Hydrogenation of nitroarenes using defined iron-phosphine catalysts.

A novel iron-catalyzed hydrogenation of nitroarenes to the corresponding amines is reported. An in situ combination of Fe(BF4)2·6H2O and phosphine allows for highly selective hydrogenation of a broad range of aromatic and nitroarenes tolerating different functional groups.

Heterogenized cobalt oxide catalysts for nitroarene reduction by pyrolysis of molecularly defined complexes.

Molecularly well-defined homogeneous catalysts are known for a wide variety of chemical transformations. The effect of small changes in molecular structure can be studied in detail and used to optimize many processes. However, many industrial processes require heterogeneous catalysts because of their stability, ease of separation and recyclability, but these are more difficult to control on a molecular level.

A molecularly defined iron-catalyst for the selective hydrogenation of α,β-unsaturated aldehydes.

A selective iron-based catalyst system for the hydrogenation of α,β-unsaturated aldehydes to allylic alcohols is presented. Applying the defined iron-tetraphos complex [FeF(L)][BF4] (L = P(PhPPh2)3) in the presence of trifluoroacetic acid a broad range of aldehydes are reduced in high yields using low catalyst loadings (0.05-1 mol %).

Ruthenium catalysts for hydrogenation of aromatic and aliphatic esters: make use of bidentate carbene ligands.

Committed carbenes: The convenient application of bidentate carbene ligands is described for the hydrogenation of carboxylic acid esters. The ligand precursors are easily synthesized through the dimerization of N-substituted imidazoles with diiodomethane. The catalyst is generated in situ and exhibits good activity and functional group tolerance for the hydrogenation of aromatic and aliphatic carboxylic acid esters.

Phosphine-imidazolyl ligands for the efficient ruthenium-catalyzed hydrogenation of carboxylic esters.

The synthesis of phosphine-imidazolyl ligands 1 and 2 in good yields is presented. In combination with [{Ru(benzene)Cl(2)}(2)], ligands 1 c and 1 e formed efficient catalyst systems for the selective hydrogenation of various carboxylic esters into their corresponding primary alcohols. Furthermore, the structures of four ruthenium complexes with ligands 1 b, 1 c, 1 d, and 1 e were determined by X-ray crystallography, which showed the formation of different coordination modes depending on the ligand structure.

Selective iron-catalyzed transfer hydrogenation of terminal alkynes.

A novel iron-catalyzed transfer hydrogenation of alkynes to the corresponding alkenes applying formic acid as a hydrogen donor is reported. An in situ combination of Fe(BF(4))(2)·6H(2)O and tetraphos allows for highly selective hydrogenation of a broad range of aromatic and aliphatic alkynes tolerating different functional groups.

A convenient and general ruthenium-catalyzed transfer hydrogenation of nitro- and azobenzenes.

An easily accessible in situ catalyst composed of [{RuCl(2)(p-cymene)}(2)] and terpyridine has been developed for the selective transfer hydrogenation of aromatic nitro and azo compounds. The procedure is general and the selectivity of the catalyst has been demonstrated by applying a series of structurally diverse nitro and azo compounds (see scheme).

Efficient and highly selective iron-catalyzed reduction of nitroarenes.

Pyrolysis of iron-phenanthroline complexes supported on carbon leads to highly selective catalysts for the reduction of structurally diverse nitroarenes to anilines in 90-99% yields. Excellent chemoselectivity for the nitro group reduction is demonstrated.