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1.
Syntheses, structures, and electrochemistry of a dialkoxo‐bridged diuranyl(VI) compound [(UO2)2(L1)2(dimethylformamide)2] ( 1 ) and a mononuclear–mononuclear cocrystalline compound [(UO2)(L2)(H2O)⊂(H2O)]·[(UO2)(L2)(H2O)] ( 2 ) derived from Schiff base ligands are reported (H2L1 = Schiff base ligand obtained on condensation of 3‐ethoxysalicylaldehyde with 2‐aminoethanol; H2L2 = N,N ′‐o ‐phenylenebis(3‐ethoxysalicylaldimine)). The compounds 1 and 2 crystallize in the space groups P 21/c and P 1, respectively. Compound 1 is a dialkoxo‐bridged dinuclear compound of uranium(VI) containing two deprotonated ligands, [L]2–, two dimethylformamide (dmf) molecules and two UO22+ centers. Three C–H···O type hydrogen bonds involving one uranyl oxygen, two dmf hydrogens, and the imine hydrogen link the dinuclear units into a two‐dimensional network. Compound 2 is a cocrystal of two mononuclear units, [(UO2)(L2)(H2O)⊂(H2O)] (unit 1) and [(UO2)(L2)(H2O)] (unit 2). In unit 1, the non‐coordinated water molecule forms hydrogen bonds with oxygens of phenoxo, ethoxy, and coordinated water molecules resulting in the formation of an inclusion product. The overall supramolecular structure of compound 2 is one‐dimensional and consists of interlinked self‐assembled dimeric unit of unit 1 and unit 2. Cyclic voltammetric measurements reveal that the uranium(VI) center in [(UO2)2(L1)2(dimethylformamide)2] ( 1 ) is reduced quasireversibly at E1/2 = –773 mV with ΔEP = 121 mV, while the metal center in [(UO2)(L2)(H2O)⊂(H2O)]·[(UO2)(L2)(H2O)] ( 2 ) is reduced reversibly with E1/2 = –765 mV with ΔEP = 68 mV. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

2.
A new coordination polymer, [Ag3hmt3(μ3 ‐btc)]·5H2O (1) (hmt = hexamethylenetetramine, btc=1,3,5‐benzenetricarboxlic), has been successfully synthesized. Crystal data: P21/a, a = 11.9906(2) Å, b = 17.3689(2) Å, c = 16.96100(10) Å, β = 101.9820(14)°, V = 3455.40(7) Å3, Z = 4, Dc = 2.002 Mg/m3. In the hexagonal structure of Ag‐hmt unit, each Ag‐hmt unit comprises three Ag atoms and three hmt ligands. The μ3 ‐btc ligands bridge adjacent two‐dimensional honeycomb‐like Ag‐hmt layers to form three‐dimensional networks. Structure analysis show that hydrogen bonds play a key role for the stable structure in the compounds. (© 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

3.
Two new Co(II) coordination polymers, [Co(Hnbta)(bth)]n ( 1 ) and {[Co3(nbta)2(bth)3(H2O)]·H2O}n ( 2 ), (H3nbta = 5‐nitro‐1,2,3‐benzenetricarboxylic acid and bth = 1,6‐bis(1,2,4‐triazole‐1‐yl)hexane), have been synthesized under different pH values through hydrothermal reactions. Both complexes were characterized by elemental analysis, IR spectra, thermogravimetric analysis (TGA), and single‐crystal X‐ray crystallography. Complex 1 exhibits a 3D polythreaded network based on 4‐connected sql 2D layer. Complex 2 has a (4,4,5)‐connected trinodal 3D pillar‐layered network with a (42·64)2(42·67·8)2(64·82) topology. Magnetic susceptibility measurements indicate that complexes 1 and 2 show weak antiferromagnetic interactions between the adjacent Co(II) ions.  相似文献   

