Zhang Rui-Bo, Li Zhao-Ji, Qin Ye-Yan, Cheng Jian-Kai, Zhang Jian, Yao Yuan-Gen
The State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, The Chinese Academy of Sciences, Fuzhou, Fujian 350002, P.R. China.
Inorg Chem. 2008 Jun 2;47(11):4861-76. doi: 10.1021/ic8001042. Epub 2008 May 2.
Nine members of a new anions-controlled Cd(II)-guanazole (3,5-diamino-1,2,4-triazole=Hdatrz) hybrid family, that is, [Cd3(datrz)6(H2O)2] (1), [Cd3(datrz)4F2] (2), [Cd5(datrz)4Cl4(OH)2] (3), [Cd5(datrz)4Br4(OH)2] (4), [Cd3(datrz)2(SO3)2].(H2O) (5), [Cd3(datrz)2(O2CMe)4] (6), [Cd(datrz)(O2CEt)] (7), [Cd(Hdatrz)(O2CtBu)2] (8), and [Cd(Hdatrz)2(H2Edta)] (9) have been synthesized by exploiting hydrothermal reactions of guanazole with suitable cadmium salts under appropriate reaction conditions. With effective control of inorganic or organic anions, the coordination diversity of the guanazole ligand in 1-9 manifests an unprecedented enrichment with five bridging modes varying from bidentate to quadridentate, two of which are first reported. Compound 1 is the first reported three-dimensional chiral complex constructed from the guanazole ligand which adopts a novel N1, N2, amino N-bridging mode. Halogen anions F-, Cl-, and Br- controlled compounds 2-4 are all three-dimensional, with their guanazole ligands possessing another novel quadridentate bridging mode. Sulfite anions controlled compound 5 displays a three-dimensional network with peculiar cage-like hexnuclear cadmium clusters. As for organic anions, low dimensional structures have been found for alkylcarboxylate anions MeCO2-, EtCO2-, and tBuCO2- controlled compounds 6, 7, and 8 (two-dimensional) and for H2Edta2- controlled compound 9 (zero-dimensional), and their guanazole ligands manifest low coordination numbers as well. These hybrid materials also present interesting structure-induced physical properties. The chiral compound 1 exhibits the second-order nonlinear optical properties at room temperature. Compounds 2-9 except 6 all exhibit photoluminescence of blue fluorescent emissions in the solid state at ambient temperature, which may be assigned to the intraligand pi-pi* transitions. Some structure related red or blue emission shifts have been investigated. Thermal studies show that most compounds of this study possess a high thermal stability.
通过在适当反应条件下利用胍唑与合适镉盐的水热反应,合成了一个新的阴离子控制的镉(II)-胍唑(3,5-二氨基-1,2,4-三唑 = Hdatrz)杂化家族的九个成员,即[Cd3(datrz)6(H2O)2](1)、[Cd3(datrz)4F2](2)、[Cd5(datrz)4Cl4(OH)2](3)、[Cd5(datrz)4Br4(OH)2](4)、[Cd3(datrz)2(SO3)2].(H2O)(5)、[Cd3(datrz)2(O2CMe)4](6)、[Cd(datrz)(O2CEt)](7)、[Cd(Hdatrz)(O2CtBu)2](8)和[Cd(Hdatrz)2(H2Edta)](9)。通过有效控制无机或有机阴离子,1-9中胍唑配体的配位多样性表现出前所未有的丰富,具有从双齿到四齿的五种桥连模式,其中两种是首次报道。化合物1是首次报道的由胍唑配体构建的三维手性配合物,其采用了新颖的N1、N2、氨基N桥连模式。卤素阴离子F-、Cl-和Br-控制的化合物2-4均为三维结构,其胍唑配体具有另一种新颖的四齿桥连模式。亚硫酸根阴离子控制的化合物5显示出具有特殊笼状六核镉簇的三维网络。至于有机阴离子,对于烷基羧酸根阴离子MeCO2-、EtCO2-和tBuCO2-控制的化合物6、7和8(二维)以及H2Edta2-控制的化合物9(零维)发现了低维结构,并且它们的胍唑配体也表现出低配位数。这些杂化材料还呈现出有趣的结构诱导物理性质。手性化合物1在室温下表现出二阶非线性光学性质。除6之外的化合物2-9在室温下固态时均表现出蓝色荧光发射的光致发光,这可能归因于配体内π-π*跃迁。已经研究了一些与结构相关的红移或蓝移发射。热学研究表明,本研究中的大多数化合物具有高的热稳定性。