Dimensional Chain Structure Research Articles

Two Calcium Coordination Polymers with Multi‐Stimuli‐Responsive Properties

AbstractTwo skeleton isomers, [CaL(H2O)(DMF)2]•DMF (1) (H2L=5‐(1,3‐dioxo‐1H‐benzo[de]isoquinolin‐2(3H)‐yl)isophthalic acid) with a 1 dimensional chain structure and [CaL(DMF)1.72]• (DMF)0.28 (2) with a 2 dimensional layer structure were synthesized. Mechanochromic luminescence studies reveal that 1 and 2 exhibit luminescent red‐shift and blue‐shift respectively under grinding stimuli. The different influence of grinding stimuli on the π⋅⋅⋅π interaction in the two structures are proposed to be the main reason for such different responses. In addition, 1 has a rare broad sensing ability for halogenated hydrocarbons and can distinguish seven halogenated hydrocarbons out of 17 solvents. 1 can also be used for rapid detection of trace water in DMF with a calculated detection limit of 0.0078 v/v %. The relevant recognition mechanism is the decomposition of the structure during the recognition process due to the water instability of the ionic bond. The above results reveal that both compounds have the potential to be used as multi‐stimulus‐responsive materials.

Synthesis, crystal structures and selective luminescence sensing property of Zn(II) coordination polymers based on semi-rigid tricarboxylic acid ligands

Herein, two novel Zn-based coordination polymers [Zn(HL)(1,10-phen)(H2O)]n (1) and [Zn2(HL)2(2,2′-bipy)2]n (2) have been successfully synthesized via solvothermal method by using the semi-rigid tricarboxylic acid ligand (H3L:3-[(1-carboxynaphthalen-2-yl)oxy] phthalic acid) and two different nitrogen-containing heterocyclic ligands (1,10-phenanthroline, 2,2′-bipyridine). A single-crystal X-ray analysis reveals that these two novel Zn-based coordination polymers 1 and 2 exhibit a one dimensional (1D) chain structures. Moreover, two novel Zn-based coordination polymers 1 and 2 exihit excellent fluorescence performances, and selectively recognition response to Ni2+, MnO4−, Cr2O72−, nitrobenzene and nitromethane through the luminescence quenching effects in aqueous solutions. The possible fluorescence recognition mechanism of 1 and 2 toward Ni2+, MnO4−, Cr2O72- are investigated, which may be attribute to the synergistic effects of energy competitive absorption and weak interaction. Whereas the fluorescence quenching behaviors of 1 and 2 toward nitrobenzene and nitromethane, owing to the existence of a strong electron-withdrawing group which can obtain excited-state electrons, and leading to the occurence of electrons transfer. These results indicating that Zn-based coordination polymers have potential application values in fluorescent recognition.

Anomalously strong viscosity behavior in mixed oxy-sulfide Na4P2S7-xOx invert glasses

In this report, the first observations of the anomalously strong viscosity behavior in the melt quenched (MQ) invert mixed oxy-sulfide Na4P2S7-xOx, 0 ≤ x ≤ 5, (NaPSO) glass series. We find that these glasses even with 67 mole% modifier, Na2S, exhibit a calorimetric fragility index, mcal, as small as 29 compared to typical values of ~ 60 to 80 for alkali silicate glasses with > 50 mole% SiO2. We find that the calorimetric fragility of these glasses varies systematically with the extent of network forming bridging oxygens (BOs) in the glasses. The mcal values were converted to kinetic fragility (mvis) values and used with the measured Tgs to produce viscosity curves for the glasses using the Mauro-Yue-Ellison-Gupta-Allan (MYEGA) model. The viscosity of the glass with a minimum mcal value of x = 2.5 was then shown to exhibit a viscosity that was as strong as some alkali aluminosilicate glasses.In this report, the first observations have been made of anomalously strong viscosity behavior and correspondingly strong bulk glass formation and resistance to crystallization in a melt quenched (MQ) prepared series of invert, modifier content greater than the glass former content, mixed oxy-sulfide Na4P2S7-xOx, 0 ≤ x ≤ 5, (NaPSO) glasses. We find that these glasses even with 67 mole % modifier, Na2S, and only 33 mole% glass former P2S5-xOx, exhibit a calorimetric fragility index, mcal, as small as 29 compared to typical values of ~ 60 to 80 for alkali silicate glasses with > 50 mole% SiO2 and the theoretical minimum mcal of ~ 15. The mcal values were converted to kinetic viscosity fragility, mvis, values and used with the measured glass transition temperatures, Tgs, to produce viscosity curves for the glasses using the Mauro-Yue-Ellison-Gupta-Allan (MYEGA) model. The viscosity of the glass with a minimum mcal value of x = 2.5 was then shown to exhibit a viscosity that was as strong as, and for some compositions stronger than, the viscosity of alkali aluminosilicate glasses which have three dimensional network structures compared to the one dimensional chain structures observed in these MOS invert glasses. Consistent with these small values of fragility indices and therefore predicted higher viscosity above the glass transition temperature, Tg, in the supercooled liquid regime, these glasses are also particularly resistant to crystallization. For example, the x = 2.5 glass composition exhibits a crystallization temperature, TC, more than 150K above its Tg. We find that the calorimetric fragility of these glasses varies systematically with the extent of network forming bridging oxygens (BOs) in the glasses. The structural change caused by incrementally replacing sulfur with oxygen has been found to have consistent, large effects on the thermal properties.

