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New strategies for the design and synthesis of novel covalent organic frameworks (COFs) and related materials

Subject Area Solid State and Surface Chemistry, Material Synthesis
Term from 2014 to 2016
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 265423569
 
Final Report Year 2017

Final Report Abstract

Covalent organic frameworks (COFs) represent a vastly emerging class of two- and three dimensional organic materials and have inspired the imagination of researchers due to their extra-large surface areas and very low density, resulting in many potential applications. The directionality and rigidity of organic molecular building units, joined together by covalent bonds, have made these extended nets particularly attractive from a design perspective. COFs show order with atomic precision and can therefore be modified with a versatility, unparalleled in traditional polymer materials. However, only a handful of covalent bond formation reactions have been utilized thus far in context of COFs. We herein aimed on a de-novo material design and synthesis approach involving mechanically bonded macrocyclic structures. The design and structure simulations were carried out using well known small molecules as building units and stitched them together computationally. The synthetic challenge was approached from three different pathways, including preformed building blocks, a hierarchical self-assembly strategy and a 2-step synthesis with subsequent photoreaction. We were finally able to isolate a material with a high level of complexity, given the simple reactants. A hierarchical assembly of [4+4] macrocycle into dimers, and subsequent crystallization, produced a compound with square nanopores. The crystal structure of these materials is strongly dependent on the packing of the dimers in ABAB or related fashion.

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