A new atom transfer radical polymerization initiator based on phenolphthalein for the synthesis of bis-allyloxy functionalized polystyrene macromonomers

• Published in: Polymer international 2015-03, Vol.64 (3), p.413-420
• Main Authors: Patil, Sachin S., Menon, Shamal K., Wadgaonkar, Prakash P.
• Format: Article
• Language: English
• Subjects: atom transfer radical polymerization; bis-allyloxy functionalized polystyrene; functional initiator; Initiators; Molecular weight; Molecular weight distribution; Monomers; Phenolphthalein; Polymerization; Polystyrene resins; Synthesis; thiol-ene click reaction
• ISSN: 0959-8103; 1097-0126
• DOI: 10.1002/pi.4804

A new ATRP initiator, namely, 2‐(1,1‐bis(4‐(allyloxy)phenyl)‐3‐oxoisoindolin‐2‐yl)ethyl 2‐bromo‐2‐methylpropanoate was conveniently synthesized starting from phenolphthalein and was utilized for the efficient synthesis of well‐defined α, α'‐bisallyloxy functionalised polystyrene macromonomers. A new atom transfer radical polymerization (ATRP) initiator, namely 2‐(1,1‐bis(4‐(allyloxy)phenyl)‐3‐oxoisoindolin‐2‐yl)ethyl 2‐bromo‐2‐methylpropanoate, was synthesized starting from phenolphthalein, a commercially available and an inexpensive chemical. Well‐ defined bis‐allyloxy functionalized polystyrene macromonomers (Mn,GPC 4800–11 700 g mol−1) with controlled molecular weight and narrow molecular weight distribution (1.05–1.09) were synthesized using ATRP by varying the monomer to initiator feed ratio. The presence of allyloxy functionality on polystyrene was confirmed by Fourier transform infrared and 1H NMR spectroscopy. A kinetic study of polymerization revealed pseudo‐first‐order kinetics with respect to monomer consumption. Initiator efficiency was found to be in the range 0.80–0.95. Matrix‐assisted laser desorption ionization time of flight spectra showed a narrow molecular weight distribution with control over the molecular weight. The reactivity of the allyloxy groups on polystyrene was successfully demonstrated by quantitative photochemical thiol‐ene click reaction with benzyl mercaptan as the model thiol reagent. Furthermore, the thiol‐ene click reaction was exploited to introduce other reactive functional groups such as hydroxyl and carboxyl by reaction of α,α′‐bis‐allyloxy functionalized polystyrene with 2‐mercaptoethanol and 3‐mercaptopropionic acid, respectively. © 2014 Society of Chemical Industry