Search results for "ammonium"
showing 10 items of 1070 documents
Crystal structure of the bis(cyclohexylammonium) succinate succinic acid salt adduct
2015
The title salt adduct comprises two cyclohexylammonium cations, one succinate anion and one molecule of succinic acid, linked together through intermolecular hydrogen-bonding interactions giving a two-dimensional layer-like self-assembly lying parallel to (010).
Crystal structure of dimethylammonium hydrogen oxalate hemi(oxalic acid)
2015
The title salt consists of a dimethylammonium cation (Me2NH2 +), an hydrogenoxalate anion (HC2O4 −), and half a molecule of oxalic acid (H2C2O4) situated about an inversion center. They are linked together through intermolecular hydrogen bonds, forming a two-dimensional bilayer-like self-assembly.
Crystal structure of bis(cyclohexylammonium) diphenyldioxalatostannate(IV)
2015
In the title salt, (CyNH3)2[Sn(Ph2)(C2O4)2] (Cy is cyclohexyl and Ph is phenyl), the SnPh2 moiety is chelated by two oxalate anions, leading to a cis arrangement within the distorted octahedral coordination sphere of the SnIV atom.
The structure of bis(trimethylammonium) undecachlorotriantimonate(III) [(CH3)3NH]2Sb3Cl11 containing a novel antimony(III) anion
1999
The structure of [(CH3)3NH]2Sb3Cl11 (space group P21/n; a = 10.374(2), b = 23.723(5), c = 11.884(2) Å, β = 113.46(3)°; V = 2682.9(9) Å3) consists of a structurally novel [Sb3Cl2−11] anion and two crystallographically nonequivalent trimethylammonium cations. The anion is composed of three deformed octahedra in the asymmetric part of the unit cell. The octahedra are connected with each other by edges and corners forming a characteristic polyanionic layer. Trimethylammonium cations, one ordered and one disordered, are connected to the inorganic sublattice by N—H· · ·Cl hydrogen bonds.
Crystal structure of allylammonium hydrogen succinate at 100 K
2014
The asymmetric unit of the title compound, C2H8N+·C4H5O4−, consists of two allylammonium cations and two hydrogen succinate anions (Z′ = 2). One of the cations has a near-perfectsyn-periplanar (cis) conformation with an N—C—C—C torsion angle of 0.4 (3)°, while the other is characterized by agaucheconformation and a torsion angle of 102.5 (3)°. Regarding the anions, three out of four carboxilic groups are twisted with respect to the central C–CH2–CH2–C group [dihedral angles = 24.4 (2), 31.2 (2) and 40.4 (2)°], the remaining one being instead almost coplanar, with a dihedral angle of 4.0 (2)°. In the crystal, there are two very short, near linear O—H...O hydrogen bonds between anions, with t…
Crystal structure of bis-(allyl-ammonium) oxalate.
2014
The title salt, 2C3H8N+·C2O42−, crystallized with six independent allylammonium cations and three independent oxalate dianions in the asymmetric unit. One of the oxalate dianions is nearly planar [dihedral angle between CO2planes = 1.91 (19)°], while the other two are twisted with angles of 11.3 (3) and 26.09 (13)°. One cation has a synperiplanar (cis) conformation with an N—C—C—C torsion angle of 0.9 (3)°, whereas the five remaining cations are characterized bygauchearrangements, with the N—C—C—C torsion angles ranging from 115.9 (12) to 128.8 (3)°. One of the allylammonium cations is positionally disordered (fixed occupancy ratio = 0.45:0.55). In the crystal, the cations and anions are co…
Structure and phase transitions in ethylenediammonium dichloride and its salts with antimony trichloride
2000
During the mixing of ethylenediammonium dichloride and antimony trichloride except of reported earlier [NH3(CH2)2NH3]5(Sb2Cl11)2 · 4 H2O a new salt [NH3(CH2)2NH3](SbCl4)2 was obtained. The crystals are monoclinic at 295 K, space group C2/m, a = 13.829(3), b = 7.408(1), c = 7.588(2) Å; β = 103.18(3)°; V = 756.9(3) Å3; Z = 2; dc = 2.585, dm = 2.56(2) g · cm–3. The structure consists of anionic sublattice built of Sb2Cl82– units composed of two SbCl52– square pyramids connected by edge. The ethylenediammonium cations are located in anionic cavities. The cations are disordered. Each methylene carbon atom is split between two positions. The X‐ray diffraction, DSC, TGA and dilatometric methods we…
CCDC 257790: Experimental Crystal Structure Determination
2005
Related Article: R.H.Laye, F.K.Larsen, J.Overgaard, C.A.Muryn, E.J.L.McInnes, E.Rentschler, V.Sanchez, S.J.Teat, H.U.Gudel, O.Waldmann, G.A.Timco, R.E.P.Winpenny|2005|Chem.Commun.||1125|doi:10.1039/b416770h
CCDC 2153375: Experimental Crystal Structure Determination
2022
Related Article: María Vicent-Morales, María Esteve-Rochina, Joaquín Calbo, Enrique Ortí, Iñigo J. Vitórica-Yrezábal, Guillermo Mínguez Espallargas|2022|J.Am.Chem.Soc.|144|9074|doi:10.1021/jacs.2c01957
Co-treatment of landfill leachate in laboratory-scale sequencing batch reactors: analysis of system performance and biomass activity by means of resp…
2014
Aged or mature leachate, produced by old landfills, can be very refractory; for this reason mature leachate is difficult to treat alone, but it can be co-treated with sewage or domestic wastewater. The aim of the study was to investigate the feasibility of leachate co-treatment with synthetic wastewater, in terms of process performance and biomass activity, by means of respirometric techniques. Two sequencing batch reactors (SBRs), named SBR1 and SBR2, were fed with synthetic wastewater and two different percentages of landfill leachate (respectively 10% and 50% v v−1 in SBR1 and SBR2). The results showed good chemical oxygen demand (COD) removal efficiency for both reactors, with average C…