The School of Chemical Sciences, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, Illinois 61801, United States.
Inorg Chem. 2012 Jul 2;51(13):7050-65. doi: 10.1021/ic201852j. Epub 2012 Jun 11.
New lanthanide N,N-dimethylaminodiboranate (DMADB) complexes of stoichiometry Ln(H(3)BNMe(2)BH(3))(3) and Ln(H(3)BNMe(2)BH(3))(3)(thf) have been prepared, where Ln = yttrium, lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, and lutetium, except that isolation of the desolvated complexes proved difficult for Eu and Yb. The tetrahydrofuran (thf) complexes are all monomeric, and most of them adopt 13-coordinate structures in which each DMADB group chelates to the metal center by means of four B-H···Ln bridges (each BH(3) group is κ(2)H; i.e., forms two B-H···Ln interactions). For the smallest three lanthanides, Tm, Yb, and Lu, the metal center is 12 coordinate because one of the DMADB groups chelates to the metal center by means of only three B-H···Ln bridges. The structures of the base-free Ln(H(3)BNMe(2)BH(3))(3) complexes are highly dependent on the size of the lanthanide ions: as the ionic radius decreases, the coordination number decreases from 14 (Pr) to 13 (Sm) to 12 (Dy, Y, Er). The 14-coordinate complexes are polymeric: each metal center is bound to two chelating DMADB ligands and to two "ends" of two ligands that bridge in a Ln(κ(3)H-H(3)BNMe(2)BH(3)-κ(3)H)Ln fashion. In the 13-coordinate complexes, all three DMADB ligands are chelating, but the metal atom is also coordinated to one hydrogen atom from an adjacent molecule. The 12-coordinate complexes adopt a dinuclear structure in which each metal center is bound to two chelating DMADB ligands and to two ends of two ligands that bridge in a Ln(κ(2)H-H(3)BNMe(2)BH(3)-κ(2)H)Ln fashion. The complexes react with water, and the partial hydrolysis product La(H(3)BNMe(2)BH(3))(2)(OH) adopts a structure in which the lanthanum and oxygen atoms form a distorted cube; each lanthanum atom is connected to three bridging hydroxyl groups and to two chelating DMADB ligands. One B-H bond of each chelating DMADB ligand forms a bridge to an adjacent metal center. Field ionization MS data, melting and decomposition points, thermogravimetric data, and NMR data, including an analysis of the paramagnetic lanthanide induced shifts (LIS), are reported for all of the complexes. The Ln(H(3)BNMe(2)BH(3))(3) compounds, which are highly volatile and sublime at temperatures as low as 65 °C in vacuum, are suitable for use as chemical vapor deposition (CVD) and atomic layer deposition (ALD) precursors to thin films.
已制备出具有化学计量比 Ln(H(3)BNMe(2)BH(3))(3) 和 Ln(H(3)BNMe(2)BH(3))(3)(thf) 的新型镧系元素 N,N-二甲基氨基二硼酸盐 (DMADB) 配合物,其中 Ln = 钇、镧、铈、镨、钕、钐、钆、铽、镝、钬、铒、铥和镥,Eu 和 Yb 除外,因为难以分离它们的去溶剂配合物。四氢呋喃 (thf) 配合物均为单体,其中大多数采用 13 配位结构,其中每个 DMADB 基团通过四个 B-H···Ln 桥螯合到金属中心(每个 BH(3) 基团为 κ(2)H;即形成两个 B-H···Ln 相互作用)。对于最小的三个镧系元素,Tm、Yb 和 Lu,金属中心为 12 配位,因为其中一个 DMADB 基团仅通过三个 B-H···Ln 桥螯合到金属中心。无碱基 Ln(H(3)BNMe(2)BH(3))(3) 配合物的结构高度依赖于镧系元素离子的大小:随着离子半径的减小,配位数从 14(Pr)减少到 13(Sm)再减少到 12(Dy、Y、Er)。14 配位配合物是聚合的:每个金属中心与两个螯合的 DMADB 配体和桥接两个“末端”的两个配体结合,形成 Ln(κ(3)H-H(3)BNMe(2)BH(3)-κ(3)H)Ln 方式。在 13 配位配合物中,所有三个 DMADB 配体均为螯合,但金属原子也与相邻分子中的一个氢原子配位。12 配位配合物采用双核结构,其中每个金属中心与两个螯合的 DMADB 配体和桥接两个配体的两个“末端”结合,形成 Ln(κ(2)H-H(3)BNMe(2)BH(3)-κ(2)H)Ln 方式。配合物与水反应,部分水解产物 La(H(3)BNMe(2)BH(3))(2)(OH) 采用其中镧和氧原子形成扭曲立方体的结构;每个镧原子与三个桥接的羟基和两个螯合的 DMADB 配体相连。每个螯合的 DMADB 配体的一个 B-H 键形成与相邻金属中心的桥接。报告了所有配合物的场致电离 MS 数据、熔点和分解点、热重数据以及 NMR 数据,包括对顺磁镧系元素诱导位移 (LIS) 的分析。Ln(H(3)BNMe(2)BH(3))(3) 化合物具有很高的挥发性,在真空中低至 65°C 即可升华,适合用作薄膜的化学气相沉积 (CVD) 和原子层沉积 (ALD) 前体。