Nickel complexes substitution

Moreover, the copper and nickel complexes substituted by eight dodecyloxy chains displayed lyotropic Ncoi and Colh mesophases in contact preparations with organic solvents (linear alkanes, cyclohexane, benzene, chloroform). The lyomesophases were stable for the copper and nickel complexes, except for the binary mixture between the nickel complex and linear alkane, for which... 

Upon treatment with suitable cobalt complexes, methylbutynol cyclizes to a 1,2,4-substituted benzene. Nickel complexes give the 1,3,5-isomer (196), sometimes accompanied by linear polymer (25) or a mixture of tetrasubstituted cyclooctatetraenes (26). 

Polymerization of alkynes by Ni" complexes produces a variety of products which depend on conditions and especially on the particular nickel complex used. If, for instance, O-donor ligands such as acetylacetone or salicaldehyde are employed in a solvent such as tetrahydrofuran or dioxan, 4 coordination sites are available and cyclotetramerization occurs to give mainly cyclo-octatetraene (cot). If a less-labile ligand such as PPhj is incorporated, the coordination sites required for tetramerization are not available and cyclic trimerization to benzene predominates (Fig. A). These syntheses are amenable to extensive variation and adaptation. Substituted ring systems can be obtained from the appropriately substituted alkynes while linear polymers can also be produced. 

To form the desired vinyl group, the methoxyethyl-substituted porphycene 9, has to be converted into its nickel complex. In the nickel porphycene the methoxyethyl side chain is... 

Stable enolates such as diethyl malonate anions react with allyl sulfones (or acetates) in the presence of nickel complexes to give a mixture of the a- and /-product83. The regioselectivity is generally poor in the nickel-catalyzed reaction, but the molybdenum-catalyzed reaction is selective for alkylation at the more substituted allylic site, thereby creating a quaternary carbon center84. 

A proline derived chiral nickel complex 1 may be used instead of oe,/J-unsaturated esters of lactones modified with a chiral alcohol as the Michael acceptor. The a,(9-unsaturated acid moiety in 1 reacts with various enolates to afford complexes 2 with diastereomcric ratios of 85 15 to 95 5. Hydrolysis of the imine moiety yields the optically active /(-substituted r-alanines. A typical example is shown296. 

A great number of nickel complexes with thiosemicarbazide (432) and thiosemicarbazone (433) ligands and their substituted derivates have been examined. Thiosemicarbazone chemistry is... 

Most studies on nickel-catalyzed domino reactions have been performed by Ikeda and colleagues [287], who observed that alkenyl nickel species, obtained from alkynes 6/4-41 and a (jr-allyl) nickel complex, can react with organometallics as 6/4-42. If this reaction is carried out in the presence of enones 6/4-43 and TM SCI, then coupling products such as 6/4-44 are obtained. After hydrolysis, substituted ketones 6/4-45 are obtained (Scheme 6/4.12). With cyclic and (5-substituted enones the use of pyridine is essential. Usually, the regioselectivity and stereoselectivity of the reactions is very high. On occasion, alkenes can be used instead of alkynes, though this is rather restricted as only norbornene gave reasonable results [288]. 

Geisler, T. Pedersen, K. Petersen, J. C. Third-harmonic Generation in Substituted Oligo-phenylene Vinylenes and Organic Square Planar Nickel Complexes. In Notions and Perspectives of Nonlinear Optics Keller, O., Eds. World Scientific Singapore, 1996 pp 580-585. 

These studies were extended to hydrosilation of cyclopentadiene with trichlorosilane (52). This is most difficult with platinum catalysts. Palladium complexes favored production of 1 1 adducts as a mixture of 3- and 4-trichlorosilylcyclopentene. Nickel complexes produced substantial amounts of 1 2 adducts as trichlorosilyl-substituted 4,7-methylene-4,7,-8,9-tetrahydroindanes, with the exception of nickel tetracarbonyl, which was very active and selectively formed almost exclusively 3-trichlorosi-lylcyclopentene with no 1 2 adduct. 

Nickel(ll) acetylacetonate catalyzes the addition of acetylacetone or ethyl acetoacetate to carbodiimides (Equation (89)).447 The acetylacetonate ligand of Ni(acac)2 may react with a carbodiimide to give a nickel complex having a 3-substituted acetylacetonate, which is then protonated by another acetylacetone to afford an adduct and Ni(acac)2. 

Hydrocyanation of aliphatic conjugated dienes in the presence of Ni(0) complexes gives diene rearrangement products and /i.y-unsaUiratcd nitriles in 10-90% yields10. Dienes other than 1,3-butadiene do not produce terminal nitriles, implying that the more highly substituted jr-allyl nickel complex is favored. Thus, reaction of 1-phenylbuta-l,3-diene (1) affords ( )-2-methyl-4-phenylbut-3-enenitrile (2) as the sole product (equation 5). The... 

