A new class of extended tetrathiafulvalene cruciform molecules for molecular electronics with dithiafulvene-4,5-dithiolate anchoring groups

Adv Mater. 2013 Jan 18;25(3):405-9. doi: 10.1002/adma.201201583. Epub 2012 Aug 20.

Abstract

Cruciform motifs with two orthogonally oriented π-extended tetrathiafulvalenes and with differently protected thiolate end-groups are synthesized by stepwise coupling reactions. The molecules are subjected to single-molecule conductivity studies in a break-junction and to conducting probe atomic force microscopy studies in a self-assembled monolayer on gold.

Publication types

  • Research Support, Non-U.S. Gov't