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1

Nishida, Yuzo. "Synthesis and Reactivity of Copper(II) Complexes with New Binucleating Ligands Derived from 16-or 20-Membered N4-Macrocycles." Zeitschrift für Naturforschung B 45, no. 1 (1990): 39–44. http://dx.doi.org/10.1515/znb-1990-0109.

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Abstract New binucleating ligands, (L1) N ,N′,N″,N‴-tetrakis(2-benzimidazolylmethyl)-1,4,9,12-tetra-azacyclohexadecane, and (L2) N ,N′,N″,N‴-tetrakis(2-benzimidazolylmethyl)-1,4,11,14-tetra-azacycloeicosane were prepared. From the reaction mixture of copper(II) salt and the ligand, new binuclear copper(II) complexes, Cu2(L1) (NO3)4 (1), Cu2(L2)(NO3)4 (2), Cu2(L2)Br4 (3), and trinuclear complexes, Cu3(L1)Cl6 (4), and Cu3(L2)Cl6 (5) were obtained. Cyclic voltammograms revealed that the trinuclear complexes 4 and 5 are composed with the binuclear complex (1 or 2) and [CuCl4]2-. The interaction be
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2

Indira Priyadarshini and Dr. Rajesh Ranjan Pandey. "Synthesis, Characterization and Antimicrobial Activity of Homonuclear Cu(II) and Ni(II) Schiff Base Complexes." Journal of Advances in Science and Technology 20, no. 2 (2024): 96–100. http://dx.doi.org/10.29070/cp5vsm97.

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The current study aimed to synthesise, characterise, and investigate the antimicrobial activity of homonuclear Cu(II) and Ni(II) Schiff base complexes. Homonuclear Schiff Base Complexes chelates of Cu(II) and Ni(II) were synthesised. It appears that the complex is a potential metallo-ligand. It forms binuclear complexes when it reacts with two different metal salts, Ni and Cu. Using a Schiff base ligand made from 4-chloro-o-phenylenediamine and 3,5-dichloro-2-hydroxyacetophenone, the homo and hetero binuclear oxygen bridging Cu(II) and Ni(II) complexes were synthesized. Numerous common physico
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3

XU, XUAN, QIN-YU LI, LIANG FANG, and ZHONG-MIN SU. "QUANTUM CHEMISTRY STUDIES ON THE Fe-Hg INTERACTIONS AND 31P NMR IN [Fe(CO)3(RPhPpy)2 (HgCl2)] (R = Me, Et, Ph)." Journal of Theoretical and Computational Chemistry 10, no. 01 (2011): 53–63. http://dx.doi.org/10.1142/s0219633611006281.

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In order to study the effects of R group on Fe-Hg interactions and 31P NMR, the structures of mononuclear complexes [Fe(CO)3(RPhPpy)2] (1: R = Me; 2: R = Et; 3: R = Ph) and binuclear complexes [Fe(CO)3(RPhPpy)2(HgCl2)] (4: R = Me; 6: R = Et; 6: R = Ph) were calculated by density functional theory (DFT) PBE0 method. Moreover, the 31P NMR chemical shifts were calculated by PBE0-GIAO method. The replacement of Ph group in Ph2Ppy ligands with Me or Et group results in higher stabilities and stronger Fe-Hg interactions. The stabilities of binuclear complexes follow the order of 5 > 4 >6. Alth
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4

Nishida, Yuzo, and Miyuki Nasu. "Redox Interaction between Binuclear Mn2(III/IV) Complexes and Binuclear Mn2(II/II) Complexes." Zeitschrift für Naturforschung B 46, no. 2 (1991): 231–34. http://dx.doi.org/10.1515/znb-1991-0217.

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Spectroscopic and ESR studies have revealed that redox interaction occurs between binuclear Mn2(III/IV) complex, [Mn2O2(2,2′-bipyridine)4]3+ and binuclear Mn2(II/II) complexes, [Mn2(L-py)(CH3COO)2]+ and [Mn2(L-py)Cl2]+, in a dilute acetonitrile solution. Electrochemical data suggest that the chloride ion plays an additional important role in the above reaction.
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5

Kazin, Pavel E., V. I. Spitsyn, and V. V. Zelentsov. "Binuclear molybdenum(III) complexes." Russian Chemical Reviews 58, no. 12 (1989): 1157–68. http://dx.doi.org/10.1070/rc1989v058n12abeh003502.

