A novel organically templated copper pentaborate, [Cu(C3N2H4)4][Cu(CH3COO)2(C3N2H4)2(H2O)2]‐ [B5O6(OH)4]2, was synthesized by hydrothermal reaction and characterized by elemental analysis, single‐crystal X‐ray diffraction, FT‐IR spectroscopy, Raman spectroscopy and TGA. The crystal structure of this compound consists of two copper‐centered polyhedra and two discrete [B5O6(OH)4]? pentaborate anions, which are linked together through intensive hydrogen bonding interactions, forming a 3D framework with large channels along c axis. The discrete pentaborate anions form infinite layers by hydrogen bonds. Moreover, the two crystallographically different octahedral coppers are connected by common oxygen atom to form an infinite chain. 相似文献
The title compound Cu2Cl2phen (phen = 1,10‐phenanthroline, C12H8N2) 1 was synthesized from CuCl2·2H2O, CuCl and phen by hydrothermal method and its structure was determined by single crystal X‐ray analysis. With phen, CuG forms one‐dimensional chains, which comprise two zigzag chains based on fused Cu‐X units and connected via covalent bonds. The compound contains two crystallographically unique monovalent copper ions, Cu(1) and Cu(2). The Cu(1) atom in the tetrahedral site, is coordinated to two bridging Cl? and two N atoms in phen. The Cu(2) atom with a slightly distorted triangular planar geometry, is coordinated to three Cl?. The compound 1 was crystallized in monoclinic, space group P21/n with a = 0.37338(4), b = 1.9510(2), c = 1.68008(19) nm, β = 95.605 (3)°, R = 0.0458, and was characterized by elemental analysis, IR spectrum and TGA analysis. 相似文献
A new hydrated lithium borate, Li4[B8O13(OH)2]·3H2O, has been hydrothermally synthesized and characterized by single crystal X‐ray diffraction, FT‐IR spectroscopy, simultaneous TGA‐DTA and chemical analysis. It crystallizes in the triclinic, space group , a=8.4578(5) Å, b=8.7877(5) Å, c=10.8058(7) Å, α=87.740(3)°, β=71.819(3)°, γ=61.569(3)°, Z=2, V=665.26(7) Å3, Dc=2.043 g/cm3. Its crystal structure features polyborate anionic layers with the larger odd 13‐membered boron rings constructed by [B8O13(OH)2]4? FBBs. Through designing the thermochemical cycle, the standard molar enthalpy of formation of this borate was determined to be ?(7953.8±6.6) kJ·mol?1 by using a heat conduction microcalorimeter. 相似文献
An organic–inorganic hybrid zinc phosphate with 28‐ring channels was synthesized by use of an organic ligand instead of organic amine template under a hydro(solvo)thermal condition. This crystalline zinc phosphate contains large channels constructed from 28 zinc and phosphate tetrahedral units. The walls of the channels consist of two types of zincophosphate chains, in which the Zn atoms are coordinated by 2,4,5‐tri(4‐pyridyl)‐imidazole ligands as pendent groups. This compound exhibits yellow emission and interesting properties of removing cobalt, cadmium, and mercury cations from aqueous solution. A new two‐dimensional organic–inorganic hybrid zincophosphate was also obtained by changing the solvent mixture ratios in the synthesis. 相似文献
1 INTRODUCTION Recently, there has been increasing interest in crystal engineering of supramolecular architectures by means of covalent bonding, hydrogen bonding or other weak intermolecular interactions[1, 2], which reflect their potential applications in host-guest che- mistry, catalysis and function materials[3~5]. The construction of such materials is mainly provided by geometry of transition metal extending through rigid ligands. The oxidation state and coordination predisposition … 相似文献
1 INTRODUCTION Transition metal oxide clusters and their deriva- tives offer an unmatched variety of structural motifs and wide ranging applications in several areas, such as analytical chemistry, materials science and cataly- sis, nanotechnology, chemical sensing, environmental decontamination, biochemical and geochemical pro- cesses, and medicine[1~3]. Polyoxovanadates or vana- dium oxide clusters constitute an important subclass of polyoxometalates and have been studied exten- sively.… 相似文献
