A new tripodal rhodamine B derivative 2 was designed and synthesized by tripodal trialdehyde and rhodamine B hydrazide for the first time. This derivative could be used as a fluorescent chemosensor for the selective a...A new tripodal rhodamine B derivative 2 was designed and synthesized by tripodal trialdehyde and rhodamine B hydrazide for the first time. This derivative could be used as a fluorescent chemosensor for the selective and sensitive determination of copper(II) in Tris-HCl buffer and ethanol aqueous mixed media. Under the optimum conditions described herein,fluorescence enhancement at 557/577 nm was linearly related to the concentration of copper(II) in the range of 0.10 to 10.00×10-5 mol·L-1,with a corre-lation coefficient of R2=0.9964 (n=15) and a detection limit of 1.129×10-7 mol·L-1 (the relative standard deviation for five repeated measurements at 4.00×10-5 mol·L-1 Cu(II) was 2.2%). The absorbance meas-urements at 557 nm were linearly related to the concentration of Cu(II) in the range of 0.50 to 25.00×10-5 mol·L-1,with a correlation coefficient of R2=0.9948 (n=13) and a detection limit of 3.338×10-7mol·L-1.展开更多
A new metal-organic coordination polymer {[Nd（tci）（H2O）2]·2H2O}n（1） has been synthesized based on the flexible tricarboxylate ligand tris（2-carboxyethyl）isocyanuric acid（H3tci） and structurally characte...A new metal-organic coordination polymer {[Nd（tci）（H2O）2]·2H2O}n（1） has been synthesized based on the flexible tricarboxylate ligand tris（2-carboxyethyl）isocyanuric acid（H3tci） and structurally characterized by single-crystal X-ray diffraction analyses, elemental analysis, infrared spectra（IR）, powder X-ray diffraction（PXRD） and thermogravimetric analysis（TGA）. Complex 1 crystallizes in triclinic, space group P1 with a = 9.1648（11）, b = 9.3326（12）, c = 12.440（2） , C（12）H（20）N3O（13） Nd, Mr = 558.55, V = 886.9（2） 3, Z = 2, Dc = 2.092 g·cm-3, μ = 3.006 mm-1, F（000） = 554, 2.56〈θ〈25.00°, λ（Mo Kα） = 0.71073 , T = 293（2） K, the final R = 0.0662 and w R = 0.2071. X-ray diffraction analysis reveals that complex 1 is a two-dimensional layer, which is further assembled into a three-dimensional supramolecular architecture through hydrogen bonding interactions. The structure of complex 1 can be simplified as a rare 2-periodic uninodal {48·62} topology and a non-interpenetrating kgd topology. Furthermore, the thermal stability and photoluminescence property of 1 were investigated.展开更多
Surface active ionic liquids (SAILs) are considered as prominent materials in enhanced oil recovery thanks to their high interfacial activity. This study reports the preparation and applications of a nanostructure Tri...Surface active ionic liquids (SAILs) are considered as prominent materials in enhanced oil recovery thanks to their high interfacial activity. This study reports the preparation and applications of a nanostructure Tripodal imidazolium SAIL as an environmentally-friendly substitute to the conventional surfactants. The product has a star-like molecular structure centered by a triazine spacer, namely [(C_(4)im)_(3)TA][Cl_(3)], prepared by a one-step synthesis method and characterized with FT-IR, NMR, XRD, and SEM analysis methods. The interfacial tension of the system was decreased to about 78% at critical micelle concentration of less than 0.08 mol·dm^(−3). Increasing temperature, from 298.2 to 323.2 K, improved this capability. The solid surface wettability was changed from oil-wet to water-wet and 80% and 77% stable emulsions of crude oil–aqueous solutions were created after one day and one week, respectively. Compared to the Gemini kind homologous SAILs, the superior effects of the Tripodal SAIL were revealed and attributed to the strong hydrophobic branches in the molecule. The Frumkin adsorption isotherm precisely reproduced the generated IFT data, and accordingly, the adsorption and thermodynamic parameters were determined.展开更多
