 | |
| Identifiers | |
|---|---|
3D model (JSmol) | |
| |
| Properties | |
| P3Sn | |
| Molar mass | 211.631 g·mol−1 |
| Appearance | black solid |
| Density | 4.25 g/cm3 |
| Melting point | 580 °C (1,076 °F; 853 K) |
| insoluble | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Tin triphosphide is a binary inorganic compound of tin metal and phosphorus with the chemical formula SnP3. [1]
X-ray crystallography reveals that tin triphosphide is not a triphosphide. It is a hexaphosphide, with P66- rings. These ruffled P6 rings form three short (2.66 Å) and three long (2.95 Å) Sn-P bonds. The result is that Sn(II) adopts highly distorted octahedral geometry. The structure of tin triphosphide resembles that of gray arsenic, which also features corrugated, linked six-membered (As6) rings, wherein each arsenic atom has a highly distorted octahedral geometry. Germanium triphosphide and tin triphosphide are similar structurally as well.
Tin triphosphide forms triclinic crystals, spatial group R3m with six formula units in a unit cell of dimensions a = 7.378 Å and c = 10.512 Å. [2] [3]
Tin triphosphide can be formed from the fusion of stoichiometric amounts of both elements at 580 °C:
SnP3 has been evaluated for use in energy storage devices. [4]
In chemistry, water(s) of crystallization or water(s) of hydration are water molecules that are present inside crystals. Water is often incorporated in the formation of crystals from aqueous solutions. In some contexts, water of crystallization is the total mass of water in a substance at a given temperature and is mostly present in a definite (stoichiometric) ratio. Classically, "water of crystallization" refers to water that is found in the crystalline framework of a metal complex or a salt, which is not directly bonded to the metal cation.
In chemistry, a phosphide is a compound containing the P3− ion or its equivalent. Many different phosphides are known, with widely differing structures. Most commonly encountered on the binary phosphides, i.e. those materials consisting only of phosphorus and a less electronegative element. Numerous are polyphosphides, which are solids consisting of anionic chains or clusters of phosphorus. Phosphides are known with the majority of less electronegative elements with the exception of Hg, Pb, Sb, Bi, Te, and Po. Finally, some phosphides are molecular.
Octahedral clusters are inorganic or organometallic cluster compounds composed of six metals in an octahedral array. Many types of compounds are known, but all are synthetic.
Copper monosulfide is a chemical compound of copper and sulfur. It was initially thought to occur in nature as the dark indigo blue mineral covellite. However, it was later shown to be rather a cuprous compound, formula Cu+3S(S2). CuS is a moderate conductor of electricity. A black colloidal precipitate of CuS is formed when hydrogen sulfide, H2S, is bubbled through solutions of Cu(II) salts. It is one of a number of binary compounds of copper and sulfur (see copper sulfide for an overview of this subject), and has attracted interest because of its potential uses in catalysis and photovoltaics.
Chromium(II) chloride describes inorganic compounds with the formula CrCl2(H2O)n. The anhydrous solid is white when pure, however commercial samples are often grey or green; it is hygroscopic and readily dissolves in water to give bright blue air-sensitive solutions of the tetrahydrate Cr(H2O)4Cl2. Chromium(II) chloride has no commercial uses but is used on a laboratory-scale for the synthesis of other chromium complexes.
Nickel(II) iodide is an inorganic compound with the formula NiI2. This paramagnetic black solid dissolves readily in water to give bluish-green solutions, from which crystallizes the aquo complex [Ni(H2O)6]I2 (image above). This bluish-green colour is typical of hydrated nickel(II) compounds. Nickel iodides find some applications in homogeneous catalysis.
Uranium pentafluoride is the inorganic compound with the chemical formula UF5. It is a pale yellow paramagnetic solid. The compound has attracted interest because it is related to uranium hexafluoride, which is widely used to produce uranium fuel. It crystallizes in two polymorphs, called α- and β-UF5.
Tin(IV) sulfide is a compound with the formula Sn S
2. The compound crystallizes in the cadmium iodide motif, with the Sn(IV) situated in "octahedral holes' defined by six sulfide centers. It occurs naturally as the rare mineral berndtite. It is useful as semiconductor material with band gap 2.2 eV.
There are three sets of Indium halides, the trihalides, the monohalides, and several intermediate halides. In the monohalides the oxidation state of indium is +1 and their proper names are indium(I) fluoride, indium(I) chloride, indium(I) bromide and indium(I) iodide.
Iridium hexafluoride, also iridium(VI) fluoride, (IrF6) is a compound of iridium and fluorine and one of the seventeen known binary hexafluorides. It is one of only a few compounds with iridium in the oxidation state +6.
