Abstract
We report the synthesis and characterization of covalent organic frameworks (COFs) incorporating thiophene-based building blocks. We show that these are amenable to reticular synthesis, and that bent ditopic monomers, such as 2,5-thiophenediboronic acid, are defect-prone building blocks that are susceptible to synthetic variations during COF synthesis. The synthesis and characterization of an unusual charge transfer complex between thieno[3,2-b]thiophene-2,5-diboronic acid and tetracyanoquinodimethane enabled by the unique COF architecture is also presented. Together, these results delineate important synthetic advances toward the implementation of COFs in electronic devices.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4923-4928 |
| Number of pages | 6 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 110 |
| Issue number | 13 |
| DOIs | |
| State | Published - Mar 26 2013 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General
Keywords
- Electronic materials
- Polymers
- Porous materials