Terbium compounds are compounds formed by the lanthanide metal terbium (Tb). Terbium generally exhibits the +3 oxidation state in these compounds, such as in TbCl3, Tb(NO3)3 and Tb(CH3COO)3. Compounds with terbium in the +4 oxidation state are also known, such as TbO2 and BaTbF6. Terbium can also form compounds in the 0, +1 and +2 oxidation states. The trivalent terbium ion (Tb3+) is generally colorless in aqueous solution, and when it is irradiated by certain wavelengths of ultraviolet light (such as 254 nm or 365 nm) in solution or crystal form, it will emit green fluorescence. This property has given rise to applications in fields such as optics. The tetravalent terbium ion (Tb4+) is non-luminescent and its coexistence with Tb3+ will reduce the green emission of Tb3+.
Properties of terbium compounds
Chalcogenides
Oxides
Terbium has a variety of oxides. The most easily obtained is terbium(III,IV) oxide, which can be produced by the decomposition of terbium compounds such as the hydroxide, the oxalate and the p-aminobenzoate. Terbium(III,IV) oxide, because the oxide contains both trivalent terbium and tetravalent terbium, can be decomposed by reacting with nitric acid to produce terbium(III) nitrate, releasing oxygen in the progress:
2 Tb4O7 + 24 HNO3 → 8 Tb(NO3)3 + 12 H2O + O2↑ It is refluxed in a mixture of acetic acid and hydrochloric acid, which can separate trivalent and tetravalent terbium:
Tb4O7 + 6 HCl → 2 TbO2 + 2 TbCl3 + 3 H2O It reacts with dicyandiamide at a high temperature to obtain Tb2O2CN2. Another common oxide of terbium is terbium(III) oxide, which can be obtained from the reduction of hydrogen from terbium(III,IV) oxide at 1300 °C. A p-type semiconductor is formed after doping with calcium. Terbium(IV) oxide can be prepared by treating terbium(III,IV) oxide with dilute hydrochloric acid, its hydrate TbO2·xH2O can be obtained by oxidizing terbium(III) hydroxide with potassium persulfate in the presence of silver nitrate. Terbium(IV) oxide can form mixed crystals with praseodymium(IV) oxide.
Other chalcogenides Terbium(III) sulfide is one of the sulfides of terbium, which can be obtained by reacting with sulfur in a stoichiometric ratio. It can also be obtained by reacting terbium(III,IV) oxide with carbon disulfide and hydrogen sulfide at high temperature. It reacts with hydrofluoric acid solution to give terbium(III) fluoride hemihydrate. Terbium(III) selenide can be obtained by the reaction of terbium polyselenide TbSe1.9 with metal terbium, which can form black needle-like crystals with U2S3 structure and space group Pnma. Terbium monochalcogenides, TbZ (Z = S, Se or Te), can be prepared by directly reacting terbium with the corresponding chalcogen. These chalcogenides are black and have a NaCl structure. They have metallic conductivity and consist of Ln3+ and Z2- ions with 1 electron from each cation delocalized in a conduction band.
Halides and halogen complexes
Terbium can form four trihalides in the form TbX3 (X=F, Cl, Br, I), which, except the fluoride, are easily soluble in water, and are strong electrolytes in water. They can be prepared by reacting terbium with the corresponding halogen:
2Tb (s) + 3F2 (g) → 2TbF3 (s) [a white substance] 2Tb (s) + 3Cl2 (g) → 2TbCl3 (s) [a white substance] 2Tb (s) + 3Br2 (g) → 2TbBr3 (s) [a white substance] 2Tb (s) + 3I2 (g) → 2TbI3 (s) Anhydrous terbium halides can be prepared by reacting oxides or halides hydrates:
Tb2O3 + 6 NH4Cl → 2 TbCl3 + 3 H2O + 6 NH3↑ TbCl3·6H2O + 6 SOCl2 → TbCl3 + 6 SO2↑ + 12 HCl↑ Terbium(II) halides are obtained by annealing Tb(III) halides in presence of metallic Tb in tantalum containers. Terbium also forms a sesquichloride Tb2Cl3, which can be further reduced to TbCl by annealing at 800 °C. This terbium(I) chloride forms platelets with layered graphite-like structure. Terbium(IV) fluoride is the only halide that tetravalent terbium can form, and has strong oxidizing properties. It is also a strong fluorinating agent, emitting relatively pure atomic fluorine when heated, rather than the mixture of fluoride vapors emitted from cobalt(III) fluoride or cerium(IV) fluoride. It can be obtained by reacting terbium(III) chloride or terbium(III) fluoride with fluorine gas at 320 °C:
2 TbF3 + F2 → 2 TbF4 When TbF4 and CsF is mixed in a stoichiometric ratio, in a fluorine gas atmosphere, CsTbF5 is obtained. It is an orthorhombic crystal, with space group Cmca, with a layered structure composed of [TbF8]4− and 11-coordinated Cs+. The compound BaTbF6 can be prepared in a similar method. It is an orthorhombic crystal, with space group Cmma. The compound [TbF8]4− also exists.
Organoterbium compounds
Organoterbium compounds are a class of organic metal compounds containing Tb-C bonds. The cyclopentadienyl complexes of terbium were studied in the early stage. They can be prepared by the reaction of sodium cyclopentadienide and anhydrous terbium halide in tetrahydrofuran, such as:
TbCl3 + 3 C5H5Na → (C5H5)3Tb + 3 NaCl TbI2 + 2 (C5HiPr4)Na → (C5HiPr4)2Tb + 2 NaI However, this compound has limited usage and academic interest. Like the other lanthanides, metal-carbon σ bonds are found in alkyls of terbium such as [TbMe6]3− and Tb[CH(SiMe3)2]3. The alkyls and aryls can be prepared by metathesis in tetrahydrofuran on ether solutions:
TbCl3 + 3 LiR → TbR3 + 3 LiCl TbCl3 + 4 LiR → Li[TbR4] + 3 LiCl3
Other compounds
Oxoacid salts
… excerpt ends here. Continue reading the full article.






