Search results for "inorganic compound"

Measurments of collisional line widths in the stimulated Raman Q-branch of the ν1 band of silane

1990

Self-broadened widths of 28SiH4 in the ν1Q-branch have been measured at room temperature (295 K) using high-resolution stimulated Raman Spectroscopy. These collisional widths have been obtained by fitting a super-position of Voigt profiles to the experimental spectra in the pressure range 28–154 Torr. No evidence for line mixing within the tetrahedral components of a Q(J) line has been found. The line broadening coefficients for J up to 13 depend weakly on the rotational quantum number. The mean value is 103.7 × 10−3 cm−1 atm−1.

Studies of the Ca4Mn3O10structure obtained using high pressure and high temperature

2002

An ideal n = 3 member of the group of Ruddlesden?Popper (RP) phases Ca4Mn3O10 was obtained by solid-state reaction under high pressure. This phase has been studied by transmission electron microscopy, convergent beam electron microscopy, high-resolution transmission electron microscopy, and parallel electron energy-loss spectroscopy. The lattice parameters are derived as a = b = 0.37 nm and c = 2.69 nm with the space group I4/mmm, which is the space group of the ideal RP phase.

Ejection of molecules from WO3 under ion bombardment: the role of the crystal structure

1992

Abstract Emission of molecular ions from WO 3 and Na x WO 3 was studied by SIMS. It was found that the phenomenon of ejection of molecules had not arisen from specific WO bond lengths and strengths in tungsten trioxide.

Solid-state NMR characterization of the structure and thermal stability of hybrid organic-inorganic compounds based on a HLaNb2O7 Dion-Jacobson layer…

2016

Dion-Jacobson phases, like MLaNb2O7, are an interesting class of ion-exchangeable layered perovskites possessing electronic and photocatalytic properties. Their protonated and organo-modified homologues, in particular, have already been indicated as promising catalysts. However, the structural analysis of these highly tailorable materials is still incomplete, and both the intercalation process and thermal stability of the included organic moieties are far from being completely understood. In this study, we present a thorough solid-state NMR characterization of HLaNb2O7·xH2O intercalated with different amounts of octylamine, or with decylamine. Samples were analyzed as prepared, and after th…

Crystal and molecular structures of hexaaquazinc(II)isonicotinate n-oxide and catena-diaquabis-μ-(isonicotinato n-oxide)cadmium(II)

1984

Abstract [Zn(H2O)6](N-inicO)2 is an ionic compound made up of hexaaqua metal cations and isonicotinate N-oxide anions. It forms an isomorphic series with the corresponding Mg2+, Fe2+, Co2+ and Ni2+ compounds. In [Cd(N-inicO)2(H2O)2]n complex, coordination takes place through the NO oxygen and one of the (COO) oxygens with ligand forming thus a double bridge between Cd2+ ions. The structure is an endless chain stretching diagonally through the unit cell. The coordination polyhedron in both compounds is almost undistorted octahedron.

119Sn Mössbauer spectroscopic studies of the products of the reaction of triorganotin(IV) derivatives with 6-thiopurine

1985

Abstract A structural study of the products of the reaction of R 3 Sn IV derivatives (R = Me, Bu n , Ph) with 6-thiopurine, 6-TPH 2 , and its sodium salt, 6-TPHNa, has been undertaken using Mossbauer spectroscopy and the point-charge model rationalization of the Mossbauer parameter nuclear quadrupole splitting. The synthetic reactions have been carried out at ca . 0 °C, 20 °C and 50 °C. The Mossbauer spectra of the complexes AlK 3 Sn(6-TPH) are consistent with the occurrence of two distinct tin(IV) sites in samples prepared at the lower temperature, while one only site appears by increasing the temperature of the reaction. Two tin sites constantly occur in the products of the reactions invo…

Electrochemical study on (NN)Fe3 (CO)9 ((NN) = 2,3-diazanorbornene) and related compounds. A new example of activation of carbon monoxide replaceme…

1985

Abstract The compound (NN)Fe 3 (CO) 9 ( 1 ) in tetrahydrofuran undergoes two reversible one-electron reduction processes in cyclic voltammetry at the platinum electrode. A rapid electron transfer-catalyzed reaction occurs when 1 is reduced in the presence of L (L = P(OMe) 3 ) and this gives (NN)Fe 3 (CO) 8 L ( 2 ), quantitatively. Only an electron-induced nucleophilic substitution is observed for compound 2 under the same conditions, yielding (NN)Fe 3 (CO) 7 L 2 , which undergoes a similar reaction but with much lower efficiency, to give (NN)Fe 3 (CO) 6 L 3 .

Synthesis and crystal structure of Na1+xV4P4O17(OH) (x ≈ 1.44)

1990

Abstract Hydrothermal synthesis starting from Na0.46VOPO4 · 1.58H2O leads to a new mixed-valence sodium vanadium phosphate: Na2.44V4P4O17(OH) (orthorhombic, space group Pnma; Z = 4; a = 13.723(5) A, b = 6.314(2) A, c = 16.139(4) A; R = 0.032 for 2659 reflections). In this phase, the interconnection of three complex types of infinite chains, built from VO6 octahedra and PO4 tetrahedra, sometimes edgeshared, defines tunnels partly occupied by a portion of the sodium atoms.

Synthesis and x-ray crystal structure of dimethyltin(IV) dithiocyanate bihydrate adduct with a crown ether

1985

Me 2 Sn(NCS) 2 (OH 2 ) 2 . 18-crown-6 cristallise dans P2 1 /n avec Z=2; affinement jusqu'a R=0,058

2,2'-BIPYRIMIDINEOXALATOCOPPER(II) COMPLEXES - FROM THE MONONUCLEAR COMPLEX TO THE 2D SHEET-LIKE POLYMER

1993