Mixed ligand coordination complexes by using multicomponent ligand: Syntheses, characterization and effect of non-covalent interactions on their framework structures

Abstract Three new coordination complexes [Mn(L1)(μ-azide)(azide)]2⋅4H2O (1), [Mn(L1)(fum)]n (2) [L1 = 2methyl-N1,N2-bis(pyridin-2yl)propane-1,2-diamine, fum = Fumaric acid] and [Co(L2)(azide)] (3) [L2 = 6 phenyl-1,3,5-triazine 2,4-diyl amino(pyridine-2yl)methanol] have been synthesized and X-ray crystallographically characterized. Complex 1, a dinuclear Mn(II) complex is formed by bridging azide ligand and other coordination sites are satisfied by tetradentate ligand L1 and terminal azide ligand. The overall structure is an incomplete supramolecular 3D cage structure, formed by intermolecular π … π interaction of pyridyl ligand and hydrogen bonding. Complex 2 comprised of eight coordinated Mn(II) centre where ligand L1 and fumarate is bridged between the metal centers that leads to a one dimensional chain structure which further extended to a 3D structure by π … π and C–H … π interactions. The overall structure is further stabilized by hydrogen bonding with the guest water molecules. Complex 3, a six coordinated mononuclear Co(II) discrete complex is consist of pentadentate ligand L2 and azide act as a terminal ligand. This Mononuclear complex is connected by π … π, C–H … π interactions and hydrogen bonding which ultimately leads to a supramolecular 2D architecture. All the complexes have been further characterized by elemental analysis, infrared spectroscopy (IR) and powder X-ray diffraction (PXRD) studies.

Cavity-induced superconducting and 4kF charge-density-wave states

We propose two experimental setups for fermionic atoms in a high-finesse optical resonator in which either a superconducting state with s-wave symmetry of the pairs or a 4k F charge density wave can self-organize. In order to stabilize the s-wave pairing, a two component attractively in- teracting fermionic gas is confined to a one dimensional chain structure by an optical lattice. The tunneling of the atoms along the chains is suppressed initially by an energy offset between neighbor- ing sites. A Raman transition using the cavity mode and a transversal pump laser then reintroduces a cavity-assisted tunneling. The feedback mechanism between the cavity field and the atoms leads to a spontaneous occupation of the cavity field and of a state of the fermionic atoms which is dominated by s-wave pairing correlations. Extending the setup to a quasi-one-dimensional ladder structure where the tunneling of atoms along the rungs of the ladder is cavity-assisted, the repul- sively interacting fermionic atoms self-organize into a 4k F charge density wave. We use adiabatic elimination of the cavity field combined with state-of-the-art density matrix renormalization group methods in finite systems in order to identify the steady state phases of the system.

