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|Title: ||Efficient access to conjugated 4,4′-bipyridinium oligomers using the Zincke reaction: Synthesis, spectroscopic and electrochemical properties|
|Authors: ||Chen, Long|
Wedge, Christopher J.
Colquhoun, Howard M.
Greenland, Barnaby W.
|Issue Date: ||2016|
|Publisher: ||© The Authors. Published by the Royal Society of Chemistry.|
|Citation: ||CHEN, L. ...et al., 2016. Efficient access to conjugated 4,4′-bipyridinium oligomers using the Zincke reaction: Synthesis, spectroscopic and electrochemical properties. Organic and Biomolecular Chemistry, 14(3), pp. 980-988.|
|Abstract: ||The cyclocondensation reaction between rigid, electron-rich aromatic diamines and 1,1′-bis(2,4-dinitrophenyl)-4,4′-bipyridinium (Zincke) salts has been harnessed to produce a series of conjugated oligomers containing up to twelve aromatic/heterocyclic residues. These oligomers exhibit discrete, multiple redox processes accompanied by dramatic changes in electronic absorption spectra.|
|Description: ||This is an Open Access Article. It is published by Royal Society of Chemistry under the Creative Commons Attribution 3.0 Unported Licence (CC BY). Full details of this licence are available at: http://creativecommons.org/licenses/by/3.0/|
|Publisher Link: ||http://dx.doi.org/10.1039/c5ob02211h|
|Appears in Collections:||Published Articles (Materials)|
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