Face-on vs. edge-on: tuning the structure of tetrathiafulvalene monolayers with solvent
Author:
Affiliation:
1. Institut National de la Recherche Scientifique (INRS) EMT Center – 1650 Boul. Lionel Boulet
2. Varennes J3X 1S2
3. Canada
4. Department of Chemistry
5. McGill University
6. Montreal
Abstract
Molecular orientation and supramolecular structure of tetrathiafulvalene derivative on graphite can be controlled by the change of deposition solvent, as revealed by scanning probe microscopy study.
Funder
Fonds de Recherche du Québec - Nature et Technologies
Natural Sciences and Engineering Research Council of Canada
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/TC/C7TC05757A
Reference37 articles.
1. Tetrathiafulvalenes, Oligoacenenes, and Their Buckminsterfullerene Derivatives: The Brick and Mortar of Organic Electronics
2. Electrical conductivity by the bis(1,3-dithiole)-bis(1,3-dithiolium) system
3. Electron transfer in a new highly conducting donor-acceptor complex
4. Tetrathiafulvalenes as building blocks in supramolecular chemistry II
5. Functionalised tetrathiafulvalenes: new applications as versatile π‐electron systems in materials chemistry
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