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6

Mashuta, Mark S., Robert M. Buchanan, and William Pierce. "Binuclear schiff base complexes." Inorganica Chimica Acta 158, no. 2 (1989): 227–37. http://dx.doi.org/10.1016/s0020-1693(00)80838-5.

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7

García, M. Esther, Daniel García-Vivó, Alberto Ramos, and Miguel A. Ruiz. "Phosphinidene-bridged binuclear complexes." Coordination Chemistry Reviews 330 (January 2017): 1–36. http://dx.doi.org/10.1016/j.ccr.2016.09.008.

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8

Zhang, Zheng-Zhi, Hsu-Kun Wang, Hung-Gen Wang, and Ru-Ji Wang. "Studies on binuclear complexes." Journal of Organometallic Chemistry 314, no. 3 (1986): 357–67. http://dx.doi.org/10.1016/0022-328x(86)80398-9.

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9

Pabitra, K. Bhattacharya. "Electronic interaction between metal centres in binuclear complexes with long bridges." Journal of Indian Chemical Society Vol. 79, Feb 2002 (2002): 105–11. https://doi.org/10.5281/zenodo.5840381.

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10

Dick, Stefan, Armin Weiss, Ursel Wagner, Friedrich Wagner, and Gerhard Große. "Einkernige und oxoverbrückte zweikernige Fe(III)-Komplexe von N-Alkyl-N,N-bis(2-pyridylmethyl)aminen / Mononuclear and Oxo-Bridged Binuclear Fe(III) Complexes of N-Alkyl-N,N-bis(2-pyridylmethyl)amines." Zeitschrift für Naturforschung B 52, no. 3 (1997): 372–84. http://dx.doi.org/10.1515/znb-1997-0313.

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Abstract Tridentate amines of the type N-alkyl-N,N -bis(2-pyridylmethyl)amine with alkyl = methyl L1, benzyl L2 and adamantyl L3 form mononuclear Fe(III) complexes LFeCl3. In the presence of various carboxylates binuclear μ-oxo-bis(μ-carboxylato) Fe(III) complexes [L2Fe2O(RCO2)2]2+ are formed. These compounds can be synthesized from mono-, bi-, tri- and tetranuclear iron complexes as starting materials.The crystal structures of three mononuclear and four binuclear complexes show that the tridentate ligand is always facially coordinated to Fe. While in binuclear complexes of L1 and L2 the Namin
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11

Singhal, Anshu, and Vimal K. Jain. "Synthesis and characterization of mono-and bi-nuclear palladium(II) and platinum(II) complexes containing acetamidine ligands." Canadian Journal of Chemistry 74, no. 11 (1996): 2018–25. http://dx.doi.org/10.1139/v96-230.

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The reactions of [M2Cl2(μ-Cl)2(PR3)2] with acetamidines in 1:2 stoichiometry afforded mononuclear complexes, [MCl2{ArNHC(Me)NAr}(PR3)] (I) (M = Pd or Pt; R3 = Et3, Bu3, Me2Ph, MePh2; Ar = Ph or 4-MeC6H4 (tol)). Treatment of [M2Cl4(PR3)2] with Li[ArNC(Me)NAr] under anerobic conditions gave acetamidino-bridged binuclear complexes, [M2Cl2(μ-ArNC(Me)NAr)2(PR3)2] (II). The reaction of [Pd2(μ-Cl)2(η3-allyl)2] with Ag[ArNC(Me)NAr] gave acetamidino-bridged allyl complexes [Pd2(μ-ArNC(Me)NAr)2(η3-allyl)2] (III). All the complexes were characterized by elemental analyses and NMR (1H, 31P, 195Pt) spectro
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12

Salishcheva, O. V., A. Yu Prosekov, N. E. Moldagulova, and V. M. Pugachev. "Platinum (II) and palladium (II) complexes: synthesis, antimicrobial and antifungal activity." Proceedings of Universities. Applied Chemistry and Biotechnology 11, no. 4 (2022): 651–62. http://dx.doi.org/10.21285/2227-2925-2021-11-4-651-662.

