Department of Chemistry Ludwig-Maximilians University, Butenandtstrasse 5-13 (Haus D), D-81377, Munich, Germany.
Inorg Chem. 2010 Mar 15;49(6):2674-83. doi: 10.1021/ic901820b.
The syntheses and characterization of uranyl complexes of nitrogen-containing ligands are reported. For the first time, an actinide complex containing dinitramide ligands coordinated to the actinide center in UO(2)(N(NO(2))(2))(2)(OP(NMe(2))(3))(2) (1) has been isolated and structurally characterized. Using an excess of OP(NMe(2))(3), the dinitramide ligands were replaced by OP(NMe(2))(3) ligands resulting in the formation of the salt [UO(2)(OP(NMe(2))(3))(4)]N(NO(2))(2) (2). Both complexes 1 and 2 were characterized using IR, Raman, as well as (1)H, (13)C, (14)N and (31)P{(1)H} NMR spectroscopy, in addition to C/H/N analysis. The structures of 1 and 2 were determined by single crystal X-ray diffraction. 1: monoclinic, P2(1)/n, a = 12.5389(3), b = 7.9496(2), c = 15.8172(4) A, beta = 110.842(3) degrees , V = 1473.48(6) A(3), Z = 2. 2: orthorhombic, Pbca, a = 14.5640(6), b = 15.3697(6), c = 45.7789(18) A, V = 10247.3(7) A(3), Z = 8. The related complex [UO(2)(N(CN)(2))(2)(OP(NMe(2))(3))(2)] (3) containing the dicyanamide ligand (N(CN)(2)(-)) coordinated to the U(VI) center was synthesized and characterized using IR, Raman, (1)H, (13)C and (31)P{(1)H} NMR spectroscopy. The structure of 3 was determined using single crystal X-ray diffraction and revealed a dinuclear complex containing both terminal and bridging N(CN)(2)(-) ligands. 3: monoclinic, P2(1)/c, a = 15.5873(9), b = 14.2132(6), c = 13.2006(5) A, beta = 100.029(3) degrees, V = 2879.8(2) A(3), Z = 2. Finally, in this investigation of the coordination of relatively nitrogen-rich ligands to uranium centers, the synthesis, characterization, and isolation of the first U(VI) complex showing coordination of the triazolate ligand via a ring nitrogen atom is reported in UO(2)((NC)(2)C(2)N(3))(2)(OPPh(3))(3) (4). Complex 4 was characterized using IR, Raman, (1)H, (13)C and (31)P{(1)H} NMR spectroscopy. The solid state structure of 4 was determined using single crystal X-ray diffraction. 4: monoclinic, P2(1)/n, a = 18.9970(2), b = 31.9500(3), c = 20.1133(2) A, beta = 111.4449(4) degrees, V = 11362.69(19) A(3), Z = 8. To the best of our knowledge, compounds 1 and 2 are the first structurally characterized complexes where a dinitramide ligand is coordinated to an f-block center. Complex 3 is the first structurally characterized actinide dicyanamide complex and a rare example of a dinuclear uranyl complex showing a 12 membered U-N-C ring formed by bridging dicyanamide ligands between two uranyl centers. Finally, complex 4 is the first isolated and structurally characterized uranium complex containing a triazolate ligand coordinated to the U(VI) center. Complexes 3 and 4 are examples of uranyl complexes containing ligands coordinated via nitrogen atoms to the U(VI) center. Whereas the dinitramide ligand can coordinate via N or O atoms, in complex 1, the N(NO(2))(2) ligand acts as a bidentate chelate ligand, and only coordination via the oxygen atoms to the U(VI) center was observed in the crystalline state.
报告了含氮配体的铀酰配合物的合成和表征。首次分离并结构表征了含有 dinitramide 配体配位到 actinide 中心的铀酰配合物 UO(2)(N(NO(2))(2))(2)(OP(NMe(2))(3))(2) (1)。通过使用过量的 OP(NMe(2))(3),将 dinitramide 配体替换为 OP(NMe(2))(3)配体,得到盐 [UO(2)(OP(NMe(2))(3))(4)]N(NO(2))(2) (2)。使用红外、拉曼以及 1H、13C、14N 和 31P{(1)H} NMR 光谱,除了 C/H/N 分析之外,还对配合物 1 和 2 进行了表征。通过单晶 X 射线衍射确定了 1 和 2 的结构。1:单斜,P2(1)/n,a = 12.5389(3),b = 7.9496(2),c = 15.8172(4) A,β = 110.842(3)°,V = 1473.48(6) A(3),Z = 2。2:正交,Pbca,a = 14.5640(6),b = 15.3697(6),c = 45.7789(18) A,V = 10247.3(7) A(3),Z = 8。合成了含有 dicyanamide 配体 (N(CN)(2)(-)) 配位到 U(VI) 中心的相关配合物 [UO(2)(N(CN)(2))(2)(OP(NMe(2))(3))(2)] (3),并通过红外、拉曼、1H、13C 和 31P{(1)H} NMR 光谱对其进行了表征。通过单晶 X 射线衍射确定了 3 的结构,结果表明它是一种含有末端和桥接 N(CN)(2)(-) 配体的双核配合物。3:单斜,P2(1)/c,a = 15.5873(9),b = 14.2132(6),c = 13.2006(5) A,β = 100.029(3)°,V = 2879.8(2) A(3),Z = 2。最后,在这项对相对富氮配体与铀中心配位的研究中,首次报道了 U(VI) 配合物 UO(2)((NC)(2)C(2)N(3))(2)(OPPh(3))(3) (4),其显示通过环氮原子配位三唑配体。通过使用红外、拉曼、1H、13C 和 31P{(1)H} NMR 光谱对 4 进行了表征。通过单晶 X 射线衍射确定了 4 的固态结构。4:单斜,P2(1)/n,a = 18.9970(2),b = 31.9500(3),c = 20.1133(2) A,β = 111.4449(4)°,V = 11362.69(19) A(3),Z = 8。据我们所知,化合物 1 和 2 是首次结构表征的含有 dinitramide 配体配位到 f 区中心的配合物。3 是第一个结构表征的 actinide dicyanamide 配合物,也是一个罕见的双核铀酰配合物的例子,其通过桥连的二氰胺配体在两个铀酰中心之间形成 12 元 U-N-C 环。最后,配合物 4 是第一个分离并结构表征的含有三唑配体配位到 U(VI) 中心的铀酰配合物。配合物 3 和 4 是含有通过氮原子配位到 U(VI) 中心的配体的铀酰配合物的例子。尽管 dinitramide 配体可以通过 N 或 O 原子配位,但在配合物 1 中,N(NO(2))(2) 配体充当双齿螯合配体,并且在晶体状态下仅观察到与 U(VI) 中心的氧原子配位。