Loading…
The mechanochemical Scholl reaction - a solvent-free and versatile graphitization tool
Herein, we report on the mechanochemical Scholl reaction of dendritic oligophenylene precursors to produce benchmark nanographenes such as hexa- peri -hexabenzocoronene (HBC), triangular shaped C 60 and expanded C 222 under solvent-free conditions. The solvent-free approach overcomes the bottleneck...
Saved in:
Published in: | Chemical communications (Cambridge, England) England), 2018, Vol.54 (42), p.537-531 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Herein, we report on the mechanochemical Scholl reaction of dendritic oligophenylene precursors to produce benchmark nanographenes such as hexa-
peri
-hexabenzocoronene (HBC), triangular shaped C
60
and expanded C
222
under solvent-free conditions. The solvent-free approach overcomes the bottleneck of solubility limitation in this well-known and powerful reaction. The mechanochemical approach allows tracking the reaction process by
in situ
pressure measurements. The quality of produced nanographenes has been confirmed by MALDI-TOF mass spectrometry and UV-Vis absorption spectroscopy. This approach paves the way towards gram scale and environmentally benign synthesis of extended nanographenes and possibly graphene nanoribbons suitable for application in carbon based electronics or energy applications.
Ball milling was applied to a Scholl reaction of dendritic oligophenylene precursors to produce benchmark nanographenes under solvent-free conditions. |
---|---|
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c8cc01993b |