A tripodal ligand, tris{2 [N (pyridine methanoyl)amino]ethyl}amine(L), and its complexes with rare earth nitrates were synthesized. These new complexes with the general formula of Ln(NO 3) 3·L·6H 2O(w...A tripodal ligand, tris{2 [N (pyridine methanoyl)amino]ethyl}amine(L), and its complexes with rare earth nitrates were synthesized. These new complexes with the general formula of Ln(NO 3) 3·L·6H 2O(where Ln=La, Nd, Eu, Tb, Y) were characterized by elemental analysis, IR spectra, thermal analysis, 1 H NMR spectra, molar conductivity and luminescent spectra. All the complexes are stable in air and their conductances in acetonitrile solution lie in the range of 142～150 S·cm 2·mol -1 , indicating 1∶1 type electrolytes. The IR and 1H NMR spectra of the ligand and its complexes show that all the C=O groups take part in coordination to the metal ions. The thermal behaviour of Eu complex shows that the weight losses at 75～120 ℃ and 120～210 ℃ correspond to the loss of four lattice water molecules and that of two coordinated water molecules, respectively. The luminescent spectra of the complexes of Eu(Ⅲ) and Tb(Ⅲ) were investigated in methanol.展开更多
Two monomeric cobalt(Ⅱ)complexes,[CoL(N3)] ClO4(1)and CoL(N3)2(2),where L is tris((3,5-dimethylpyrazol-1-yl)methyl)amine,were synthesized and their crystal structures were determined by X-ray diffraction technique.C... Two monomeric cobalt(Ⅱ)complexes,[CoL(N3)] ClO4(1)and CoL(N3)2(2),where L is tris((3,5-dimethylpyrazol-1-yl)methyl)amine,were synthesized and their crystal structures were determined by X-ray diffraction technique.Complex 1 is five coordinated with one azide nitrogen atom and four nitrogen atoms of the tris((3,5-dimethylpyrazol-l-yl)-methyl)amine ligand,and the metal center is in distorted trigonal bipyramidal environment.Complex 2 is six coordinated distorted octahedron with the two azide nitrogen atoms and four nitrogen donors of the tris((3,5-dimethylpyrazol-1-yl)-methyl)amine ligand.The solution behaviors of the title complexes have been further investigated by UV-Vis,and 1H NMR analysis.It is found that the formation of 1 and 2 depends on the molar ratio of the azide ion to metal salt and ligand Complex 1 attached with one azide group is more stable and easy to generate than complex 2 incorporated with two azide groups,and the reasons were well discussed.展开更多
A new cadmium(Ⅱ) coordination polymer, [Cd(TITMB)_2]-(SO_4 )·21H_2O, whereTITMB = 1, 3, 5-tris (imidazol-1-yl-methyl) -2, 4, 6-trimethylbenzene, was obtained by self-assemblyof tripodal ligand TITMB with CdSO_4&...A new cadmium(Ⅱ) coordination polymer, [Cd(TITMB)_2]-(SO_4 )·21H_2O, whereTITMB = 1, 3, 5-tris (imidazol-1-yl-methyl) -2, 4, 6-trimethylbenzene, was obtained by self-assemblyof tripodal ligand TITMB with CdSO_4·2.7H_2O in acetonitrile, and characterized by X-raycrystallography. The crystal data belongs to monoclinic space group C_c with cell parameters a =1.16891(4) nm, b= 2.06671(6) nm, c = 2.48185(7) nm, β= 97.8560(10)°, R = 0.0487, wR =0.1211. Theresults of structure analysis indicate that each TITMB ligand coordinates three metal atoms and inturn each Cd(Ⅱ) atom with octahedral coordination geometry connects six nitrogen atoms of imidazolegroup from six different TITMB ligands to produce a 2D honeycomb network structure. There are a lotof water molecules linked by hydrogen bonds and occupied the channels formed intra- andinter-sheets.展开更多
Treatment of Ru(CO)(Cl)(H)(PPh3)3 with NaLOEt (LOEt-= [CpCo{P(O)(OEt)2}3]-) afforded the hydride complex (PPh3)(CO)-LOEtRu(H) (1), which has been characterized by X-ray crystallography. Similarly, the tricyclohexylpho...Treatment of Ru(CO)(Cl)(H)(PPh3)3 with NaLOEt (LOEt-= [CpCo{P(O)(OEt)2}3]-) afforded the hydride complex (PPh3)(CO)-LOEtRu(H) (1), which has been characterized by X-ray crystallography. Similarly, the tricyclohexylphosphine analogue, (PCy3)(CO)LOEtRu(H) (2), was synthesized from Ru(CO)Cl(H)(PCy3)2 and NaLOEt. Treatment of complex 1 with R'SO2N3 afforded the (arylsulfonyl)amido complexes LOEtRu(CO)(PPh3)(NHSO2R) (R = 2,4,6-i-Pr3C6H2 (3), 4-t-BuC6H4 (4)). The crystal structure of complex 3 has been determined. The Ru-N distance and Ru-N-S angle in 3 are 2.076(3) and 126.14(16)°, respectively. Reactions of complex 1 with acids have been studied.展开更多
A new tripodal ligand, N, N, N′, N′, N″, N″ hexaisopropyl 2, 2′, 2″ nitrilotris (2,1 ethoxy) triacetamide (L) and its new erbium picrate complex were prepared. The structure of the complex was determined by...A new tripodal ligand, N, N, N′, N′, N″, N″ hexaisopropyl 2, 2′, 2″ nitrilotris (2,1 ethoxy) triacetamide (L) and its new erbium picrate complex were prepared. The structure of the complex was determined by X ray crystal structure analysis. The result reveals that the Er 3+ is encapsulated by the three arms of the tripodal ligand, and nine coordinated by the bridged head nitrogen atom, all ether oxygen atoms and carbonyl oxygen atoms of the ligand, and two oxygen atoms of the bidentate picrate. The coordination polyhedron is a distorted mono-capped square antiprism.展开更多
