This work was supported by EPSRC. We thank Johannes K. Sprafke for preliminary experiments on the synthesis of the template, and the EPSRC Mass Spectrometry Service (Swansea) for mass spectra.
Communication
Enhanced π Conjugation around a Porphyrin[6] Nanoring†
Article first published online: 28 MAY 2008
DOI: 10.1002/anie.200801188
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Hoffmann, M., Kärnbratt, J., Chang, M.-H., Herz, Laura M., Albinsson, B. and Anderson, Harry L. (2008), Enhanced π Conjugation around a Porphyrin[6] Nanoring. Angew. Chem. Int. Ed., 47: 4993–4996. doi: 10.1002/anie.200801188
- †
Publication History
- Issue published online: 16 JUN 2008
- Article first published online: 28 MAY 2008
- Manuscript Revised: 26 APR 2008
- Manuscript Received: 12 MAR 2008
Funded by
- EPSRC
Keywords:
- conjugation;
- molecular electronics;
- porphyrinoids;
- self-assembly;
- template synthesis

Strong cycle: The cyclic hexamer–template complex 3 obtained through template-directed trimerization of a porphyrin dimer 2, using a hexapyridyl template 1, is extremely stable (Kf=7×1038 M−1), but the free macrocycle 4 can be liberated using amine ligands. Spectroscopic data and DFT calculations show that the cyclic hexamer is more conjugated than its linear analogue.

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