| |||
Names | |||
---|---|---|---|
IUPAC name bismuth bromide | |||
Other names bismuth tribromide tribromobismuth tribromobismuthine tribromobismuthane bismuth(III) bromide | |||
Identifiers | |||
3D model (JSmol) | |||
ChemSpider | |||
ECHA InfoCard | 100.029.201 | ||
EC Number |
| ||
PubChem CID | |||
UNII | |||
CompTox Dashboard (EPA) | |||
| |||
| |||
Properties | |||
BiBr3 | |||
Molar mass | 448.692 g·mol−1 | ||
Appearance | white to light yellow or golden deliquescent crystals [1] | ||
Density | 5.72 g/cm3 at 25 °C [1] | ||
Melting point | 219 °C (426 °F; 492 K) [1] | ||
Boiling point | 462 °C (864 °F; 735 K) [1] | ||
Soluble, slow hydrolysis | |||
Solubility | diethyl ether, THF | ||
-147.0·10−6 cm3/mol | |||
Thermochemistry | |||
Std enthalpy of formation (ΔfH⦵298) | −276 [1] | ||
Hazards | |||
Occupational safety and health (OHS/OSH): | |||
Main hazards | corrosive [2] | ||
GHS labelling: | |||
Danger | |||
H314 | |||
P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, P501 | |||
NFPA 704 (fire diamond) | |||
Related compounds | |||
Other anions | bismuth trifluoride bismuth trichloride bismuth triiodide | ||
Other cations | nitrogen tribromide phosphorus tribromide arsenic tribromide antimony tribromide aluminium tribromide iron(III) bromide | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Bismuth tribromide is an inorganic compound of bismuth and bromine with the chemical formula BiBr3.
It may be formed by the reaction of bismuth oxide and hydrobromic acid. [1]
Bismuth tribromide can also be produced by the direct oxidation of bismuth in bromine. [1]
Bismuth tribromide adopts two different structures in the solid state: a low-temperature polymorph α-BiBr3 that is stable below 158 °C and a high-temperature polymorph β-BiBr3 that is stable above this temperature. Both polymorphs are monoclinic, but α-BiBr3 is in space group P21/a whereas β-BiBr3 is in C2/m. α-BiBr3 consists of pyramidal molecules whereas β-BiBr3 is polymeric and adopts the AlCl3 structure. BiBr3 is the only group 15 trihalide that can adopt both molecular and polymeric structures. [3]
Bismuth bromide is highly water-soluble. It is a Lewis acid and accepts bromide ions to form monomeric and oligomeric anionic complexes (bromobismuthates), e.g. [BiBr6]3−, [Bi2Br10]4−, (BiBr−
4)n and (BiBr2−
5)n. [4]
Bromine is a chemical element; it has symbol Br and atomic number 35. It is a volatile red-brown liquid at room temperature that evaporates readily to form a similarly coloured vapour. Its properties are intermediate between those of chlorine and iodine. Isolated independently by two chemists, Carl Jacob Löwig and Antoine Jérôme Balard, its name was derived from the Ancient Greek βρῶμος (bromos) meaning "stench", referring to its sharp and pungent smell.
Phosphorus tribromide is a colourless liquid with the formula PBr3. The liquid fumes in moist air due to hydrolysis and has a penetrating odour. It is used in the laboratory for the conversion of alcohols to alkyl bromides.
Phosphorus pentabromide is a reactive, yellow solid of formula PBr5, which has the structure [PBr4]+Br− in the solid state but in the vapor phase is completely dissociated to PBr3 and Br2. Rapid cooling of this phase to 15 K leads to formation of the ionic species phosphorus heptabromide.
Carbon tetrabromide, CBr4, also known as tetrabromomethane, is a bromide of carbon. Both names are acceptable under IUPAC nomenclature.
Gold(III) bromide is a dark-red to black crystalline solid. It has the empirical formula AuBr3, but exists primarily as a dimer with the molecular formula Au2Br6 in which two gold atoms are bridged by two bromine atoms. It is commonly referred to as gold(III) bromide, gold tribromide, and rarely but traditionally auric bromide, and sometimes as digold hexabromide. As is similar with the other gold halides, this compound is unique for being a coordination complex of a group 11 transition metal that is stable in an oxidation state of +3 whereas copper or silver complexes persist in oxidation states of +1 or +2.