A novel tripodal receptor,1,3,5-tri((5,7-dimethyl-1,8-naphthyridin-2-yl-amino)methyl)-2,4,6-triethylbenzene(1) was synthesized from starting materials 2,6-diamino-pyridine(2) and 1,3,5-triethylbenzene(4) by three step...A novel tripodal receptor,1,3,5-tri((5,7-dimethyl-1,8-naphthyridin-2-yl-amino)methyl)-2,4,6-triethylbenzene(1) was synthesized from starting materials 2,6-diamino-pyridine(2) and 1,3,5-triethylbenzene(4) by three steps with an overall yield of 25%,and characterized by ESI-MS,FT-IR and ~1H NMR spectra.Additionally,its absorption and emission spectra were investigated.展开更多
An N-hydroxyl peptide unit of H-L-Pro-L-Ala-L-Ala-β-（BnO）Ala-OMe was synthesized by stepwise chain building method in solution. Then, based on nitrilotriacetic acid backbone and this N-hydroxyl peptide unit, a nove...An N-hydroxyl peptide unit of H-L-Pro-L-Ala-L-Ala-β-（BnO）Ala-OMe was synthesized by stepwise chain building method in solution. Then, based on nitrilotriacetic acid backbone and this N-hydroxyl peptide unit, a novel chiral tripodal ligand P as an analogue of desferrichrome, has been synthesized. In neutral pH, ligand P formed stable tri（hydroxamato）- iron（Ⅲ） complexes which showed a maximum absorptiota （∑max=2750 M^-lcm^-1） at 422 nm in UV-Vis spectra. The characteristic absorption spectra are similar to those of natural trihydroxamate-type siderophores.展开更多
Solid complexes [REL(NO3)3]n with novel (10,3)-a type three-dimensional networks structure have been assembled using rare earth nitrates and an amide type semirigid tripodal bridging ligand, 1,3,5-tris {[(2′-benzylam...Solid complexes [REL(NO3)3]n with novel (10,3)-a type three-dimensional networks structure have been assembled using rare earth nitrates and an amide type semirigid tripodal bridging ligand, 1,3,5-tris {[(2′-benzylaminoformyl)phenoxyl]methyl}benzene (L), as building blocks. The complexes were crys- tallized in the orthorhombic system with chiral space group P212121. The whole structure consists of an infinite array of trigonal RE(III) ions bridged by tridentate ligands, and a novel (10,3)-a net is formed, which is very uncommon in the rare earth complexes. At room temperature, the Sm(III), Eu(III), Tb(III), Dy(III) complexes all exhibited characteristic luminescence emissions of central metal ions under UV light excitation.展开更多
The tris（2-aminoethyl）amine （tren）-based tris（4-pyridylurea） receptor L has been synthesized and its anion binding properties were studied. The ligand forms a 2 ： 1 （host/guest） complex with MgSO4, [SO4^2 L2]...The tris（2-aminoethyl）amine （tren）-based tris（4-pyridylurea） receptor L has been synthesized and its anion binding properties were studied. The ligand forms a 2 ： 1 （host/guest） complex with MgSO4, [SO4^2 L2], in which a sulfate ion is encapsulated by six urea groups from the two ligands through multiple hydrogen bonds. The metal ions do not coordinate to the pyridyl groups but exist as the hydrate [Mg（H2O）6]2＋ and interact with the [SO4 L2] capsules in the outer coordination sphere to form a three dimensional extended structure. The anion binding behav- ior of ligand L in solution was studied.展开更多
The mixed complex [Ni（L）（L＇）]（ClO4）2 has been synthesized using 2-aminoethyl- bi（3-bi-aminopropyl）amine with phen （1,10-phenanthroline） in the presence of Ni（Ⅱ） ion, and its structure was determined by X...The mixed complex [Ni（L）（L＇）]（ClO4）2 has been synthesized using 2-aminoethyl- bi（3-bi-aminopropyl）amine with phen （1,10-phenanthroline） in the presence of Ni（Ⅱ） ion, and its structure was determined by X-ray diffraction. The crystal crystallizes in monoclinic, space group P21/c with a = 13.713（2）, b = 13.1466（19）, c = 14.780（2） A°, β= 97.620（3）°, V = 2640.9（7） A °^3, F（000） = 1272, Z = 4, Dc = 1.540 g/cm^3, R = 0.0536 and wR = 0.1207. The Ni^2＋ ion is sixcoordinated to furnish a distorted octahedral geometry.展开更多
