A novel indolocarbazole-based chemosensor 1 containing hydrogen bond donor moieties has been established as a selective colorimetric and fluorometric sensor for F⁻ in CH₃CN/H₂O (4:1 v/v). Upon the addition of a series of tetrabutylammonium salts to receptor 1 in aqueous CH₃CN, only when the counter ion was F⁻ was a significant color change (from light violet to dark orange) observed.

2,2,2-Trichloro-1-aryl-ethanones can be reduced by RMgX to the corresponding 2,2-dichloro-1-arylethen-1-olates and trapped with a range of electrophiles resulting in either reduction, reduction/aldol, reduction/Claisen condensation or reduction/aldol-Tishchenko products. In addition we demonstrate that 2,2-dichloro-1-arylethen-1-olates undergo counter-ion controlled Darzens condensations, which...

In the title compound, [CoBr(CH5N)(C3H10N2)2]Br2, the cobalt(III) ion has a distorted octa-hedral coordination environment and is surrounded by four N atoms in the equatorial plane, with an additional N atom and the Br atom occupying the axial positions. In the crystal, the complex cation and the two counter anions are linked via N-H⋯Br and C-H⋯Br hydrogen bonds, forming a three-dimensional net...

In the title compound, [Ni(C(24)H(16)N(6))(2)](NCS)(2)·2H(2)O, the central Ni(II) ion is octahedrally coordinated by six N atoms of two tridentate 2,3,5,6-tetra-2-pyridyl-pyrazine ligands (tppz). Two thio-cyanate anions act as counter-ions and two water mol-ecules act as solvation agents. O-H⋯N hydrogen bonds are observed in the crystral structure.

The asymmetric unit of the title salt, C(28)H(28)O(3)P(+)·Cl(-)·H(2)O, contains a benzyl-triphenyl-phospho-nium cation, a chloride counter-ion, and a water mol-ecule of crystallization. The 3,4,5-trimeth-oxy substituents of the benzylic functionality are arranged with the 3,5-methyl groups lying approximately in the aromatic ring plane while the 4-methyl group is out of the plane.

The interaction of passing-ion drift orbits with spatially inhomogeneous but purely diffusive radial transport is demonstrated to cause spontaneous toroidal spin-up in a simple model of the tokamak edge. Physically, major-radial orbit shifts cause orbit-averaged diffusivities to depend on v(∥), including its sign, leading to residual stress. The resulting pedestal-top intrinsic rotation scales ...

Aryl(alkynyl)iodonium salts have been demonstrated to be valuable precursors to a diverse range of heteroaromatic ring systems including aryl[1,2-a]imidazopyridines. Successful application, using the recently described aryl(alkynyl)iodonium trifluoroacetate salts, is described, highlighting for the first time that the regioselectivity of this process is both counter-ion and concentration depend...

In the title complex, [CrCl(2)(C(12)H(8)N(2))(2)]Cl, the Cr(III) ion is situated on a twofold rotation axis and displays a slightly distorted octa-hedral CrCl(2)N(4) coordination geometry. The Cr environment is composed of a cis arrangement of two 1,10-phenanthroline and two chloride ligands. The chloride counter-anion exhibits half-occupation and is equally disordered over two positions.

In the title compound, [CoBr(2)(C(14)H(24)N(4))]·Br, the Co(III) ion is located on an inversion centre and possesses a distorted octa-hedral coordination geometry in which four nitro-gen donors of the ligand mol-ecule are in the equatorial plane and two Br(-) ions occupy both the axial sites to give a trans isomer. The Br(- )counter- anion is also located on an inversion centre.

The asymmetric unit of the title salt, [Mn(C2H6OS)6]I2, consists of one Mn(II) ion, six O-bound dimethyl sulfoxide (DMSO) ligands and two I(-) counter-anions. The isolated complex cations have an octa-hedral configuration and are grouped in hexa-gonally arranged rows extending parallel to [100]. The two I(-) anions are located between the rows and are linked to the cations through two weak C-H⋯...