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Journal articles on the topic 'Metallo bis-ditiolene sulphur-based ligands'

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1

Hladysh, Sviatoslav, Daniela Václavková, David Vrbata, et al. "Synthesis and characterization of metallo-supramolecular polymers from thiophene-based unimers bearing pybox ligands." RSC Advances 7, no. 18 (2017): 10718–28. http://dx.doi.org/10.1039/c6ra26665g.

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A series of novel metallo-supramolecular polymers was prepared, based on 2,6-bis(2-oxazolinyl)pyridine chelating groups bridged with thiophene, bithiophene and thienothiophene as a linker, beginning from commercially available (chelidamic) acid.
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2

Xu, Xiaowen, Anne K. Seiffert, Ruben Lenaerts, et al. "[2 × 2] metallo-supramolecular grids based on 4,6-bis((1H-1,2,3-triazol-4-yl)-pyridin-2-yl)-2-phenylpyrimidine ligands: from discrete [2 × 2] grid structures to star-shaped supramolecular polymeric architectures." Dalton Transactions 50, no. 25 (2021): 8746–51. http://dx.doi.org/10.1039/d1dt01373d.

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[2 × 2] metallo-supramolecular grids were readily obtained by complexation of novel 4,6-bis(6-ethynylpyridin-2-yl)-2-phenylpyrimidine ligands with Fe<sup>2+</sup> or Zn<sup>2+</sup> in acetonitrile, allowing for constructing discrete grids and star-shaped polymers.
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3

Chaur Valencia, Manuel Noé, Héctor Fabio Zuluaga Corrales, and Gabriel Martínez. "Electronic and electrochemical properties of grid-type metal ion complexes (Fe+2 and Co2+) with a pyridine-pyrimidine-pyridine based bis(hydrazone)." Revista Colombiana de Química 47, no. 2 (2018): 45–53. http://dx.doi.org/10.15446/rev.colomb.quim.v47n2.66081.

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Se reporta la síntesis de nuevos complejos metálicos de Co2+ y Fe2+ tipo rejilla que contienen como ligando orgánico una doble hidrazona altamente soluble en solventes orgánicos. Los datos obtenidos de resonancia magnética nuclear (RMN 1H), espectroscopía infrarroja con transformada de Fourier (FT-IR) y análisis elemental indican que los complejos adoptaron una estructura de tipo rejilla. Las propiedades electrónicas de las metalo-rejillas fueron analizadas a través de espectroscopía UV-Vis en cloroformo, metanol y diclorometano. Adicionalmente, se realizaron medidas de voltamperometría cíclica y voltametría de onda cuadrada en DMF. Los complejos exhibieron dos procesos de oxidación atribuidos al ligando orgánico y a varios eventos reductivos que comprometían al ligando y a los centros metálicos, por tanto, la interacción entre la naturaleza del ion metálico y la estructura del ligando fue analizada en detalle. Estos resultados representan un avance en la química de metalo-rejillas no solo por los escasos reportes de propiedades electroquímicas encontrados en la literatura, sino también por el diseño de nuevos ligandos hidrazónicos de alta solubilidad y fácil preparación.
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4

Zhang, Ying-Ying, Yue-Jian Lin, and Guo-Xin Jin. "Nano-sized heterometallic macrocycles based on 4-pyridinylboron-capped iron(ii) clathrochelates: syntheses, structures and properties." Chem. Commun. 50, no. 18 (2014): 2327–29. http://dx.doi.org/10.1039/c3cc49038f.

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A series of nano-scaled Ir–Fe heterometallic rectangles were prepared from 4-pyridinylboron-capped iron(ii) clathrochelates and bis(amidine) ligands. The cavity size could be controlled easily by the length of the organic ligand.
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5

Satapathy, Rudrakanta, Mohan Ramesh, Harihara Padhy, et al. "Novel metallo-dendrimers containing various Ru core ligands and dendritic thiophene arms for photovoltaic applications." Polym. Chem. 5, no. 18 (2014): 5423–35. http://dx.doi.org/10.1039/c4py00444b.