A new Co（Ⅲ） complex with a tripodal amide ligand [CoL（N3）3] （L = N-acetyl- N＇,N＇-bis-[（2-pyridyl）methyl]-ethylenediamine） has been synthesized and characterized structurally by X-ray diffraction. It crystal...A new Co（Ⅲ） complex with a tripodal amide ligand [CoL（N3）3] （L = N-acetyl- N＇,N＇-bis-[（2-pyridyl）methyl]-ethylenediamine） has been synthesized and characterized structurally by X-ray diffraction. It crystallizes in orthorhombic, space group Pnma with a = 9.2515（19）, b = 12.729（3）, c = 17.273（4） A, V = 2034.0（7） A3, C16H20CoN13O, Mr = 469.38, Dc = 1.533 g/cm3, μ（MoKα） = 0.884 mm^-1, F（000） = 968, Z = 4, the final R = 0.0392 and wR = 0.0818 for 2430 observed reflections. In the complex, the amide ligand L acts as a tridentate fashion and coordinates to the Co（Ⅲ） ion through three nitrogen atoms, while the other three positions of the Co（Ⅲ） center are occupied by three terminal azide anions. The complex is connected as a 1D chain structure by intermolecular hydrogen bonds between the uncoordinated amide groups. In order to investigate the coordination ability, thermodynamic stability of the ligand L with the first-series transition metal ions （Co（Ⅱ）, Ni（Ⅱ）, Cu（Ⅱ） and Zn（Ⅱ）） has been studied by potentiometric titration, and the results show that the order of their stability constants conforms to the Irving-Williams sequence.展开更多
A new tripodal P,N ligand （C63H48N3O3P3） was prepared and characterized by elemental analysis, IR and single-crystal X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/c with a = 13.013...A new tripodal P,N ligand （C63H48N3O3P3） was prepared and characterized by elemental analysis, IR and single-crystal X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/c with a = 13.013（3）, b = 28.406（6）, c = 14.911（3） A^°, β= 111.04（3）°, V= 5144.6（18） A^°^3 Z = 4, Dc = 1.276 g/cm^3, Mr = 987.95, λ（MoKa） = 0.71073 A^°,μ = 0.17 mm^-1, F（000） = 2064, R = 0.0786 and wR = 0.1545. A total of 43260 unique reflections were collected, of which 5112 with I 〉 2σ（I） were observed. The title compound has a central benzene ring, which is linked by -NH-CO- bonds to three 2-aminophenyltriphenylphosphium moieties, of which two with P（1） and P（2） centers are pointing to the same face of the central aryl ring, while the third one directs oppositely, forming a pseudo-propeller. In the crystal structure, there exist face-to-face π-π stacking interactions which increase the stability of the crystal structure.展开更多
A new manganese compound [Mn8（tmp）2（Htmp）4（（CH3）3CCO2）4（py）2Cl2]·2py （1·2py, H3tmp = 1,1,1-tri（hydroxymethyl）propane, py = pyramid） has been synthesized and its structure was characterized by I...A new manganese compound [Mn8（tmp）2（Htmp）4（（CH3）3CCO2）4（py）2Cl2]·2py （1·2py, H3tmp = 1,1,1-tri（hydroxymethyl）propane, py = pyramid） has been synthesized and its structure was characterized by IR, elemental analysis and X-ray diffraction. Compound 1 belongs to the triclinic system, space group P1 with a = 13.378（5）, b = 14.334（5）, c = 15.012（6） , α = 107.637（5）, β = 95.635（3）, γ = 92.825（4）°, V = 2720.7（17） 3, Z = 1, C76H124N4O26Cl2Mn8, Mr = 2022.23, Dc = 1.234 Mg/m3, μ = 1.007 mm-1, F（000） = 1052, T = 293（2） K, the final R = 0.0755 and wR = 0.2163 for all 6463 observed reflections （I 〉 2σ（I））. X-ray analysis shows that the core of 1 contains a [Mn8] mixed-valence rod-like unit consisting of six edge-sharing triangles （Mn3）, each of which is bridged by a μ3-oxygen atom.展开更多
Five complexes ([Cu(tpc)] 2+ 1, [Cu(tpa)] 2+ 2, [Co(tpa)] 2+ 3, [Fe(tpa)] 2+ 4 and [Mn(tpa)] 2+ 5) (tpc = N, N', N' tris[(2 pyridyl)methyl] 1,4,7 triaza cyclononane(L1) and tp...Five complexes ([Cu(tpc)] 2+ 1, [Cu(tpa)] 2+ 2, [Co(tpa)] 2+ 3, [Fe(tpa)] 2+ 4 and [Mn(tpa)] 2+ 5) (tpc = N, N', N' tris[(2 pyridyl)methyl] 1,4,7 triaza cyclononane(L1) and tpa = tris[2 ((2 pyridyl)methyl imino)ethyl]amine(L2)) were synthesized and characterized. The crystal structures of 1, 3 and 4 were determined by X ray crystallography. Electrochemical investigations over two cupric complexes reveal that 2 has a less negative redox potential than that of 1. Electronic spectra of 2, 3, 4 and 5 show that the distinction in metal ion results in a shift of the ligand based π*←π transition.展开更多
Reaction of Cu(ClO4)2'6H2O with tripodal ligand tri s (2-benzi nd dazol yl methyl ) aInine(ntb) and sodium isonicotinate (Iso) yielded a mononuclear complex lCu(ntb)(lso)]ClO4.3.5H2O. Thestructure has been establi...Reaction of Cu(ClO4)2'6H2O with tripodal ligand tri s (2-benzi nd dazol yl methyl ) aInine(ntb) and sodium isonicotinate (Iso) yielded a mononuclear complex lCu(ntb)(lso)]ClO4.3.5H2O. Thestructure has been established by X-ray crystallography The Cu (Ⅱ) atom is in a distorted trigonalbipyranddal environment with three benzimindazole N atoms of ntb defining the equatorial plane, oneandne N atom of ntb, and one O atom of the carboxylate group of isonicotinate occupying the axialpositions.展开更多
