Tris borate ligands

Properties of nickel poly(pyrazol-l-yl)borate complexes such as solubility, coordination geometry, etc., can be controlled by appropriate substituent groups on the pyrazol rings, in particular in the 3- and 5-positions. Typical complexes are those of octahedral C symmetry (192)°02-604 and tetrahedral species (193). In the former case, two different tris(pyrazolyl)borate ligands may be involved to give heteroleptic compounds.602,603 Substituents in the 5-position mainly provide protection of the BH group. Only few representative examples are discussed here. 

During the course of modeling copper dioxygen chemistry, Kitajima et al. reported the synthesis of a yu-peroxo dinuclear complex with a 3,5-dimethyl-substituted tris(pyrazolyl)borate ligand, which showed remarkable physicochemical similarities to oxy-Hc and oxy-Tyr. Using a 3,5-di-isopropyl-substituted terminal ligand, they provided the first structural proof of the existence of peroxo dicopper(II) core (108) (copper geometry distorted square pyrami-... 

Using a fluorinated tris(pyrazolyl)borate ligand, Gorun and co-workers126 synthesized a complex (117) (t = 0.06). This group very successfully isolated and structurally characterized a dinuclear oxygenated complex, revealing that the crystal contains about 80% peroxo... 

A large body of work with particular reference to the mimicry of mononuclear zinc enzymes has utilized tris(pyrazolyl)borate ligands. This ligand class offers a facial coordination mode of three pyrazole A-donors and can be functionalized in the three and five positions on the rings to increase steric bulk and vary the electronic properties of the ligand. The synthesis and complex formation with these ligands has been extensively reviewed.2,21 219... 

Pyridyl functionalized tris(pyrazolyl)borate ligands show some interesting properties including the formation of polynuclear zinc complexes.23,1 Some of these contain extensive H bonding and have potential as models for multinuclear zinc enzymes such as phospholipase C or PI nuclease.235 A bis-ligand complex of the hydrotris(5-methyl-3-(3-pyridyl)pyrazolyl)borate ligand (23) shows octahedral coordination of all six pyrazole nitrogen donors despite the steric bulk. 

The zinc acetate complex of tris(3-/-butyl-5-methylpyrazol-l-yl)borate was prepared as a structural model for carbonic anhydrase and comparison with the enzyme active site structures confirmed that the complexes are excellent structural models.239 A mononuclear zinc hydroxide complex can also be formed with the tris(pyrazolyl) borate ligand system as a structural model for carbonic anhydrase.240... 

A structurally characterized example of a dinuclear zinc complex with a bridging phosphate monoester was provided by Kitajima and co-workers using the tris(pyrazolyl)borate ligand system. The P—O bond in a tris- or bis-phosphate ester is cleaved by a hydroxo zinc complex resulting in the monoester compound.443... 

The substituted tris(2-thioimidazolyl)borate ligands with l-R-2-thioimidazole groups where R = tBu and CgH4-/>-CH(CH3)2 yielded tetrahedral complexes on reaction with zinc salts. The... 

A Cd2 complex with one of the tris(pyrazolyl)borate ligands mentioned in Section 6.9.4.2.3(ii) has been identified in solution by its large coupling constant 1/(113Cd,111Cd) of 20.626 kHz also a Cd11 hydride complex has been detected by NMR.410... 

Using a similar strategy, Dias and coworkers were able to prepare classical AgI-CO and AgJ-C2H4 complexes supported by the mesityl-substituted tris(pyrazolyl)borate ligand L9 (Fig. 11) (102). The isolation of such complexes is a challenging task because silver(I) is a poor u-acceptor, a poor 7t-donor, and in... 

Although the poly(pyrazolyl)borate complexes of iron(II) have been well known for many years, [1] it is only recently that the complexes with the tris(l-pyrazolylmethane ligand, HC(pz)3, [45-48] have been studied in detail. It should be noted that poly(pyrazolyl)methane ligands, such as the tris(l-pyrazolylmethane ligand, are neutral, whereas the poly(pyrazolyl)bo-rate ligands, such as the tris(l-pyrazolyl)borate ligand, HB(pz)3", are monoanions. As a consequence, the metal(II) poly(pyrazolyl)methane complexes are dications and often have quite different properties from those of the analogous metal(II) poly(pyrazolyl)borate molecular complexes. But, in spite of these differences there are often very close structural similarities between the dicationic complexes and the neutral complexes. Therefore the study of the pyrazolylmethane complexes will parallel that of the borate complexes discussed above. 

Recently, a somewhat different synthetic approach has been reported. Halcrow et al. (215) synthesized a series of five-coordinate copper(II) complexes comprising a tridentate tris(pyrazolyl)borate ligand and a bidentate phenol derivative. Neutral complexes [Cun(TpPh)(bidentate phenolate)] were synthesized and structurally characterized [Tpph] = hydrido-tris(3-phenylpyrazol-l-yl)borate. The species [Cun(TpPh)(2-hydroxy-5-methyl-3-methylsulfanylbenzaldehydato)] can electro-chemically be converted to the (phenoxyl)copper(II) monocation, which has been characterized in solution by UV-vis spectroscopy. It displays two intense absorption maxima at 907 nm (e = 1.2 x 103 M 1 cm-1), and 1037 (1.1 x 103 M l cm-1), resembling in this respect the radical cofactor in GO (Fig. 7). 

A dimethylaluminum complex [HB(3,5-(CF3)2Pz)3]AlMe2 (Figure 22) of the highly fluorinated tris(pyrazolyl)borate ligand [HB(3,5-(CF3)2Pz3] was obtained from the reaction between the silver adduct [HB(3,5-(GF3)2Pz)3]Ag(THF)... 

As previously discussed, the binuclear Cu(I) haemocyanins constitute another important class of dioxygen carriers. The first model compound whose structure in the oxygenated form resembles most closely that of oxyhaemocyanin is the dicopper(II) complex with the tris(3,5-diisopro-pylpyrazolyl)borate ligand shown in Figure 26.29... 

NMR (CeDg, 125.7 MHz, 25°C) 139.8, 132.5, 128.8-129.1 (overlapping resonances), 124.6, 17.0 (br). B NMR (CgDg, 128.3 MHz, 25°C) -10.96 ppm. The compound is a versatile precursor to a wide range of transition metal complexes supported by the tris(phosphino)borate ligand. It is air- and water-stable for extended periods, and, unlike the lithium and ammonium salts of [PhB(CH2PPh2)3] , it is both soluble and stable in chloroform and dichloromethane for days, making these useful solvents available for subsequent trans-metallation chemistry. 

The tris(N-(3-tm-butyl)pyrazolyl)methane ligand, with an extremely bulky 3-substituent, favors the formation of tetrahedral complexes2 in much the same way as observed in the chemistry of the hydrotris(3-tert-butyl-pyrazolyl)borate ligand.1... 

A side-on p,-Tq2 Tq2-peroxo dicopper(II) complex. A very important development in copper-dioxygen chemistry occurred in 1989 with the report by Kitajima et al. [10,108] that another Cu202 species could be prepared and structurally characterized by using copper complexes with a substituted anionic tris(pyrazolyl)borate ligand. This intensely purple compound, Cu[HB(3,5-iPr2pz)3] 2(02) (5), was prepared either by reaction of Cu[HB(3,5-iPr2pz)3] (4) with 02 or by careful addition of aqueous hydrogen peroxide to the p-dihydroxo... 

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