Skip to content

Chemistry · Ch 11 — The p-Block Elements

Chemical Properties

11.1.6

Chemical Properties

Chemical Properties of Group 13

Oxidation states and the inert-pair effect. Boron is so small that the sum of its first three ionisation enthalpies is enormous — far too costly for boron to simply lose three electrons and form a bare B3+B^{3+} ion. Boron therefore forms only covalent compounds. Moving to aluminium, that combined ionisation cost drops sharply, so aluminium readily loses three electrons to give Al3+Al^{3+} and behaves as a strongly electropositive metal.

Further down the group, though, the poorly-shielding d and f electrons in Ga, In and Tl hold the outer ns2ns^2 electron pair unusually tightly against the nucleus — this reluctance of the ns2ns^2 pair to take part in bonding is called the inert-pair effect. It leaves mainly the single npnp electron free to bond, so Ga, In and Tl show BOTH +1 and +3 states, and the +1 state becomes progressively more stable in the order:

Al<Ga<In<TlAl < Ga < In < Tl

For thallium, +1 is actually the more stable state, while Tl3+Tl^{3+} is a strong oxidising agent. As a general rule, +1-state compounds are more ionic than the corresponding +3-state compounds.

Electron deficiency and Lewis acidity. In the +3 state, these elements form compounds (e.g. BF3BF_3) with only six electrons around the central atom — an incomplete octet. Such "electron-deficient" species readily accept a lone pair from a donor to complete their octet, i.e. they act as Lewis acids. Boron trichloride is the classic example: it accepts the lone pair on ammonia's nitrogen to form an adduct, going from planar BCl3BCl_3 to a tetrahedral adduct:

BCl3+:NH3→Cl3B←NH3BCl_3 + :NH_3 \rightarrow Cl_3B \leftarrow NH_3

Because boron has no d orbitals available, its covalence is capped at 4 — it can never exceed four bonds. Aluminium and the heavier members DO have accessible d orbitals, so their covalence can expand past 4. This is why most other Group 13 trihalides dimerise: AlCl3AlCl_3 exists as Al2Cl6Al_2Cl_6, with each aluminium centre becoming tetrahedral by accepting a lone pair from a bridging chlorine on the neighbouring molecule.

Hydrolysis. Being covalent, most +3 compounds hydrolyse in water. The trichlorides give tetrahedral [M(OH)4]−[M(OH)_4]^- (M is sp3sp^3-hybridised). Aluminium chloride in acidified water instead forms the octahedral complex [Al(H2O)6]3+[Al(H_2O)_6]^{3+}, in which aluminium's 3d orbitals participate and the hybridisation is sp3d2sp^3d^2.

Reactivity toward air. Boron in its crystalline form is unreactive. Aluminium develops a thin, tightly-adherent oxide film that protects the metal underneath. On strong heating in air, both form the trioxide, and with nitrogen they form nitrides:

4E(s)+3O2(g)→Δ2E2O3(s)2E(s)+N2(g)→Δ2EN(s)4E(s) + 3O_2(g) \xrightarrow{\Delta} 2E_2O_3(s) \qquad 2E(s) + N_2(g) \xrightarrow{\Delta} 2EN(s)

The acid–base character of these oxides changes down the group: B2O3B_2O_3 is acidic (reacts with basic oxides to form borates); Al2O3Al_2O_3 and Ga2O3Ga_2O_3 are amphoteric; In2O3In_2O_3 and Tl2O3Tl_2O_3 are basic.

Reactivity toward acids and alkalis. Boron resists both acids and alkalis even on heating. Aluminium is amphoteric — it dissolves in dilute HCl liberating hydrogen: …