A new Mn（Ⅱ） coordination polymer {[Mn（timb）2（H2O）2]·（Cl）2·（H2O）2}n（1,timb = 1,3,5-tris-（imidazol-1-ylmethyl）benzene） has been synthesized and characterized by elemental analysis,IR,TG and sing...A new Mn（Ⅱ） coordination polymer {[Mn（timb）2（H2O）2]·（Cl）2·（H2O）2}n（1,timb = 1,3,5-tris-（imidazol-1-ylmethyl）benzene） has been synthesized and characterized by elemental analysis,IR,TG and single-crystal X-ray diffraction.The title compound crystallizes in the triclinic system,space group P1 with a=9.0774（13）,b=9.8720（15）,c=11.4898（16）A,α=93.378（3）,β= 95.471（3）,γ=101.101（3）°,V=1002.6（3）A^3,Mr=834.67,Dc=1.382 g/cm^3,μ（MoKα）=0.517mm^-1,F（000）=435,GOF=0.986,Z=1,the final R=0.0506 and wR=0.1139 for 3517 observed reflections I〉2σ（I）.It consists of one-dimensional double stranded chains formed through bridging bidentate timb ligands,and these chains are further connected to yield a 3D supramolecular framework by hydrogen bonding interactions and π…π stacking interactions.展开更多
基金Supported by the Foundation of the Governor of Guizhou Province, China (Grant No. 200617)the Talented Person Foundation of Guizhou University (Grant No. 2007039)
文摘A new tripodal rhodamine B derivative 2 was designed and synthesized by tripodal trialdehyde and rhodamine B hydrazide for the first time. This derivative could be used as a fluorescent chemosensor for the selective and sensitive determination of copper(II) in Tris-HCl buffer and ethanol aqueous mixed media. Under the optimum conditions described herein,fluorescence enhancement at 557/577 nm was linearly related to the concentration of copper(II) in the range of 0.10 to 10.00×10-5 mol·L-1,with a corre-lation coefficient of R2=0.9964 (n=15) and a detection limit of 1.129×10-7 mol·L-1 (the relative standard deviation for five repeated measurements at 4.00×10-5 mol·L-1 Cu(II) was 2.2%). The absorbance meas-urements at 557 nm were linearly related to the concentration of Cu(II) in the range of 0.50 to 25.00×10-5 mol·L-1,with a correlation coefficient of R2=0.9948 (n=13) and a detection limit of 3.338×10-7mol·L-1.
文摘A new metal-organic coordination polymer {[Nd（tci）（H2O）2]·2H2O}n（1） has been synthesized based on the flexible tricarboxylate ligand tris（2-carboxyethyl）isocyanuric acid（H3tci） and structurally characterized by single-crystal X-ray diffraction analyses, elemental analysis, infrared spectra（IR）, powder X-ray diffraction（PXRD） and thermogravimetric analysis（TGA）. Complex 1 crystallizes in triclinic, space group P1 with a = 9.1648（11）, b = 9.3326（12）, c = 12.440（2） , C（12）H（20）N3O（13） Nd, Mr = 558.55, V = 886.9（2） 3, Z = 2, Dc = 2.092 g·cm-3, μ = 3.006 mm-1, F（000） = 554, 2.56〈θ〈25.00°, λ（Mo Kα） = 0.71073 , T = 293（2） K, the final R = 0.0662 and w R = 0.2071. X-ray diffraction analysis reveals that complex 1 is a two-dimensional layer, which is further assembled into a three-dimensional supramolecular architecture through hydrogen bonding interactions. The structure of complex 1 can be simplified as a rare 2-periodic uninodal {48·62} topology and a non-interpenetrating kgd topology. Furthermore, the thermal stability and photoluminescence property of 1 were investigated.
基金The authors would like to acknowledge the Bu Ali Sina University and the Iran National Science Foundation:INSF,under Grant number of 99031559,for their financial supports.
文摘Surface active ionic liquids (SAILs) are considered as prominent materials in enhanced oil recovery thanks to their high interfacial activity. This study reports the preparation and applications of a nanostructure Tripodal imidazolium SAIL as an environmentally-friendly substitute to the conventional surfactants. The product has a star-like molecular structure centered by a triazine spacer, namely [(C_(4)im)_(3)TA][Cl_(3)], prepared by a one-step synthesis method and characterized with FT-IR, NMR, XRD, and SEM analysis methods. The interfacial tension of the system was decreased to about 78% at critical micelle concentration of less than 0.08 mol·dm^(−3). Increasing temperature, from 298.2 to 323.2 K, improved this capability. The solid surface wettability was changed from oil-wet to water-wet and 80% and 77% stable emulsions of crude oil–aqueous solutions were created after one day and one week, respectively. Compared to the Gemini kind homologous SAILs, the superior effects of the Tripodal SAIL were revealed and attributed to the strong hydrophobic branches in the molecule. The Frumkin adsorption isotherm precisely reproduced the generated IFT data, and accordingly, the adsorption and thermodynamic parameters were determined.
