Diiron bis‐cyclopentadienyl complexes as transfer hydrogenation catalysts: The key role of the bridging aminocarbyne ligand
نویسندگان
چکیده
The catalytic activity of a series diiron complexes based on the {Fe 2 Cp (CO) x } core (x = 2–3) and containing bridging aminocarbyne ligand was screened in transfer hydrogenation reaction cyclohexanone from isopropanol. includes cationic tricarbonyl complexes, [1a – d]CF 3 SO , neutral derivatives obtained by substitution one carbonyl with hydride ( 2a c ), cyanide 3a d ) or chloride 4a ligands. novel compounds b were characterized analytical spectroscopic techniques, single crystal X‐ray structure isomer determined. In general, exhibited moderate combination potassium hydroxide; [Fe (CN)(CO)(μ‐CO){μ‐CN (Me)(4‐C 6 H 4 OMe)}], emerged as best catalyst, study its extended to range other ketones. DFT calculations suggest an unusual carbyne‐centred mechanism, better performance displayed is ascribable stabilizing effect provided co‐ligand, which experimentally supported IR analyses.
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ژورنال
عنوان ژورنال: Applied Organometallic Chemistry
سال: 2022
ISSN: ['0268-2605', '1099-0739']
DOI: https://doi.org/10.1002/aoc.6990