Syntheses, structures and properties of four Cd(II) coordination polymers induced by the pH regulator

Four new coordination polymers [Cd2(CHDC)2(APYZ)(H2O)2](H2O) (1), [Cd(HCHDC)2(APYZ) (H2O)] (2), [Cd2(CHDC)2(PYZ)(H2O)2](H2O) (3), and [Cd(HCHDC)2(PYZ)(H2O)] (4) (H2CHDC = 1,4-cyclohexanedicarboxylic acid, APYZ = 2-aminopyrazine, PYZ = pyrazine) have been synthesized under the hydrothermal conditions by changing the pH regulator and the N-containing ligands. The pH regulator impacted on the degree of deprotonation of the 1,4-cyclohexanedicarboxylic acid ligand and resulted in the formation of the two pairs of different networks. Polymers 1 and 3 crystallize in monoclinic, space group P21/c, exhibit two dimensional 63 net, which further formed three-dimensional supramolecular structure by the CH⋯O hydrogen bond interactions. While polymers 2 and 4 possess one dimensional chain structures and further link into two dimensional layered supramolecular structures by intermolecular hydrogen bonding interactions. From all three conformers of H2CHDC, e,a-cis is consistently present in the Cd coordination polymers. Furthermore, photoluminescence properties of four polymers are also investigated, the luminescent intensity of polymer 1 (or 2) with amino group in pyrazine is dramatically stronger than that of the similar structure of polymer 3 (or 4) without amino group in pyrazine, the results shown that the presence of the amino group from 2-aminopyrazine play a key role in increasing the luminescence properties.

Structural Diversity in Zn(II) Coordination Polymers Constructed by Linear N,N′‐Donor Linker and Different Pseudohalides: Sorption Study and Luminescent Properties

AbstractReaction of a linear N,N′‐donor ligand, (4‐bpdh) with Zn(NO3)2⋅6H2O and four different pseudohalides [NCS−, NCO−, N3− and N(CN)2−]; afforded five complexes, namely {Zn(4‐bpdh)(H‐4‐bpdh)(SCN)3]}n (1), {Zn(4‐bpdh)(CNO)2]}n (2), {Zn(4‐bpdh)(N3)2]}n (3), {Zn3(4‐bpdh)3(N3)6(H2O)]⋅(4‐bpdh)0.5 (H2O)4}n (4) and {[Zn(4‐bpdh)2(N(CN)2)](N(CN)2) ⋅x(H2O)}n (5). All the complexes 1–5 were characterized by single crystal X‐ray analysis and other physicochemical methods. From X‐ray structural analysis, 1 is a discrete zero dimensional monomer, extended to a one dimensional supramolecular structure by H‐bonding and C−H⋅⋅⋅π interactions. Isostructural 2–3 are showing one dimensional chain structure. On the other hand, 4 shows a two dimensional structure linked by both bridging azide, and 4‐bpdh, whereas 5 forms a two‐fold interpenetrated α‐polonium type three‐dimensional network having two different types of channels occupied by the water molecule and free dicyanamide. The sorption study was performed for compound 2, 4 and 5 with different gases and vapors. Both 2 and 4 shows surface adsorption for the gases but evacuated framework of 5 selectively adsorbs CO2 over N2 and H2. Both 4 and 5 also exhibit interesting sorption behavior for the vapors. Solid state luminescence studies of all the complexes have also been performed at room temperature which shows ligand based emission in all the cases.

Structurally Different Calcium(II) Complexes with 5‐Substituted Tetrazole Ligands

AbstractThree different tetrazole‐carboxylate ligands, Hpymtza, Hpytza, and H2dtzeda were chosen to be reacted with Ca(NO3)2·4H2O, resulting in the formation of three coordination compounds, [Ca(pymtza)2(H2O)4] (1), [Ca(pytza)2(H2O)2] (2), and [Ca(dtzeda)(H2O)2] (3) [Hpymtza = 5‐(2‐pyrimidyl)tetrazole‐1‐acetic acid, Hpytza = 5‐(3‐pyridyl)tetrazole‐2‐acetic acid, and H2dtzeda = 1, 2‐bis(tetrazol‐5‐yl)ethane‐N1, N1′‐diacetic acid]. X‐ray diffraction analysis revealed that compound 1 displays a mononuclear structure, compound 2 is a one dimensional zigzag chain structure, whereas 3 shows a three‐dimensional structure. The structures were controlled by not only the different substituents of the tetrazolyl ring, but also the complementary hydrogen bonds. Furthermore, the luminescence properties of compounds 1–3 were investigated at room temperature in the solid state. These emissions can be tentatively attributed to the ligand centered emission.