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A polymer solar cell device containing an active layer of BTRu2G3 : PC70BM = 1 : 3 (by wt), i.e., the third generation of the bis-Ru-based dendritic complex BTRu2G3 showed the highest PCE value of 0.77%.
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6

Chagas, Rafael César Russo, José Roberto da Silveira Maia, and Vany P. Ferraz. "Synthesis and characterisation of organotin(IV) derivatives of ambidentate ligands containing nitrogen and sulphur donor atoms." Main Group Metal Chemistry 34, no. 5-6 (2011): 131–37. http://dx.doi.org/10.1515/mgmc-2012-0904.

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Abstract A series of organotin(IV) derivatives of bis(pyrimidin-2-ylthio)methane (ptm), 1,2-bis(pyrimidin-2-ylthio)ethane (pte) and 1,6-bis(pyrimidin-2-ylthio)hexane (pth) have been prepared in dichloromethane at room temperature. The 2:1 (M/L) molar ratio compounds have a general formula of [Sn2ClxPh8-xL] (x=2, 4, 6, 8; L=ptm, pte and pth). A 1:1 complex was also obtained by reacting SnClPh3 with pth. The organotin derivatives were characterised by multinuclear NMR (1H, 13C and 119Sn) and infrared spectroscopy, gel permeation chromatography (GPC), microanalysis and melting point. In the triphenyltin derivatives, 1, 5, 9 and 10 the tin atoms show a distorted trigonal-bipyramidal configuration where the ligand is monodentate towards the metal atom. In the compounds 2–4, 6–8 and 11–13, the tin atoms each exhibit a distorted octahedral configuration. Chelation is formed between the tin nucleus and the coordinating sulphur and nitrogen atoms. The correlation between the 1J(13C-119Sn) and C-Sn-C bond angle indicates formation of 5-coordinate compounds.
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7

Awal, Abdul, Shifa Sarker, Md Mia, Md Delwar Hossain, and A. J. Saleh Ahammad. "Fe(II)-Based Metallo-Supramolecular Polymer Film as a Sensing Material for the Detection of Nitrite." ECS Transactions 107, no. 1 (2022): 14783–90. http://dx.doi.org/10.1149/10701.14783ecst.

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In this work, we report the synthesis of a mono metallic supramolecular polymer for constructing a new nonenzymatic electrochemical nitrite sensor. Metallo supramolecular polymer have been prepared by the complexation reaction of a ligand bearing terpyridine moieties [4′,4′′′′-(1,4 Phenylene) bis (2,2′:6′,2′′-terpyridine] with Fe(II) salts (Fe salt: Ligand-1:1) (polyFe). The polyFe was characterized with the UV/Vis titration and FTIR. The glassy carbon electrode (GCE) was used for fabricating ployFe_GCE via a drop casting method that was used for detecting nitrite through the oxidation process. The kinetics of the irreversible oxidation mechanism was studied using scan rate. Amperometry and CV techniques were used for studying the effectiveness of the polyFe_GCE for detecting nitrite at different concentrations. The polyFe_GCE was also used for interference, reproducibility, and stability study. We utilized the proposed sensor further for analyzing nitrite in tap water. The recovery obtained was satisfactory with relatively low value of standard deviation.
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8

Macedi, Eleonora, Daniele Paderni, Mauro Formica, et al. "Playing with Structural Parameters: Synthesis and Characterization of Two New Maltol-Based Ligands with Binding and Antineoplastic Properties." Molecules 25, no. 4 (2020): 943. http://dx.doi.org/10.3390/molecules25040943.

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Two maltol-based ligands, N,N′-bis((3-hydroxy-4-pyron-2-yl)methyl)-1,4-piperazine (L1) and N,N′,N′-tris((3-hydroxy-4-pyron-2-yl)methyl)-N-methylethylendiamine (L2), were synthesized and characterized. L1 and L2, containing, respectively, two and three maltol units spaced by a diamine fragment, were designed to evaluate how biological and binding features are affected by structural modifications of the parent compound malten. The acid-base behavior and the binding properties towards transition, alkaline-earth (AE) and rare-earth (RE) cations in aqueous solution, studied by potentiometric, UV-Vis and NMR analysis, are reported along with biological studies on DNA and leukemia cells. Both ligands form stable complexes with Cu(II), Zn(II) and Co(II) that were studied as metallo-receptors for AE and RE at neutral pH. L1 complexes are more affected than L2 ones by hard cations, the L1-Cu(II) system being deeply affected by RE. The structural modifications altered the mechanism of action: L1 partially maintains the ability to induce structural alterations of DNA, while L2 provokes single strand (nicks) and to a lesser extent double strand breaks of DNA.
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9

