2, 2, 6, 6‐Tetramethylpiperydinyl‐1‐oxyl (TEMPO) Functionalized Benzoxazines Prepared with a One‐Pot Synthesis for Reactive/Crosslinkable Initiators of Nitroxide Mediated Polymerization. Issue 15 (5th June 2017)

• Record Type: Journal Article
• Authors: Han, Yi‐Jen; Liu, Ying‐Ling
• Is Part Of: Macromolecular rapid communications. Volume 38:Issue 15(2017)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-06-05
• Subjects: benzoxazine -- functionalization of polymers -- initiator -- living polymerization -- nitroxide mediated polymerization; Macromolecules -- Periodicals; Polymers -- Periodicals; Chemistry -- Periodicals; 547.705
• DOI: 10.1002/marc.201700078
• Languages: English
• ISSNs: 1022-1336

Abstract

Abstract : An effective approach to incorporating TEMPO groups on polymer chains in a one‐pot synthesis is demonstrated for the preparation of reactive/crosslinkable macroinitiators of nitroxide‐mediated polymerization (NMP) and the corresponding graft copolymers. Abstract : In this work, the incorporation of a 2, 2, 6, 6‐tetramethylpiperydinyl‐1‐oxyl (TEMPO) group to a benzoxazine ring is performed using a one‐pot synthesis for the preparation of TEMPO‐functionalized benzoxazine compounds and polymers as reactive and crosslinkable initiators for nitroxide‐mediated polymerization (NMP). The TEMPO‐functionalization reaction of benzoxazine, traced with 1 H NMR, is conducted with sequential radical transfer and coupling reactions. Moreover, polystyrene‐grafted polybenzoxazine copolymers are prepared with the TEMPO‐benzoxazine initiator and NMP of styrene. The polymerization system exhibits the characteristics of controlled radical polymerization, including controlled molecular weights of products and ability for sequential polymerization. Moreover, based on the chemical reactivity and crosslinking ability of benzoxazine groups, the synthesis route developed in this work will widen the scope of the design and synthesis of functional and high‐performance polymers.