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The study aims to synthesize and examine the biological activity of mono- and binuclear platinum (II) and palladium (II) complexes containing terminal and bridging nitrite ligands against the test cultures of Bacillus subtilis B4647, Aspergillus brasiliensis (niger) F679, Pseudomonas aeruginosa B8243, and Escherichia coli. Through the interaction of mononuclear platinum (II) and palladium (II) complexes, dimeric complexes having nitrite ligands were synthesized. The composition and structure of these complexes were established using elemental analysis, conductometry, potentiometry, cryoscopy,
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13

Prakash, Shivani, Anju Kumari Gupta, Sachin Prakash, and D. Prakash. "Studies on Some Hetero Binuclear Copper(II) Schiff base Complexes." Oriental Journal Of Chemistry 36, no. 05 (2020): 954–57. http://dx.doi.org/10.13005/ojc/360522.

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A series of new hetero binuclear complexes of copper(II) and lead(II) using Schiff base have been synthesized. The Schiff base has been derived from the condensation reaction between Salicylaldehyde and 1,2-Ethylenediamine. The hetero binuclear complexes have been characterized by using elemental analysis, molar conductance measurement, magnetic susceptibility studies, UV-Vis and IR spectra. The studies revealed square planar geometry for the complexes with coordination number four.
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14

Surucic, Ljiljana, Aleksandra Nastasovic, Antonije Onjia, Goran Janjic, and Aleksandra Rakic. "Design of amino-functionalized chelated macroporous copolymer [poly(GMA-EDGMA)] for the sorption of Cu (II) ions." Journal of the Serbian Chemical Society 84, no. 12 (2019): 1391–404. http://dx.doi.org/10.2298/jsc190125031s.

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Polymer-based, highly porous nanocomposites with functionalized ligands attached to the core structure are extremely efficient in the detection, removal and recovery of metals through the process of sorption. Quantumchemical models could be helpful for sorption process analyses. The sorption of Cu(II) ions by amino-functionalized chelating macroporous copolymers poly(GMA-co-EGDMA)-amine and sorption selectivity of the subject copolymers, ethylenediamine (en), diethylenetriamine (dien) and triethylenetetramine (trien), were successfully modelled by quantum chemical calculations. Considering the
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15

Prakash, Sachin, Anju K. Gupta, Shivani Prakash, K. R. R. P. Singh, and D. Prakash. "Synthesis and characterization of heterobinuclear copper(II) complexes derived from Schiff base with organosilver(I)." Research Journal of Chemistry and Environment 26, no. 2 (2022): 126–30. http://dx.doi.org/10.25303/2602rjce126130.

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Copper(II) ion can form complexes with varied ligands. The present study describes the synthesis of a series of new hetero binuclear Schiff base complexes of copper(II) and organic chelates of silver(I). The Schiff base ligand was derived from salicylaldehyde and ophenylenediamine. For the characterization of the hetero binuclear complexes, various physicoanalytical and spectral studies viz. elemental analysis, magnetic moment measurements, molar conductance, FTIR and electronic spectral recordings were applied. Evidences from these analyses reveal square geometry for the complexes.
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16

Liu, Yu, Shan Shan Zhang, Da Jun Song, Tian Zhu Yang, Hong Xiao Tian, and Jian Gao. "Structure Studies on Order Assemblage of Manganese II Isovanillin Complexes." Applied Mechanics and Materials 618 (August 2014): 193–97. http://dx.doi.org/10.4028/www.scientific.net/amm.618.193.

