The reduction of the Cd(2,2,2)2+ complex has been studied in acetonitrile using polarography, chronocoulometry, and cyclic voltammetry. The corresponding kinetic parameters have been calculated and are compared with those obtained for the solvated cadmium cation in the same solvent. The study of the eiectrochemical reduction mechanism showed that the final stable products are the free ligand (2...

[reaction: see text] The Morita-Baylis-Hillman reaction of a variety of conjugated nitroalkenes with activated nonenolizable carbonyl compounds such as glyoxylate, trifluoropyruvate, pyruvaldehyde, and ninhydrin in the presence of 40-100 mol % of DMAP in acetonitrile or 100 mol % of imidazole in CHCl(3) or THF provided the adducts in decent to good yields. In most cases, the reactions catalyzed...

In the title compound, [Cu(C(2)H(3)N)(2)(C(22)H(28)N(2)O(6))]ClO(4), the Cu atom is coordinated by two N atoms from one bidentate Schiff base ligand and two N atoms from two acetonitrile groups. The Cu atom adopts a tetra-hedral geometry. The Cu-N(ligand) distances are 2.076 (3) and 2.089 (3) Å, and the Cu-N(acetonitrile) distances are 1.964 (4) and 1.975 (4) Å.

In the title compound, bis({6-ethylamino-10-[2-(methoxycarbonyl)phenyl]-2,7-dimethylxanthen-3-ylidene}ethanaminium) hexachloridotin(IV) acetonitrile disolvate, (C(27)H(29)N(2)O(3))(2)[SnCl(6)]·2C(2)H(3)N, the octa-hedral SnCl(6) (2-) anion lies on an inversion center. The xanthene ring system is essentially planar, with an average deviation of 0.020 Å, and the substituent benzene ring forms a d...

The title compound, C(36)H(30)NP(2) (+)·Br(-)·C(2)H(3)N, crystallized from a CH(3)CN/OEt(2) solution as an acetonitrile solvate. The central P-N-P angle [142.88 (10)°] is significantly larger than in the corresponding chloride and iodide structures.

The conductance o f N al in acetonitrile-water mixtures was measured at 25.000 ± 0.001 °C for the whole com position range o f the mixed solvent, the salt molarity ranging from 5 • 10“ 5 to 1 • 10-2 . Using the Fuoss-Hsia equation with the Femandez-Prini parameters, the association constants were computed for several values o f the ion-ion distances. The influence o f the mixed solvent composit...

In the title compound, [TeBr(4)(C(22)H(23)OP)]·CH(3)CN, the Te atom exhibits a square-pyramidal coordination with an apical Te-C bond and four basal Te-Br bonds. The conformation of the aliphatic C-C-C-C chain is gauche [torsion angle = -67.7 (8)°]. A weak C-H⋯Br inter-action helps to establish the conformation. In the crystal, there is a weak secondary bonding inter-action [Te⋯N = 3.456 (11) Å...

The structure of the title compound, [Li(BF(4))(CH(3)CN)](n), consists of a layered arrangement parallel to (100) in which the Li(+) cations are coordinated by three F atoms from three tetra-fluoridoborate (BF(4) (-)) anions and an N atom from an acetonitrile mol-ecule. The BF(4) (-) anion is coordinated to three different Li(+) cations though three F atoms. The structure can be described as be...

The asymmetric unit of the title compound, C(10)H(6)N(2)O(2), contains two independent mol-ecules. The dihedral angles between the acetonitrile and the 1H-isoindole-1,3(2H)-dione units are 69.0 (7)° and 77.0 (5)° in the two mol-ecules. One of the two terminal N atoms is disordered over two positions in a 0.66 (8):0,34 (8) ratio. In the crystal structure, the mol-ecules are linked by inter-molec...

In the title compound, C(26)H(23)BrP(+)·Br(-)·C(2)H(3)N, the dihedral angles between the plane of the benzylic phenyl ring attached to the P atom and the planes of the three directly attached phenyl rings are 34.04 (12), 45.48 (13) and 87.18 (9)°. In the crystal, centrosymmetric pairs of cations and anions are linked into dimeric aggregates via C-H⋯Br hydrogen bonds. There is also a C-H⋯N hydro...