EFFECT OF MIXING PROPORTION ON COMPRESSIVE STRENGTH OF FLY-ASH BASED GEOPOLYMER PASTE AND MORTAR USING TAGUCHI’S METHOD

Alkali activated pozzolan are known low carbon cementitious binders which can be used to replace cement. The material is also known as geopolymer because of its three dimensional polymeric chain and ring like structure consisting silica and alumina. A common type of pozzolan used is fly ash because of its rich silica content; therefore the term alkali activated fly-ash based binders is adopted. Despite much research and development of this material, there is no specific standard for design mix proportion. This research used the Taguchi’s design of experiment method to determine the optimum mix proportion of alkali activated fly ash based cement paste and mortar. Four factors were considered in the tests, silica fume, sand to cementitious ratio, liquid to solid ratio, and percentage of superplasticiser. Tests were conducted on the 9 batches of alkali activated fly-ash based paste and mortar samples to determine the compressive strength under ambient condition. Tests were also conducted to determine the residual strength of the samples after exposed to elevated temperatures. ANOVA analysis of the test results revealed the main factors contribution on the tested properties and led to the determination of the optimum design proportion of the factors considered in these tests.

Synthesis, Crystal Structure and Antibacterial Activity of Mg(II) Complex [Mg(H2O)6]·(4-amino-3-methylbenzenesulfonate)2

A Mg(II) complex, [Mg(H2O)6]·L2 (H2L = 4-amino-3-methylbenzenesulfonate), has been synthesized and characterized by elemental analysis, Infrared (IR) and single-crystal X-ray diffraction. The results indicated that the Mg(II) complex was monoclinic with P21/n, a = 6.3184(16) Å, b = 7.0522(18) Å, c = 24.434(6) Å, β = 93.946(3)°, V = 1086.2(5) Å3, Z = 2, Mr = 504.81, Dc = 1.544 g/cm3, T = 296(2) K, F(000) = 532, μ(MoKa) = 0.338 mm−1, R = 0.0339 and wR =0.1194. The Mg(II) ion lies in a distorted octahedral geometry. The hydrogen bonds and π-π stacking interaction play an important role in the forming of one dimensional chain structure. The antibacterial activity against Escherichia coli, Bacillus subtilis and Staphylococcus white of the Mg(II) complex has also been investigated.

Hydrothermal synthesis and characterization of one dimensional chain structures of monolacunary Keggin polyoxoanions substituted with copper

Two novel polymeric polyoxometallates constructed from transition metal substituted heteropolytungstates, [(4,4′bpyH2)2(4,4′bpyH)][PCuW11O39]·H2O (1), and [(4,4′bpyH2)(pyH)3][PCuW11O39]·2H2O (2), (4,4′bpy=4,4′bipyridine, py=pyridine) have been synthesized under hydrothermal conditions and characterized by IR, TGA, single crystal X-ray diffraction and magnetic measurements. The product formation showed a high sensitivity toward experimental factors including pH and stirring. Compounds 1 crystallizes in the monoclinic space group P2(1)/n with a=13.503(3)Å, b=26.726(5)Å, c=15.168(3)Å, β=99.61(3)° and Z=4. The second compound also crystallizes in space group P2(1)/n, but with a=13.519(3)Å, b=20.431(4)Å, c=18.655(4)Å, β=96.52(3)° and Z=4. Compound 1 exhibits a zigzag chain structure, while compound 2 exhibits a straight chain structure. Compound 2 is the first example of a polyoxometallate containing 1D chains of transition-metal-substituted heteropolytungstate designed with two significantly different organic units as the countercations. The Cu2+ ions in 1 exhibit paramagnetic behavior.

Crystal Structure of Na(I) Complex with 1,5-Naphthalenedisulfonate

A new Na (I) complex, [Na (H2O)5(DMF)]·(L) (L=1,5-naphthalenedisulfonate) has been obtained in the CH3CH2OH and a little DMF solution. The complex was characterized by X-ray single crystal diffraction analysis. The results showed that the local geometry around central Na (I) ion can be described a distorted octahedral environment which connected by five water molecules and one DMF molecule. The complex formed one dimensional chain structure through intramolecule and intermolecule hydrogen bonds and π-π stacking.

