Exploring RAFT polymerization for the synthesis of bipolar diblock copolymers and their supramolecular self-assembly
Literature Information
Joseph P. Patterson, Saghar Khodabakhsh, Rachel K. O'Reilly
Until recently, the primary controlled radical polymerization (CRP) technique used to synthesize side chain semi-conducting block copolymers from vinyl monomer species has been nitroxide-mediated polymerization (NMP). The potential exploitation of reversible addition fragmentation chain transfer (RAFT) polymerization for the preparation of semi-conducting diblocks has not yet been fully realized. In this work a trithiocarbonate chain transfer agent (CTA) has been shown to polymerize both hole transporting (HT) monomers m-vinyltriphenyl amine and p-vinyltriphenyl amine and also a new fluorinated triphenylamine monomer for the first time, affording both homopolymers and diblock copolymers with good control over molecular weight (Mn) and narrow polydispersities (Mw/Mn). The electronic properties of these blocks and diblocks were explored using UV-vis and cyclic voltammetry analysis. The selective self-assembly of these diblocks into solution nanostructures has been explored and characterized by DLS and TEM analysis.
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![(2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure (2E)-4-[(1R,2S,8R,19S,21R)-14-Hydroxy-11-isopropenyl-8,23,23-trimethyl-5-(3-methyl-2-buten-1-yl)-16,20-dioxo-3,7,22-trioxaheptacyclo[17.4.1.1~8,12~.0~2,17~.0~2,21~.0~4,15~.0~6,13~]pentacosa-4(15),5,13
,17-tetraen-21-yl]-2-methyl-2-butenoic acid structure](https://static.chemtradehub.com/structs/173/173867-04-4-d2d3.webp)
![4-[(2,4-Dihydroxyphenyl)diazenyl]-5-hydroxy-2,7-naphthalenedisulfonic acid structure 4-[(2,4-Dihydroxyphenyl)diazenyl]-5-hydroxy-2,7-naphthalenedisulfonic acid structure](https://static.chemtradehub.com/structs/362/3627-01-8-79ac.webp)