1979
DOI: 10.1002/ange.19790910732
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Einfacher Zugang zu Li- oder Zn-metallierten η5-Cyclopentadienyleisen-Olefin-Komplexen

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Cited by 12 publications
(7 citation statements)
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“…1 H and 13 C NMR spectra of 1 in solution are unexceptional and entirely consistent with its formulation, and showed resonances characteristic of η 4 ‐naphthalene7, 8 and η 4 ‐1,5‐cyclooctadiene3, 12 groups bound in a 1:1 ratio to an electron‐rich metal center. A single‐crystal X‐ray study on 1 , as the [K([18]crown‐6)] salt, revealed an undistorted cation that was well‐separated from the cobalt center of the anion and had no significant effect on its structure 13.…”
Section: Methodsmentioning
confidence: 78%
“…1 H and 13 C NMR spectra of 1 in solution are unexceptional and entirely consistent with its formulation, and showed resonances characteristic of η 4 ‐naphthalene7, 8 and η 4 ‐1,5‐cyclooctadiene3, 12 groups bound in a 1:1 ratio to an electron‐rich metal center. A single‐crystal X‐ray study on 1 , as the [K([18]crown‐6)] salt, revealed an undistorted cation that was well‐separated from the cobalt center of the anion and had no significant effect on its structure 13.…”
Section: Methodsmentioning
confidence: 78%
“…Analogous reactions of 1 with excess 1,5‐cyclooctadiene (cod) gave no evidence for the formation of unknown paramagnetic [Fe(η 4 ‐cod) 2 ] − or reported [Fe(η 4 ‐cod) 2 ] 2− ,26 but instead afforded the first example of a mixed‐ligand or heteroleptic Fe −I complex, [Fe(η 4 ‐C 14 H 10 )(η 4 ‐cod)] − ( 5 ). This species was isolated in good yield as teal or dichroic red‐violet microcrystals of the [K([18]crown‐6)] + ( 5 a ) or [K([2.2.2]cryptand)] + ( 5 b ) salts, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Although the mechanisms of iron‐catalyzed cross‐coupling reactions have not been elucidated (see Section 3.3), it has been postulated that highly reduced iron–magnesium clusters containing an iron(−II) center, such as [Fe(MgX) 2 ] n , may play an important role in the catalytic cycle. Martin and Fürstner probed this theory by testing the known, well‐defined iron(−II) complex [Li(tmeda)] 2 [Fe(C 2 H 4 ) 4 ] ( 8 ), which was first described by Jonas and co‐workers,30a, b as a catalyst for cross‐coupling reactions 30c. Indeed, 8 is a very active catalyst for the coupling of aryl Grignard reagents with alkyl electrophiles, including secondary alkyl bromides (Scheme ).…”
Section: Iron‐catalyzed Reactionsmentioning
confidence: 99%