Two coordination compounds containing tetra-n-butyl-ammonium cations and bis-tfd-chelated molybdenum(IV) [tfd2- = S2C2(CF3)22-] and oxalate (ox2-, C2O42-) in complex anions are reported, namely bis-(tetra-n-butyl-ammonium) bis-(1,1,1,4,4,4-hexa-fluoro-but-2-ene-2,3-di-thiol-ato)oxalatomolybdate(IV)-chloro-form-oxalic acid (1/1/1), (C16H36N)2[Mo(C4F6S2)2(C2O4)]·CHCl3·C2H2O4 or (N n Bu4)2[Mo(tfd)...

The title compound, ammonium potassium iron(III) phosphate fluoride, (NH(4))(0.875)K(0.125)FePO(4)F, is built from zigzag chains (∞) (1){[FeO(4)F(2)](7-)}, with Fe(3+) in a distorted octahedral coordination, extending along both the [011] and [01] directions. These chains are made up of alternating trans-[FeO(4)F(2)] and cis-[FeO(4)F(2)] octa-hedra via shared F-atom corners, and are linked by P...

In the title compound, C(8)H(20)N(+)·CHO(3) (-)·3H(2)O, the bicarbon-ate anion, which has a small mean deviation from the plane of 0.0014 Å, fully utilises its three O and one H atom to form various O-H⋯O hydrogen bonds with the three water mol-ecules in the asymmetric unit, generating a hydrogen-bonded layer, which extends along (10[Formula: see text]). The tetra-ethyl-ammonium cations, as the...

The title salt, C2H8N+·C10H5O8-, was the unexpected product of an attempt to prepare a ZrIV metal-organic framework with benzene-1,2,4,5-tetra-carb-oxy-lic acid (1,2,4,5-H3B4C). In the reaction, the DMF solvent has been decarb-on-yl-ated, forming the di-methyl-ammonium cation, with one proton lost from the tetra-carb-oxy-lic acid. It is proposed that the ZrIV salt acts as a Tsotsi or robber, pl...

The crystal structure of the title compound, poly[bis-(tri-methyl-ammonium) hexa-μ(1,1)-azido-tetra-azido-tricobalt-ate(II,III)], [(CH(3))(3)NH](2)[Co(II)Co(III) (2)(N(3))(10)], consists of anionic chains [Co(II)Co(III) (2)(N(3))(10)](2-) extending parallel to the c axis and [(CH(3))(3)NH](+) counter-cations situated between the chains. In the anionic chain, one tetra-hedrally coordinated Co(II...

In recent years, there has been a growing interest in green solvents to dissolve and shape cellulose into microspheres. However, development of suitable for room temperature dissolution shaping spheres is very limited. this work, novel process fabricate microspheres presented. First, the effect ethanol-hydrochloric acid pulp pretreatment on solubility aqueous tetra-n‑butyl phosphonium hydroxide...

In the title compound, C(10)H(19)N(3) (2+)·2Br(-), the plane of the three butyl C atoms nearest to the pyridine ring is almost perpendicular to the ring [dihedral angle = 84.80 (2)°]. The N atom of the ammonium group is displaced by 1.150 (8) Å from the plane of these three C atoms. The iminium N atom lies on the opposite side of this plane. The crystal structure is stabilized by hydrogen bonds...

The asymmetric unit of the title compound, NH(4) (+)·CF(2)NO(4)S(2) (-), consists of two crystallographically independent ammonium cations and two 4,4-difluoro-1,3,2-dithia-zetin-2-ide 1,1,3,3-tetra-oxide anions all located in general positions. The S-C-S-N rings of both crystallographically independent anions are almost planar, with the N atom bent out of the plane by 9.82 (5) and 12.82 (4)°. ...

In the title salt, (C(16)H(36)N)[Fe(C(3)H(9)OSi)(4)], the cation contains a central N atom bonded to four n-butyl alkyl groups in a tetra-hedral arrangement, while the anion contains a central Fe(III) atom tetra-hedrally coordinated by four trimethyl-silanolate ligands.

In the structure of the title coordination polymer, {(C(8)H(20)N)[Sn(3)(CH(3))(9)(SO(4))(2)]}(n), each of the three Sn(IV) atoms is coordinated in a trigonal-bipyramidal manner by three methyl groups in the equatorial plane and by two O atoms of SO(4) (2-) anions in the axial positions. The μ(3)-bridging mode of the sulfate anions leads to the formation of corrugated anionic layers parallel to ...