Abstract

Dynamic Covalent Chemistry, consisting in the use of dynamic covalent bonds (DCBs) to create complex objects by working at the thermodynamic equilibrium, has undeniable advantages for the preparation of conjugated systems with tailored optoelectronic properties for organic electronics. Chemists can combine simple building blocks with simple functional groups of appropriate geometry, structure and stoichiometry to build multidimensional conjugated architectures. Dynamic covalent reactions are often precious metal‐free, generate little to no side products and are very efficient. DCBs however afford sensitive materials, and consequently a balance needs to be found between the ease of synthesis, the stability and the performances. The dynamicity of the target materials hence can considerably reduce their applicability in organic electronics where strongly stable materials are needed, but opens the door to stimuli‐responsive behaviour and recyclability. A way to overcome dynamicity issues is to lock DCBs, but often at the cost of decreased conjugation. In this review, we will highlight how DCBs are employed to prepare functional optoelectronically active materials, such as discrete molecules, polymers or covalent organic frameworks, applied in fields ranging from organic light‐emitting diodes and solar cells to organic batteries and transistors. We will also discuss their limitations, benefits and  current challenges to overcome.

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