Addition of an excess of t-butyl isocyanide to solid Mo2 (0, CCF3 )4 or MO?_ (0, CMe)4 gives (t-BuNC), Mo(Oz CCF3 )* or (t-BuNC), Mo(Oz CMe), , respectively. The quadruple bond in K4 MO* Cl8 or Cl4 MO, (n-Bus P)4 also can be cleaved by an excess of t-butyl isocyanide to yield (t-BuNC), MoCl, _ The anionic ligands can be exchanged with ammonium hexafluorophosphate in presence of excess t-BuNC to...

Bimolecular reactions of the antimony(V) porphyrin complexes SbO(tpp)OH, 1 and SbO(oep)OH, 2 with tetra-n-butylammonium hydroxide were investigated at 298 K in acetonitrile solution (tpp, dianion of 5,10,15,20-tetraphenylporphyrin and oep, dianion of 2,3,7,8,12,13,17,18-octaethylporphyrin). Spontaneous nucleophilic addition of hydroxide ions to the non-oxidized porphyrin macrocycle leads to nov...

The crystal structure of the title compound, [Hf(C10H15)2(C4H9)2], reveals two independent mol-ecules in the asymmetric unit. The diffraction experiment was performed with a racemically twinned crystal showing a 0.529 (5):0.471 (5) component ratio. Each Hf(IV) atom is coordinated by two penta-methyl-cyclo-penta-dienyl and two n-butyl ligands in a distorted tetra-hedral geometry, with the cyclo-...

In the title compound, [N(C4H9)4]2[Ni(C11H3F3N2O6)] or [N(n-Bu)4]2[Ni(topbo)] [n-Bu = n-butyl and topbo = 4-tri-fluoro-methyl-1,2-phenyl-enebis(oxamate)], the Ni(2+) cation is coordinated by two deprotonated amido N atoms and two carboxyl-ate O atoms, setting up a slightly distorted square-planar coordination environment. The [Ni(topbo](2-) anion lies on a twofold rotation axis. Due to an incom...

Silica aerogels prepared by the sol-gel process are often used as solid desiccants in enthalpy wheels for dehumidifying ventilation air in air-conditioning systems. These hygroscopic materials have good moisture adsorption and desorption characteristics due to their porous structure. The current study is focused on the evaluation of the mass diffusivity of solid silica aerogels and silica aerog...

Ionosilica ionogels have been lately introduced as emerging all-ionic designer materials. They consist of an ionic liquid (IL) guest trapped within a solid ionosilica support host. In this work, we investigate the influence (i) nature and (ii) ionosilica/IL ratio on mobility confined IL. We report elaboration various via nonhydrolytic sol–gel process, using namely tris(3-(trimethoxysilyl)propyl...

The structure of the title salt, (C(6)H(14)N)(2)[CuBr(4)], is built up from cyclo-hexyl-ammonium cations and tetra-bromidocuprate anions, the latter being located on an inversion center. In the crystal, anions and cations are inter-connected by N-H⋯Br hydrogen bonds, forming ribbons parallel to [0-11].

Four mol-ecular salts made from hexa-methyl-ene-tetra-minium and 2-chloro-4-nitro-benzoate have been synthesized and are reported, namely ammonium hexa-methyl-ene-tetra-minium bis-(2-chloro-4-nitro-benzoate), NH4+·C6H13N4+·2C7H3ClNO4-, (I), hexa-methyl-ene-tetra-minium hydrogen bis-(2-chloro-4-nitro-benzoate), 0.5C6H13N4+·C7H3.50ClNO4-, (II), hexa-methyl-ene-tetra-minium 2-chloro-4-nitro-benzoa...

In the title compound, [Sn2(CH3)6(NCS)2(C24H22N4)], the 1,2,3,4-tetra-kis-(pyridin-4-yl)butane ligand uses the pyridine N atoms at the ends of the butyl chain to coordinate to two trimethylthiocyanatotin(IV) units, forming a dinuclear structure. The Sn(IV) atom in the mol-ecule shows a distorted trans-trigonal-bipyramidal coordination with the methyl groups in equatorial positions. The mol-ecul...

In the title mol-ecule, C21H20BrClN6O2, the chloro-substituted benzene ring forms a dihedral angle of 77.84 (7)° with the tetra-zole ring and the bromo-substituted ring forms a dihedral angle of 43.95 (6)° with the imidazole ring. The dihedral angle between the tetra-zole and imidazole rings is 67.42 (8)°. The terminal methyl group of the butyl substituent is disordered over two sets of sites, ...