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1.
The new silver(I) triple salt 2Ag2C2·AgF·9AgNO3·H2O was prepared by dissolving Ag2C2 in an aqueous solution of AgNO3 and AgBF4. Its crystal structure contains two kinds of monocapped trigonal prismatic C2@Ag7 cages, with the capping atom occurring on one triangular face or one rectangular face. 相似文献
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将N,N-二甲基乙醇胺、N-甲基二乙醇胺分别接枝到1,3-二溴丙烷的两端进行季铵化反应,得到N1,N3-二羟乙基-N1,N1,N3,N3-四甲基-1,3-丙二胺二溴盐(QAS-1)和N1,N1,N3,N3-四羟乙基-N1,N3-二甲基-1,3-丙二胺二溴盐(QAS-2)。采用傅立叶变换红外光谱(FTIR)、核磁共振(NMR)和元素分析确证了其结构,以抑菌圈法和试管二倍稀释法评价了两者对5种菌株的抗菌活性。结果显示,它们对所选菌株均具有一定的抗菌活性,其中对白色念珠菌的最小抑菌浓度(MIC)分别为100 mg·L~(-1)和50 mg·L~(-1)。扫描电子显微镜(SEM)和透射电子显微镜(TEM)显示,QAS-1对金黄色葡萄球菌的抗菌作用机理可能为,带正电荷的季铵盐吸附在细菌表面,破坏细胞膜,导致细胞质外流从而杀灭细菌。细胞毒性显示QAS-1对人正常肝细胞(LO2)和人永生化表皮细胞(HaCat)的IC_(50)值分别为110.34 mg·L~(-1)和92.68 mg·L~(-1),细胞毒性显著低于阳性药。该研究说明该类季铵盐在抗菌领域具有潜在的应用价值。 相似文献
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《Analytical letters》2012,45(12):2545-2551
ABSTRACT A spectrochemical method has been developed for the quantitative determination of metallic silver in silver nitrate and silver chloride or bromide matrices exposed to light. The method is based on the oxidation of silver(0) by iron(III) at pH 3.5 in the presence of ferrozine. The resulting absorbance of the iron ferrozine complex is measured at 562 nm. Less than 0.1 mg of metallic silver can be determined with a relative standard deviation better than 6%. 相似文献
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Jin-Sen Yang Zhen Han Xi-Yan Dong Peng Luo Hui-Lin Mo Prof. Dr. Shuang-Quan Zang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(29):11996-12000
Luminescent metal clusters show promise for applications in imaging and sensing. However, promoting emission from metal clusters at room temperature is a challenging task owing to the lack of an efficient approach to suppress the nonradiative decay process in metal cores. We report herein that the addition of a silver atom into a metal interstice of the radarlike thiolated silver cluster [Ag27(StBu)14(S)2(CF3COO)9(DMAc)4]⋅DMAc ( NC1 , DMAc=dimethylacetamide), which is non-emissive under ambient conditions, produced another silver cluster [Ag28(AdmS)14(S)2(CF3COO)10(H2O)4] ( NC2 ) that displayed bright green room-temperature photoluminescence aided by the new ligand 1-adamantanethiol (AdmSH). The 28th Ag atom, which hardly affects the geometrical and electronic structures of the Ag–S skeleton, triggered the emission of green light as a result of the rigidity of the cluster structure. 相似文献
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Ten polymeric silver(I) double salts containing embedded acetylenediide: [(Ag2C2)2(AgCF3CO2)9(L1)3] (1), [(Ag2C2)2(AgCF3CO2)10(L2)3]H2O (2), [(Ag2C2)(AgCF3CO2)4(L3)(H2O)]0.75 H2O (3), [(Ag2C2)(1.5)(AgCF3CO2)7(L4)2] (4), [(Ag2C2)(AgCF3CO2)7(L5)2(H2O)] (5), [(Ag2C2) (AgC2F5CO2)7(L1)3(H2O)] (6), [(Ag2C2)(AgCF3CO2)7(L1)3(H2O)]2 H2O (7), [(Ag2C2)(AgC2F5CO2)6(L3)2] (8), [(Ag2C2)2(AgC2F5CO2)12(L4)2(H2O)4]H2O (9), and [(Ag2C2)(AgCF3CO2)6(L3)2(H2O)]H2O (10) have been isolated by varying the types of betaines, the perfluorocarboxylate ligands employed, and the reaction conditions. Single-crystal X-ray analysis has shown that 1-4 all have a columnar structure composed of fused silver(I) double cages, with C2(2-) species embedded in its stem and an exterior coat comprising anionic and zwitterionic carboxylates. For 5 and 6, single silver(I) cages are