Chemical reactions may be triggered by light at room temperature. This effect was used by KIT scientists to specifically link molecules to defined polymer chains under light. “In many conventional processes, polymer chains of variable length are produced. The building blocks are arranged randomly along the chain,” says Professor Christopher Barner-Kowollik of the KIT Institute for Chemical Technology and Polymer Chemistry (ITCP). “We wanted to develop a light-induced method for polymer structuring, which reaches the precision of nature,” the Holder of the Chair for Preparative Macromolecular Chemistry adds. The models in nature, e.g. proteins, have an exactly defined structure. The new, light-induced synthesis method allows for customized molecule design, with the building blocks being arranged at the positions desired similar to a string of colored pearls.
“By controlling the structure of the molecule, the so-called sequence, properties of macromolecules can be controlled,” Barner-Kowollik says. “Sequence-defined polymers might also be used as molecular data and information storage systems.” Information might be encoded by the sequence of monomers, similar to the genetic information of the DNA.
The team of Barner-Kowollik now presents the new light-induced and highly precise polymerization method in Nature Communications under the heading of “Coding and Decoding Libraries of Sequence Defined Functional Copolymers Synthesized via Photoligation.” The developers expect the fundamental method to become a tool for chemists, biologists, and materials scientists and to be the key to future macromolecular chemistry.
The new method was developed under the Collaborative Research Center 1176 “Molecular Structuring of Soft Matter” which is funded by the German Research Foundation (DFG) and coordinated by KIT. For the first four years, a budget of EUR 9 million is available to the Collaborative Research Center that started in January 2016.