Synthesis and Characterization of Solvated Lanthanide(II) Bis(triisopropylsilyl)phosphide Complexes

被引:2
作者
Baldwin, Jack [1 ]
Brookfield, Adam [1 ]
Whitehead, George F. S. [1 ]
Natrajan, Louise S. [1 ]
Mcinnes, Eric J. L. [1 ]
Oakley, Meagan S. [1 ]
Mills, David P. [1 ]
机构
[1] Univ Manchester, Dept Chem, Manchester M13 9PL, England
基金
英国工程与自然科学研究理事会; 欧盟地平线“2020”; 欧洲研究理事会;
关键词
CRYSTAL-STRUCTURE DETERMINATION; STRUCTURAL-CHARACTERIZATION; RARE-EARTH; PLANAR COORDINATION; MOLECULAR-STRUCTURE; PHOSPHIDO COMPLEX; BASIS-SETS; 4-COORDINATE; EU; CHEMISTRY;
D O I
10.1021/acs.inorgchem.4c03135
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Lanthanide (Ln) silylamide chemistry is well-developed, but the corresponding silylphosphide chemistry is immature; there are only ten structurally characterized examples of Ln(II) bis(trimethylsilyl)phosphide complexes to date and no reported derivatives with bulkier R-groups. Here, we report the synthesis of the first f-block bis(triisopropylsilyl)phosphide complexes, [Ln{P((SiPr3)-Pr-i)(2)}(2)(THF)(x)] (1-Ln; Ln = Sm, Eu, x = 3; Ln = Yb, x = 2), by the respective salt metathesis reactions of parent [LnI(2)(THF)(2)] with 2 equiv of [Na{P((SiPr3)-Pr-i)(2)}](n) in toluene. Complexes 1-Ln were characterized by a combination of NMR, EPR, ATR-IR, electronic absorption and emission spectroscopies, elemental analysis, SQUID magnetometry, and single crystal X-ray diffraction. These data contrast with those obtained for related Ln(II) bis(trimethylsilyl)phosphide complexes due to the bulkier ligands in 1-Ln and also with Ln(II) bis(triisopropylsilyl)amide complexes due to a combination of longer Ln-P vs. Ln-N bonds and the softer nature of P- vs. N-donor ligands.
引用
收藏
页码:20295 / 20306
页数:12
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