Mixed Methyl/Chlorido Yttrium(III) Complexes Supported by a Neutral Tridentate N-Donor Ligand

被引:5
作者
Mortis, Alexandros [1 ]
Maichle-Moessmer, Caecilia [1 ]
Anwander, Reiner [1 ]
机构
[1] Eberhard Karls Univ Tubingen, Inst Anorgan Chem, D-72076 Tubingen, Germany
关键词
RARE-EARTH-METALS; ORGANOMETALLIC COMPLEXES; TRIMETHYLSILYLMETHYL COMPLEXES; STRUCTURAL-CHARACTERIZATION; POLYMERIZATION CATALYSTS; CRYSTAL-STRUCTURE; METHYL COMPLEXES; ALKYL; REACTIVITY; SCANDIUM;
D O I
10.1021/acs.organomet.2c00636
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Trimethylyttrium, supported by the neutral tridentate ligand Me3TACN (1,4,7-trimethyl-1,4,7-triazacyclononane), is readily synthesized from (Me3TACN)YCl3 (via salt metathesis with MeLi in THF) or [YMe3]n (via Me3TACN-donor addition in toluene). Such discrete complex (Me3TACN)YMe3 reacts with trimethylchlorosilane according to a silane elimination protocol, affording well-defined mixed methyl/chlorido complexes of the composition [(Me3TACN)YMe3-xClx] (x = 1, 2, 3). All complexes were characterized by X-ray diffraction, homo-and heteronuclear NMR (especially 89Y) and FTIR spectroscopies, and elemental analysis. The reaction of heteroleptic complex [(Me3TACN)YMe2Cl] with dibenzyl ketone was investigated.
引用
收藏
页码:1158 / 1165
页数:8
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