Abstract: | I‐Type La2Si2O7: According to La6[Si4O13][SiO4]2 not a Real Lanthanum Disilicate In attempts to synthesize lanthanum telluride silicate La2Te[SiO4] (from La, TeO2, SiO2 and CsCl, molar ratio: 1 : 1: 1 : 20, 950 °C, 7 d) or fluoride‐rich lanthanum fluoride silicates (from LaF3, La2O3, SiO2 and CsCl, molar ratio: 5 : 2 : 3 : 17, 700 °C, 7 d) in evacuated silica tubes, colourless lath‐shaped single crystals of hitherto unknown I‐type La2Si2O7 (monoclinic, P21/c; a = 726.14(5), b = 2353.2(2), c = 1013.11(8) pm, β = 90.159(7)°) were found in the CsCl‐flux melts. Nevertheless, this new modification of lanthanum disilicate does not contain any discrete disilicate groups [Si2O7]6‐ but formally three of them are dismutated into one catena‐tetrasilicate ([Si4O13]10‐ unit of four vertex‐linked [SiO4]4‐ tetrahedra) and two ortho‐silicate anions (isolated [SiO4]4‐ tetrahedra) according to La6[Si4O13][SiO4]2. This compound can be described as built up of alternating layers of these [SiO4]4‐ and the horseshoe‐shaped [Si4O13]10‐ anions along [010]. Between and within the layers the high‐coordinated La 3+ cations (CN = 9 ‐ 11) are localized. The close structural relationship to the borosilicates M3[BSiO6][SiO4](M = Ce ‐ Eu) is discussed and structural comparisons with other catena‐tetrasilicates are presented. |