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Facile Strategy to Well-Defined Water-Soluble Boronic Acid (Co)polymers

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TLDR
The pinacol ester derivatized (co)polymers were easily deprotected by a mild and convenient strategy to yield free boronic acid polymers.
Abstract
A facile route to well-defined boronic acid (co)polymers from stable and easily manipulated boronic ester monomers is presented. The polymerization of 4-pinacolatoborylstyrene by reversible addition−fragmentation chain transfer (RAFT) yielded polymeric boronic acid precursors. Selection of stoichiometry allowed tuning of polymerization kinetics and targeting specific molecular weights in the range of Mn = 17000−32000 g/mol. The resulting low polydispersity poly(4-pinacolatoborylstyrene) homopolymers were employed as macro-chain transfer agents for block copolymerization with N,N-dimethylacrylamide to yield amphiphilic block copolymers that formed micelles in aqueous media. The pinacol ester derivatized (co)polymers were easily deprotected by a mild and convenient strategy to yield free boronic acid polymers

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Future perspectives and recent advances in stimuli-responsive materials

TL;DR: It is the goal to emphasize underutilized adaptive behaviors of stimuli-responsive polymers so that novel applications and new generations of smart materials can be realized.
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Advances in the Synthesis of Organoborane Polymers for Optical, Electronic, and Sensory Applications

TL;DR: The past decade has witnessed renewed interest and numerous unexpected discoveries in the area of main group organometallic chemistry, and unusual bonding modes have been uncovered and new materials have been developed and new applications are being pursued.
Journal ArticleDOI

Bioapplications of RAFT polymerization.

TL;DR: The control of molecular weight and molecular weight distribution has enabled access to complex architectures and site specific functionality that were previously impossible to achieve via traditional free radical polymerizations.
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Synthesis of functional polymers by post-polymerization modification.

TL;DR: This Review surveys different classes of reactive polymer precursors bearing chemoselective handles and discusses issues related to the preparation of these reactive polymers by direct polymerization of appropriately functionalized monomers as well as the post-polymerization modification of these precursor into functional polymers.
References
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Journal ArticleDOI

Living free-radical polymerization by reversible addition - Fragmentation chain transfer: The RAFT process

TL;DR: The authors proposed a reversible additive-fragmentation chain transfer (RAFT) method for living free-radical polymerization, which can be used with a wide range of monomers and reaction conditions and in each case it provides controlled molecular weight polymers with very narrow polydispersities.
BookDOI

Handbook of radical polymerization

TL;DR: Krzysztof Matyjaszewski and Thomas P. Davis as discussed by the authors discussed the fundamental concepts and history of living radical polymers and their application in industrial applications and processes.
Journal ArticleDOI

Reversible addition–fragmentation chain transfer (RAFT) radical polymerization and the synthesis of water-soluble (co)polymers under homogeneous conditions in organic and aqueous media

TL;DR: The applicability of reversible addition-fragmentation chain transfer (RAFT) radical polymerization to the synthesis of water-soluble/dispersible (co) polymers under homogeneous reaction conditions in both aqueous and organic media is discussed in this paper.
Journal ArticleDOI

Synthesis and volume phase transitions of glucose-sensitive microgels.

TL;DR: The effects of pH, ionic strength, and PBA content on the glucose sensitivity of the P(NIPAM-PBA) microgels were investigated.
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