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The ManganeseII Isovanillin complex [Mn2(C8H7O3)4(H2O)2], Diaqua-tetra (isovanillinato-O,O')-bis (manganeseII),the MnII atom is coordinated by three isovanillinate anions and one water molecule in a distorted trigonal bipyramidal configuration with five-coordinations geometry. And one isovanillinate ligand chelates to the MnII atom through its methyl and hydroxy O atoms, the other two isovanillinate ligand chelates to the MnII atom only through its hydroxy O atoms. The same as another MnII atom. So we get a Binuclear MnII metal complexe. The fact clearly suggests not so much significant contri
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17

Gallio, Andrea E., Leonardo Brustolin, Nicolò Pettenuzzo, and Dolores Fregona. "Binuclear Heteroleptic Ru(III) Dithiocarbamate Complexes: A Step towards Tunable Antiproliferative Agents." Inorganics 10, no. 3 (2022): 37. http://dx.doi.org/10.3390/inorganics10030037.

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Binuclear dithiocarbamate complexes of Ru(III) are promising candidates in the search for outstanding metal-based anticancer agents. While different dithiocarbamates have shown ligand-dependent cytotoxicity in homoleptic binuclear Ru(III) complexes, the properties of heteroleptic analogues with different dithiocarbamate (DTC) ligands have yet to be explored. We herein propose the introduction of heteroleptic ligands as tunable features for the development of improved ruthenium-based antiproliferative agents and report a synthetic strategy for their synthesis as well as the evaluation of the cy
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18

Asekunowo, Patrick O., Rosenani A. Haque, and Mohd R. Razali. "A comparative insight into the bioactivity of mono- and binuclear silver(I)-N-heterocyclic carbene complexes: synthesis, lipophilicity and substituent effect." Reviews in Inorganic Chemistry 37, no. 1 (2017): 29–50. http://dx.doi.org/10.1515/revic-2016-0007.

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AbstractSilver(I)-N-heterocyclic carbene (Ag(I)-NHC) complexes of mononuclear and binuclear species, synthesised by our group and others in recent years, offer a fascinating outlook on their bioactivity. These complexes advance a range of adaptable structural patterns, leading to intra-specific variation in anticancer and antimicrobial activities. This study therefore reviews the synthesis, structural analysis and bioactivity of Ag complexes derived from mononuclear-NHC complexes either with coordinating or non-coordinating anions and binuclear NHC complexes. Specifically, the effect of stabil
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19

Pidko, Evgeny A., Emiel J. M. Hensen, and Rutger A. van Santen. "Self-organization of extraframework cations in zeolites." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 468, no. 2143 (2012): 2070–86. http://dx.doi.org/10.1098/rspa.2012.0057.

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Structural properties of a series of mordenite and ZSM-5 zeolites with different framework Al distribution modified with oxygenated extraframework Ga, Zn, Al, Cu and Fe complexes were investigated by means of periodic density functional theory calculations. It is demonstrated that mononuclear oxygenated and hydroxylated cationic metal complexes in high-silica zeolites tend to self-organize into binuclear complexes. In the cases of Ga- and Fe-modified zeolites, it is shown that the catalytic activity of the most stable binuclear extraframework cations is much higher than that of the hypothetica
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20

Pabitra, K. Bhattacharya. "Electronic interaction between metal centres in binuclear complexes with long bridges." Journal of Indian Chemical Society Vol. 79, Feb 2002 (2002): 105–11. https://doi.org/10.5281/zenodo.5846005.

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21

Wang, Guang Hui, Da Jun Song, Hong Xiao Tian, Jian Gao, and Yu Liu. "Structure Studies on Order Assemblage of CadmiumII Isophthalicacid Benzimidazole Complexes." Applied Mechanics and Materials 713-715 (January 2015): 2872–75. http://dx.doi.org/10.4028/www.scientific.net/amm.713-715.2872.

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The CadmiumII Isophthalicacid Benzimidazole complex [Cd2(C8H4O4)2 (C7H6N2)4(H2O)3], Triqua-bis (isophthalicacidato-O,O')-tetra (benzimidazole) bis (CadmiumII),the CdII atom is coordinated by two isophthalicacid anions and two benzimidazole and one water molecule in a distorted octahedral configuration with six-coordinations geometry. And one isophthalicacid ligand chelates to the CdII atom through its one carboxylic O atoms, but the other isophthalicacid ligand chelates to the CdII atom through its two carboxylic O atoms. The same as another CdII atom. So we get a Binuclear CdII metal complexe
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22

Nishida, Yuzo, Izumi Watanabe, and Kei Unoura. "Interaction between Binuclear Copper(I) Complexes and the Dioxygen Molecule Investigated by Electrochemical Methods." Zeitschrift für Naturforschung B 47, no. 1 (1992): 109–14. http://dx.doi.org/10.1515/znb-1992-0120.

