Graft copolymer synthesis grafting from polymer surfaces

A dense polymer brush is obtained using the grafting from techniques. Surface-initiated polymerization in conjunction with a living polymerization technique is one of the most useful synthetic routes for the precise design and functionalization of the surfaces of various solid materials with well-defined polymers and copolymers. Above all, surface-initiated living radical polymerization (LRP) is particularly promising due to its simplicity and versatility and it has been applied for the synthesis of Au NPs. 

Scheme 5.10 Synthesis of norbornene-functionalized MWCNTs, and the subsequent grafting polymer and block copolymer from CNT surfaces by ROMP. ...

Due to the relative ease of control, temperature is one of the most widely used external stimuli for the synthesis of stimulus-responsive bmshes. In this case, thermoresponsive polymer bmshes from poly(N-isopropylacrylamide) (PNIPAM) are the most intensively studied responsive bmshes that display a lower critical solution temperature (LOST) in a suitable solvent. Below the critical point, the polymer chains interact preferentially with the solvent and adopt a swollen, extended conformation. Above the critical point, the polymer chains collapse as they become more solvophobic. Jayachandran et reported the synthesis of PNIPAM homopolymer and block copolymer brushes on the surface of latex particles by aqueous ATRP. Urey demonstrated that PNIPAM brushes were sensitive to temperature and salt concentration. Zhu et synthesized Au-NPs stabilized with thiol-terminated PNIPAM via the grafting to approach. These thermosensitive Au-NPs exhibit a sharp, reversible, dear opaque transition in solution between 25 and 30 °C. Shan et al. prepared PNIPAM-coated Au-NPs using both grafting to and graft from approaches. Lv et al. prepared dual-sensitive polymer by reversible addition-fragmentation chain transfer (RAFT) polymerization of N-isopropylacrylamide from trithiocarbonate groups linked to dextran and sucdnoylation of dextran after polymerization. Such dextran-based dual-sensitive polymer is employed to endow Au-NPs with stability and pH and temperature sensitivity. 

While end-functional polymers are clearly important industrial products for materials synthesis, they are also interesting from an academic point of view. Many complex macromolecular architectures can be realized from end-functional polymeric starting materials. Two mono-telechelic polymers can, for example, be joined to form a diblock copolymer, or several such polymers can be joined to form star-like polymers. Mono-telechelic polymers can also be attached to a linear, multifunctional polymer to yield graft copolymers. Depending on the functional end group, such polymers can attach to macroscopic or nanoparticle surfaces or form conjugates with bio-oligomers [5] or biomacromolecules [6]. 

Recently, the investigation of polymer brushes has been focused on the synthesis of new tethered polymer systems primarily through surface-initiated polymerization (SIP). Previously, the term polymer brushes has been limited to the investigation of block copolymers (qv) or end-functional linear polymers that have been physically or chemically adsorbed to surfaces, respectively (3,4). Recent synthetic efforts using different polymerization mechanisms have resulted in the discovery of many novel properties of polymer brushes. This has been aided no less than the use of innovative and unique surface-sensitive analysis methods as applied to flat substrates and particles. The study of polymer brushes has benefited from improved dielectric, optical, spectroscopic, and microscopic characterization methods. Understanding the chemistry of these grafting reactions and how... 

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