Amido complexes synthesis

Amidinato-amido chloro complexes, with Ti(IV), 4, 335-336 Amidinato-imido titanium complexes, synthesis, 4, 431 -32 Amidinato ligands... 

Ferrocenyl amido complexes, with Zr(IV), 4, 773 Ferrocenyl amino alcohols, synthesis, 6, 202 Ferrocenylated ODN, characteristics, 1, 909—910 Ferrocenyl diols, chiral, synthesis, 6, 204 Ferrocenyldiphenylphosphines, preparation, 6, 202 Ferrocenylimines mercuration, 2, 433 into platinacycles, 8, 511... 

Hydrocarbonyl compounds, lanthanide complexes, 4, 4 ( -Hydrocarbyl)bis(zirconocene), preparation, 4, 906 Hydrocarbyl-bridged cyclopentadienyl-amido complexes, with Zr(IV), 4, 864 Hydrocarbyl complexes bis-Cp Ti hydrocarbyls reactions, 4, 551 structure and properties, 4, 551 synthesis, 4, 542 cobalt with rf-ligands, 7, 51 cobalt with rf-ligands, 7, 56 cobalt with ]4-ligands, 7, 59 cobalt with rf-ligands, 7, 71 heteroleptic types, 4, 192 homoleptic types, 4, 192 into magnetic metal nanoparticles via ligand stabilization, 12, 87 via polymer stabilization, 12, 87 into noble metal nanoparticles... 

Mono(cyclooctatetraenyl) lanthanide(III) compounds, synthesis and characteristics, 4, 124 Mono(cyclooctatetraenyl) zirconium(III) compounds, preparation and reactions, 4, 743 Mono(cyclopentadienyl) amido complexes alkane elimination, 4, 446 amine elimination, 4, 442 HCL elimination, 4, 446 metathesis reactions, 4, 438 miscellaneous reactions, 4, 448 properties, 4, 437... 

The extensive chemistry of amido complexes, and, more particularly, of alkylamido complexes, reveals that the planar form is almost invariably found, along with bridging amides (221). Much attention has been paid to the synthesis of metal amido complexes of early transition metals, lanthanides and actinides. The amido group, particularly where it is bulky, confers unusual low coordination numbers on the metals and can also produce materials with considerable kinetic stability toward attack by nucleophiles (42, 67). However, the relevance of this extensive and fascinating chemistry to nitrogen fixation is somewhat problematic. 

The transition metal catalyzed synthesis of arylamines by the reaction of aryl halides or tri-flates with primary or secondary amines has become a valuable synthetic tool for many applications. This process forms monoalkyl or dialkyl anilines, mixed diarylamines or mixed triarylamines, as well as N-arylimines, carbamates, hydrazones, amides, and tosylamides. The mechanism of the process involves several new organometallic reactions. For example, the C-N bond is formed by reductive elimination of amine, and the metal amido complexes that undergo reductive elimination are formed in the catalytic cycle in some cases by N-H activation. Side products are formed by / -hydrogen elimination from amides, examples of which have recently been observed directly. An overview that covers the development of synthetic methods to form arylamines by this palladium-catalyzed chemistry is presented. In addition to the synthetic information, a description of the pertinent mechanistic data on the overall catalytic cycle, on each elementary reaction that comprises the catalytic cycle, and on competing side reactions is presented. The review covers manuscripts that appeared in press before June 1, 2001. This chapter is based on a review covering the literature up to September 1, 1999. However, roughly one-hundred papers on this topic have appeared since that time, requiring an updated review. 

Amido Complexes. The compounds of the general type MNHR and MNR2, especially those of Li, are important reagents in both organic and organometallic chemistry as well as starting materials for the synthesis of other metallic amido and... 

Gribkov, D.V., Hultzsch, K.C., and Hampel, F. (2003) Synthesis and characterization of new biphenolate and binaphtholate rare-earth-metal amido complexes catalysts for asymmetric olefin hydroamination/cyclization. Chemistry - A European Journal, 9, 4796. 

Functionalized tertiary aryl phosphines play an important role in transition metal coordination chemistry. These compounds have been used as ligands in synthesis, catalysis, mechanistic studies, and in the study of coordination compounds as structural models. In this contribution the syntheses of two new types of these ligands, tertiary aryl phosphines functionalized by an amide group, are detailed. The published coordination chemistry of these compounds includes the study of intramolecular N—H oxidative addition, the synthesis of chelates stabilized amido complexes, and the preparation of complexes with both ftve- and six-membered chelate rings. ... 

The zirconocene bis(arylamido) complex 787 was obtained by the reaction of Cp2ZrCl2 with 2 equiv. of the lithium amide605 (Scheme 195). When the reaction is carried out in a 1 1 ratio, the monoamide zirconocene chloride is generated as the major product. Reaction of in situ-generated Cp 2Zr with 2-(methylmercapto)aniline yields monoamido zirconocene hydride 788, the spectroscopic data of which suggest an interaction between the S atom and the Zr center in this complex. The bis(amido) complex 787 serves as a precursor for the synthesis of amido rhodium and iridium complexes. 

Scheme 4 Synthesis of bis (ureate) chloro, alkyl, or amido complexes of group 4 metals. DME= 1,2-dimethoxyethane...

Hydroamination is an atom-economical process for the synthesis of industrially and pharmaceutically valuable amines. The hydroamination reaction has been studied intensively, including asymmetric reactions, and a variety of catalytic systems based on early and late transition metals as well as main-group metals have been developed." However, Group 5 metal-catalysed hydroaminations of alkenes had not been reported until Hultzsch s work in 2011. Hultzsch discovered that 3,3 -silylated binaphtho-late niobium complex 69 was an efficient catalyst for the enantioselective hydroaminoalkylation of iV-methyl amine derivatives 70 with simple alkenes 71, giving enantioselectivities up to 80% (Scheme 9.30). Enantiomerically pure (l )-binaphtholate niobium amido complex 69 was readily prepared at room temperature in 5 min via rapid amine elimination reactions between Nb(NMe2)5 and l,l-binaphthyl-2-ol possessing bullqr 3,3 -silyl substituents. Since the complex prepared in situ showed reactivity and selectivity identical... 

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