文摘A tripodal ligand, tris{2 [N (pyridine methanoyl)amino]ethyl}amine(L), and its complexes with rare earth nitrates were synthesized. These new complexes with the general formula of Ln(NO 3) 3·L·6H 2O(where Ln=La, Nd, Eu, Tb, Y) were characterized by elemental analysis, IR spectra, thermal analysis, 1 H NMR spectra, molar conductivity and luminescent spectra. All the complexes are stable in air and their conductances in acetonitrile solution lie in the range of 142～150 S·cm 2·mol -1 , indicating 1∶1 type electrolytes. The IR and 1H NMR spectra of the ligand and its complexes show that all the C=O groups take part in coordination to the metal ions. The thermal behaviour of Eu complex shows that the weight losses at 75～120 ℃ and 120～210 ℃ correspond to the loss of four lattice water molecules and that of two coordinated water molecules, respectively. The luminescent spectra of the complexes of Eu(Ⅲ) and Tb(Ⅲ) were investigated in methanol.
基金Project (No. 973602311) supported by the Tianjin Natural Science Foundation of China
文摘 Two monomeric cobalt(Ⅱ)complexes,[CoL(N3)] ClO4(1)and CoL(N3)2(2),where L is tris((3,5-dimethylpyrazol-1-yl)methyl)amine,were synthesized and their crystal structures were determined by X-ray diffraction technique.Complex 1 is five coordinated with one azide nitrogen atom and four nitrogen atoms of the tris((3,5-dimethylpyrazol-l-yl)-methyl)amine ligand,and the metal center is in distorted trigonal bipyramidal environment.Complex 2 is six coordinated distorted octahedron with the two azide nitrogen atoms and four nitrogen donors of the tris((3,5-dimethylpyrazol-1-yl)-methyl)amine ligand.The solution behaviors of the title complexes have been further investigated by UV-Vis,and 1H NMR analysis.It is found that the formation of 1 and 2 depends on the molar ratio of the azide ion to metal salt and ligand Complex 1 attached with one azide group is more stable and easy to generate than complex 2 incorporated with two azide groups,and the reasons were well discussed.
文摘A new cadmium(Ⅱ) coordination polymer, [Cd(TITMB)_2]-(SO_4 )·21H_2O, whereTITMB = 1, 3, 5-tris (imidazol-1-yl-methyl) -2, 4, 6-trimethylbenzene, was obtained by self-assemblyof tripodal ligand TITMB with CdSO_4·2.7H_2O in acetonitrile, and characterized by X-raycrystallography. The crystal data belongs to monoclinic space group C_c with cell parameters a =1.16891(4) nm, b= 2.06671(6) nm, c = 2.48185(7) nm, β= 97.8560(10)°, R = 0.0487, wR =0.1211. Theresults of structure analysis indicate that each TITMB ligand coordinates three metal atoms and inturn each Cd(Ⅱ) atom with octahedral coordination geometry connects six nitrogen atoms of imidazolegroup from six different TITMB ligands to produce a 2D honeycomb network structure. There are a lotof water molecules linked by hydrogen bonds and occupied the channels formed intra- andinter-sheets.
基金supported by the Hong Kong Research Grants Council (602209)
文摘Treatment of Ru(CO)(Cl)(H)(PPh3)3 with NaLOEt (LOEt-= [CpCo{P(O)(OEt)2}3]-) afforded the hydride complex (PPh3)(CO)-LOEtRu(H) (1), which has been characterized by X-ray crystallography. Similarly, the tricyclohexylphosphine analogue, (PCy3)(CO)LOEtRu(H) (2), was synthesized from Ru(CO)Cl(H)(PCy3)2 and NaLOEt. Treatment of complex 1 with R'SO2N3 afforded the (arylsulfonyl)amido complexes LOEtRu(CO)(PPh3)(NHSO2R) (R = 2,4,6-i-Pr3C6H2 (3), 4-t-BuC6H4 (4)). The crystal structure of complex 3 has been determined. The Ru-N distance and Ru-N-S angle in 3 are 2.076(3) and 126.14(16)°, respectively. Reactions of complex 1 with acids have been studied.
文摘A new tripodal ligand, N, N, N′, N′, N″, N″ hexaisopropyl 2, 2′, 2″ nitrilotris (2,1 ethoxy) triacetamide (L) and its new erbium picrate complex were prepared. The structure of the complex was determined by X ray crystal structure analysis. The result reveals that the Er 3+ is encapsulated by the three arms of the tripodal ligand, and nine coordinated by the bridged head nitrogen atom, all ether oxygen atoms and carbonyl oxygen atoms of the ligand, and two oxygen atoms of the bidentate picrate. The coordination polyhedron is a distorted mono-capped square antiprism.
基金the National Natural Science Foundation of China(Nos.20671094 and 90610034)the foundation (No.GJHZ05) for Bureau of International Co-operation of Chinese Academy of Science.
