摘要:
The present disclosure relates to a method for preparing a metal catalyst comprising at least one ligand that is coordinated to the metal through at least one phosphorous (P) atom and at least one nitrogen (N) atom, the method comprising reacting a metal pre-cursor complex with an acid addition salt of an aminophosphine, diaminophosphine, aminodiphosphine or diaminodiphosphine, in the presence of a base.
摘要:
The present disclosure relates to a process for the hydrogenation of compounds comprising one or more carbon-oxygen (C═O) double bonds, to provide the corresponding alcohol, comprising contacting the compound with hydrogen gas at and a catalyst comprising a ruthenium-aryl-aminophosphine complex.
摘要:
The present disclosure relates to processes and methods of generating hydrogen via the hydrolysis or solvolyis of a compound of the formula (I), R1R2HNBHR3R4, using ligand-stabilized homogeneous metal catalysts.
摘要:
The present disclosure relates to processes and methods of generating hydrogen via the dehydrocoupling of amine boranes using ligand-stabilized homogenous metal catalysts. The amine-borane is shown by the formula (I), R1R2N—BHR3R4. A process is also shown for the preparation of a linear, branched or cyclic polymer which comprises a repeating unit of the formula (II), —[R1R2N—BR3R4]-n, by reacting HR1R2N—BHR3R4 in the presence of at least one ligand-stabilized metal catalyst.
摘要:
The present disclosure relates to processes and methods of generating hydrogen via the hydrolysis or solvolyis of a compound of the formula (I), R1R2HNBHR3R4, using ligand-stabilized homogeneous metal catalysts.
摘要:
The present disclosure includes catiome complexes of iron, ruthenium, and osmium, and their use as catalysts in organic synthesis transformations including the hydrogenation of unsaturated compounds. The complexes are represented by the following formulae I, II, III, IV, and V, wherein M is Fe, Ru or Os, P is a monodentate ligand with a phosphorus donor atom, P2 is a bidentate neutral ligand with two phosphorus donor atoms, N2 is a bidentate neutral ligand with two nitrogen donor atoms, PN is a bidentate neutral ligand with phosphorus and nitrogen donor atoms, PNNP is a tetradentate neutral ligand bonded to M via two phosphorus and two nitrogen atoms, X is any anionic ligand, LB is any neutral Lewis base, Y is any non-coordinating anion, n is 0, 1, or 2, m is 1 or 2, q is 0 or 1, r is 1 or 2 and q+r=2.
摘要翻译:本公开内容包括铁,钌和锇的配合物,以及它们在有机合成转化中的用途,包括不饱和化合物的氢化。 络合物由下式I,II,III,IV和V表示,其中M是Fe,Ru或Os,P是具有磷供体原子的单齿配体,P2是具有两个磷给体原子的二齿中性配体 N 2是具有两个氮供体原子的二齿中性配体,PN是具有磷和氮给体原子的二齿中性配体,PNNP是通过两个磷和两个氮原子与M键合的四齿中性配体,X是任何阴离子配体,LB 是任何中性路易斯碱,Y是任何非配位阴离子,n是0,1或2,m是1或2,q是0或1,r是1或2,q + r = 2。
摘要:
The present application is directed to i) a method for synthesizing aminophosphine (P,N) and phosphine-aminophosphine (P,N,P) ligands, ii) the use of such ligands in the preparation of metal complexes as hydrogenation catalysts, and iii) aminophosphine (P,N) and phosphine-aminophosphine (P,N,P) ligands of various structures. In particular, the methods in i) involve reacting a protected tertiary amine of formula (I) with a metal phosphide of the formula Y—PR8R9 to afford an aminophosphine of formula (II), which can then be optionally further reacted with a phosphine of the formula (III) to afford the phosphine-aminophosphine of formula (IV).