Tantalum(V) bromide is the inorganic compound with the formula Ta2Br10. Its name comes from the compound's empirical formula, TaBr5. It is a diamagnetic, orange solid that hydrolyses readily. The compound adopts an edge-shared bioctahedral structure, which means that two TaBr5 units are joined by a pair of bromide bridges. There is no bond between the Ta centres. Niobium(V) chloride, niobium(V) bromide, niobium(V) iodide, tantalum(V) chloride, and tantalum(V) iodide all share this structural motif.
Tin(II) bromide is a chemical compound of tin and bromine with a chemical formula of SnBr2. Tin is in the +2 oxidation state. The stability of tin compounds in this oxidation state is attributed to the inert pair effect.
Bromine compounds are compounds containing the element bromine (Br). These compounds usually form the -1, +1, +3 and +5 oxidation states. Bromine is intermediate in reactivity between chlorine and iodine, and is one of the most reactive elements. Bond energies to bromine tend to be lower than those to chlorine but higher than those to iodine, and bromine is a weaker oxidising agent than chlorine but a stronger one than iodine. This can be seen from the standard electrode potentials of the X2/X− couples (F, +2.866 V; Cl, +1.395 V; Br, +1.087 V; I, +0.615 V; At, approximately +0.3 V). Bromination often leads to higher oxidation states than iodination but lower or equal oxidation states to chlorination. Bromine tends to react with compounds including M–M, M–H, or M–C bonds to form M–Br bonds.
Indium(I) bromide is a chemical compound of indium and bromine. It is a red crystalline compound that is isostructural with β-TlI and has a distorted rock salt structure. Indium(I) bromide is generally made from the elements, heating indium metal with InBr3. It has been used in the sulfur lamp. In organic chemistry, it has been found to promote the coupling of α, α-dichloroketones to 1-aryl-butane-1,4-diones. Oxidative addition reactions with for example alkyl halides to give alkyl indium halides and with NiBr complexes to give Ni-In bonds are known. It is unstable in water decomposing into indium metal and indium tribromide. When indium dibromide is dissolved in water, InBr is produced as a, presumably, insoluble red precipitate, that then rapidly decomposes.
Lead(II) bromide is the inorganic compound with the formula PbBr2. It is a white powder. It is produced in the burning of typical leaded gasolines.
Niobium(V) bromide is the inorganic compound with the formula Nb2Br10. Its name comes from the compound's empirical formula, NbBr5. It is a diamagnetic, orange solid that hydrolyses readily. The compound adopts an edge-shared bioctahedral structure, which means that two NbBr5 units are joined by a pair of bromide bridges. There is no bond between the Nb centres. Niobium(V) chloride, niobium(V) iodide, tantalum(V) chloride, tantalum(V) bromide, and tantalum(V) iodide all share this structural motif.
Bismuth pentafluoride is an inorganic compound with the formula BiF5. It is a white solid that is highly reactive. The compound is of interest to researchers but not of particular value.
Sodium bismuthate is an inorganic compound, and a strong oxidiser with chemical formula NaBiO3. It is somewhat hygroscopic, but not soluble in cold water, which can be convenient since the reagent can be easily removed after the reaction. It is one of the few water insoluble sodium salts. Commercial samples may be a mixture of bismuth(V) oxide, sodium carbonate and sodium peroxide.
Praseodymium(III) bromide is a crystalline compound of one praseodymium atom and three bromine atoms.
Neodymium(III) bromide is an inorganic salt of bromine and neodymium the formula NdBr3. The anhydrous compound is an off-white to pale green solid at room temperature, with an orthorhombic PuBr3-type crystal structure. The material is hygroscopic and forms a hexahydrate in water (NdBr3· 6H2O), similar to the related neodymium(III) chloride.
Selenium tetrabromide is an inorganic compound with a chemical formula SeBr4.
Rhodium(III) bromide refers to inorganic compounds of the formula RhBr3(H2O)n where n = 0 or approximately three. Both forms are brown solids. The hydrate is soluble in water and lower alcohols. It is used to prepare rhodium bromide complexes. Rhodium bromides are similar to the chlorides, but have attracted little academic or commercial attention.
Ruthenium(III) bromide is a chemical compound of ruthenium and bromine with the formula RuBr3. It is a dark brown solid that decomposes above 400 °C.
Praseodymium compounds are compounds formed by the lanthanide metal praseodymium (Pr). In these compounds, praseodymium generally exhibits the +3 oxidation state, such as PrCl3, Pr(NO3)3 and Pr(CH3COO)3. However, compounds with praseodymium in the +2 and +4 oxidation states, and unlike other lanthanides, the +5 oxidation state, are also known.
Zirconium(III) bromide is an inorganic compound with the formula ZrBr3.