The title compound, C(26)H(34)NSi(2) (+)·Cl(-), shows chirality at silicon. Because of its highly selective synthesis with an e.r. of >99:1 by means of a racemic resolution with mandelic acid, the free disilane is of great importance to the chemistry of highly enanti-omerically enriched lithio-silanes and their trapping products. N-H⋯Cl hydrogen bonding is present between the protonated nitro-g...

The scope of cross-coupling reactions using tertiary carbon-centered radicals has expanded rapidly over the past decade. In this review, we outline development that involve persistent as a powerful toolbox to synthesize molecules containing quaternary carbon(s) and/or tetra-substituted carbon(s). particular, focus on derived from carbonyl- or related compounds. We first describe historical back...

The structure of the title compound, poly[di-μ-penta-noato-zinc(II)], [Zn{CH(3)(CH(2))(3)COO}(2)](n), consists of a three-dimensional polymeric layered network with sheets parallel to the (100) plane, in which tetra-hedrally coordinated zinc(II) ions are connected by penta-noate bridges in a syn-anti arrangement. The hydro-carbon chains are in the fully extended all-trans conformation and are a...

Quantitative results are reported for gas-liquid chromatography of mixtures of free tetra-, hexa-, and octadecanals and cis-9-octadecenal on polar and nonpolar liquid phases. Stability of the fatty aldehydes during chromatographic analysis and up to 1 year of storage appears to be related to the solvent (carbon disulfide) used. Analysis of the free aldehydes by gas-liquid chromatography elimina...

In the title compound, C(14)H(11)BrF(3)N(5)O(2), the pyrimidine ring adopts a flattened envelope conformation with sp(3)-hybridized carbon as the flap [deviation = 0.177 (3) Å]. The dihedral angle between tetra-zole and bromo-phenyl rings is 84.3 (1)°. In the crystal, mol-ecules are linked into centrosymmetric dimers by pairs of N-H⋯N hydrogen bonds.

The title compound, [Ni(C(5)H(9)N)(3)(CO)], was prepared from Ni(CO)(4) and a tenfold excess of tert-butyl isocyanide. It crystallizes with two symmetry-independent mol-ecules per asymmetric unit. The central Ni atom of each independent mol-ecule has a nearly perfect tetra-hedral coordination environment, comprising one carbon monoxide and three isocyanide ligands. The title compound is the fir...

The title compound, C(16)H(14)Cl(2)N(4), is isomorphous with 2,9-dimethyl-6H,13H-5:12,7:14-dimethano-dibenzo[d,i]-[1,3,6,8]tetra-azecine [Rivera et al. (2009 ▶). Acta Cryst. E65, o2553] and has twofold symmetry, with two carbon atoms located on a twofold axis. Only van der Waals forces occur between molecules in the crystal. In the isomorphous compound the crystal structure is stabilized by wea...

In the crystal structure of the title compound, CH(6)N(+)·C(9)H(3)Cl(4)O(4) (-), the N atom of the methyl-amine mol-ecule is protonated and hydrogen bonded to the carboxyl group of the 3,4,5,6-tetra-chloro-2-(meth-oxy-carbon-yl)benzoate anion. The anions are linked by the cations via inter-molecular N-H⋯O inter-actions into chains extending along the c axis.

The title compound, C(31)H(44)N(3)O(10) (+)·Cl(-)·CH(4)O, is the methanol solvate of 8-benzo-yloxy-,9,11,11a-tetra-hydroxy-6,10,13-trimeth-oxy-3-meth-oxy-methyl-1-methyl-tetra-deca-hydro-1H-3,6a,12-(epiethane-1,1,2-tri-yl)-7,9-methanona-phtho[2,3-b]azocin-1-ium chloride, the amine-protonated hydro-chloride of 14-benzoyl-mesaconine hydro-chloride. The cation has an aconitine carbon skeleton with...