Format

Send to

Choose Destination
See comment in PubMed Commons below
Adv Mater. 2013 Jan 18;25(3):405-9. doi: 10.1002/adma.201201583. Epub 2012 Aug 20.

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

Author information

1
Department of Chemistry, Nano-Science Center, University of Copenhagen & Sino-Danish Centre for Education and Research (SDC), Universitetsparken 5, DK-2100 Copenhagen Ø, Denmark.

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.

PMID:
22903744
DOI:
10.1002/adma.201201583
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Wiley
    Loading ...
    Support Center