Halogen bonds in 2D supramolecular self-assembly of organic semiconductors


Autoria(s): Gutzler, Rico; Fu, Chaoying; Dadvand, Afshin; Hua, Yun; MacLeod, Jennifer M.; Rosei, Federico; Perepichka, Dmitrii F.
Data(s)

13/09/2012

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

http://eprints.qut.edu.au/89956/

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