linked into a beaded chain through both types of carboxylate ligands. In 7, two different coordination modes of L1 connect the silver(I) polyhedra into a chain. For 8, the mu(2)-O,O' coordination mode of L3 connects the silver(I) double cages into a chain. Compound 9 exhibits a two-dimensional architecture generated from the cross-linkage of double cages by C2F5CO2-, L4, and [Ag2(C2F5CO2)2] units. Similar to 9, 10 is also a two-dimensional structure, which is formed by connecting the chains of linked double cages through [Ag2(CF3CO2)2] bridging. 相似文献
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1 INTRODUCTION Great attention has currently been paid to com-pounds formed by the reaction between phosphineand metal alkynyl building blocks[1]. The ligand NP3contains one tertiary nitrogen atom as well as threephosphorous atoms and bonds to the metal ions as atetradentate ligand, affording tetrahedral[2] or triangle-bipyrimidal geometry[3, . In other coordination ca- 4]ses, one[5, , two[7], three P donors[8, 6] … 相似文献
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Two silver(I) complexes were prepared by the reaction of [Ag(C(CPh)]n with NP3 [NP3 = N(CH2CH2PPh2)3] or with NP3 and [Cu(CH3CN)4]ClO4. Complex 1 [(Ag2Cl(NP3)2)(Ag5(C(CPh)6)] contains both NP3 and PhC(C- ligands. The complex cation is (Ag2Cl(NP3)2)+, in which two Ag(NP3)+ cations were bridged by a Cl- donor. The anion is (Ag5(C(CPh)6)-, where five Ag+ ions are linked by six C(CPh- to form a pentanuclear cluster. Complex 2 only contains NP3 ligand, where the silver center adopts a trigonal-bipyramidal geometry. Crystal data for 1: C133H116Ag7Cl3N2P6, Mr = 2789.54, triclinic, space group P, a = 13.0780(2), b = 15.3678(2), c = 31.2041(3) (A), α = 91.3928(7), β = 90.9328(8), γ = 96.0244(4)o, V = 6233.8(1) (A)3, T = 293(2) K, Z = 2, Dc = 1.486 g/cm3, F(000) = 2796, μ = 1.266 mm-1, the final R = 0.0746 and wR = 0.1953 for 16475 observed reflections with I > 2σ(I). Crystal data for 2: C42H42AgClNO4P3, Mr = 861.00, trigonal, space group R3, a = 17.451(1), b = 17.451(1), c = 11.3985(7) (A), V = 3006.0(3) (A)3, T = 293(2) K, Z = 3, Dc = 1.427 g/cm3, F(000) = 1326, μ = 0.731 mm-1, the final R = 0.0251 and wR = 0.0663 for 1499 observed reflections with I > 2σ(I). 相似文献
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Jin‐Sen Yang Zhen Han Xi‐Yan Dong Peng Luo Hui‐Lin Mo Shuang‐Quan Zang 《Angewandte Chemie (International ed. in English)》2020,59(29):11898-11902
Luminescent metal clusters show promise for applications in imaging and sensing. However, promoting emission from metal clusters at room temperature is a challenging task owing to the lack of an efficient approach to suppress the nonradiative decay process in metal cores. We report herein that the addition of a silver atom into a metal interstice of the radarlike thiolated silver cluster [Ag27(StBu)14(S)2(CF3COO)9(DMAc)4]?DMAc ( NC1 , DMAc=dimethylacetamide), which is non‐emissive under ambient conditions, produced another silver cluster [Ag28(AdmS)14(S)2(CF3COO)10(H2O)4] ( NC2 ) that displayed bright green room‐temperature photoluminescence aided by the new ligand 1‐adamantanethiol (AdmSH). The 28th Ag atom, which hardly affects the geometrical and electronic structures of the Ag–S skeleton, triggered the emission of green light as a result of the rigidity of the cluster structure. 相似文献
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Modeling of Structural,Energetic, and Dynamic Properties of Few‐Atom Silver Clusters Embedded in Polynucleotide Strands by Using Molecular Dynamics 下载免费PDF全文
