A New Family of Lanthanide Borate Halides with Unusual Coordination and a New Neodymium-Containing Cationic Framework

Abstract

The reactions of Ln(2)O(3)/CeO(2)/Pr(6)O(11) (Ln = La-Nd, Sm), molten boric acid, and concentrated HBr or HI result in the formation of La[B(7)O(10)(OH)(3)(H(2)O)Br], Ln[B(6)O(9)(OH)(2)(H(2)O)(2)Br]·0.5H(2)O (Ln = Ce, Pr), Nd(2)[B(12)O(17.5)(OH)(5)(H(2)O)(4)Br(1.5)]Br(0.5)·H(2)O (NdBOBr), Sm(4)[B(18)O(25)(OH)(13)Br(3)], and Ln[B(7)O(11)(OH)(H(2)O)(3)I] (Ln = La-Nd, Sm). The lanthanide(III) centers in these compounds are found with 9-coordinate hula hoop or 10-coordinate capped triangular cupola geometries, where there are six approximately coplanar oxygen donors provided by the polyborate sheet. The sheets are formed into three-dimensional frameworks via BO(3) triangles that are roughly perpendicular to the layers. Additionally, a new cationic framework, NdBOBr, has been isolated. NdBOBr is unusual in that not only is it a cationic framework, but it is also the first trivalent f-element borate to have terminal halides bound exclusively to the base site of the hula hoop. The Ln[B(7)O(11)(OH)(H(2)O)(3)I] (Ln = La-Nd, Sm) structures require two corner-shared BO(3) units in order to tether the layers together because of the large size of the capping iodine atom.