文摘A novel tripodal receptor,1,3,5-tri((5,7-dimethyl-1,8-naphthyridin-2-yl-amino)methyl)-2,4,6-triethylbenzene(1) was synthesized from starting materials 2,6-diamino-pyridine(2) and 1,3,5-triethylbenzene(4) by three steps with an overall yield of 25%,and characterized by ESI-MS,FT-IR and ~1H NMR spectra.Additionally,its absorption and emission spectra were investigated.
文摘An N-hydroxyl peptide unit of H-L-Pro-L-Ala-L-Ala-β-（BnO）Ala-OMe was synthesized by stepwise chain building method in solution. Then, based on nitrilotriacetic acid backbone and this N-hydroxyl peptide unit, a novel chiral tripodal ligand P as an analogue of desferrichrome, has been synthesized. In neutral pH, ligand P formed stable tri（hydroxamato）- iron（Ⅲ） complexes which showed a maximum absorptiota （∑max=2750 M^-lcm^-1） at 422 nm in UV-Vis spectra. The characteristic absorption spectra are similar to those of natural trihydroxamate-type siderophores.
基金Supported by the National Natural Science Foundation of China (Grant No. 20401008)the Program for New Century Excellent Talents in University (Grant No. NCET-06-0902)the Natural Science Foundation of Gansu Province (Grant No. 3ZS061-A25-003)
文摘Solid complexes [REL(NO3)3]n with novel (10,3)-a type three-dimensional networks structure have been assembled using rare earth nitrates and an amide type semirigid tripodal bridging ligand, 1,3,5-tris {[(2′-benzylaminoformyl)phenoxyl]methyl}benzene (L), as building blocks. The complexes were crys- tallized in the orthorhombic system with chiral space group P212121. The whole structure consists of an infinite array of trigonal RE(III) ions bridged by tridentate ligands, and a novel (10,3)-a net is formed, which is very uncommon in the rare earth complexes. At room temperature, the Sm(III), Eu(III), Tb(III), Dy(III) complexes all exhibited characteristic luminescence emissions of central metal ions under UV light excitation.
基金the National Natural Science Foundation of China
文摘The tris（2-aminoethyl）amine （tren）-based tris（4-pyridylurea） receptor L has been synthesized and its anion binding properties were studied. The ligand forms a 2 ： 1 （host/guest） complex with MgSO4, [SO4^2 L2], in which a sulfate ion is encapsulated by six urea groups from the two ligands through multiple hydrogen bonds. The metal ions do not coordinate to the pyridyl groups but exist as the hydrate [Mg（H2O）6]2＋ and interact with the [SO4 L2] capsules in the outer coordination sphere to form a three dimensional extended structure. The anion binding behav- ior of ligand L in solution was studied.
基金This project was supported by the National Natural Science Foundation of China (No. 50372028) and the Foundation of hhit Marine-Technology lab.
文摘The mixed complex [Ni（L）（L＇）]（ClO4）2 has been synthesized using 2-aminoethyl- bi（3-bi-aminopropyl）amine with phen （1,10-phenanthroline） in the presence of Ni（Ⅱ） ion, and its structure was determined by X-ray diffraction. The crystal crystallizes in monoclinic, space group P21/c with a = 13.713（2）, b = 13.1466（19）, c = 14.780（2） A°, β= 97.620（3）°, V = 2640.9（7） A °^3, F（000） = 1272, Z = 4, Dc = 1.540 g/cm^3, R = 0.0536 and wR = 0.1207. The Ni^2＋ ion is sixcoordinated to furnish a distorted octahedral geometry.
基金supported by the National Natural Science Foundation of China (No.20771083)
文摘A new Co（Ⅲ） complex with a tripodal amide ligand [CoL（N3）3] （L = N-acetyl- N＇,N＇-bis-[（2-pyridyl）methyl]-ethylenediamine） has been synthesized and characterized structurally by X-ray diffraction. It crystallizes in orthorhombic, space group Pnma with a = 9.2515（19）, b = 12.729（3）, c = 17.273（4） A, V = 2034.0（7） A3, C16H20CoN13O, Mr = 469.38, Dc = 1.533 g/cm3, μ（MoKα） = 0.884 mm^-1, F（000） = 968, Z = 4, the final R = 0.0392 and wR = 0.0818 for 2430 observed reflections. In the complex, the amide ligand L acts as a tridentate fashion and coordinates to the Co（Ⅲ） ion through three nitrogen atoms, while the other three positions of the Co（Ⅲ） center are occupied by three terminal azide anions. The complex is connected as a 1D chain structure by intermolecular hydrogen bonds between the uncoordinated amide groups. In order to investigate the coordination ability, thermodynamic stability of the ligand L with the first-series transition metal ions （Co（Ⅱ）, Ni（Ⅱ）, Cu（Ⅱ） and Zn（Ⅱ）） has been studied by potentiometric titration, and the results show that the order of their stability constants conforms to the Irving-Williams sequence.