Dr. Nicolas Staelens Dr. Laurence Leherte Prof. Benoît Champagne Prof. Daniel P. Vercauteren 《Chemphyschem》2015,16(2):360-369
This work concerns the study of the structural, energetic, and dynamic properties of fluorescent systems composed of silver clusters stabilized by polynucleotide strands. To do so, classical interaction potentials relative to silver, neutral and cationic, were introduced in the AMBER force field. Molecular dynamics simulations allowed analysis of the nature and force of the interactions between the various parts of the nucleic oligomers and the silver clusters. Conformational analyses were necessary to explore the flexibility of the supramolecular assemblies, specifically by radial distribution functions and Ramachandran‐type maps. 相似文献
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Dr. Sebastian Bestgen Dr. Xiaoxun Yang Dr. Ibrahim Issac Dr. Olaf Fuhr Prof. Dr. Peter W. Roesky Prof. Dr. Dieter Fenske 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(29):9933-9937
The silver salts of 1‐adamantanethiol (AdSH) and furan‐2‐ylmethanethiol (FurCH2SH) were successfully applied as building blocks for ligand‐protected Ag2S nanoclusters. The reaction of the silver thiolates [AgSAd]x and [AgSCH2Fur]x with S(SiMe3)2 and 1,5‐bis(diphenylphosphino)pentane (dpppt) afforded three different clusters with 58, 94 and, 190 silver atoms. The intensely colored compounds [Ag58S13(SAd)32] ( 1 ), [Ag94S34(SAd)26(dpppt)6] ( 2 ), and [Ag190S58(SCH2Fur)74(dpppt)8] ( 3 ) were structurally characterized by single‐crystal X‐ray diffraction and exhibit different cluster core geometries and ligand shells. The diameters of the well‐defined sphere‐shaped nanoclusters range from 2.2 nm to 3.5 nm. 相似文献
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由2-硝基-1,4-对苯二甲酸和4,4'-联吡啶作为起始原料合成了4个金属银的配位聚合物,{[Ag(4,4'-bipy)]·2-Hnbdc·2H2O·CH3OH}n (1),{[Ag(4,4'-bipy)(2-Hnbdc)]}n (2),{[Ag2(4,4'-bipy)2(2-nbdc)]·2H2O}n (3),和{[Ag2(4,4'-bipy)2(2-nbdc)(H2O)]·2H2O}n (4)。通过IR、元素分析、TG、UV和荧光光谱以及粉末衍射等手段,对配合物进行了表征和性质研究。单晶衍射分析显示,配合物1为1D阴-阳离子型聚合物,配合物2为1D双链结构,且结构中不存在溶剂分子。配合物3和4均为1D链状结构。结构的多样性主要是由配体构象、硝基对苯二甲酸的配位模式以及弱作用(如π-π堆积、Ag…Ag作用以及氢键等)导致的。结构的不同也使得它们的稳定性、紫外吸收以及荧光光谱存在着差异。 相似文献
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由2-硝基-1, 4-对苯二甲酸和4, 4'-联吡啶作为起始原料合成了4个金属银的配位聚合物, {[Ag(4, 4'-bipy)]·2-Hnbdc·2H2O ·CH3OH}n (1), {[Ag(4, 4'-bipy)(2-Hnbdc)]}n (2), {[Ag2(4, 4'-bipy)2(2-nbdc)]·2H2O}n (3), 和{[Ag2(4, 4'-bipy)2(2-nbdc)(H2O)]·2H2O}n (4)。通过IR、元素分析、TG、UV和荧光光谱以及粉末衍射等手段, 对配合物进行了表征和性质研究。单晶衍射分析显示, 配合物1为1D阴-阳离子型聚合物, 配合物2为1D双链结构, 且结构中不存在溶剂分子。配合物3和4均为1D链状结构。结构的多样性主要是由配体构象、硝基对苯二甲酸的配位模式以及弱作用(如π-π堆积、Ag…Ag作用以及氢键等)导致的。结构的不同也使得它们的稳定性、紫外吸收以及荧光光谱存在着差异。 相似文献
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铜盐与二甲氧基嘧啶胺配合物的合成及其结构表征 总被引:2,自引:0,他引:2
利用氯化苄基三乙基胺(TEBA)为催化剂,改进文献方法提高2-氨基-4,6 -二甲氧基嘧啶(AMP)的产率。无水乙醇中回流制得水合氯化铜和硝酸铜与AMP的 物质的量比为1:2的固态配合物,用化学分析和元素分析确定它们的组成为Cu (AMP)2Cl2(1)和Cu(AMP)2(NO3)2(2);用IR,XPS和^1H NMR等手段研究了它们的成 键情况;配合物中配体通过氨基N原子和嘧啶环上一个N原子与Cu^2+双齿配位,配 合物2中NO3^-未参与配位,中心离子Cu^2+分别为sp^3d^2和sp^3杂化,配位数为6 和4。据此,推测了它们的可能结构。 相似文献
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Dr. David Buceta Dr. Blanca Dominguez Dr. Sara Vieitez Dr. Iria R. Arias Dr. J. Manuel Ageitos Prof. M. Carmen Blanco Prof. Giampaolo Barone Prof. Fernando Domínguez Prof. M. Arturo López-Quintela 《ChemistryOpen》2021,10(8):760-763
