Accessing New Materials through Polymerization and Modification of a Polycarbonate with a Pendant Activated Ester

详细信息    查看全文

• 作者：Amanda C. Engler ; Julian M. W. Chan ; Daniel J. Coady ; Jeannette M. O鈥橞rien ; Haritz Sardon ; Alshakim Nelson ; Daniel P. Sanders ; Yi Yan Yang ; James L. Hedrick
• 刊名：Macromolecules
• 出版年：2013
• 出版时间：February 26, 2013
• 年：2013
• 卷：46
• 期：4
• 页码：1283-1290
• 全文大小：338K
• 年卷期：v.46,no.4(February 26, 2013)
• ISSN：1520-5835

文摘

Functionalized polycarbonates were synthesized by organocatalytic ring-opening polymerization (ROP) of a cyclic monomer with a pendant activated ester (MTC-OC₆F₅) followed by a postpolymerization modification with both small molecules and macromolecules. Controlled ROP to form homopolymers and diblock copolymers was realized using catalytic quantities of triflic acid. For the homopolymers, a linear relationship between [M]₀/[I]₀ and molecular weight (by GPC) demonstrated the living nature of the polymerization. Poly(MTC-OC₆F₅) was functionalized under mild reaction conditions with a variety of amines to obtain polymers with pendant primary, secondary, and tertiary amides. Graft polymers with a high grafting density of over 87% were synthesized using amine-terminated poly(ethylene glycol) of two different molecular weights (2 and 5 kDa). The preparation of poly(MTC-OC₆F₅) provides a means of accessing a wide range of functional polycarbonates with minimal synthetic steps. This new methodology for the formation of functionalized polycarbonates provides a simple and versatile platform for the synthesis of new and innovative materials.