Alkali Metal Reduction of 1,2-Bis[(2,6-dibenzhydryl-4-methylphenyl)imino]acenaphthene (ArBIG-bian) to Radical-Anion

被引:9
作者
Moskalev, Mikhail V. [1 ]
Razborov, Danila A. [1 ]
Skatova, Alexandra A. [1 ]
Bazanov, Andrey A. [1 ]
Fedushkin, Igor L. [1 ]
机构
[1] Russian Acad Sci, GA Razuvaev Inst Organometall Chem, Tropinina Str 49, Nizhnii Novgorod 603137, Russia
基金
俄罗斯基础研究基金会;
关键词
Alkali metals; Bulky ligands; Acenaphthene-1; 2-diimines; ESR spectroscopy; Structure elucidation; ALPHA-DIIMINE NICKEL; INSERTION POLYMERIZATION; CRYSTAL-STRUCTURES; GALLIUM COMPLEXES; CATALYTIC HYDROSILYLATION; ELECTRONIC COMMUNICATION; MOLECULAR-STRUCTURES; MONOMERIC MAGNESIUM; CALCIUM COMPLEXES; SOLUTION BEHAVIOR;
D O I
10.1002/ejic.202000909
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reduction of Ar-BIG-bian (1, 1,2-bis[(2,6-dibenzhydryl-4-methylphenyl)imino]acenaphthene) with one molar equivalent of Li, Na or K in tetrahydrofuran (THF) affords corresponding radical-anionic salts (Ar-BIG-bian)M(THF) (M=Li, 2; Na, 3; K, 4). Compounds 2-4 were isolated in good yields and characterized by the elemental analysis, IR and ESR spectroscopy as well as the single-crystal X-Ray analysis. Bulky Ph-2(H)C groups in Ar-BIG-bian ligand prevent dimerization of complexes 2-4 and limit a number of coordinated THF molecules to one. In all three products a saturation of the alkali metal coordination sphere is achieved through an interaction with Ph rings of Ph-2(H)C substituents.
引用
收藏
页码:458 / 463
页数:6
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