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Alkali Metal Reduction of 1,2‐Bis[(2,6‐dibenzhydryl‐4‐methylphenyl)imino]acenaphthene (Ar BIG ‐bian) to Radical‐Anion
Author(s) -
Moskalev Mikhail V.,
Razborov Danila A.,
Skatova Alexandra A.,
Bazanov Andrey A.,
Fedushkin Igor L.
Publication year - 2021
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.202000909
Subject(s) - acenaphthene , chemistry , tetrahydrofuran , alkali metal , medicinal chemistry , ligand (biochemistry) , molecule , metal , inorganic chemistry , coordination sphere , molar conductivity , crystal structure , crystallography , photochemistry , elemental analysis , organic chemistry , biochemistry , receptor , solvent , anthracene
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.
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