4.
Two novel layered CrIII containing metal‐hedp compounds, Na20AlCrIII[CH3C(O)P2O6]6·O3·(H2O)26·(H3O)10 (CH3 CH2 OH) and Na6CrIII[CH3C(OH)P2O6]3·(H2O)21(H3O)3 (designated as DLES‐AlCr and DLES‐CrIII respectively), were hydrothermally synthesized. Their structures were determined by single‐crystal X‐ray diffraction. The two crystals are isostructural with propeller‐like chiral motifs and hexagonal rings along [001]. DLES‐AlCr crystal exhibits interesting hollow tubular hexagonal morphology, while DLES‐Cr crystal possesses solid hexagonal morphology. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

5.
Two new inorganic‐organic complexes, namely, [Ag2(hmt)2]Cr2O7·H2O ( 1 ) and [Ag(hmt)(tar)0.5]·H2O ( 2 ), (hmt = hexamethylenetetramine, Tar = tartarate,), have been synthesized in H2O/CH3CN solvent at room temperature. Both molecules have the common [Ag3hmt3]3+ layers. Compound 1 is a two‐dimensional structure, and Complex 2 shows three‐dimensional topology. In complex 2 , the tartarate molecules are connected with adjacent layers to form parallelogram pores of 18.55×7.44 Å, which are occupied by two water molecules. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

6.
A new complex of Zinc(II) and guanidinium pyridine–2,6–dicarboxylate proton transfer compound, (GnH)2 (pydc), was synthesized and characterized using IR, 1H NMR and 13C NMR spectroscopy and single crystal X–ray diffraction. The chemical formula and space group of the resulting complex is (GnH)[Zn(pydc)(pydcH)] · (pydcH2) · 4H2O, P 1 where the final R value is 0.0310 for 13287 reflections collected. The [Zn(pydc)(pydcH)] anions and the (GnH)+ counter‐cations form a three‐dimensional solid‐state structure by a variety of noncovalent interactions such as ion pairing, hydrogen bonding and π–π stacking which are going to be discussed. (© 2007 WILEY ‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

7.
The crystal structure of 1‐allyl‐5‐(4‐methylbenzoyl)‐4‐(4‐methylphenyl)pyrimidine‐2(1H)‐thione (C22H20N2OS) has been determined from three dimensional single crystal X‐ray diffraction data. The title compound crystallizes in the monoclinic space group P 21/c, with a = 10.6674(13), b = 10.1077(7), c = 17.9467(19) Å, β = 98.460(9)°, V = 1914.0(3) Å3, Dcalc = 1.251 g cm–3, Z = 4. In the title compound, the allyl group shows positional disorder. Molecules are linked by C‐H···O, C‐H···N and C‐H···S intermolecular interactions forming two‐dimensional network. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

8.
The compound [UO2(NO3)2(H2O)2] · 2C12H18O was synthesized and studied by IR spectroscopy and X-ray diffraction. The structure consists of the neutral island groups [UO2(NO3)2(H2O)2], which belong to the crystal-chemical group AB 01 2 M 1 2 (A = UO2 2+, B 01 = NO3, M 1 = H2O) of uranyl complexes, and 1-adamantyl methyl ketone molecules. The characteristic features of the association of the complexes [UO2(NO3)2(H2O)2] and 1-adamantyl methyl ketone molecules in the crystal structure via hydrogen bonds are considered with the use of Voronoi-Dirichlet polyhedra.  相似文献   

9.
The effects of initial supersaturation, cooling rate, and stirring rate on the morphology of strontium chloride hexahydrate (SrCl2·6H2O) crystals were investigated by batch‐cooling crystallization, providing optimal operating conditions. Uniform needle‐like crystals with a length of 1200.50 μm and a width of 100.92 μm on average were obtained. The corresponding aspect ratio of length to width was about 11.90. Moreover, the morphological modification of SrCl2·6H2O crystals using cetyltrimethylammonium chloride (CTAC) was studied. When 20.30 mmol·L−1 of CTAC was added, the length and width of crystals were 792.71 μm and 233.25 μm, respectively, and the corresponding aspect ratio decreased to 3.40. The shape of SrCl2·6H2O crystal changed to granule‐like, probably because of the strong interaction of CTAC with the SrCl2·6H2O facets with a denser distribution of Cl ions. This study offers a simple, flexible, and highly efficient approach to regulate the morphology of SrCl2·6H2O crystals and opportunities for multiple applications of SrCl2·6H2O.  相似文献   