Kanao, Miki, and Masayoshi Higuchi. "Synthesis of Ni-Based Metallo-Supramolecular Polymer with Bis-NNO-Tridentate Ligand for Electrochromic Devices." Journal of Photopolymer Science and Technology 29, no. 2 (2016): 295–300. http://dx.doi.org/10.2494/photopolymer.29.295.

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10

Feng, Tao, Li-Li Li, Ya-Juan Li, and Wen-Kui Dong. "A half-salamo-based pyridine-containing ligand and its novel NiII complexes including different auxiliary ligands: syntheses, structures, fluorescence properties, DFT calculations and Hirshfeld surface analysis." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 77, no. 1 (2021): 168–81. http://dx.doi.org/10.1107/s2052520620016157.

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Three novel multinuclear NiII complexes, namely, bis{μ-2-methoxy-6-[8-(pyridin-2-yl)-3,6-dioxa-2,7-diazaocta-1,7-dien-1-yl]phenolato}bis[thiocyanatonickel(II)], [Ni2(L)2(NCS)2], 1, bis{μ-2-methoxy-6-[8-(pyridin-2-yl)-3,6-dioxa-2,7-diazaocta-1,7-dien-1-yl]phenolato}bis[azidonickel(II)], [Ni2(L)2(N3)2], 2, and catena-poly[[{2-methoxy-6-[8-(pyridin-2-yl)-3,6-dioxa-2,7-diazaocta-1,7-dien-1-yl]phenolato}nickel(II)]-μ-dicyanamidato], [Ni(L)(dca)] n , 3 {dca is dicyanamide, C2N3, and HL is 2-methoxy-6-[8-(pyridin-2-yl)-3,6-dioxa-2,7-diazaocta-1,7-dien-1-yl]phenol, C16H17N3O4}, with a half-salamo-based pyridine-containing HL ligand have been synthesized and characterized by FT–IR, UV–Vis absorption spectroscopy, X-ray crystallography, Hirshfeld surface analysis and density functional theory (DFT) calculations. The central NiII ions in complexes 1–3 are hosted in the half-salamo-based N3O-donor cavity of the organic ligand. Complex 1 is a centrosymmetric dimer and two [Ni(L)(NCS)] units form a centrosymmetric dimeric structure, which is bridged by two phenolate O atoms. The two N atoms at the axial ends are provided by two NCS− ligands. In complex 1, each NiII ion has a six-coordinated octahedral geometry. Complex 2 is similar to 1, but they differ in that the auxiliary NCS− ligand is replaced by N3 −. However, complex 3 is a one-dimensional coordination polymer constructed from [Ni(L)(dca)] units, which are connected by the auxiliary bidentate dca ligand via N-donor atoms. As with complexes 1 and 2, the NiII ion in 3 has a six-coordinated octahedral geometry.
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11

Fujii, Kazuko, Manas Kumar Bera, Dines Chandra Santra, and Masayoshi Higuchi. "Nanocomposites of Fe(II)-Based Metallo-Supramolecular Polymer and a Layered Inorganic–Organic Hybrid for Improved Electrochromic Materials." Polymers 14, no. 5 (2022): 915. http://dx.doi.org/10.3390/polym14050915.

