Halogen bonds in 2D supramolecular self-assembly of organic semiconductors
Data(s) |
13/09/2012
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Resumo |
Weak interactions between bromine, sulphur, and hydrogen are shown to stabilize 2D supramolecular monolayers at the liquid–solid interface. Three different thiophene-based semiconducting organic molecules assemble into close-packed ultrathin ordered layers. A combination of scanning tunneling microscopy (STM) and density functional theory (DFT) elucidates the interactions within the monolayer. Electrostatic interactions are identified as the driving force for intermolecular Br⋯Br and Br⋯H bonding. We find that the S⋯S interactions of the 2D supramolecular layers correlate with the hole mobilities of thin film transistors of the same materials. |
Identificador | |
Publicador |
Royal Society of Chemistry |
Relação |
DOI:10.1039/C2NR31648J Gutzler, Rico, Fu, Chaoying, Dadvand, Afshin, Hua, Yun, MacLeod, Jennifer M., Rosei, Federico, & Perepichka, Dmitrii F. (2012) Halogen bonds in 2D supramolecular self-assembly of organic semiconductors. Nanoscale, 4(19), pp. 5965-5971. |
Direitos |
Copyright 2012 The Royal Society of Chemistry |
Fonte |
School of Chemistry, Physics & Mechanical Engineering; Science & Engineering Faculty |
Tipo |
Journal Article |