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Challenges in chelating positron emitting copper isotopes: tailored synthesis of unsymmetric chelators to form ultra stable complexes

Silversides, Jon D.; Smith, Rachel; Archibald, Stephen J.

Authors

Jon D. Silversides

Rachel Smith



Abstract

The synthesis of chelators that form high stability complexes with copper(II) isotopes and do not suffer from transchelation in vivo has been a goal for many chemists. Such chelators will facilitate the exploitation of the Cu-64 isotope (t(1/2) = 12.7 h, beta(+) (19%); beta(-) (39%); EC (41%)) for positron emission tomography imaging studies, which has a longer half life relative to the more commonly used F-18 (t(1/2) = 109.8 min) and C-11 (t(1/2) = 20.4 min) isotopes. One option is the CBTE2A chelator, which has been championed by Weisman, Wong and Anderson, and, more recently, alternate bifunctional chelator (BFC) versions have been synthesised. Improved synthetic methods are required for unsymmetric derivatisation of these chelators to allow more selective biomolecule attachment. This work investigates synthetic routes to form new unsymmetric chelating ligands via stepwise reaction of the bisaminal precursor, determines their X-ray structures and demonstrates cold copper(II) isotope complex formation.

Citation

Silversides, J. D., Smith, R., & Archibald, S. J. (2011). Challenges in chelating positron emitting copper isotopes: tailored synthesis of unsymmetric chelators to form ultra stable complexes. Dalton Transactions : an international journal of inorganic chemistry, 40(23), 6289-6297. https://doi.org/10.1039/c0dt01395a

Journal Article Type Article
Acceptance Date Mar 9, 2011
Online Publication Date Apr 1, 2011
Publication Date Jun 21, 2011
Deposit Date Nov 13, 2014
Journal Dalton Transactions
Print ISSN 1477-9226
Electronic ISSN 1477-9234
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 40
Issue 23
Pages 6289-6297
DOI https://doi.org/10.1039/c0dt01395a
Keywords Inorganic Chemistry
Public URL https://hull-repository.worktribe.com/output/462804