Nickel(II) bis(acetylacetonate) is a coordination complex with the formula [Ni(acac)2]3, where acac is the anion C5H7O2− derived from deprotonation of acetylacetone. It is a dark green paramagnetic solid that is soluble in organic solvents such as toluene. It reacts with water to give the blue-green diaquo complex Ni(acac)2(H2O)2.
Metal acetylacetonates are coordination complexes derived from the acetylacetonate anion (CH
3COCHCOCH−
3) and metal ions, usually transition metals. The bidentate ligand acetylacetonate is often abbreviated acac. Typically both oxygen atoms bind to the metal to form a six-membered chelate ring. The simplest complexes have the formula M(acac)3 and M(acac)2. Mixed-ligand complexes, e.g. VO(acac)2, are also numerous. Variations of acetylacetonate have also been developed with myriad substituents in place of methyl (RCOCHCOR′−). Many such complexes are soluble in organic solvents, in contrast to the related metal halides. Because of these properties, acac complexes are sometimes used as catalyst precursors and reagents. Applications include their use as NMR "shift reagents" and as catalysts for organic synthesis, and precursors to industrial hydroformylation catalysts. C
5H
7O−
2 in some cases also binds to metals through the central carbon atom; this bonding mode is more common for the third-row transition metals such as platinum(II) and iridium(III).
Magnesium iron hexahydride is an inorganic compound with the formula Mg2FeH6. It is a green diamagnetic solid that is stable in dry air. The material is prepared by heating a mixture of powdered magnesium and iron under high pressures of hydrogen:
Lithium tungstate is the inorganic compound with the formula Li2WO4. It is a white solid that is soluble in water. The compound is one of the several orthotungstates, compounds that feature the tetrahedral WO42− anion.
Cobalt phosphate is the inorganic compound with the formula Co3(PO4)2. It is a commercial inorganic pigment known as cobalt violet. Thin films of this material are water oxidation catalysts.
Bismuth oxynitrate is the name applied to a number of compounds that contain Bi3+, nitrate ions and oxide ions and which can be considered as compounds formed from Bi2O3, N2O5 and H2O. Other names for bismuth oxynitrate include bismuth subnitrate and bismuthyl nitrate. In older texts bismuth oxynitrate is often simply described as BiONO3 or basic bismuth nitrate. Bismuth oxynitrate was once called magisterium bismuti or bismutum subnitricum, and was used as a white pigment, in beauty care, and as a gentle disinfectant for internal and external use. It is also used to form Dragendorff's reagent, which is used as a TLC stain.
Iridium disulfide is the binary inorganic compound with the formula IrS2. Prepared by the direct reaction of the elements, the compound adopts the pyrite crystal structure at high pressure. At normal atmospheric pressures, an orthorhombic polymorph is observed.. The high- and low-pressure forms both feature octahedral Ir centers, but the S–S distances are pressure dependent. Although not practical, IrS2 is a highly active catalyst for hydrodesulfurization.
Hexaphosphabenzene is a valence isoelectronic analogue of benzene and is expected to have a similar planar structure due to resonance stabilization and its sp2 nature. Although several other allotropes of phosphorus are stable, no evidence for the existence of P6 has been reported. Preliminary ab initio calculations on the trimerisation of P2 leading to the formation of the cyclic P6 were performed, and it was predicted that hexaphosphabenzene would decompose to free P2 with an energy barrier of 13−15.4 kcal mol−1, and would therefore not be observed in the uncomplexed state under normal experimental conditions. The presence of an added solvent, such as ethanol, might lead to the formation of intermolecular hydrogen bonds which may block the destabilizing interaction between phosphorus lone pairs and consequently stabilize P6. The moderate barrier suggests that hexaphosphabenzene could be synthesized from a [2+2+2] cycloaddition of three P2 molecules. Currently, this is a synthetic endeavour which remains to be conquered.
Arsenic in the solid state can be found as gray, black, or yellow allotropes. These various forms feature diverse structural motifs, with yellow arsenic enabling the widest range of reactivity. In particular, reaction of yellow arsenic with main group and transition metal elements results in compounds with wide-ranging structural motifs, with butterfly, sandwich and realgar-type moieties featuring most prominently.
Sulfidostannates, or thiostannates are chemical compounds containing anions composed of tin linked with sulfur. They can be considered as stannates with sulfur substituting for oxygen. Related compounds include the thiosilicates, and thiogermanates, and by varying the chalcogen: selenostannates, and tellurostannates. Oxothiostannates have oxygen in addition to sulfur. Thiostannates can be classed as chalcogenidometalates, thiometallates, chalcogenidotetrelates, thiotetrelates, and chalcogenidostannates. Tin is almost always in the +4 oxidation state in thiostannates, although a couple of mixed sulfides in the +2 state are known,
