The mononuclear title complex, [Mo(C9H9NO2)O2(H2O)], contains an Mo(VI) atom in a distorted octa-hedral coordination sphere defined by an Mo=O and an Mo-(OH2) bond to the axial ligands and two Mo-O bonds to phenolate and alcoholate O atoms, another Mo=O bond and one Mo-N bond to the imino N atom in the equatorial plane. The five-membered metalla-ring shows an envelope conformation. In the cryst...

In the title polymer, {[Co(C(14)H(10)N(2)O(4))(H(2)O)]·3.5H(2)O}(n), the Co(2+) ion is coordinated by three carboxyl-ate O atoms from two 5-[(pyridin-2-ylmeth-yl)amino]-isophthalate anions, two N atoms from a (pyridin-2-ylmeth-yl)amino group and an O atom from a water mol-ecule, furnishing a distorted CoO(4)N(2) octa-hedral geometry. Each anion acts as a μ(3)-bridge, linking cobalt ions into a ...

During the process of transformation in Hemophilus influenzae integration of donor DNA, i.e. the formation of recombinant DNA, involves the incorporation of single-stranded DNA. Evidence was obtained from cesium chloride density gradient centrifugation of DNA from donor-recipient complexes that integration was accompanied by the formation of hybrid DNA with a density intermediate with respect t...

A series of luminescent fac-[Re(CO)3(L)(NN)](+) complexes, where L is a pyridine or an imidazole and NN is the 1,10-phenanthroline subunit of mixed donor pentadentate thioether crowns have been synthesised and their luminescence properties have been analysed. Then, heterometallic Re(i)/Au(i) complexes, with the Au(i) fragment bonded directly to the imidazole ligand, and heterometallic Re(i)/Ag(...

In the title diorganotin dicarboxyl-ate, [Sn(CH(3))(2)(C(17)H(17)N(2)O(3))(2)], the tin(IV) atom is six-coordinated by four O atoms derived from asymmetrically coordinating carboxyl-ate ligands, and two methyl-C atoms. The resulting C(2)O(4) donor set defines a skew-trapezoidal bipyramid with the Sn-C bonds disposed over the weaker Sn-O bonds. Within each carboxyl-ate ligand, the hydroxyl-H ato...

In the title compound, [Cu(C11H10N3O)2(C8H4O5)2]·4H2O, the Cu(II) ion, located on a crystallographic inversion center, is coordinated in a square-planar environment by two trans-O atoms belonging to two monodentate 5-hy-droxy-isophthalate (hip) dianions and two trans nicotinamide pyridyl N-donor atoms from monodentate protonated pendant N-(pyridin-4-yl)nicotinamide (4-pnaH) ligands. The protona...

Z. Naturforsch. 54 b, 8-12 (1999); received September 1, 1998 Silylamines, Silylamides, Crystal Structure Lithiation of tris(methylamino)wt'f/7v/silane using an excess of n -butyllithium affords the cor­ responding trifunctional lithium amide in high yield. The compound crystallizes from tetrahydrofuran as a dimer with six donor molecules: {[MeSi(NMeLi)3]2(thf)6}. The cluster is a cage structur...

In the title compound, [V(C(7)H(3)NO(4))O(C(10)H(8)N(2))]·C(2)H(5)OH, the V(IV) atom exhibits a distorted octa-hedral coordination environment formed by two pyridyl N atoms of 2,2'-bipyridine (bpy), the vanadyl O atom, and two carboxyl-ate O atoms and one pyridyl N atom of the tridentate pyridine-2,6-dicarboxyl-ate (pydc(2-)) ligand. The pyridyl N atom of the pydc(2-) anion and one pyridyl N at...

Reaction of three phenolate ligands, viz. 2,4,6-tribromophenol (HL, where H stands for the phenolic proton), 2-nitrophenol (HL) and 2,4,6-trinitrophenol (HLO), with [Ru(PPh3)3Cl2] in a 2:1 molar ratio in the presence of a base gives complexes of type [Ru(PPh3)2(L)2] (L=L , L and L). The 2,4,6-tribromophenolate ligand (L) binds to ruthenium as a bidentate O,Br-donor, while the 2-nitrophenolate l...

Проведен расчет структуры комплексов ампициллина с катионами лантаноидов методом DFT, определены длины связей ионов донорными атомами лигандов, получены энергии комплексов. Установлено, что энергия комплексов, рассчитанная находится в монотонной зависимости от экспериментально определенных констант их образования. The structure of ampicillin complexes with lanthanide cations was calculated by t...