Abstract: | LaCl(BO2)2 and Er2Cl2[B2O5]: Two Chloride Oxoborates of Trivalent Lanthanides Er2Cl2[B2O5] is obtained as single crystals by the reaction of ErCl3, Er2O3 and B2O3 with an excess of ErCl3 as flux in evacuated silica tubes after two weeks at 850 °C. The compound crystallizes as long, pale pink needles and appears to be air‐ and water‐resistant. Single‐crystalline LaCl(BO2)2 emerges from the reaction of La2O3, LaCl3, and B2O3 with an excess of B2O3 as flux in evacuated silica tubes after four weeks at 900 °C. LaCl(BO2)2 crystallizes as thin, colourless, air‐ and water‐resistant needles which tend to severe twinning due to their fibrous habit. The crystal structure of Er2Cl2[B2O5] (orthorhombic, Pbam; a = 1489.65(9), b = 1004.80(6), c = 524.86(3) pm; Z = 4) contains two crystallographically different erbium cations. (Er1)3+ resides in pentagonal‐bipyramidal coordination of seven anions while (Er2)3+ is surrounded by only six anions with the shape of an octahedron. The planar oxodiborate units [B2O5]4— consisting of two vertex‐shared [BO3]3— triangles are isolated according to {([BOO]2)4—}. LaCl(BO2)2 crystallizes isostructurally with PrCl(BO2)2 in the triclinic space group P1¯ (a = 423.52(4), b = 662.16(7), c = 819.33(8) pm; α = 82.081(8), β = 89.238(9), γ = 72.109(7)°; Z = 2). The characteristic unit consists of endless chains built up by corner‐linked [BO3]3— triangles. These quasi‐planar zigzag chains of the composition {[(B1)OO(B2)OO]2—} (≡ {[BO2]—} run parallel [100]. The La3+ cations exhibit coordination numbers of ten and are coordinated by three Cl— and seven O2— anions. |