| Literature DB >> 20540511 |
Scott R Burks1, Mallory A Makowsky, Zachary A Yaffe, Chad Hoggle, Pei Tsai, Sukumaran Muralidharan, Michael K Bowman, Joseph P Y Kao, Gerald M Rosen.
Abstract
Nitroxides with narrow linewidths are essential for low-frequency EPR spectroscopy and in vivo EPR imaging. In developing a framework for designing narrow-line nitroxides, we sought to understand the unexpectedly narrow line width of 4-oxo-2,2,6,6-tetramethyl-1-piperidinyloxyl (5). Computational modeling revealed that the carbonyl double bond in the 4-position allows conformational diversity that results in the observed narrowing of the EPR spectral line. In view of this finding, we synthesized two new nitroxides bearing an exocyclic double bond: 4-methoxycarbonylmethylidene-2,2,6,6-tetramethyl-1-piperidinyloxyl (7) and 4-acetoxymethoxycarbonylmethylidene-2,2,6,6-tetramethyl-1-piperidinyloxyl (9). These nitroxides, like nitroxide 5, exhibited narrow linewidths-consistent with the results of modeling. Nitroxide 8 (4-carboxymethylidene-2,2,6,6-tetramethyl-1-piperidinyloxyl), as a prototype, allows for a variety of structural diversity, such as nitroxide 9,that can, for instance, target tissue compartments for in vivo EPR imaging.Entities:
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Year: 2010 PMID: 20540511 PMCID: PMC2914483 DOI: 10.1021/jo1005747
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354