Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation

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Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation. / Tochwin, Anna; El-Betany, Alaa; Tai, Hongyun et al.
In: Polymer, 13.09.2017.

Research output: Contribution to journalArticlepeer-review

HarvardHarvard

Tochwin, A, El-Betany, A, Tai, H, Chan, K, Blackburn, C & Wang, W 2017, 'Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation', Polymer.

APA

Tochwin, A., El-Betany, A., Tai, H., Chan, K., Blackburn, C., & Wang, W. (2017). Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation. Polymer.

CBE

Tochwin A, El-Betany A, Tai H, Chan K, Blackburn C, Wang W. 2017. Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation. Polymer.

MLA

VancouverVancouver

Tochwin A, El-Betany A, Tai H, Chan K, Blackburn C, Wang W. Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation. Polymer. 2017 Sept 13.

Author

Tochwin, Anna ; El-Betany, Alaa ; Tai, Hongyun et al. / Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation. In: Polymer. 2017.

RIS

TY - JOUR

T1 - Thermoresponsive and Reducible Hyperbranched Polymers Synthesized by RAFT Polymerisation

AU - Tochwin, Anna

AU - El-Betany, Alaa

AU - Tai, Hongyun

AU - Chan, Kai

AU - Blackburn, Chester

AU - Wang, Wenxin

PY - 2017/9/13

Y1 - 2017/9/13

N2 - Abstract: Here, we report the synthesis of new thermoresponsive hyperbranched polymers (HBPs) via one-pot reversible addition-fragmentation chain transfer (RAFT) copolymerisation of poly(ethylene glycol)methyl ether methacrylate (PEGMEMA, Mn = 475 g/mol), poly(propylene glycol)methacrylate (PPGMA, Mn = 375 g/mol), and disulfide diacrylate (DSDA) using 2-cyanoprop-2-yl dithiobenzoate as a RAFT agent. DSDA was used as the branching agent and to afford the HBPs with reducible disulfide groups. The resulting HBPs were characterised by Nuclear Magnetic Resonance Spectroscopy (NMR) and Gel Permeation Chromatography (GPC). Differential Scanning Calorimetry (DSC) was used to determine lower critical solution temperatures (LCSTs) of these copolymers, which are in the range of 17–57 °C. Moreover, the studies on the reducibility of HBPs and swelling behaviours of hydrogels synthesized from these HBPs were conducted. The results demonstrated that we have successfully synthesized hyperbranched polymers with desired dual responsive (thermal and reducible) and crosslinkable (via thiol-ene click chemistry) properties. In addition, these new HBPs carry the multiplicity of reactive functionalities, such as RAFT agent moieties and multivinyl functional groups, which can afford them with the capacity for further bioconjugation and structure modifications.

AB - Abstract: Here, we report the synthesis of new thermoresponsive hyperbranched polymers (HBPs) via one-pot reversible addition-fragmentation chain transfer (RAFT) copolymerisation of poly(ethylene glycol)methyl ether methacrylate (PEGMEMA, Mn = 475 g/mol), poly(propylene glycol)methacrylate (PPGMA, Mn = 375 g/mol), and disulfide diacrylate (DSDA) using 2-cyanoprop-2-yl dithiobenzoate as a RAFT agent. DSDA was used as the branching agent and to afford the HBPs with reducible disulfide groups. The resulting HBPs were characterised by Nuclear Magnetic Resonance Spectroscopy (NMR) and Gel Permeation Chromatography (GPC). Differential Scanning Calorimetry (DSC) was used to determine lower critical solution temperatures (LCSTs) of these copolymers, which are in the range of 17–57 °C. Moreover, the studies on the reducibility of HBPs and swelling behaviours of hydrogels synthesized from these HBPs were conducted. The results demonstrated that we have successfully synthesized hyperbranched polymers with desired dual responsive (thermal and reducible) and crosslinkable (via thiol-ene click chemistry) properties. In addition, these new HBPs carry the multiplicity of reactive functionalities, such as RAFT agent moieties and multivinyl functional groups, which can afford them with the capacity for further bioconjugation and structure modifications.

M3 - Article

JO - Polymer

JF - Polymer

SN - 0032-3861

ER -