Kawano M, Bacon J W, Campana C F, Winger B E, Dudek J D, Sirchio S A, Scruggs S L, Geiser U, Dahl L F
Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, USA.
Inorg Chem. 2001 May 21;40(11):2554-69. doi: 10.1021/ic000979p.
Pd(16)Ni(4)(CO)(22)(PPh(3))(4)(-) (1) and Pd(33)Ni(9)(CO)(41)(PPh(3))(6)(-) (2) were obtained as the two major products from the reduction of PdCl(2)(PPh(3))(2) with Ni(6)(CO)(12)(-). Their crystal structures as PPh(4) salts were unambiguously determined from CCD X-ray crystallographic analyses; the resulting stoichiometries were ascertained from elemental analyses. Infrared, multinuclear (1)H, (31)P[(1)H] NMR, UV-vis, CV, variable-temperature magnetic susceptibility, and ESI FT/ICR mass spectrometric measurements were performed. The Pd(16)Ni(4) core of 1 ideally conforms to a ccp nu(3) tetrahedron of pseudo-T(d)() (4 3m) symmetry. Its geometry normal to each tetrahedral Pd(7)Ni(3) face (i.e., along each of the four 3-fold axes) may be viewed as a four-layer stacking of 20 metal atoms in a ccp [a(Ni(1)) b(Pd(3)) c(Pd(6)) a(Pd(7)Ni(3))] sequence. A comparative analysis of the different ligand connectivities about the analogous metal-core geometries in 1 and the previously reported Os(20)(CO)(40)(-) has stereochemical implications pertaining to the different possible modes of carbon monoxide attachment to ccp metal(111) surfaces. The unique geometry of the Pd(33)Ni(9) core of 2, which has pseudo-D(3)(h)() (6 2m) symmetry, consists of five equilateral triangular layers that are stacked in a hcp [a(Pd(7)Ni(3)) b(Pd(6)) a(Pd(7)Ni(3)) b(Pd(6)) a(Pd(7)Ni(3))] sequence. Variable-temperature magnetic susceptibility measurements indicated both 1 and 2 to be diamagnetic over the entire temperature range from 5.0 to 300 K. Neutral Pd(12)(CO)(12)(PPh(3))(6) (3) and Pd(29)(CO)(28)(PPh(3))(7)(-) (4) as the PPh(4) salt were obtained as minor decomposition products from protonation reactions of 1 and 2, respectively, with acetic acid. Compound 3 of pseudo-D(3)(d)() (3 2/m) symmetry represents the second highly deformed hexacapped octahedral member of the previously established homopalladium family of clusters containing uncapped, monocapped, bicapped, and tetracapped Pd(6) octahedra. The unprecedented centered 28-atom polyhedron for the Pd(29) core of 4 of pseudo-C(3)(v)() (3m) symmetry may be described as a four-layer stacking of 29 metal atoms in a mixed hcp/ccp [a(Pd(1)) b(Pd(3)) a(Pd(10)) c(Pd(15))] sequence.
Pd(16)Ni(4)(CO)(22)(PPh(3))(4)(-)(1)和Pd(33)Ni(9)(CO)(41)(PPh(3))(6)(-)(2)是用Ni(6)(CO)(12)(-)还原PdCl(2)(PPh(3))(2)得到的两种主要产物。通过电荷耦合器件X射线晶体学分析明确确定了它们作为PPh(4)盐的晶体结构;通过元素分析确定了所得的化学计量比。进行了红外、多核(1)H、(31)P[(1)H]核磁共振、紫外可见、循环伏安、变温磁化率和电喷雾傅里叶变换/离子回旋共振质谱测量。1的Pd(16)Ni(4)核理想地符合具有伪-T(d)()(4 3m)对称性的面心立方nu(3)四面体。其垂直于每个四面体Pd(7)Ni(3)面(即沿着四个3重轴中的每一个)的几何形状可视为20个金属原子以面心立方[a(Ni(1)) b(Pd(3)) c(Pd(6)) a(Pd(7)Ni(3))]序列的四层堆叠。对1中类似金属核几何形状周围不同配体连接性与先前报道的Os(20)(CO)(40)(-)进行的比较分析具有与一氧化碳附着到面心立方金属(111)表面的不同可能模式相关的立体化学意义。2的具有伪-D(3)(h)()(6 2m)对称性的Pd(33)Ni(9)核的独特几何形状由五个等边三角形层组成,这些层以六方密堆积[a(Pd(7)Ni(3)) b(Pd(6)) a(Pd(7)Ni(3)) b(Pd(6)) a(Pd(7)Ni(3))]序列堆叠。变温磁化率测量表明1和2在5.0至300 K的整个温度范围内都是抗磁性的。中性的Pd(12)(CO)(12)(PPh(3))(6)(3)和Pd(29)(CO)(28)(PPh(3))(7)(-)(4)作为PPh(4)盐分别是1和2与乙酸质子化反应的次要分解产物。具有伪-D(3)(d)()(3 2/m)对称性的化合物3代表了先前建立的包含未封端、单封端、双封端和四封端Pd(6)八面体的同钯簇家族中的第二个高度变形的六帽八面体成员。4的具有伪-C(3)(v)()(3m)对称性的Pd(29)核的前所未有的中心28原子多面体可描述为29个金属原子以混合六方密堆积/面心立方[a(Pd(1)) b(Pd(3)) a(Pd(10)) c(Pd(15))]序列的四层堆叠。