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Fe-based metallo-supramolecular polymer (polyFe), composed of Fe(II) ions and bis(terpyridyl)benzene, is known as a good electrochromic (EC) material. For the first time, to improve the EC properties, we prepared nanocomposites comprising polyFe and a layered inorganic–imidazoline covalently bonded hybrid (LIIm) by simply mixing them in methanol and then examined the effect of the nanocomposition on EC properties. The obtained blue/purple-colored composites (polyFe/LIIm composites) were demonstrated by scanning electron microscopy (SEM) to comprise a structure of LIIm nanoparticles coated with amorphous polyFe. Interestingly, X-ray diffraction (XRD) measurements suggested that there was no intercalation of polyFe in the interlayer space of LIIm. Ultraviolet-visible (UV-vis) spectroscopy measurements demonstrated that light absorption close to 600 nm was attributed to metal-to-ligand charge transfer (MLCT) from the Fe(II) ion to the bisterpyridine ligand and was influenced by LIIm in the composites. The composites exhibited a pair of redox waves, assigned to the redox between Fe(II) and Fe(III), in the cyclic voltammograms; moreover, the composites were estimated to be diffusion controlled. Thin composite films demonstrated reversible EC changes, triggered by the redox reaction of the metal. Furthermore, the results show that the nano-scale composition of the metallo-supramolecular polymers with LIIm can effectively improve the memory properties without reducing the contrast in transmittance (ΔT) of 70–76% in EC changes after applying 1.2 V vs. Ag/Ag+. The EC properties varied with varying ratios (3/0.1, 0.5, 1, and 5) of the polyFe/LIIm, and the ratio of 3/1 exhibited the longest memory and largest MLCT absorption peak among composites. The results show that the polyFe/LIIm composites are useful EC materials for dimming glass applications, such as smart windows.
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12

Lai, Po-Ni, Sungwon Yoon, and Thomas S. Teets. "Efficient near-infrared luminescence from bis-cyclometalated iridium(iii) complexes with rigid quinoline-derived ancillary ligands." Chemical Communications 56, no. 62 (2020): 8754–57. http://dx.doi.org/10.1039/d0cc02745f.

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13

Perdih, Franc. "CuIIand ZnIIβ-diketonate coordination polymers based on pyrimidin-2-amine, pyrazine and 1,2-bis(4-pyridyl)ethane". Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 72, № 6 (2016): 828–35. http://dx.doi.org/10.1107/s2052520616014566.

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Copper(II) and zinc(II) bis(4,4,4-trifluoro-1-phenylbutane-1,3-dionato) compounds with pyrimidin-2-amine (pyr2a), pyrazine (pyz) and 1,2-bis(4-pyridyl)ethane (dpet) were prepared and solid-state structures of coordination polymers [M(tfpb)2(pyr2a)]∞[M= Cu (1), Zn (2); tfpb = 4,4,4-trifluoro-1-phenylbutane-1,3-dionate], [M(tfpb)2(pyz)]∞[M= Cu (3), Zn (4a, 4b)] and [Cu(tfpb)2(dpet)]∞(5), respectively, were determined by single-crystal X-ray analysis. The coordination of metal centers in all compounds is octahedral with nitrogen ligands occupying the axial positions. Compound (1) crystallizes in the triclinic space group P\bar 1, whereas (2) crystallizes in the monoclinic space groupP2/n. Differences are due to the different orientation of adjacentM(tfpb)2units, whereas the orientation of pyrimidin-2-amine is the same in both compounds. Polymeric chains in (1) and (2) contain intramolecular N—H...O hydrogen bonding between amino and carbonyl groups. Room-temperature structures (3) and (4a) are isomorphous adopting the monoclinic space groupC2/m; however, on cooling crystals (4a) to 150 K a single-crystal-to-single-crystal transformation to (4b) possessing the triclinic space group P\bar 1 was observed. Compound (5) crystallizes in the triclinic space group P\bar 1 and contains a parallel aggregation of chains in contrast to the known structure of the non-fluorinated benzoylacetonato ligand, where chains aggregate in a perpendicular fashion. In the compounds studied intramolecular C—H...O and/or C—H...F interactions are present. The neighboring chains are linked by π...π interactions and in some compounds also by C—H...π interactions [(1), (4b), (5)].
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14

Ding, Junqiao, Jia Gao, Qi Fu, Yanxiang Cheng, Dongge Ma, and Lixiang Wang. "Highly efficient phosphorescent bis-cyclometalated iridium complexes based on quinoline ligands." Synthetic Metals 155, no. 3 (2005): 539–48. http://dx.doi.org/10.1016/j.synthmet.2005.08.034.

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15

Wang, Xiuli, Xiang Pan, Xiang Wang, Guocheng Liu, Hongyan Lin, and Shan Zhang. "Polyoxometalate-based complexes with a flexible bis-imidazole-bis-amide ligand: structures, electrochemical and photocatalytic properties." Transition Metal Chemistry 44, no. 3 (2018): 207–17. http://dx.doi.org/10.1007/s11243-018-0284-7.

