Conducting polymers are commonly used materials in chemical and biological sensors. These materials possess receptor as well as transducer functions [1]. Typical examples of conducting polymers (CPs) include polythiophenes, polypyrroles, polyanilines, and polyphenylenes. Such polymers show some intrinsic receptor properties towards analytes that can react/interact with the polymer, like, for example, redox active or acidic/basic gases. Oxidation/reduction and in some cases protonation/ deprotonation introduces/removes charge carriers in the conjugated backbone, whereas conformational changes alter the planarity of the conjugated backbone, which leads to changes in the mobility of the charge carriers. Figure 12.1 demonstrates the example of PANI (polyaniline), showing the influence of redox potential and pH on the interconversion between the different forms of PANI.These changes can be detected by in situ resistance, UV-vis, IR, or fluorescence measurements. Direct interactions with the p-system often produce very large signal changes; however, they are quite non-specific. A possible way to introduce some selectivity in these polymers is to modify their conjugated backbone with receptors.Usually, receptors can be introduced into a polymer backbone either after polymerization or directly to monomer, which is polymerized or copolymerized. The synthetic availability and the ability to polymerize the monomer under certain conditions are the most common limitations in the choice of a derivative with receptor group. Some classes of these receptors are discussed in Section 12.4. Doping of CPs by counter ions bearing the required receptor [2-8], the inclusion of ionophores into the polymer matrix [9], and the chemical linkage of ligands or receptor units to the polymer backbone [10] are also applied to enhance the selectivity and sensitivity of CPs. Receptors attached to the p-system via some short side chain can communicate with the p-system of the polymer by, for example, electron donating/withdrawing, electrostatic interactions or by inducing conformational changes upon analyte binding. As there is no direct interaction with the polymer backbone, the signal change may be smaller, but also much more specific.
Artificial Receptors for Chemical Sensors. Edited