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The cyclic voltammograms of some binuclear copper(II) compounds with binucleating ligands where two molecules of tridentate ligand, N, N -bis(benzimidazol-2-ylmethyl)amine are linked by several alkyl chains, were measured under both argon and dioxygen. The results demonstrate that the binuclear copper(I) species produced by electrochemical reduction exhibit high reactivity towards dioxygen, while the reaction of the corresponding mononuclear species with oxygen is very slow. Thin-layer coulometry ([binuclear copper(I)]/[O2] = 0.47 - 10.6) and thin-layer cyclic voltammetry ([binuclear copper(I)
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23

Gao, Yue, Yu-Qin Li, Yao Li, et al. "Diverse Magnetic Properties of Two New Binuclear Complexes Affected by [FeN6] Octahedral Distortion: Two-Step Spin Crossover versus Antiferromagnetic Interactions." Magnetochemistry 9, no. 3 (2023): 69. http://dx.doi.org/10.3390/magnetochemistry9030069.

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Polymetallic complexes with covalently bridged metal centers that interact magnetically are important in the molecular magnetism field, with binuclear compounds receiving special attention because they represent the simplest type of multinuclear species with covalently bridged metal centers. Herein, we report the synthesis and properties of two new binuclear FeII complexes, namely, {[Fe(abpt-TPE)(NCS)2]2(bpym)}·2MeOH·2MeCN (1) and {[Fe(abpt-TPE)(NCS)2]2(bpym)}·2CH2Cl2 (2) (bpym = 2,2′-bipyrimidine). The crystal structure is analyzed at different temperatures, and its properties are analyzed by
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24

Kumar, Sanjay. "Studies on Hetero Binuclear Complexes derived from Rubidium and Caesium salt of Acetyl salicylic acid (ASPIRIN) with N, N’-1,2-ethylenebis(5-nitrosalicylaldiminato) nickel(II)." Oriental Journal Of Chemistry 38, no. 1 (2022): 193–97. http://dx.doi.org/10.13005/ojc/380124.

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Hetero binuclear complexes, [NiE5NSRbAp] and [NiE5NSCsAp], have been synthesized from Rubidium(I) and Caesium(I) salt of Acetyl salicylic acid (ASPIRIN) and N,N’-1,2-ethylenebis(5-nitrosalicylaldiminato) nickel(II) as ligand, respectively. This ligand [NiE5NS] has been prepared from Nickel(II) acetate and salen type dibasic Schiff base derived from 5-nitrosalicylaldehyde and Ethylenediamine. These novel hetero binuclear complexes obtained in pure solid state and their structures have been characterized with the help of Elemental analysis, Solubility, Magnetic property, Molar conductance measur
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25

Zlatar, Matija, Filip Vlahovic, Dragana Mitic, Mario Zlatovic, and Maja Gruden. "Assessment of density functional approximations for calculation of exchange coupling constants in thiocyanato and cyanato double bridged binuclear Ni(II) complexes." Journal of the Serbian Chemical Society, no. 00 (2020): 71. http://dx.doi.org/10.2298/jsc201106071z.

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In the present work, we examine the magnetic properties of 8 "endto-end" thiocyanato, and 3 "end-to-end" cyanato double bridged Ni(II) binuclear complexes. Thiocyanato complexes are weakly ferromagnetic. Cyanato bridged complexes exhibit weak antiferromagnetic coupling. Therefore, it is a challenge for computational chemistry to calculate the exchange coupling constant in these systems accurately. 17 different Density Functional Approximations with different flavors are used to find the method of choice to study magnetic properties in binuclear Ni(II) complexes within the Broken-Symmetry appro
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26

Baar, Cliff R., Michael C. Jennings, Richard J. Puddephatt, and Kenneth W. Muir. "Electrophilic Binuclear Methylplatinum(II) Complexes." Organometallics 18, no. 21 (1999): 4373–79. http://dx.doi.org/10.1021/om990218y.