Designed synthesis of copper(II) and nickel(II) complexes with a tridentate N2O donor Schiff base: Modulation of crystalline architectures through C[sbnd]H⋯π and anion⋯π interactions

Two copper(II) complexes, Cu(L1)Cl (1), Cu(L1)NCS (3) and two nickel(II) complexes Ni(L1)Cl (2), Ni(L1)NCS (4), where HL1=1-[(2-diethylamino-ethylimino)-methyl]-naphthalen-2-ol act as tridentate N2O donor ligand, have been prepared and characterized by elemental analysis, IR and UV–Vis spectroscopy and single crystal X-ray diffraction studies. The geometry of the central metal ion in each of the four complexes is square planar. The existence of CH⋯π interactions in 2 gives rise to one dimensional chain structure. Complex 3 shows two CH⋯π interactions and one anion⋯π interactions which leads to a two dimensional layer structure. Each mononuclear unit of 4 has two CH⋯π interactions along b axis to form a double strand one dimensional array of the molecules in crystal packing.

Synthesis, structure, magnetic properties and biological activity of supramolecular copper(ii) and nickel(ii) complexes with a Schiff base ligand derived from vitamin B6

Three new complexes of Cu(II) and Ni(II), [Cu(II)(H(2)pydmedpt)](2+)·2Cl(-) (1), [Ni(II)(H(2)pydmedpt)](2+)·2Cl(-) (2) and [Ni(II)(pydmedpt)(OH)](-)·K(+) (3) of the Schiff base ligand [H(2)pydmedpt](2+)·2Cl(-) were synthesized by the in situ reaction of pyridoxal (pyd), a vitamer of vitamin B(6), N,N-bis[3-aminopropyl]methylamine (medpt) and copper(II) acetate or nickel(II) acetate, respectively. The molecular structures of 1 and 2 were determined by single crystal X-ray diffraction studies. The structure of 3 in the solid state was inferred by elemental analysis, diffuse reflectance spectrum, variable temperature magnetic moment studies and DFT calculations. The binding of the Schiff base ligand to the metal centers involves two phenolato oxygens, two imine nitrogens and one amine nitrogen. The coordination geometry around Cu in 1 is distorted square pyramidal and that around the Ni atom in 2 is intermediate between square-pyramidal and trigonal-bipyramidal. In the crystals the compounds form supramolecular one dimensional chain structures stabilized by hydrogen bonding and π-π stacking interactions. Variable temperature magnetic moment data of 2 indicate the presence of a momomeric high spin Ni(II) centre in the complex. The solid state diffuse reflectance spectrum, conductance and elemental analysis suggest that 3 is a Ni(II) complex with a tetragonally distorted octahedral field, the sixth position being occupied by the oxygen atom of a hydroxyl group. The variable temperature magnetic moment of 3 indicates the presence of a ferromagnetic dinuclear species (29.2%) along with the major monomeric species, the intra-dimer exchange term J value being 14.3 cm(-1). The competitive binding of 1 and 2 with DNA was studied in the concentration range 40 to 400 μM, the apparent binding constants being K = 2.9 × 10(3) and 6.7 × 10(3) M(-1), respectively. Human Serum Albumin (HSA) binding studies were carried out at concentrations of 800-1000 μM and 400-500 μM for the complexes and HSA, respectively, in PBS buffer at pH 7.4. Complex 1 binds to HSA, while no binding is observed in case of 2, instead, the complex hydrolyses under the experimental conditions used and the resulting Ni(2+) ions bind with HSA.

Synthesis, Crystal Structure and Luminescent Property of Cd (II) Complex with N-Benzenesulphonyl-L-leucine

A new trinuclear Cd (II) complex [Cd3(L)6(2,2-bipyridine)3] [L = N-phenylsulfonyl-L-leucinato] has been synthesized and characterized by elemental analysis, IR and X-ray single crystal diffraction analysis. The results show that the complex belongs to the orthorhombic, space group P212121 with a = 16.877(3) Å, b = 22.875(5) Å, c = 29.495(6) Å, α = β = γ = 90°, V = 11387(4) Å3, Z = 4, Dc= 1.416 μg·m−3, μ = 0.737 mm−1, F (000) = 4992, and final R1 = 0.0390, ωR2 = 0.0989. The complex comprises two seven-coordinated Cd (II) atoms, with a N2O5 distorted pengonal bipyramidal coordination environment and a six-coordinated Cd (II) atom, with a N2O4 distorted octahedral coordination environment. The molecules form one dimensional chain structure by the interaction of bridged carboxylato groups, hydrogen bonds and π-π interaction of 2,2-bipyridine. The luminescent properties of the Cd (II) complex and N-Benzenesulphonyl-L-leucine in solid and in CH3OH solution also have been investigated.

Synthesis, Crystal Structure and Luminescent Property of Mg(II) Complex with N-Benzenesulphonyl-L-Leucine and 1,10-Phenanthroline.

