Wu Ting, Fitchett Christopher M, Downard Alison J
School of Physical and Chemical Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand.
Langmuir. 2021 Sep 28;37(38):11397-11405. doi: 10.1021/acs.langmuir.1c02012. Epub 2021 Sep 14.
A new coupling reaction, the -fluoro-thiol (PFT) reaction, activated by base at room temperature, is reported for carbon surface functionalization. 4-Nitrothiophenol (4-NTP) and (3-nitrobenzyl)mercaptan (3-NBM) were coupled to pentafluorophenyl (F-Ph) anchor layers grafted from the aryldiazonium ion formed . The relative yields of the PFT reactions, estimated from the electrochemical responses of coupled nitrophenyl (NP) and nitrobenzyl (NB) groups, depended on the nucleophilicity of the thiolate and the strength of the base. The highest surface concentration (4.6 × 10 mol cm) was obtained using 3-NBM in the presence of [BuN]OH; this concentration corresponds to the maximum that is typically achieved for other high-yielding coupling reactions at aryldiazonium ion anchor layers. The PFT reaction is expected to be applicable to the numerous thiol derivatives commonly restricted to self-assembled monolayer (SAM) formation at gold and other noble metals, thereby opening a simple new approach for interface design on carbon substrates. The strategy may also have advantages for modification of gold surfaces: the layer prepared by coupling 3-NBM to F-Ph films on gold was found to be more stable to storage under ambient conditions than self-assembled monolayers of 3-NBM.