10.
The recrystallization of Heptakis[6‐O‐tert ‐butyldimethylsilyl)]‐β ‐cyclodextrin ( 1 ) from ethyl acetate gave single crystals of 1 2·(ethyl acetate)3 complex. The superstructure of 12·(ethyl acetate)3 complex was investigated by 1H NMR spectroscopy, molecular modeling, and single crystal/powder X‐ray diffractions. Encapsulation of ethyl acetate molecules with 1 and a unique hexagonal columnar superstructure in its crystal were found. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

11.
An exploration of the mixed‐ligand system under hydrothermal condition, has led to the isolation of a 3‐D novel framework {[Cu2(mp)L2)(H2O)2]·6H2O}n ( 1 ) (mp = benzene‐1,2,4,5‐ tetracarboxylate tetraanion, L = 4‐(5‐(pyridin‐4‐yl)‐1,3,4‐thiadiazol‐2yl)pyridine). Single‐crystal X‐ray analyses reveal that it crystallizes in the triclinic space group P‐1, a = 8.807(4) Å, b =11.139(6) Å, c = 11.291(5) Å, α=75.337(7), β = 73.584(5), γ= 66.795(5)°. The CuII ions are linked into an extended 2‐D grid net via mp molecules. Further these layers are united together through the bridging L to form a 3‐D structure, which exhibits a new 4‐connected topological network. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

12.
Large single crystals of optical quality of the non‐centrosymmetric orthorhombic potassium rare earth nitrate mixed crystals K2(La1–x Cex)(NO3)5 · 2 H2O were grown at 38 °C from diluted HNO3. For crystals with x = 0.0, 0.19, 0.38 and 0.66 refractive indices and their dispersion were determined with an error less than 1 · 10–4 in the wavelength range 0.404 – 1.083 μm by the prism method. Phase matching conditions for collinear SHG frequency conversion were analysed in detail, including calculation of the effective nonlinear optical susceptibility. By an appropriate choice of the fraction x of cerium the mixed crystals K2(La1–x Cex)(NO3)5 · 2 H2O allow an adjustment of non‐critical type I phase matching conditions to a desired wavelength of the fundamental wave within the range 1.055(4) – 1.107(6) μm. Non‐critical type II phase matching can be tuned in the wavelength range 0.949(2) – 0.931(2) μm. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

13.

Abstract  

Two complexes [Cd2(dpe)3(H2O)8]·(dpe)·(hssal)2·(H2O)2 1, [Mn(dpe)2(Hpcmb)2·(H2O)2] 2, (dpe = trans-1,2-di(4-pyrindyl)ethylene; H2hssal = sulphosalicylic acid; H2pcmb = p-(carboxyl-methyloxy)-benzenecarboxylic acid) has been prepared, and was characterized by elemental analysis, FT-IR and single-crystal X-ray diffraction. Structure indicates in complex 1 that Cd(II) is a distorted octahedral coordination geometry. The hssal2− anions are localized between 2-D sheets {[Cd(dpe)2(H2O)4]2+(dpe)}n and {{[Cd(dpe)2(H2O)4]2+}n as count anions and bridge to further connect these 2-D sheets through hydrogen bond O–H···O to form 3-D structure. The complex 2 is a single molecule structure. In 2, Each Mn(II) atom is six-coordinated with a distorted octahedral coordination geometry. The single molecule units are extended into three-dimensional structure via π–π, hydrogen bonding interactions. The thermogravimetric behavior and luminescent property of complex 1 were investigated.  相似文献   

