The Key Role of Side Chain Linkage in Structure Formation and Mixed Conduction of Ethylene Glycol Substituted Polythiophenes.

Functionalizing conjugated polymers with polar ethylene glycol side chains enables enhanced swelling and facilitates ion transport in addition to electronic transport in such systems. Here, we investigate three polythiophene homopolymers (P3MEET, P3MEEMT, and P3MEEET) having differently linked (without spacer and with methyl and ethyl spacer, respectively) diethylene glycol side chains. All the polymers were tested in organic electrochemical transistors (OECTs). They show drastic differences in the device performance. The highest µOECT C* product of 11.5 F/cm·V·s was obtained for ethyl-spaced P3MEEET. How the injection and transport of ions is influenced by the side-chain linkage was studied with electrochemical impedance spectroscopy, which shows a dramatic increase in volumetric capacitance from 80 ± 9 up to 242 ± 17 F/cm3 on going from P3MEET to P3MEEET. Thus, ethyl-spaced P3MEEET exhibits one of the highest reported volumetric capacitance values among p-type polymers. Moreover, P3MEEET exhibits in dry thin films an organic field-effect transistor (OFET) hole mobility of 0.005 cm2/V·s, highest among the three, which is one order of magnitude higher than that for P3MEEMT. The extracted hole mobility from OECT (oxidized swollen state) and the hole mobility in solid-state thin films (OFET) show contradictory trends for P3MEEMT and P3MEEET. In order to understand exactly the properties in the hydrated and dry states, the crystal structure of the polymers was investigated with wide-angle X-ray scattering (WAXS) and grazing incidence WAXS, and the water uptake under applied potential was monitored using electrochemical quartz crystal microbalance with dissipation monitoring (E-QCMD). These measurements reveal an amorphous state for P3MEET and a semicrystalline state for P3MEEMT and P3MEEEET. On the other hand, E-QCMD confirms that P3MEEET swells 10 times more than P3MEEMT in the oxidized state. Thus, the importance of the ethyl spacer toward crystallinity and mixed-conduction properties was clearly demonstrated, emphasizing the impact of side chain linkage of diethylene glycol. This detailed study offers a better understanding of how to design high-performance organic mixed conductors.

Principles of Structural Design of Conjugated Polymers Showing Excellent Charge Transport toward Thermoelectrics and Bioelectronics Applications.

Conjugated polymers, especially their second generation with a donor-acceptor alternating structure, have promising properties. These are suitable for two emerging fields, thermoelectrics and bioelectronics, if appropriate structural designs are implemented. This review aims to give a perspective for the potential and challenges of novel conjugated polymers in such applications. In particular, the aspects of synthetic design and the consequences of modifications of the chemical structure on the charge transport in selected second-generation conjugated polymers are reviewed. By understanding the effects of structural motifs on the overall material properties, polymers can be specifically tailored for the respective application. The basics of charge transport measurements are briefly summarized, as the charge transport plays an important role for thermoelectrics as well as for bioelectronics. In particular, the correlation between the reported charge carrier mobility values and the structural design of the polymers is reviewed. Examples of the application of second-generation conducting polymers in thermoelectrics and bioelectronics are shown to demonstrate the current state of research. Finally, the prospect of a purposeful design of new materials for these two emerging fields is discussed.

Functional Brush Poly(2-ethyl-2-oxazine)s: Synthesis by CROP and RAFT, Thermoresponsiveness and Grafting onto Iron Oxide Nanoparticles.

Brush polymers are highly functional polymeric materials combining the properties of different polymer classes and have found numerous applications, for example, in nanomedicine. Here, the synthesis of functional phosphonate-ester-bearing brush polymers based on poly(2-oxazine)s is reported through a combination of cationic ring-opening polymerization (CROP) of 2-ethyl-2-oxazine and reversible addition-fragmentation chain transfer (RAFT) polymerization. In this way, a small library of well-defined (D ≤ 1.17) poly(oligo(2-ethyl-2-oxazine) methacrylate) P(OEtOzMA)n brushes with tunable lower critical solution temperature (LCST) behavior and negligible cell toxicity is prepared. Upon deprotection, the phosphonic acid end-group of the P(OEtOzMA)n brush enables the successful grafting-onto iron oxide nanoparticles (IONPs). Colloidal stability of the particle suspension in combination with suitable magnetic resonance imaging (MRI) relaxivities demonstrates the potential of these particles for future applications as negative MRI contrast agents.