Polymer Brushes via Surface-Initiated Polymerization catalysts in the final polymer brushes might have undesirable consequences for applications, such as in the biomedical or electronic industry. However, some methods, in particular A(R)GET ATRP, have been developed that allow to reduce the amount of copper to the level of a few ppm. 72
Surface-Initiated Reversible-Addition Fragmentation Chain Transfer (SI-RAFT) PolymerizationIn contrast to ATRP, where the equilibrium between the dormant and active, propagating chains is based on reversible termination, reversible-addition fragmentation chain transfer (RAFT) polymerization is based on reversible chain transfer. [114][115][116] A distinct advantage of RAFT polymerization is its relative simplicity and versatility, since conventional free radical polymerizations can be readily converted into a RAFT process by adding an appropriate RAFT agent, such as a dithioester, dithiocarbamate, or trithiocarbonate compound, while other reaction parameters, such as monomer, initiator, solvent, and temperature, can be kept constant. RAFT polymerization has also been successfully used to prepare polymer brushes via surface-initiated polymerization. SI-RAFT can be performed using two different strategies, which use either surface-immobilized conventional free radical initiators or surface-immobilized RAFT agents (Scheme 2). These two different strategies will be discussed in more detail in the following paragraphs.
The pH-induced swelling and collapse of surface-tethered, weak polyelectrolyte brushes is of interest for the development of actuators or to allow pH controlled transport or adsorption. This contribution discusses results of an extensive series of quartz crystal microbalance (QCM) experiments that aimed at (i) further understanding the influence of brush thickness and density on the pH responsiveness of poly(methacrylic acid) (PMAA) brushes and (ii) developing strategies that allow one to engineer the pH responsiveness and dynamic response range of PMAA based brushes. It was observed that, due to their high grafting density, the apparent pK(a) of surface-tethered PMAA differs from that of the corresponding free polymer in solution and also covers a broader pH range. The pK(a) of the PMAA brushes was found to depend on both brush thickness and density; thicker brushes showed a higher pK(a) value, and brushes of higher density started to swell at higher pH. The second part of the paper demonstrates the feasibility of the N-hydroxysuccinimide-mediated post-polymerization modification to engineer the pH responsiveness of the PMAA brushes. By using appropriate amine functionalized acids, it was possible to tune both the pH of maximum response as well as the dynamic response range of these PMAA based polyelectrolyte brushes.
Benzo‐15‐crown‐5 functionalized polymer brushes prepared via surface‐initiated atom transfer radical polymerization are used as the active layer in a potassium‐selective quartz crystal microbalance sensor. The polymer brushes allow the selective detection of potassium ions, even in the presence of a large excess of sodium ions and the sensitivity of the sensor can be tuned by varying the brush thickness.
In this review, we provide a bird's eye view of recent developments in the field of pressure-sensitive adhesives (PSAs) derived from renewable monomeric building blocks. This emerging research field has been driven by increasing sustainability requirements in the adhesive industry and bridges the gap existing between highly optimized petroleum-based synthetic PSA systems, which display superior performance but lack biobased content, and historical PSAs derived from naturally occurring biopolymers (e.g., starch and natural rubber), which provide more environmentally friendly bonding solutions but have inherent technical limitations that prevent their more widespread implementation in today's technically demanding applications. We critically reviewed a representative (and exhaustive) survey of recent synthetic approaches to the development of biobased PSAs from the academic (articles) and industrial (patents) literature categorized in two families: chain-growth and step-growth polymerization routes. Finally, we draw a parallel between renewable synthetic PSAs and nature's selfadhesive glues, highlighting how the synergy between green chemistry and biomimetic concepts could inspire the emergence of a new generation of smart, synthetic, biobased PSAs with differentiated properties that approach the ones that are found in the natural world and with a wide spectrum of potential applications in the industrial and medical sectors.
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