Lanthanum(III) iodide can be synthesised by the reaction of lanthanum metal with mercury(II) iodide:[2][3]
2 La + 3 HgI2 → 2 LaI3 + 3 Hg
It can also be prepared from the elements, that is by the reaction of metallic lanthanum with iodine:[2]
2 La + 3 I2 → 2 LaI3
While lanthanum(III) iodide solutions can be generated by dissolving lanthanum oxide in hydroiodic acid, the product will hydrolyse and form polymeric hydroxy species:[4]
Lanthanum(III) iodide is very soluble in water and is deliquescent.[4] Anhydrous lanthanum(III) iodide reacts with tetrahydrofuran to form a photoluminescent complex, LaI3(THF)4, with an average La–I bond length of 3.16 Å.[6][7] This complex is a starting material for amide and cyclopentadienyl complexes of lanthanum.[6][8]
Related compounds
Lanthanum also forms a diiodide, LaI2. It is an electride and is best formulated {LaIII,2I−,e−}, with the electron delocalised in a conduction band.[4] Several other lanthanides form similar compounds, including CeI2, PrI2 and GdI2.[9] Lanthanum diiodide adopts the same tetragonal crystal structure as PrI2.[10]
Lanthanum(III) iodide reacts with lanthanum metal under an argon atmosphere in a tantalum capsule at 1225 K to form the mixed-valence compound La2I5.[11]
Reduction of LaI2 or LaI3 with metallic sodium in an argon atmosphere at 550 °C gives lanthanum monoiodide, LaI, which has a hexagonal crystal structure.[12]
^ abCorbett, John D. & Simon, Arndt (1984). "Chapter 6: Lanthanum Triiodide (and Other Rare Earth Metal Triiodides)". In Holt Jr., Smith L. (ed.). Inorg. Synth. Vol. 22. pp. 11–16. doi:10.1002/9780470132531.ch6.
^Li, Yangjuan; Chen, Xiuting; Gong, Yu (2021). "Photoluminescence of LaI3 switched on and off by association and dissociation of non-luminescent tetrahydrofuran". Dalton Trans.50 (11): 3797–3800. doi:10.1039/D1DT00162K. PMID33720234. S2CID232232544.
^Windorff, Cory J.; Dumas, Megan T.; Ziller, Joseph W.; Gaunt, Andrew J.; Kozimor, Stosh A.; Evans, William J. (2017). "Small-Scale Metal-Based Syntheses of Lanthanide Iodide, Amide, and Cyclopentadienyl Complexes as Analogues for Transuranic Reactions". Inorg. Chem.56 (19): 11981–11989. doi:10.1021/acs.inorgchem.7b01968. PMID28915015.
^Wells, A. F. (1984). Structural Inorganic Chemistry (5th ed.). Oxford University Press. p. 1250. ISBN978-0-19-965763-6.
^Burrow, J. H.; Maule, C. H.; Strange, P.; Tothill, J. N.; Wilson, J. A. (1987). "The electronic conditions in the 5d1 layer-metal LaI2 making comparison with the iso-electronic tantalum dichalcogenides, with the other RE di-iodides, and with the RE monochalcogenides". J. Phys. C: Solid State Phys.20 (26): 4115–4133. Bibcode:1987JPhC...20.4115B. doi:10.1088/0022-3719/20/26/014.