As mentioned in Sections 3.1.6 and 4.1.3, cyclopropenes can also be suitable starting materials for the generation of carbene complexes. Cyclopropenone di-methylacetal [678] and 3-alkyl- or 3-aryl-disubstituted cyclopropenes [679] have been shown to react, upon catalysis by Ni(COD)2, with acceptor-substituted olefins to yield the products of formal, non-concerted vinylcarbene [2-1-1] cycloaddition (Table 3.6). It has been proposed that nucleophilic nickel carbene complexes are formed as intermediates. Similarly, bicyclo[1.1.0]butane also reacts with Ni(COD)2 to yield a nucleophilic homoallylcarbene nickel complex [680]. This intermediate is capable of cyclopropanating electron-poor alkenes (Table 3.6). 

Water NMRD profiles acquired for other complexes and proteins always exhibit the same features of hexaaqua nickel(II). As an example, we report here the profile of the hexa-coordinate nickel(II)-substituted bovine carbonic anhydrase II 54,55) (Fig. 15). As in the aqua complex, (i) the low-field profile is flat, (ii) no dispersion appears, the cOg dispersion being quenched in S = 1 complexes with large static ZFS 56) (see Section I.A.5) and the... 

Fig. 17 Optimized geometries at BP86/SVP of the nickel complexes N-Ni(CO)3 (N = 1-9). Experimental values are given in italics. Bond lengths in A, angles in degrees. Hydrogen atoms of the phenyl rings are omitted for clarity. Experimental values from X-ray analysis taken from [107]. Experimental values from X-ray analysis of a substituted analog taken from [111]...

Nickel forms a large number of complexes with various anions (monoden-tate, bidentate, and polydentate) and many neutral ligands. The most common coordination numbers of the metal in these complexes are six and four while the metal is usually in +2 oxidation state, Ni2+. Also, some complexes of three and five coordinations exist. Several zero valent nickel complexes, such as nickel tetracarbonyl, and a number of substituted carbonyl complexes are well known. 

The corresponding nickel complexes of these ligands were synthesized through deprotection of the acetyl groups via saponification in methanol, followed by addition of Ni(H20)6Cl2 and air oxidation. The monoanions 4a-e were then precipitated by treatment with tetrabutylammonium bromide, and recrystallized to give shiny, crystalline materials. 7V-Methylpyridinium salts were also produced by substituting A -methylpyridinimn iodide for tetrabutylammonimn bromide. 

The cross-coupling route to allylsilanes is effective with either aromatic or aliphatic a-silylated Grignard reagents16, and palladium catalysts are more reactive and stereoselective than the corresponding nickel complexes. Unsubstituted or i+monosubstituted alkenyl bromides work well but the Z-substituted bromides give lower yields and an inferior enantiomeric excess. The enantiomeric excess increases quite markedly with decreasing temperature, and optimum results are obtained at 0 C or below. 

Dale Margerum Ralph Wilkins has mentioned the interesting effect of terpyridine on the subsequent substitution reaction of the nickel complex. I would like to discuss this point—namely the effect of coordination of other ligands on the rate of substitution of the remaining coordinated water. However, before proceeding we should first focus attention on the main point of this paper-which is that a tremendous amount of kinetic data for the rate of formation of all kinds of metal complexes can be correlated with the rate of water substitution of the simple aquo metal ion. This also means that dissociation rate constants of metal complexes can be predicted from the stability constants of the complexes and the rate constant of water exchange. The data from the paper are so convincing that we can proceed to other points of discussion. 

Nickel complexes are observed to undergo substitution much faster than platinum complexes. Offer an explanation. 

The synthesis of substituted glutamic acid analogues has been pursued by many routest94-106 using asymmetric alkylation, Simmons-Smith reactions, Diels-Alder reactions, and nickel complexes of glycine or alanine equivalents. 

The formation in solution of nickel complexes with TV-substituted ethylenediamines has been studied over a long period by many authors.707 Solutions of nickel(II) complexes with TV-substituted diamines often exhibit equilibria between pseudotetrahedral and pseudo-octahedral species. These equilibria are displaced towards the pseudotetrahedral species when the temperature increases. Complexes Ni(TV,TV-Et2en)2X2691 with poorly coordinating anions are thermochromic. This behaviour has been investigated by means of calorimetric and NMR studies.708,709... 

Thiazole, C3H3NS, and substituted thiazoles coordinate through the nitrogen atom in nickel complexes as imidazole does.901-903... 

A number of nickel complexes with substituted and unsubstituted tetrazoles910-913 and with pyrazole- and imidazole-derived ligands have also been reported recently.914-916... 

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