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Iron carbonyls reductive cleavage

Iron-substituted mesoporous aluminophosphate was used as a novel, efficient and ecofriendly catalyst for reductive cleavage of azo dyes and reduction in nitroarenes and catalytic transfer hydrogenation of nitro and carbonyl compounds. Unlike most of the iron-containing molecular sieves, dislodgement of tetrahedral Fe(III) was not observed upon various process treatments such... [Pg.1638]

The commercially available (tj5-cyclopentadienyl)iron dicarbonyl dimer 1 is the source of the carbonyl(//5-cyclopentadienyl)iron(L) moiety. Reductive or oxidative cleavage of 1 provides reactive monomeric species that may be converted into iron-acyl complexes as described in the following sections (see also Houben-Weyl, Vol. 13/9a, p208). [Pg.518]

The reductive dehalogenation of haloalkanes has also been achieved in high yield using polymer supported hydridoiron tetracarbonyl anion (Table 11.15). In reactions where the structure of the alkyl group is such that anionic cleavage is not favoured, carbonylation of the intermediate alkyl(hydrido)iron complex produces an aldehyde (see Chapter 8) [3]. [Pg.500]

Ill) Iron and Ruthenium. w-Allyliron complexes are not readily prepared directly from olefins by cleavage of an allylic C—H bond, but Jt-allylhydridoiron complexes are intermediates in olefin isomerization catalyzed by Fe(0) carbonyl complexes ". The intermediate 7i-allyliron hydride complexes formed are too reactive to be isolated and undergo a fast reductive elimination to give the isomerized or the starting olefin ... [Pg.120]


See other pages where Iron carbonyls reductive cleavage is mentioned: [Pg.246]    [Pg.188]    [Pg.173]    [Pg.188]    [Pg.281]    [Pg.153]    [Pg.131]    [Pg.231]    [Pg.153]    [Pg.341]    [Pg.246]    [Pg.210]    [Pg.213]    [Pg.238]    [Pg.51]    [Pg.213]    [Pg.44]    [Pg.90]    [Pg.293]    [Pg.4243]    [Pg.287]   


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