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Abstract
The synthesis of rigid symmetric polyradical model systems with inter-spin distances between 1.4 and 4 nm and their room temperature continuous wave (CW) EPR spectra are reported. Conditions for attachment of the spin-label via esterification have been optimized on the direct synthesis of polyradicals from commercially available polyphenols and the carboxylic acid functionalized nitroxide TPC. A common synthetic protocol utilizing 4-hydroxy-4′-iodobiphenyl as a key building block has been used to synthesize an equilateral biradical and a triradical in only two steps from commercially available starting materials. The first synthesis of a tetraradical based upon an adamantane core bearing six equivalent nitroxide–nitroxide distances is also reported. These systems are very promising candidates for studying multi-spin effects in pulsed EPR distance measurements.
Original language | English |
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Pages (from-to) | 8313–8323 |
Number of pages | 11 |
Journal | The Journal of Organic Chemistry |
Volume | 79 |
Issue number | 17 |
Early online date | 7 Aug 2014 |
DOIs | |
Publication status | Published - 20 Aug 2014 |
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