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16

Irmak, Mustafa, Annika Groschner, and Mike M. K. Boysen. "glucoBox ligand—a new carbohydrate-based bis(oxazoline) ligand. Synthesis and first application." Chem. Commun., no. 2 (2007): 177–79. http://dx.doi.org/10.1039/b612986b.

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17

Ligny, Romain, Mikko M. Hänninen, Sophie M. Guillaume та Jean-François Carpentier. "Steric vs. electronic stereocontrol in syndio- or iso-selective ROP of functional chiral β-lactones mediated by achiral yttrium-bisphenolate complexes". Chemical Communications 54, № 58 (2018): 8024–31. http://dx.doi.org/10.1039/c8cc03842b.

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18

Gun, Jenny, Irina Ekeltchik, Ovadia Lev, Rimma Shelkov, and Artem Melman. "Bis-(hydroxyamino)triazines: highly stable hydroxylamine-based ligands for iron(iii) cations." Chemical Communications, no. 42 (2005): 5319. http://dx.doi.org/10.1039/b508138f.

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19

Li, Peng, Ting Zhang, Li-Li Li, and Wen-Kui Dong. "Self-assembling of three rare structurally various homomultinuclear CuII complexes derived from a bis(salamo)-based multioxime ligand." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 77, no. 5 (2021): 848–60. http://dx.doi.org/10.1107/s2052520621008441.

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A family of rare structurally different homometal multinuclear CuII bis(salamo)-based complexes, [Cu4(L)2(MeOH)2](ClO4)2·2MeOH (1), [Cu4(L)2(EtOH)2](NO3)2·2EtOH (2) and [Cu2(HL)(EtOH)Br2]·CHCl3 (3), has been successfully synthesized by the reactions of cupric salts with a bis(salamo)-based multidentate chelate ligand (H3 L). The salamo-based ligand [R-CH=N—O—(CH2) n —O—N=CH—R] is a new type of salen-based analog. Complexes (1) and (2) are isostructural structures, and crystallize in monoclinic space group P21/n with centrosymmetric spiral structures, where the main structures contain two fully deprotonated ligand (L)3− units, a charged tetranuclear CuII folding center and two coordinated solvent molecules. Complex (3) crystallizes in monoclinic space group Cc and consists of two CuII cations, one incompletely deprotonated ligand (HL)2− unit and one coordinated ethanol molecule, and forms a novel homo-binuclear CuII complex structure due to Br− counter anions. Complexes (1)–(3) have zero-dimensional cluster-based structures and are further assembled into three-dimensional frameworks via intermolecular interactions. Because of the different solvents and counter anions which have a significant influence on the structures of complexes (1)–(3), the interactions were quantitatively evaluated by Hirshfeld surfaces analyses. Complexes (1)–(3) have been characterized by elemental analyses, IR spectra, UV–vis spectra and X-ray crystallography analyses. In addition, fluorescence properties are evaluated and DFT calculations are performed.
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20

Ying, Jun, Xiuyan Wang, and Yaguang Chen. "Four octamolybdate- and Keggin-based compounds constructed by flexible bis(triazole) ligands with different spacers." Transition Metal Chemistry 45, no. 5 (2020): 343–52. http://dx.doi.org/10.1007/s11243-020-00385-w.

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Wang, Xiu-Li, Jun-Jun Sun, Hong-Yan Lin, et al. "Effect of N-donor sites of bis-pyridyl-bis-amide ligands on the architectures of three Anderson-type polyoxometalate-based metal–organic complexes." Transition Metal Chemistry 42, no. 2 (2017): 145–52. http://dx.doi.org/10.1007/s11243-017-0119-y.

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22

Hao, Jin Ming, Yue Hua Li, Huan Huan Li, and Guang Hua Cui. "Erratum to: Two cobalt(II) metal–organic frameworks based on mixed 1,2,4,5-benzenetetracarboxylic acid and bis(benzimidazole) ligands." Transition Metal Chemistry 39, no. 1 (2013): 9. http://dx.doi.org/10.1007/s11243-013-9774-9.

