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Cammidge, Andrew N. 
ORCID: https://orcid.org/0000-0001-7912-4310, Goddard, Victoria H. M., Will, Geoffrey, Arnold, Dennis P. and Cook, Michael J.
(2009)
Mixed cyclisations giving phthalocyanine–naphthalocyanine hybrids.
Tetrahedron Letters, 50 (25).
pp. 3013-3016.
Abstract
Mixed cyclisations have been performed to give phthalocyanine–naphthalocyanine hybrids bearing solubilising substituents. Reactivity differences between the two phthalonitrile precursors result in inefficient mixed-macrocyclisation under standard, non-templating conditions leading to predominant formation of symmetrical phthalocyanine. Templated mixed-macrocyclisation leads to the hybrids. However, the reaction proceeds with unexpected selectivity with only one of the possible 2:2 products observed.
| Item Type: | Article |
|---|---|
| Faculty \ School: | Faculty of Science > School of Chemistry (former - to 2024) Faculty of Science > School of Chemical Sciences and Pharmacy (former - to 2009) |
| UEA Research Groups: | Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Materials and Catalysis Faculty of Science > Research Groups > Chemistry of Light and Energy |
| Depositing User: | Rachel Smith |
| Date Deposited: | 22 Mar 2011 13:32 |
| Last Modified: | 24 Sep 2024 09:19 |
| URI: | https://ueaeprints.uea.ac.uk/id/eprint/26871 |
| DOI: | 10.1016/j.tetlet.2009.03.193 |
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