Synthesis and purification of metal clusters without strong binding agents by wet chemical methods are very attractive for their potential applications in many research areas. However, especially challenging is the separation of uncharged clusters with only a few number of atoms, which renders the usual techniques very difficult to apply. Herein, we report the first efficient separation of Ag2 and Ag3 clusters using the different entropic driving forces when such clusters interact with DNA, into which Ag3 selectively intercalates. After sequential dialysis of the samples and denaturalizing the DNA-Ag3 complex, pure Ag2 can be found in the dialysate after extensive dialysis. Free Ag3 is recovered after DNA denaturation. 相似文献
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Zhi Wang Xiao‐Yu Li Li‐Wei Liu Si‐Qi Yu Zhen‐Yu Feng Prof. Chen‐Ho Tung Dr. Di Sun 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(20):6830-6836
Assembly of small clusters into rigid bodies with precise shape and symmetry has been witnessed by the significant advances in cluster‐based metal–organic frameworks (MOFs), however, nanosized silver cluster based MOFs remain largely unexplored. Herein, two anion‐templated silver clusters, CO3@Ag20 and SO4@Ag22, were ingeniously incorporated into a 2D sql lattice ( 1 , [CO3@Ag20(iPrS)10(NO3)8(DMF)2]n) and an unprecedented 3D two‐fold interpenetrated dia network ( 2 , [SO4@Ag22(iPrS)12(NO3)6 ? 2 NO3]n), respectively, under mild solvothermal conditions. Their atomically precise structures were confirmed by single‐crystal X‐ray diffraction analysis and further consolidated by IR spectroscopy, thermogravimetric analysis (TGA), and elemental analysis. Each drum‐like CO3@Ag20 cluster is extended by twelve NO3? ions to form the 2D sql lattice of 1 , whereas each ball‐shaped SO4@Ag22 cluster with a twisted truncated tetrahedral geometry is pillared by four [Ag6(NO3)3] triangular prisms to form the 3D interpenetrated dia network of 2 . Notably, 2 is the first interpenetrated 3D MOF constructed from silver clusters. These results demonstrate the dual role of the anions, which not only internally act as anion templates to induce the formation of silver thiolate clusters but also externally extend the cluster units into the rigid networks. The photoluminescent and electrochemical properties of 2 are discussed in detail. 相似文献
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S. G. Kozlova S. P. Gabuda V. P. Isupov L.É. Chupakhina 《Journal of Structural Chemistry》2003,44(2):198-205
The effect of the anion charge on the structure of [LiAl2(OH)6]nX (X = Cl-, Br-, I-, SO4
2-, C6H8O4
2-) intercalation compounds and the water effect on the structure of [LiAl2(OH)6]Cl·nH2O have been studied using 1H, 7Li, and 27Al NMR. A change in the charge on the anion leads to significant changes in the asymmetry parameter for the lithium and aluminum nuclei with relatively small changes in the quadrupolar coupling constant and the broadening factor. The structure of the intermediate [LiAl2(OH)6]Cl·0.5H2O hydrate can be represented as a derivative of the structure of the anhydrous [LiAl2(OH)6]Cl intercalate with a slightly increased layer thickness and a minor orthorhombic distortion of the hexagonal cell; the water molecules partially fill the interlayer voids and participate in the diffusion process. Further hydration of the intercalate (x 1) leads to a minor (0.2) increase in the layer thickness and is accompanied by disordering of chloride ions and water molecules in the interlayer space. 相似文献