A one-dimensional zigzag chain complex of Cd(FA)(pyim)(H2O) (1) (H2FA=4,4′-(hexafluoroisopropylidene)bis(benzoic acid) and pyim=2-(2-pyridyl)imidazole) was hydrothermal synthesized from Cd(NO3)2·4H2O, 4,4′- (hexafluoroisopropylidene)bis (benzoic acid) and 2-(2-pyridyl)imidazole. Single-crystal X-ray analysis revealed that the zigzag chains of 1 are linked into three-dimensional supramolecular networks by both O-H …O hydrogen- bonds and π…π stacking interactions. The crystal is of monoclinic, space group P21/n with a=0.856 34(10) nm, b=1.020 49(12) nm, c=2.809 0(3) nm, β=98.115(2)°, V=2.430 2(5) nm3, Dc=1.820 g·cm-3, Z=4, F(000)=1 320, Goof= 1.009, R1 =0.047 0, wR2 =0.115 5. In addition, complex 1 exhibits strong photoluminescent emission at room temperature. CCDC: 733837.
A novel compound [Cl2Bz(3-MeQl) ](TCNQ) ([Cl2Bz(3-MeQl) ]+ = 1-(3,4-dichlo-robenzyl) 3-methlquinoline cation,TCNQ-= 7,7,8,8-tetracyanoquinodimethanide anion) has been synthesized by the reaction of [Cl2Bz(3-MeQl) ]Br and LiTCNQ,and its structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic,space group P21/c. The structure analysis shows that the anions are stacked into a column with isolated π-dimers,and there is one type of TCNQ entries(TCNQ) ,in agreement with the IR spectra analysis and density functional theory calculations of the compound. The most prominent structural features are the completely segregated stacking columns of the TCNQ- anions and [Cl2Bz(3-MeQl)]+ cations.
One novel neodymium-tartrate complex exhibiting distinctive rare topology,name-ly,[Nd(TTA)1.5(H2O)]·H2O(1,H2TTA = tartaric acid),was successfully synthesized by the reaction of neodymium-oxide with H2TTA under hydrothermal conditions.Single-crystal X-ray diffraction analysis reveals that 1 belongs to the monoclinic system,space group P21/c with a = 6.0357(13),b = 7.6106(17),c = 24.389(5) ,β = 100.136(5)°,V = 1102.8(4) 3,Z = 4,Dc = 2.423 g·cm-3,μ = 4.763 mm-1,F(000) = 776,the final R = 0.0689 and wR = 0.2191.In complex 1,the 2D layer consisting of μ4-ligands and 4-connected Nd(III) centers is a rare example of uni-nodal net of(42.64) topology.The 2D layers are further connected by μ2-TTA2-ligands to give a 3D(42.64)(42.67.8) topological structure,where the Nd(III) atoms act as rare 5-connected topological blocks.
One Cd(Ⅱ) complex based on dicarboxylate and N-auxiliary ligand, namely, [Cd(aip)(m-bix)]n(1, H2aip=5-aminoisophthalic acid, m-bix=1,3-bis(imidazol-1-yl-methyl)benzene), was successfully synthesized under hydrothermal conditions. Single-crystal X-ray diffraction analysis reveals that 1 belongs to the orthorhombic system, space group Pbca with a=14.0790(11), b=17.0038(15), c=17.3191(16), V=4146.1(6)3 ,Z=8, Dc=1.698 g·cm-3 ,μ=1.095 mm-1 , F(000)=2128, the final R=0.0268 and wR=0.0623. Complex 1 is a three-dimensional architecture with fsc-3,5-Cmce-1 topology, in which the metal ions act as rare 5-connected nodes. The TGA, XRD and luminescent properties of 1 were studied.
A novel compound [(IBz)2Im](TCNQ) [(IBz)2Im=1,3-bis(4-iodobenzyl) imidazole cation, TCNQ-=7,7,8,8-tetracyanoquinodimethanide anion] was synthesized by the reaction of [(IBz)2Im]Br and LiTCNQ in CH3OH and its structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/c with a=1.147 35(18) nm, b=2.028 1(3) nm, c=1.264 1(2) nm, β=104.73(0)°, V=2.666(65) nm3, Z=4, C29H19I2N6, Mr= 705.30, Dc=1.757 g·cm-3, R1=0.053 2 and wR2=0.111 2. The structure analysis shows that the anions are stacked into column with isolated π-dimers, and there is one type of TCNQ entries (TCNQ-), in agreement with the IR spectra analysis of the compound. The most prominent structural features are the completely segregated stacking columns of the TCNQ-anions and [(IBz)2Im]+ cations. CCDC: 759523.
Two new alkaline earth metal coordination polymers constructed from the deriva-tive of 1,2,4-triazole are presented herein,namely,{[Sr(AmTAZAc)2(H2O)]}(1) and {[Ba(AmTAZAc)2(H2O)]}(2)(AmTAZAc = 3-amino-1H-1,2,4-triazole-5-carboxylate),which have been synthesized by using the layering method and structurally characterized by elemental analysis,IR,and single-crystal X-ray diffraction.Complexes 1 and 2 are isostructural,and both crystallize in the orthorhombic system,space group Fdd2.X-ray structural analysis shows that 1 or 2 has an intriguing 3-D infinite network of(318.438.510) topology based on a 2-D sheet structure of(4,4) net.The result shows that noncovalent interactions play an important role in strengthening the whole structures of the compounds.
A novel pyridyl-dicarboxylate Schiff-base ligand (5-((pyridin-3-ylmethyl)amino)isophthalic acid,H2L) and its Zinc(Ⅱ) complex,namely,ZnL (1),were synthesized. The ligand was characterized by NMR analysis. The X-ray crystallographic analysis on complex 1 shows that 1 crystallizes in homoclinic,space group P21/c with a= 0.753 83(10) nm,b=1.040 52(14) nm,c=1.734 67(19) nm,β=112.123(5)°,V=1.260 5(3) nm3,Z=4,Dc=1.769 g· cm-3,F(000)=680,μ=1.966 mm-1,the final R=0.030 8,wR=0.085 6. In complex 1,the coordination environment of Zn(Ⅱ) is distorted tetragonal-pyramid with N1O4 set. The 2D 4,4-topological sheets in 1 packed along a axis to form its 3D framework,which was stabilized by the π…π interactions between the adjacent aromatic rings on the neighbouring sheets. The photoluminescent property of 1 was also investigated.