基金Supported by the Natural Science Foundation of Fujian Province (2007J0216, U0750004)the Key Project of Chinese Ministry of Education (No. 208066)+1 种基金the Education Department of Fujian Province (JA07029)State Key Laboratory of Structural Chemistry (No. 20080053)
文摘A new tripodal P,N ligand （C63H48N3O3P3） was prepared and characterized by elemental analysis, IR and single-crystal X-ray diffraction. The crystal belongs to the monoclinic system, space group P21/c with a = 13.013（3）, b = 28.406（6）, c = 14.911（3） A^°, β= 111.04（3）°, V= 5144.6（18） A^°^3 Z = 4, Dc = 1.276 g/cm^3, Mr = 987.95, λ（MoKa） = 0.71073 A^°,μ = 0.17 mm^-1, F（000） = 2064, R = 0.0786 and wR = 0.1545. A total of 43260 unique reflections were collected, of which 5112 with I 〉 2σ（I） were observed. The title compound has a central benzene ring, which is linked by -NH-CO- bonds to three 2-aminophenyltriphenylphosphium moieties, of which two with P（1） and P（2） centers are pointing to the same face of the central aryl ring, while the third one directs oppositely, forming a pseudo-propeller. In the crystal structure, there exist face-to-face π-π stacking interactions which increase the stability of the crystal structure.
基金Supported by the National Natural Science Foundation of China (Nos. 20633020 and 20973172)the National Basic Research Program of China (No. 2009CB220009)+1 种基金the Natural Science Foundation of Fujian Province (No. 2008J0175)the Fujian Province Youth Foundation (No. 2007F3112)
文摘A new manganese compound [Mn8（tmp）2（Htmp）4（（CH3）3CCO2）4（py）2Cl2]·2py （1·2py, H3tmp = 1,1,1-tri（hydroxymethyl）propane, py = pyramid） has been synthesized and its structure was characterized by IR, elemental analysis and X-ray diffraction. Compound 1 belongs to the triclinic system, space group P1 with a = 13.378（5）, b = 14.334（5）, c = 15.012（6） , α = 107.637（5）, β = 95.635（3）, γ = 92.825（4）°, V = 2720.7（17） 3, Z = 1, C76H124N4O26Cl2Mn8, Mr = 2022.23, Dc = 1.234 Mg/m3, μ = 1.007 mm-1, F（000） = 1052, T = 293（2） K, the final R = 0.0755 and wR = 0.2163 for all 6463 observed reflections （I 〉 2σ（I））. X-ray analysis shows that the core of 1 contains a [Mn8] mixed-valence rod-like unit consisting of six edge-sharing triangles （Mn3）, each of which is bridged by a μ3-oxygen atom.
文摘Five complexes ([Cu(tpc)] 2+ 1, [Cu(tpa)] 2+ 2, [Co(tpa)] 2+ 3, [Fe(tpa)] 2+ 4 and [Mn(tpa)] 2+ 5) (tpc = N, N', N' tris[(2 pyridyl)methyl] 1,4,7 triaza cyclononane(L1) and tpa = tris[2 ((2 pyridyl)methyl imino)ethyl]amine(L2)) were synthesized and characterized. The crystal structures of 1, 3 and 4 were determined by X ray crystallography. Electrochemical investigations over two cupric complexes reveal that 2 has a less negative redox potential than that of 1. Electronic spectra of 2, 3, 4 and 5 show that the distinction in metal ion results in a shift of the ligand based π*←π transition.
文摘Reaction of Cu(ClO4)2'6H2O with tripodal ligand tri s (2-benzi nd dazol yl methyl ) aInine(ntb) and sodium isonicotinate (Iso) yielded a mononuclear complex lCu(ntb)(lso)]ClO4.3.5H2O. Thestructure has been established by X-ray crystallography The Cu (Ⅱ) atom is in a distorted trigonalbipyranddal environment with three benzimindazole N atoms of ntb defining the equatorial plane, oneandne N atom of ntb, and one O atom of the carboxylate group of isonicotinate occupying the axialpositions.
基金Supported by the National Basic Research Program of China (2006CB806104)Science Foundation for Youths of Guangxi Province (No 0991089)Initiation Found of Hechi University (No 2008QS-N022)
文摘A new Mn（Ⅱ） coordination polymer {[Mn（timb）2（H2O）2]·（Cl）2·（H2O）2}n（1,timb = 1,3,5-tris-（imidazol-1-ylmethyl）benzene） has been synthesized and characterized by elemental analysis,IR,TG and single-crystal X-ray diffraction.The title compound crystallizes in the triclinic system,space group P1 with a=9.0774（13）,b=9.8720（15）,c=11.4898（16）A,α=93.378（3）,β= 95.471（3）,γ=101.101（3）°,V=1002.6（3）A^3,Mr=834.67,Dc=1.382 g/cm^3,μ（MoKα）=0.517mm^-1,F（000）=435,GOF=0.986,Z=1,the final R=0.0506 and wR=0.1139 for 3517 observed reflections I〉2σ（I）.It consists of one-dimensional double stranded chains formed through bridging bidentate timb ligands,and these chains are further connected to yield a 3D supramolecular framework by hydrogen bonding interactions and π…π stacking interactions.