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Grätz, Maik, Andreas Bäcker, Lisa Vondung, Leon Maser, Arian Reincke, and Robert Langer. "Donor ligands based on tricoordinate boron formed by B–H-activation of bis(phosphine)boronium salts." Chemical Communications 53, no. 53 (2017): 7230–33. http://dx.doi.org/10.1039/c7cc02335a.

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Bowlas, C. J., A. E. Underhill, and D. Thetford. "The synthesis and properties of metal bis-dithiolenes based on the new DMAD ligand." Synthetic Metals 56, no. 1 (1993): 2158–63. http://dx.doi.org/10.1016/0379-6779(93)90391-9.

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Yoshidomi, Tetsushi, Yasutomo Segawa, and Kenichiro Itami. "Pyridine-based dicarbene ligand: synthesis and structure of a bis-2-pyridylidene palladium complex." Chemical Communications 49, no. 50 (2013): 5648. http://dx.doi.org/10.1039/c3cc42655f.

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Zhu, Hui, Dong Liu, Yue-Hua Li, and Guang-Hua Cui. "Two silver(I) complexes based on dicarboxylate and flexible bis(benzimidazole) ligands: synthesis, crystal structures, sensing and photocatalytic properties." Transition Metal Chemistry 45, no. 1 (2019): 19–29. http://dx.doi.org/10.1007/s11243-019-00352-0.

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Singla, Manisha, Pavan Mathur, Manisha Gupta, and M. S. Hundal. "Oxidation of electron deficient olefins using a copper(II) complex based on a bis-benzimidazole diamide ligand." Transition Metal Chemistry 33, no. 2 (2007): 175–82. http://dx.doi.org/10.1007/s11243-007-9029-8.

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Leovac, Vukadin M., and Valerija I. Cešljević. "Transition metal complexes with thiosemicarbazide-based ligands, Part II, Synthesis and characterisation of nickel(II), cobalt(II), manganese(II) and zinc(II) complexes with the pentadentate ligand, 2,6-diacetylpyridine bis(S-methylisothiosemicarbazone)." Transition Metal Chemistry 12, no. 6 (1987): 504–7. http://dx.doi.org/10.1007/bf01023835.

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Qin, Li, Yu Gu, Guang Yue Li, Shu Lin Xiao, and Guang Hua Cui. "Preparation and crystal structure of a triple parallel interpenetrated copper coordination polymer based on a flexible bis(imidazole) ligand." Transition Metal Chemistry 38, no. 4 (2013): 407–12. http://dx.doi.org/10.1007/s11243-013-9705-9.

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Wang, Xiao Xiao, Ying Na Zhao, Guang Yue Li, and Guang Hua Cui. "Self-assembly of two 2D cobalt(II) coordination polymers constructed from 5-tert-butyl isophthalic acid and flexible bis(benzimidazole)-based ligands." Transition Metal Chemistry 39, no. 6 (2014): 653–60. http://dx.doi.org/10.1007/s11243-014-9846-5.

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Chen, Zhuo-Ling, Youzhen Dong, Qing-Wen Liu, et al. "Two coordination polymers based on mixed 1,4-bis(benzimidazo-1-yl)benzene and O-donor linker ligands: syntheses, crystal structures and properties." Transition Metal Chemistry 44, no. 5 (2019): 445–54. http://dx.doi.org/10.1007/s11243-019-00323-5.

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Zhang, Guo-Qi, Guo-Qiang Yang, Lin-Na Zhu, Qing-Qi Chen, and Jin-Shi Ma. "A potential fluorescent sensor for Zn2+ based on a selective bis-9-anthryldiamine ligand operating in buffer." Sensors and Actuators B: Chemical 114, no. 2 (2006): 995–1000. http://dx.doi.org/10.1016/j.snb.2005.08.014.

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Pan, Rong-Kai, Jiang-Li Song, Guo-Bi Li, San-Qing Lin, Sheng-Gui Liu, and Gui-Zhen Yang. "Copper(II), cobalt(II) and zinc(II) complexes based on a tridentate bis(benzimidazole)pyridine ligand: synthesis, crystal structures, electrochemical properties and antitumour activities." Transition Metal Chemistry 42, no. 3 (2017): 253–62. http://dx.doi.org/10.1007/s11243-017-0129-9.