The reaction of CuBr2 with 1,10‐phen‐H2O (1,10‐phen = 1,10‐phenanthroline) gave two compounds: CuBr2(C12H8N2) and Cu3Br3(C12H8N2)2. Their structures have been characterized by single‐crystal X‐ray diffraction analysis, elemental analyses, thermogravimetric analyses (TGA) and measurement of variable temperature magnetic susceptibility. Crystal data for CuBr2(C12‐H8N2): monoclinic, space group P21/n, a = 0.9977(3) nm, b = 0.65138(14) nm, c = 1.8207(4) nm, β = 91.624(18)°, V = 1.1828(5) nm3, Z = 2. Crystal data for Cu3Br3(C12H8N2)2: monoclinic, space group C2/c, a = 1.00167(11) nm, b = 1.4523(4) nm, c = 1.6295(3) nm, β = 94.386(14)°, V = 2.3635(8) nm3, Z = 3. 相似文献
Chiral coordination polymers have attracted intense interest mainly due to their potential applications. Hence, two new chiral copper(II) coordination polymers {[Cu(tsgluO)(H2O)]2·3H2O}n ( 1 ) and [Cu(tsgluO)(2,2′‐bipy)]n ( 2 ) (H2tsglu?(+)‐N‐tosyl‐l‐glutamic acid; 2,2′‐bipy?2,2′‐bipyridine) were synthesized in the absence or presence of 2,2′‐bipy ligand and structurally characterized. A single crystal X‐ray diffraction study revealed that compound 1 consists of a paddle‐wheel dicopper(II) core, which links other equivalents via four tsgluO2? ligands to form a 1D double chain. Such a chain is further interconnected through weak π‐π stacking and hydrogen bonding interactions to form a 3D H‐bonded supramolecular structure with 1D channels hosting lattice water molecules. Whereas, compound 2 , containing the coordinating 2,2′‐bipy, gives rise to a ladder‐like 1D double chain. Antiferromagnetic interactions were observed in 1 and 2 . 相似文献
The title compound (H3NCH2CH2NH3)4[(VO)6(B10O22)2](H3O)7 1 has been synthe- sized by the hydrothermal method and determined by X-ray crystallography.Crystallographic data: monoclinic, space group C2/c, a = 20.250(4), b = 13.448(3), c = 21.655(4) (A), β = 97.05(3)°, Mr = 851.74 (C4H30.5B10N4O28.5V3), V = 5852(2) (A)3, Z = 8, Dc = 1.933 g/cm3, μ = 1.057 mm-1, F(000) = 3436, R = 0.0500 and wR = 0.1442 for 4511 observed reflections with I > 2δ(I).The structure con- sists of [(VO)6(B10O22)2]15- cluster anions that have a central band of six trans-edge-sharing VO5 square pyramids capped by two [B10O22]14- polyborate ligands.Other characterizations are also describ- ed by elemental analysis, IR spectrum and thermal analysis. 相似文献
Herein, gelated thermoresponsive large‐compound vesicles (LCVs) are reported for the first time. The LCVs are prepared by self‐assembly of poly(ethylene oxide)‐block‐poly[N‐isopropylacrylamide‐random‐3‐(trimethoxysilyl)propyl methacrylate] [PEO‐b‐P(NIPAM‐r‐TMPM)] in DMF‐water mixture. Then, sol‐gel reaction of the reactive PTMPM block is performed to stabilize the LCVs. LCVs with higher cross‐linking density keep almost the same size under different temperatures while LCVs with lower cross‐linking density display obviously thermoresponsive size transition between 22 and 36 °C. The gelated LCVs exhibit enhanced permeability with temperature elevation and their permeabilities at different temperatures all elevate with increasing the cross‐linking density.
Two isostructural layered coordination polymers constructed from mixed ligands, [Ln2(tdc)3(phen)2(H2O)2] (Ln = Sm 1, Eu 2, H2tdc = thiophene-2,5-dicarboxylic acid, phen = 1,10-phenanthroline), have been hydrothermally synthesized and characterized by elemental analysis, IR and single-crystal X-ray diffraction. Crystal data for 1: triclinic, space group P1 with a = 10.546(2), b = 11.201(2), c = 18.644(4)A, α = 106.69(3), β = 91.27(3), γ = 94.43(3)°, Dc = 1.909 g·cm-3, F(000) = 1180, μ = 2.992 mm^-1, Z = 2, the final R = 0.0300 and wR = 0.0656 for 6968 observed reflections with I 〉 2σ(I). And those for 2: triclinic, space group P1^- with a = 10.557(2), b = 11.159(2), c = 18.588(2) A, α = 106.945(6), β = 91.255(6), γ = 94.359(6)°, Dc = 1.927 g·cm^-3, F(000) = 1184, μ = 3.204 mm^-1, Z = 2, the final R = 0.0221 and wR = 0.0459 for 6328 observed reflections with I 〉 2σ(I). The title complexes show a two-dimensional (2D) square grid structure constructed from paddle-wheel-like [Ln2(CO2)4] dimers and tdc ligands. The 2D layers were further assembled into a 3D supramolecular assembly via O-H…O hydrogen bond. The photoluminescence properties of complexes 1 and 2 were investigated. 相似文献