化学
异核分子
配体(生物化学)
钇
盐变质反应
硅烷
药物化学
酮
复分解
甲苯
核磁共振波谱
立体化学
有机化学
聚合
氧化物
聚合物
受体
生物化学
作者
Alexandros Mortis,Cäcilia Maichle‐Mößmer,Reiner Anwander
出处
期刊:Organometallics
[American Chemical Society]
日期:2023-02-28
卷期号:42 (11): 1158-1165
被引量:6
标识
DOI:10.1021/acs.organomet.2c00636
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI