Complexes of zinc

Electroplating. Aluminum can be electroplated by the electrolytic reduction of cryoHte, which is trisodium aluminum hexafluoride [13775-53-6] Na AlE, containing alumina. Brass (see COPPERALLOYS) can be electroplated from aqueous cyanide solutions which contain cyano complexes of zinc(II) and copper(I). The soft CN stabilizes the copper as copper(I) and the two cyano complexes have comparable potentials. Without CN the potentials of aqueous zinc(II) and copper(I), as weU as those of zinc(II) and copper(II), are over one volt apart thus only the copper plates out. Careful control of concentration and pH also enables brass to be deposited from solutions of citrate and tartrate. The noble metals are often plated from solutions in which coordination compounds help provide fine, even deposits (see Electroplating). 

An equilibrium among polysulfido complexes of zinc, ZnS (TMEDA) ( =4, 5, 6), has also been observed in MeCN solution (see Scheme 39), although solutions in pyridine or CH2CI2 do not show such an equilibrium [111]. The equilibrium ratio among these three complexes is ZnS4(TMEDA) ZnS5(TMEDA) ZnS6(TMEDA)=l 1.5 12. 

The resulting water helps to extend the life of the dry cell by providing moisture for the movement of the ionic species. A second reaction, that extends the usefulness of this cell, is the formation of an amine complex of zinc ions in the cell ... 

The value of the tris(pyrazolyl)hydroborato complexes [TpRR ]ZnOH is that they are rare examples of monomeric four-coordinate zinc complexes with a terminal hydroxide funtionality. Indeed, [TpBut]ZnOH is the first structurally characterized monomeric terminal hydroxide complex of zinc (149). As such, the monomeric zinc hydroxide complexes [TpRR ]ZnOH may be expected to play valuable roles as both structural and functional models for the active site of carbonic anhydrase. Although a limitation of the [TpRR ]ZnOH system resides with their poor solubility in water, studies on these complexes in organic solvents... 

Lewis-Acid Catalyzed. Recently, various Lewis acids have been examined as catalyst for the aldol reaction. In the presence of complexes of zinc with aminoesters or aminoalcohols, the dehydration can be avoided and the aldol addition becomes essentially quantitative (Eq. 8.97).245 A microporous coordination polymer obtained by treating anthracene- is (resorcinol) with La(0/Pr)3 possesses catalytic activity for ketone enolization and aldol reactions in pure water at neutral pH.246 The La network is stable against hydrolysis and maintains microporosity and reversible substrate binding that mimicked an enzyme. Zn complexes of proline, lysine, and arginine were found to be efficient catalysts for the aldol addition of p-nitrobenzaldehyde and acetone in an aqueous medium to give quantitative yields and the enantiomeric excesses were up to 56% with 5 mol% of the catalysts at room temperature.247... 

The biphenyl ligand functionalized with two imidazoles (6) was used to produce distorted tetrahedral complexes of zinc.119 2,2 -Biimidazole can act as a bidentate ligand coordinating to one zinc ion (7) or as a bridging ligand in the formation of dimeric species (8) with X-ray structures of both binding motifs.120... 

Studies of the thermodynamics of formation of complexes of zinc with 2,2 -bipyridine in the presence of halide and thiocyanate ions in DMF has been carried out.205 The zinc complexes of 2,2 -bipyridine with A-(benzenesulfonyl)glycine and A-(toluene- -sulfonyl)glycine were synthesized and infrared data implied a structural analogy with the cadmium complexes. This suggests that the zinc promotes sulfonamide nitrogen deprotonation in the amino acid ligands in the solid state.206... 

A triazacyclononane ligand with a diphenyl phosphine pendant connected via a propyl linker formed a dimeric complex of zinc [Zn2L2Cl3][C104], 10... 

Bis-phosphaallyl complexes of zinc have been prepared and characterized from cyclic amino-phosphazanes and aminoiminophosphanes. The structure of the bis(l,3-diaza-2-phosphaallyl)zinc complex [Zn(RNPNR )2] (R = R = C6H3Pr2i-2,6) was determined.311... 

The trigonal planar zinc phenoxide complex [K(THF)6][Zn(0-2,6-tBu2C6H3)3] is formed by the reaction of a zinc amide complex, via a bis phenoxide, which is then further reacted with potassium phenoxide. TheoX-ray structure shows a nearly perfect planar arrangement of the three ligands with zinc only 0.04 A out of the least squares plane defined by the three oxygen atoms.15 Unlike the bisphenoxide complexes of zinc with coordinated THF molecules, these complexes are not cataly-tically active in the copolymerization of epoxides with C02. The bisphenoxide complex has also been structurally characterized and shown to be an effective polymerization catalyst. 43... 

Markies et al. have studied the coordination of zinc to cyclic and acyclic polyether ligands. In some cases the zinc is not coordinated within the ligand cavity but only through two of the ether donors in the macrocyclic ring.360 The bis(methoxyethyl)ether complex of zinc diphenyl (41) is five-coordinate with three ether oxygens coordinating from the acyclic ligand.361... 

Di-t-butyl phosphate complexes of zinc were synthesized as precursors for ceramic material formation. A tetrameric zinc complex was characterized from the treatment of zinc acetate with the phosphate resulting in a compound with a bridging oxo at the center, [Zn4(/i4-0)(di-t-butyl phosphate)6]. In the presence of auxiliary donor ligands such as imidazole or ethylenediamine, monomeric complexes are formed, [Zn(di-t-butyl phosphate)2(imidazole)4]. It is also possible to convert the tetramer into the monomer by treating with a large excess of imidazole.41... 

A number of zinc-bound bidentate bis(thioether) donor ligands were characterized as distorted tetrahedral complexes of zinc dichloride. The complexes 2,3-bis(methylthio)hexane,l,2-bis (methylthio) cyclohexane, and m-[5,6-bis(methylthio)-l,3-cycloheptadiene showed a variation in S—Zn—S angles.539... 

Zinc dithiocarbamates have been used for many years as antioxidants/antiabrasives in motor oils and as vulcanization accelerators in rubber. The crystal structure of bis[A, A-di- -propyldithio-carbamato]zinc shows identical coordination of the two zinc atoms by five sulfur donors in a trigonal-bipyramidal environment with a zinc-zinc distance of 3.786 A.5 5 The electrochemistry of a range of dialkylthiocarbamate zinc complexes was studied at platinum and mercury electrodes. An exchange reaction was observed with mercury of the electrode.556 Different structural types have been identified by variation of the nitrogen donor in the pyridine and N,N,N, N -tetra-methylenediamine adducts of bis[7V,7V-di- .vo-propyldithiocarbamato]zinc. The pyridine shows a 1 1 complex and the TMEDA gives an unusual bridging coordination mode.557 The anionic complexes of zinc tris( V, V-dialkyldithiocarbamates) can be synthesized and have been spectroscopically characterized.558... 

Complexes of zinc dialkyldithiocarbamates with bidentate nitrogen ligands such as 1,10-phen-anthroline have been structurally characterized.563 The related complexes (4,4 -bipyridyl)... 

A monomeric selenolato complex of zinc (65) was synthesized with a chelating oxazoline ligand.587 The complex was characterized by X-ray crystal structure, 1H, 13C, and 77Se NMR. These studies demonstrate that the compound is helically chiral and solution studies appear to show retention of chirality in solution. The zinc complex is tetrahedral with a Zn—Se average bond length of 2.378(1) A. 

Macrocyclic complexes of zinc have inspired interest in varied areas such as supramolecular and biomimetic chemistry including hydrolysis enzymes, such as phosphatases and esterases, and also for the fluorescent detection of zinc. The polyaza macrocycles and their A--functionalized derivatives are particularly well represented. An important aspect of macrocycle synthesis is the use of metal templates to form the ligand. Examples of zinc as a template ion will be discussed where relevant. 

Moore and co-workers have also studied the complexation of zinc with other tetraaza macrocycles and pendent arm derivatives. Zinc complexes of 11-(2 -dimethylaminoethyl)-1,4,7-trimethyl-1,4,7,11-tetra-azacyclotetradecane have been characterized.695 A pyridine analog of this... 

Lippard characterized the structural effect of variation in the alkyl bridge length in tropocoro-nand complexes of zinc (80). Six complexes of ligands with bridge lengths from n = m = 3 to n = m = 6 were structurally characterized.702 The complexes had distorted tetrahedral-square planar geometries, with the exception of the m = n = 3 adduct which was five-coordinate with an additional pyridine ligand. 

The catecholate and semiquinonate complexes of zinc with tetraaza macrocycles have been synthesized and CD spectra recorded.710... 

The complexes of zinc with pyridylphenylketone and pyridylphenylmethanol are stabilized by the chelate effect. The complexes formed were dependent on anions present and the ratio of the... 

V,/V-bis(2-hydroxy-di-3,5-/-butylphenyl)amine forms complexes of zinc which have ligand-based redox processes with four oxidation levels of the coordinated anion.864 2 1 and 1 1 complexes are formed in the presence of zinc with the 2 1 complex coordinated in an octahedral geometry and the 1 1 complex square planar with a triethylamine ligand completing the coordination sphere. The complexes, at the different redox levels, have been investigated by EPR, spectro-electrochemistry, l I NMR, and magnetochemistry, as appropriate. 

Hodgson J.F., Lindsay W.L., Trierweiler J.F. Micronutrient cation complexing in soil solution. II. Complexing of zinc and copper in displaced solution from calcareous soils. Soil Sci Soc A Proc 1966 30 723-726. 

To increase precursor volatility, interest focused on using ligands of considerable bulk to reduce the degree of molecular association. This was of limited success, with mercury proving to be an exception. Bradley and Kunchur218 reported that Hg(SBu )2 has only weak intermolecular interactions and occurs as discrete Hg(SR)2 units even in the solid state. Other attempts to prepare complexes of zinc or cadmium with limited degrees of polymerization have been undertaken. 

In contrast to the Simmons-Smith reagent and similar carbenoids, which are reactive and therefore difficult to characterize, adducts of the fV-heterocyclic l,3-diorganylimidazol-2-ylidenes are remarkably stable. The first iV-heterocyclic carbene complex of zinc, namely the l,3-di(l-adamantyl)imidazol-2-ylidene diethylzinc complex 48 (Figure 22), was reported by Arduengo et al. in 1993.98 Because of the general utility of these iV-heterocyclic... 

ZnxZryFz. A fluoro complex of zirconium, ZrF62, and an ammine complex of zinc, ZnfNFF), have been used to grow ZnxZryFz films on silicon. The Zn/Zr/F ratio was 0.08/1/0.32, and the films contained hydroxyl groups and physisorbed water.128... 

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