14.
Abstract A new complex containing two different substituted pyridine ligands, viz. 4-CNpy (4-cyanopyridine) and pdc (pyridine-2,6-dicarboxylate), [Ni(H2O)2(pdc)(4-CNpy)] · 2H2O (1), has been prepared using [Ni(4-CNpy)2(H2O)3(SO4)] · H2O (2) as the starting compound. Crystal data on 1 are: monoclinic, P21/c, a = 11.533(2) ?, b = 20.114(4) ?, c = 7.306(1) ?, β = 93.777(3)°, V = 1,691.1(5) ?3, Z = 2, D calc. = 1.57 g cm−3, R 1 = 0.0585, w R 2 = 0.1236 for reflections with I > 4σ(F 0) and 268 parameters (R 1 = 0.0859, wR 2 = 0.1336 for all 4,024 reflections). The discrete molecules of the title complex remain hydrogen-bonded to assemble into supramolecular layers interleaved by disordered water molecules. In an attempt to obtain the cationic complex species cis-[Ni(H2O)4(4-CNpy)2]2+ we have isolated the compound [Ni(H2O)4(4-CNpy)2] · (BPh4)2 · 2(4-CNpy) · 4H2O (3) by adding NaBPh4 to an aqueous solution of 2. Crystal data on 3 are: monoclinic, P21/n, a = 10.5002(1) ?, b = 21.1692(3) ?, c = 15.3249(2) ?, β = 95.120(1)°, V = 3392.84(7) ?3, Z = 2, D calc. = 1.231 g cm−3, R 1 = 0.0453, wR 2 = 0.1217 for reflections with I > 4σ (F 0) and 556 parameters (R 1 = 0.0688, wR 2 = 0.1364 for all 9,257 reflections). Index Abstract Synthesis and Crystal Structure of [Ni(H2O)2(pdc)(4-CNpy)] · 2H2O (pdc = Pyridine-2,6-dicarboxylate, 4-CNpy = 4-cyanopyridine) Manjit K. Bhattacharyya, Sanchay J. Bora and Birinchi K. Das Crystal structure of a new nickel(II) complex displaying a supramolecular layered structure is described. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

15.
Many explorations of transition metal (M)‐L system under solvothermal condition, have led to the syntheses of two new 4‐heterocyclic acylpyrazolone complexes [Co(L)2(CH3OH)2] (HL = 1‐phenyl‐3‐methyl‐4‐(2‐furoyl)‐5‐pyrazolone) ( 1 ) and [Cr(L)3] ( 2 ). Single‐crystal X‐ray analyses reveal that crystal structures of compound 1 and 2 are respectively orthorhombic, Pbca, a = 15.0378(6) Å, b = 9.8405(4) Å, c = 20.7321(8) Å, V = 3067.9(2) Å3, Z = 8 and triclinic, P‐1, a = 10.7966(18) Å, b = 13.023(2) Å, c = 15.520(3) Å, α = 73.011(4)°, β = 84.884(4)°, γ = 70.267(4)°, V = 1964.3(6) Å3, Z = 2. Complex 1 has a two‐dimensional (2D) network structure that is formed by O–H···N H‐bonding interactions. Complex 2 makes a one‐dimensional (1D) zigzag chain structure by intermolecular π···π interactions, which is further interlinked via C–H···N H‐bonding interactions to generate a 2D sheet, and then a three‐dimensional (3D) supramolecular network structure is further linked by intermolecular C–H···π interactions. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

16.
Self‐assembly of Cd(NO3)2 with o ‐phthalic acid monopotassium salt (KHphth) in the presence of ethylenediamine (en) produced a new heterometallic coordination polymer [CdK2(phth)2(en)0.5(H2O)]n ( 1 ). Single‐crystal X‐ray analyses reveal that it crystallizes in a monoclinic space group P 21/c. a = 11.6707(6) Å, b = 8.1019(4) Å, c = 20.9503(11) Å, β = 94.6640(10)o. The complex displays an en‐pillared 3D framework, which is constructed from 2D [CdK2(phth)2(H2O)]n layers featuring uncommon inorganic cadmium‐potassium‐oxide layers containing potassium‐oxide layers. In the solid state, complex 1 shows photoluminescence with the maximum emission intensities at 355 nm upon excitation at 312 nm. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

