Synthesis and Characterization of Homo- and Heteroleptic Neptunium(IV) Heteroarylalkenolate Complexes

被引:0
作者
Groedler, Dennis [1 ]
Kaden, Peter [1 ]
Sperling, Joseph M. [2 ,3 ]
Rotermund, Brian M. [2 ,3 ]
Scheibe, Benjamin [2 ,3 ]
Beck, Nicholas B. [2 ,3 ]
Lichtenberg, Andreas [4 ]
Albrecht, Thomas E. [2 ,3 ]
Mathur, Sanjay [4 ]
Gericke, Robert [1 ]
机构
[1] Helmholtz Zentrum Dresden Rossendorf, Inst Resource Ecol, D-01328 Dresden, Germany
[2] Colorado Sch Mines, Dept Chem & Nucl Sci, Golden, CO 80401 USA
[3] Engn Ctr, Colorado Sch Mines, Golden, CO 80401 USA
[4] Univ Cologne, Inst Inorgan & Mat Chem, Dept Chem, D-50939 Cologne, Germany
关键词
CHEMICAL-VAPOR-DEPOSITION; ORGANIC-COMPOUNDS; URANIUM; CHEMISTRY; ALKOXIDES;
D O I
10.1021/acs.inorgchem.4c04521
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Heteroleptic AnIV (An = U, Np) chlorido-ketoenaminate complexes of the type [AnCl2(TFB-tBuA)2(THF)] (An-1 type: U-1, Np-1; TFB-tBuA = 4-(tert-butylamino)-1,1,1-trifluorobut-3-en-2-one) and the homoleptic NpIV heteroarylalkenolate complexes [Np(PyTFP)4] (Np-2, PyTFP = 1-(pyridin-2-yl)-3,3,3-trifluoroprop-1-en-2-ol) and [Np(DMOTFP)4] (Np-3, DMOTFP = 1-(4,5-dimethyloxazol-2-yl)-3,3,3-trifluoroprop-1-en-2-ol) were synthesized and characterized (SC-XRD, NMR, Vis-NIR, MS). While their solid-state structures compare well to those of their uranium analogues, the behavior in solution showed significant differences. The binding motif of the DMOTFP ligand in complex Np-3 can change to form two different complex isomers, as seen by paramagnetic chemical shifts in NMR experiments. Furthermore, the flexibility and the influence of the steric effects at the N-side of the ligands are discussed and compared with its uranium counterpart.
引用
收藏
页码:2321 / 2328
页数:8
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