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34

Tasada, Andres, Francisca M. Albertí, Antonio Bauzá, et al. "Metallomacrocycles as anion receptors: combining hydrogen bonding and ion pair based hosts formed from Ag(i) salts and flexible bis- and tris-pyrimidine ligands." Chemical Communications 49, no. 43 (2013): 4944. http://dx.doi.org/10.1039/c3cc40772a.

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Lin, Hong-Yan, Na Han, Xiu-Li Wang, Jian Luan, and Guo-Cheng Liu. "Two copper(II) complexes based on N,N′-bis(4-pyridinecarboxamide)-1,2-ethane and tricarboxylate ligands: a 5-fold interpenetrating 3 D network and a 1 D ribbon-like chain." Transition Metal Chemistry 39, no. 3 (2014): 343–51. http://dx.doi.org/10.1007/s11243-014-9807-z.

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Rodriguez-Zubiri, Mireia, Vito Gallo, Jacky Rosé, Richard Welter, and Pierre Braunstein. "Assembling metals and clusters around an octaphosphine ligand based on N-substituted bis(diphenylphosphanyl)amines: structural characterization of dendrimer-like Co12and Co16branched clusters." Chem. Commun., no. 1 (2008): 64–66. http://dx.doi.org/10.1039/b713540h.

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37

Braga, Dario, Marco Polito, Marco Bracaccini та ін. "Novel hetero-bimetallic metalla-macrocycles based on the bis-1-pyridyl ferrocene [Fe(η5-C5H4-1-C5H4N)2] ligand. Design, synthesis and structural characterization of the complexes [Fe(η5-C5H4-1-C5H4N)2](Agi)22+/(Cuii)24+/(Znii)24+". Chemical Communications, № 10 (18 квітня 2002): 1080–81. http://dx.doi.org/10.1039/b200344a.

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38

Leovac, Vukadin M., Vladimir Divjaković, Refik Fazlić, and Peter Engel. "Transition metal complexes with thiosemicarbazide-based ligands, Part IX. Cobalt(II) and nickel(II) complexes with 2-furaldehydeS-methylisothiosemicarbazone; crystal and molecular structure of aqua-bis(2-furaldehydeS-methylisothiosemicarbazone)cobalt(II)-diperchlorate." Transition Metal Chemistry 14, no. 2 (1989): 139–42. http://dx.doi.org/10.1007/bf01040609.

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39

Komuro, Takashi, та Hiromi Tobita. "Thermal reaction of a ruthenium bis(silyl) complex having a lutidine-based Si,N,Si ligand: formation of a μ-silyl(μ-silylene) diruthenium complex involving a 3c–2e Ru–Si–C interaction". Chemical Communications 46, № 7 (2010): 1136. http://dx.doi.org/10.1039/b915395k.

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40

Awal, Abdul, Md Mithu Mia, Shifa Sarkar, et al. "Fe(II)-Based Metallo-Supramolecular Polymer Film for Electrochemical Detection of Nitrite: Studies of Kinetics and Reaction Mechanisms." Journal of The Electrochemical Society, March 1, 2023. http://dx.doi.org/10.1149/1945-7111/acc01a.

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Abstract Here, a monometallic supramolecular polymer (SMP) was synthesized for the fabrication of an electrochemical nitrite sensor, and a mechanism for nitrite detection was proposed based on the experimental findings. The SMP (polyFe) was synthesized using a symmetrical ligand containing terpyridine moieties [4′,4′′′′-(1,4- Phenylene) bis(2,2′:6′,2′′-terpyridine)] and ferrous acetate. Various analytical methods, such as ultraviolet/visible titration, field-emission scanning electron microscopy, Fourier transform infrared spectroscopy, and energy dispersive X-ray spectroscopy, were used to characterize polyFe. The molecular weight of polyFe was calculated from the intrinsic viscosity measurement using the Mark-Houwink-Sakurada equation. The electrochemical behavior of the fabricated sensor was investigated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy. The variation in scan rate from CV was used to investigate the kinetics of nitrite oxidation. A possible reaction mechanism was proposed based on the kinetic studies. The proposed sensor showed a good linear range of 2.49 µM to 1.23 mM and a limit of detection of 0.17 µM. Stability, interference, and reproducibility of the proposed sensor were also investigated. The CV technique was used to demonstrate the applicability of the nitrite sensor for real sample analysis. A satisfactory recovery with a low relative standard deviation was achieved.
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41

