Chalcogen bridged pyrene derivatives: Synthesis, crystal−packing structures and field effect transistors properties
Source abstract
Abstract
Abstract To explore how the different intermolecular non-covalent interactions synergistically affect the molecular packing and properties when they existed at the same molecules. A series of new pyrene derivatives with chalcogen atoms as bridges were designed and synthesized. The single crystal structures of the compounds revealed the significant effect of different intermolecular non-covalent interactions on the molecular packing. The thin film transistor devices were fabricated and exhibit high mobility over 0.04 cm2 V−1 s−1. The distinct difference of the OFETs performance suggests that the intermolecular non-covalent interactions have very important effect on gearing the molecular packing and properties.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Thin-Film Transistor Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (27)
Show source-provided references
1. Murphy · Chem. Rev. · 2007 · 107 · 106610.1021/cr0501386 ↗
2. Hu · 2013
3. Sirringhaus · Adv. Mater. · 2014 · 26 · 131910.1002/adma.201304346 ↗
4. Yan · Nature · 2009 · 457 · 67910.1038/nature07727 ↗
5. Mei · J. Am. Chem. Soc. · 2013 · 135 · 672410.1021/ja400881n ↗
6. Wang · Chem. Rev. · 2012 · 112 · 220810.1021/cr100380z ↗
7. Jiang · Nanoscale · 2010 · 2 · 265210.1039/c0nr00466a ↗
8. Figureueira-Duarte · Chem. Rev. · 2011 · 111 · 726010.1021/cr100428a ↗
9. Oh · Angew. Chem. Int. Ed. · 2009 · 48 · 252210.1002/anie.200804669 ↗
10. Zöphel · Chem. Commun. · 2011 · 47 · 696010.1039/c1cc11827g ↗
11. Bernhardt · Chem. Eur. J. · 2006 · 12 · 611710.1002/chem.200500999 ↗
12. Oh · Org. Electron. · 2009 · 10 · 16310.1016/j.orgel.2008.10.015 ↗
13. Zhang · Chem. Commun. · 2006 · 42 · 75510.1039/b515433b ↗
14. Cho · ACS Appl. Mater. Interfaces · 2013 · 5 · 385510.1021/am4005368 ↗
15. Kim · Chem. Commun. · 2011 · 47 · 890710.1039/c1cc11589h ↗
16. Li · J. Mater. Chem. · 2011 · 21 · 1766210.1039/c1jm12977e ↗
17. Wang · J. Am. Chem. Soc. · 2006 · 128 · 1305810.1021/ja064580x ↗
18. Kwon · New J. Chem. · 2012 · 36 · 181310.1039/c2nj40348j ↗
19. Kwon · New J. Chem. · 2013 · 37 · 288110.1039/c3nj00295k ↗
20. Oniwa · Chem. Commun. · 2016 · 52 · 480010.1039/C6CC00948D ↗
21. Moggia · J. Mater. Chem. · 2006 · 16 · 238010.1039/b601870j ↗
22. Huang · Cryst. Growth Des. · 2007 · 7 · 254210.1021/cg070447k ↗
23. Hotta · J. Phys. Chem. B · 2000 · 104 · 1031610.1021/jp002166s ↗
24. Würthner · Angew. Chem. Int. Ed. · 2011 · 50 · 337610.1002/anie.201002307 ↗
25. Bard · 1984
26. Dai · J. Mater. Chem. C · 2016 · 4 · 875810.1039/C6TC02601J ↗
27. Chi · Macromol. Rapid Commun. · 2005 · 26 · 153210.1002/marc.200500437 ↗