| Literature DB >> 26376768 |
Keunhong Jeong1,2, Clancy C Slack1,2, Christophoros C Vassiliou1,2, Phuong Dao1,2, Muller D Gomes1,2, Daniel J Kennedy1,2, Ashley E Truxal1,2, Lindsay J Sperling3, Matthew B Francis1,2, David E Wemmer1,4, Alexander Pines5,6.
Abstract
Recent work has shown that xenon chemical shifts in cryptophane-cage sensors are affected when tethered chelators bind to metals. Here, we explore the xenon shifts in response to a wide range of metal ions binding to diastereomeric forms of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) linked to cryptophane-A. The shifts induced by the binding of Ca(2+) , Cu(2+) , Ce(3+) , Zn(2+) , Cd(2+) , Ni(2+) , Co(2+) , Cr(2+) , Fe(3+) , and Hg(2+) are distinct. In addition, the different responses of the diastereomers for the same metal ion indicate that shifts are affected by partial folding with a correlation between the expected coordination number of the metal in the DOTA complex and the chemical shift of (129) Xe. These sensors may be used to detect and quantify many important metal ions, and a better understanding of the basis for the induced shifts could enhance future designs.Entities:
Keywords: DOTA; NMR spectroscopy; cryptophane; metal-ion sensors; xenon
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Year: 2015 PMID: 26376768 DOI: 10.1002/cphc.201500806
Source DB: PubMed Journal: Chemphyschem ISSN: 1439-4235 Impact factor: 3.102