used to form hyperbranched polymers from both small organic molecules
and polymeric chains bearing an alkyne and a thiol. The UV-catalyzed reaction is fast …
A new synthesis of hyperbranched polymers is outlined. This paper presents the synthesis of hyperbranched polymers by the recently highlighted thiol−yne reaction. In the thiol−yne reaction, a catalytic amount of photoinitiator and UV radiation are used to add two thiols across one alkyne bond at room temperature. This work demonstrates how the thiol−yne reaction can be used to form hyperbranched polymers from both small organic molecules and polymeric chains bearing an alkyne and a thiol. The UV-catalyzed reaction is fast, forming high-molecular-weight polymers after 20 min of UV irradiation. Hyperbranched polymers made by the thiol−yne reaction have the potential to serve as new materials for a variety of applications from catalytic support and drug delivery to viscosity modification.
ACS Publications
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