Law, Wayne W. H., Voula Kanelis, and Deborah B. Zamble. "Biochemical studies highlight determinants for metal selectivity in the Escherichia coli periplasmic solute binding protein NikA." Metallomics, October 18, 2022. http://dx.doi.org/10.1093/mtomcs/mfac084.

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Abstract Nickel is an essential micronutrient for the survival of many microbes. On account of the toxicity of nickel and its scarcity in the environment, microbes have evolved specific systems for uptaking and delivering nickel to enzymes. NikA, the solute binding protein for the ATP binding cassette (ABC) importer NikABCDE, plays a vital role in the nickel homeostasis of Escherichia coli by selectively binding nickel over other metals in the metabolically complex periplasm. While the endogenous ligand for NikA is known to be the octahedral bis(L-histidinato)nickel(II) complex (Ni[II]-[L-His]2), the molecular basis by which NikA selectively binds Ni(II)-(L-His)2 is unclear, especially considering that NikA can bind multiple metal-based ligands with comparable affinity. Here we show that, regardless of its promiscuous binding activity, NikA preferentially interacts with Ni(II)-(L-His)2, even over other metal-amino acid ligands with an identical coordination geometry for the metal. Replacing both the Ni(II) and the L-His residues in Ni(II)-(L-His)2 compromises binding of the ligand to NikA, in part because these alterations affect the degree by which NikA closes around the ligand. Replacing H416, the only NikA residue that ligates the Ni(II), with other potential metal-coordinating amino acids decreases the binding affinity of NikA for Ni(II)-(L-His)2 and compromises uptake of Ni(II) into E. coli cells, likely due to altered metal selectivity of the NikA mutants. Together, the biochemical and in vivo studies presented here define key aspects of how NikA selects for Ni(II)-(L-His)2 over other metal complexes, and can be used as a reference for studies into the metal selectivity of other microbial solute binding proteins.
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42

Tobón Zapata, Gloria Elena, Dina Marcela Martínez Carmona, Gustavo Alberto Echeverría, and Oscar Enrique Piro. "Molecular structures of two copper complexes with the pharmaceuticals norfloxacin and tinidazole, when powder X-ray diffraction assists multi-domain single-crystal X-ray diffraction." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 78, no. 3 (2022). http://dx.doi.org/10.1107/s2052520622003766.

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The crystal structures of bis[1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-ium-4-yl)-1,4-dihydroquinoline-3-carboxylato]copper(II) sulfate heptahydrate, [Cu(C16H18FN3O3)2]SO4·7H2O or [Cu(nor)2]SO4·7H2O (nor is norfloxacin), and bis{1-[2-(ethylsulfonyl)ethyl]-2-methyl-5-nitroimide}dinitratocopper(II), [Cu(NO3)2(C8H13N3O4S)2] or [Cu(NO3)2(tnz)2] (tnz is tinidazole), were solved by X-ray diffraction. Both complexes crystallize in the space group P21/c, with Z = 4 (for nor) and Z = 2 (for ntz) molecules per unit cell. In [Cu(nor)2]SO4·7H2O, the CuII ion is at the centre of a square-planar environment, trans coordinated to two independent norfloxacin molecules in the zwitterionic form acting as bidentate ligands through one of the carboxyl (cbx) and the carbonyl (cb) O atoms. The solid is further stabilized by an extensive network of N—H...O(sulfate), N—H...O(cbx), N—H...OW, OW—H...O(sulfate) and OW—H...OW hydrogen bonds. The [Cu(NO3)2(tnz)2] complex is centrosymmetric, with the CuII ion in a square planar environment, coordinated to a tinidazole molecule acting as a monodentate ligand through its imidazole N atom and to one nitrate O atom. The vibrational FT–IR absorption spectra and thermal behaviour of the complexes were also studied and are briefly discussed based on the crystal structures.
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