| Literature DB >> 26014854 |
Asish Pal1, Morteza Malakoutikhah1,2, Giulia Leonetti1, Meniz Tezcan1, Mathieu Colomb-Delsuc1, Van Duc Nguyen3, Jasper van der Gucht4, Sijbren Otto5.
Abstract
Directing self-assembly processes out-of-equilibrium to yield kinetically trapped materials with well-defined dimensions remains a considerable challenge. Kinetically controlled assembly of self-synthesizing peptide-functionalized macrocycles through a nucleation-growth mechanism is reported. Spontaneous fiber formation in this system is effectively shut down as most of the material is diverted into metastable non-assembling trimeric and tetrameric macrocycles. However, upon adding seeds to this mixture, well-defined fibers with controllable lengths and narrow polydispersities are obtained. This seeded growth strategy also allows access to supramolecular triblock copolymers. The resulting noncovalent assemblies can be further stabilized through covalent capture. Taken together, these results show that self-synthesizing materials, through their interplay between dynamic covalent bonds and noncovalent interactions, are uniquely suited for out-of-equilibrium self-assembly.Entities:
Keywords: block co-fibers; dynamic covalent chemistry; nucleation and growth; self-replication; systems chemistry
Year: 2015 PMID: 26014854 DOI: 10.1002/anie.201501965
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336