Variable temperature and EPR frequency study of two aqueous Gd(III) complexes with unprecedented sharp lines

被引:35
作者
Borel, Alain [1 ]
Kang, Hoon
Gateau, Christelle
Mazzanti, Marinella
Clarkson, R. B.
Belford, R. Linn
机构
[1] Univ Illinois, Illinois EPR Res Ctr, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Vet Clin Med, Urbana, IL 61801 USA
[4] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
[5] CEA Grenoble, Serv Chim Inorgan & Biol, UMR E 3, UJF,Dept Rech Fondamentale Mat Condensee,Lab Reco, F-38054 Grenoble 09, France
关键词
D O I
10.1021/jp065445+
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present an EPR study of two Gd(III) complexes in aqueous solution at multiple temperatures and EPR frequencies. These two complexes, [Gd(TPATCN)] and [Gd(DOTAM)(H2O)](3+), display remarkably sharp lines (i.e. slow transverse electron spin relaxation) in comparison with all complexes studied in the past, especially at X-band (similar to 9.08 GHz). These unprecedented spectra even show, for the first time in solution, a distinct influence of hyperfine coupling to two magnetically active Gd isotopes (Gd-155 14.8%, I = 3/2, gamma = -0.8273 x 10(7) s(-1) T-1 and Gd-157, 15.65%, I = 3/2, -1.0792 x 10(7) s(-1) T-1). The hyperfine coupling splitting in [Gd(TPATCN)] was determined accurately for a Gd-157-enriched complex, and the value A(Gd-157)/g mu(B) = 5.67 G seems to be a good estimation for most chelates of interest. Consequently, we can safely assert that neglecting the Gd isotopes in line shape studies is not a significant source of error as long as the apparent peak-to-peak width is greater than 10-20 G. This is generally the case, except at very high EPR frequencies (> 150 GHz). Analyzing the spectra within the physical model of Rast et al. we find that the slow electron spin relaxation is due to a nearly zero static ZFS. We discuss some structural features that might explain this interesting electron structure.
引用
收藏
页码:12434 / 12438
页数:5
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