“…Light green, moisture- and air-sensitive crystals grown from a concentrated solution in toluene at 4 °C revealed a trigonal arrangement of praseodymium atoms (Figure ) supported by three doubly bridging alkoxy ligands present along the sides of the hypothetical triangle (O3, O4, and O5). Two additional μ 3 -bridging alkoxy ligands (O1 and O2) are present below and above the triangular plane, resulting in a 6-fold oxygen coordination around each of the Pr centers as generally favored by this class of lanthanide compounds. , The obtained molecular structure is similar to those reported for yttrium, lanthanum, terbium, and gadolinium tert -butoxides. ,,, Herein, the Pr–O bond lengths (Table ) fit well with the trend of the Ln–O bond lengths within the lanthanide series, exhibiting shorter bond lengths with increasing atomic number (selected bond lengths between Ln and μ 3 -bridging O: La, 2.505 (13) Å; Pr, 2.4721(17) Å; Nd, 2.409 (13) Å; Gd, 2.3610 (15) Å; Tb, 2.343(3) Å; Er, 2.305(3) Å) (selected bond lengths between Ln and μ 2 -bridging O: La, 2.449(14) Å; Pr, 2.4137(18) Å; Nd, 2.399(3) Å; Gd, 2.3313(16) Å; Tb, 2.320(4) Å; Er, 2.269(3) Å) (selected bond lengths between Ln and terminal alkoxy as well as tert -butyl alcohol (with the exception of the Nd complex where THF was reported as a molecule ligate) ligands: La, 2.195(13) Å/2.604(15) Å; Pr, 2.1912(18) Å/2.6639(19) Å; Nd, 2.147(4) Å/2.661(4) Å; Gd, 2.1223(16) Å/2.5567(16) Å; Tb, 2.114(4) Å/2.609(4) Å; Er, 2.067(3) Å/2.525(4) Å). Despite its discrete molecular structure, 1 cannot be vaporized due to coordinated alcohol ligands that are removed under vacuum, thus producing higher agglomerates with evidently low vapor pressure.…”