Oxygen bridged neutral annulenes: a novel class of materials for organic field-effect transistors
- 20 October 2011
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 48 (1) , 121-123
Abstract
New, neutral, meso-substituted tetraoxa[22]annulene[2,1,2,1] aromatic macrocycles are synthesised and disclosed as new p-type semiconductors with reproducible bulk-like carrier mobility (as high as 0.40 cm2 V−1 s−1) on highly crystalline thin films deposited on octadecyltrichlorosilane modified SiO2.Keywords
This publication has 16 references indexed in Scilit:
- Towards “green” electronic materials. α-Oligofurans as semiconductorsChemical Communications, 2010
- New sulfur bridged neutral annulenes. Structure, physical properties and applications in organic field-effect transistorsChemical Communications, 2010
- The photophysical properties of expanded porphyrins: relationships between aromaticity, molecular geometry and non-linear optical propertiesChemical Communications, 2008
- Tetrathia[22]annulene[2,1,2,1]: physical properties, crystal structure and application in organic field-effect transistorsJournal of Materials Chemistry, 2007
- Porphycenes: synthesis and derivativesChemical Society Reviews, 2007
- Synthetic Expanded Porphyrin ChemistryAngewandte Chemie International Edition, 2003
- Tetra-phenyl porphyrin based thin film transistorsSynthetic Metals, 2003
- Effect of Molecular Orientation of Epitaxially Grown Platinum(II) Octaethyl Porphyrin Films on the Performance of Field‐Effect TransistorsAdvanced Materials, 2003
- Organic field-effect transistors with high mobility based on copper phthalocyanineApplied Physics Letters, 1996
- Five redox stages of tetraoxaporphyrin: a UV/visible/near-IR, ESR, and MO theoretical studyJournal of the American Chemical Society, 1992