A new complex [Mg(L)2(phen)(H2O)2](phen)(H2O)2 [L= N-benzenesulphonyl-L-leucine] was synthesized by the reaction of magnesium chloride hexahydrate with N-benzenesulphonyl-L-leucine and 1,10-phenanthroline in the CH3CH2OH/H2O (v:v = 5:1). It was characterized by elemental analysis, IR and X-ray single crystal diffraction analysis. The crystal of the title complex [Mg(L)2(phen)(H2O)2](phen)(H2O)2 belongs to triclinic, space group P-1 with a = 0.72772(15) nm, b = 1.4279(3) nm, c = 1.4418(3) nm, α = 63.53(3)°, β = 79.75(3)°, γ = 81.83(3)°, V = 1.3163(5) nm3, Z =1, Dc= 1.258 μg·m−3, μ = 0.177 mm−1, F(000) = 526, and final R1 = 0.0506, ωR2 = 0.1328. The complex comprises a six-coordinated magnesium(II) center, with a N2O4 distorted octahedron coordination environment. The molecules are connected by hydrogen bonds and π-π stacking to form one dimensional chain structure. The luminescent property of the Mg(II) complex has been investigated in solid.

Research on the Structure of One-Dimensional Chain Calcium (ΙΙ) Complex Material

A new Ca(II) complex material has been prepared by the reaction of calcium perchlorate with 4-amino-3-methyl-benzenesulfonic acid and sodium hydroxide, and was characterized by single-crystal X-ray diffraction. The results showed that the complex crystallizes in monoclinic, space group P2(1)/n with a = 0.63090(10) nm, b = 0. 70513(11) nm, c = 2.4262(4) nm, V = 1.0766(3) nm3, Z = 2, F (000) = 562, Rint = 0.0252. Single-crystal X-ray diffraction analysis revealed that each calcium ion lies in six-coordinated environments, and the complex formed one dimensional chain structure through intramolecule and intermolecule hydrogen bonds and π-π stacking interaction.

Preparation and Structural Characterization of Chain Ni (II) Coordination Polymer Material

A chain Ni (II) coordination polymer material was prepared and characterized by elemental analysis and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group C2/c with a = 1.24348(13) nm, b = 1.29477(12) nm, c = 1.51480(17) nm and Dc = 1.401 g•cm-3. The results of structural analysis indicated that each Ni (II) ion forms six-coordinated with nitrogen atoms of pyridine and thiocyanate, and the Ni (II) coordination polymer material formed one dimensional chain structure by the interaction of pyridine rings.

Synthesis and Crystal Structure of the Azoxydichinyl Helicene, Pyrido[3,2-f]quinolino[6,5-c]cinnoline 5-Oxide Monohydrate.

The helicene, pyrido[3,2-f]quinolino[6,5-c]cinnoline 5-oxide, was prepared by treatment of 6-hydroxylaminoquinoline with xanthine oxidase or treatment of 6-nitroquinoline with glucose in 30% NaOH and the product characterized using NMR, high resolution mass spectrometry, and X-ray crystallography. The hydrogens on carbons 7 and 12 of the terminal aromatic rings are separated by 2.495 Å creating an angle of 25.0° between the planes of the two quinoline ring systems. In the crystal, water molecules serve to link the helicenes into a one dimensional chain structure forming a hydrogen bonded bridge between N2 of one molecule and N4 of another. The molecule (C(18)H(10)N(4)O•H(2)O) crystallized in the monoclinic P2(1)/n space group. Unit cell parameters for pyrido[3,2-f]quinolino[6,5-c]cinnoline 5-oxide monohydrate: a = 7.0829(12), b = 18.559(3), c = 11.0985(19) Å, β = 107.736(2)°, and Z = 4.

Synthesis, Crystal Structure and Antibacterial Activity of 1D Chain Ca(II) Coordination Polymer

1D chain Ca(II) coordination polymer was synthesized and characterized by elemental analysis, molar conductance, IR and single-crystal X-ray diffraction, The results of crystal structure show that each Ca(II) ion forms eight-coordinated and the complex formed one dimensional chain structure by the oxygen atoms of carboxylate and water bridged. The antibacterial activity of the Ca(II) coordination polymer and the ligand were tested, the results show that the complex show considerable antibacterial activity against escherichia coli, bacillus subtilis and staphylococcus white.