17.
A novel complex, namely [RuII(PPh3)(CO)(H)(Hbpdc)]·2MeOH ( 1 ) (H2bpdc = 2,2′‐bipyridyl‐5,5′‐dicarboxylic acid), has been synthesized from the reaction of H2bpdc with [RuII(PPh3)3(CO)(H)2] in methanol under mild condition and characterized by elemental analysis, IR spectrum, ESI mass spectrometry, and single crystal X‐ray diffraction. The structure shows that the complex crystallizes in the monoclinic space group P21/c with unit cell parameters a = 11.8984(13) Å, b = 16.5180(18) Å, c = 25.5322(19) Å, β = 115.302(4)°, V = 4536.6(8) Å3, Z = 4. This compound features a 1‐D supramolecular chain constructed via hydrogen bonds. Its photophysical properties have been investigated in MeOH solution and in the solid state at room temperature.  相似文献   

18.
Compounds K2[UO2(C3H2O4)2] · H2O (I) and Rb2[UO2(C3H2O4)2] · H2O (II) are synthesized and their crystal structures are determined by X-ray diffraction. The compounds crystallize in the monoclinic crystal system; for I, a = 7.1700(2) ?, b =12.3061(3) ?, c = 14.3080(4) ?, β = 95.831(2)°, space group P21/n, Z = 4, and R = 0.0275; for II, a = 7.1197(2) ?, b = 12.6433(4) ?, c = 14.6729(6) ?, β = 96.353(2)°, space group P21/n, Z = 4, and R = 0.0328. It is found that I and II are isostructural. The main structural units of the crystals are the [UO2(C3H2O4)2]2− chains, which belong to the AT 11 B 01 (A = UO22+, T 11, and B 01 = C3H2O42−) crystal chemical group of uranyl complexes. The chains and alkali metal ions R (R = K or Rb) are connected by electrostatic interactions and hydrogen bonds. Some specific structural features of [UO2(C3H2O4)2]2− complex groups are discussed.  相似文献   

19.
To explore the possibility of obtaining the metal‐organic frameworks (MOFs) bearing the 2‐bromo‐1,4‐benzenedicarboxylate ligand, one new Mn(II) and one Co(II) coordination polymers, [Mn(HL)2(bipy)2·2H2O]·bipy ( 1 ) and [Co(L)(bpe)] ( 2 ) (bipy=4,4′‐bipyridine; bpe=1,2‐bis(4‐pyridyl)ethene) were synthesized and characterized by elemental analysis and X‐ray diffraction analysis. Compounds 1 exhibits one‐dimensional coordination chains, which are further connected to form two dimensional supramolecular networks through hydrogen bonding interactions. Compound 2 presents a two‐fold interpenetrating two‐dimensional layer structure. The 2‐bromo‐1,4‐benzenedicarboxylate anion exhibits different coordination modes in the two complexes. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

20.
A supramolecular compound, {[CuMn(pydc)2(H2O)5]·2H2O} ( 1 ) (pydc = pyridine‐2,6‐dicarboxylate dianion), has been synthesized and characterized by single‐crystal X‐ray diffraction. Single‐crystal X‐ray analysis reveals that it crystallizes in the triclinic space group P‐1, a = 8.4763(17) Å, b = 9.7715(19) Å, c = 13.909(3) Å, α =101.234(3)°, β =102.520(3)°, γ= 97.375(4)°. Two mixed‐metal ions exhibit similar coordinated geometries with octahedron. 1 possesses a 3‐D unusual supramolecular network featuring 1D water tape. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   

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