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27

Solomon, Edward I., Felix Tuczek, David E. Root, and Carl A. Brown. "Spectroscopy of Binuclear Dioxygen Complexes." Chemical Reviews 94, no. 3 (1994): 827–56. http://dx.doi.org/10.1021/cr00027a013.

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28

Crause, Chantelle, Helmar Görls, and Simon Lotz. "Binuclear biscarbene complexes of furan." Dalton Trans., no. 9 (2005): 1649–57. http://dx.doi.org/10.1039/b419148j.

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29

Smith, David C., and Harry B. Gray. "Photochemistry of binuclear d8 complexes." Coordination Chemistry Reviews 100 (April 1990): 169–81. http://dx.doi.org/10.1016/0010-8545(90)85009-h.

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30

Vogel, Emanuel, Martin Michels, Lars Zander, Johann Lex, Nurcan S. Tuzun, and Kendall N. Houk. "Spirodiporphyrins—As Binuclear Metal Complexes." Angewandte Chemie International Edition 42, no. 25 (2003): 2857–62. http://dx.doi.org/10.1002/anie.200250690.

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31

Li, Huidong, Hao Feng, Weiguo Sun, Yaoming Xie, R. Bruce King, and Henry F. Schaefer. "Binuclear Pentalene Iron Carbonyl Complexes." European Journal of Inorganic Chemistry 2011, no. 17 (2011): 2746–55. http://dx.doi.org/10.1002/ejic.201100155.

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32

Degtyareva, S. S., D. A. Bardonov, K. A. Lysenko, M. E. Minyaev, I. E. Nifant’ev, and D. M. Roitershtein. "Praseodymium and Erbium 1,2,4-Triphenylcyclopentadienyl Complexes." Координационная химия 49, no. 8 (2023): 504–12. http://dx.doi.org/10.31857/s0132344x22600540.

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The reaction of triphenylcyclopentadienyl potassium with praseodymium and erbium chloride tetrahydrofuranates gives, depending on the reactant ratio, tetranuclear ate complexes, [{(Ph3C5H2)-Pr(THF)}2(µ2-Cl)2(µ3-Cl)3K]2(C7H8)4 (I) and [{(Ph3C5H2)Er(THF)}2(µ2-Cl)2(µ3-Cl)3K(THF)]2 (III), or binuclear ate complexes [(Ph3C5H2)2LnCl(KCl)]2 Ln = Pr (II), Er (IV) (CCDC nos. 2224244 (I), 2224243 (II), 2224245 (III), 2224242 (IV)). The structurally similar complexes I and III are based on the {[Ln2(µ-Cl)3]2(µ-Cl)2K2} core, and in III, the potassium cation is additionally coordinated to the THF molecule.
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Al-Mandhary, Muna R. A., Christopher M. Fitchett, and Peter J. Steel. "Discrete Metal Complexes of Two Multiply Armed Ligands." Australian Journal of Chemistry 59, no. 5 (2006): 307. http://dx.doi.org/10.1071/ch06116.

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The syntheses and metal complexes of 1,2,4,5-tetrakis(8-quinolyloxymethyl)benzene 1 and hexakis(8-quinolyloxymethyl)benzene 2 are described. X-Ray crystal structures are reported of the free ligand 1, a binuclear silver(i) and a tetranuclear copper(i) complex of 1, as well as a binuclear cobalt(ii) and trinuclear palladium(ii) and silver(i) complexes of 2. Within these discrete metal complexes the ligands are found to adopt a range of coordination modes, with considerable variation in the relative orientations of the ligand arms as a result of the flexibility imparted by the CH2O linker units.
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Sönmez, Mehmet, and Memet Şekerci. "The template synthesis, spectral characterization and thermal behavior of new binuclear Schiff base complexes derived from N-aminopyrimidine with 2,3-butandion." Journal of the Serbian Chemical Society 72, no. 3 (2007): 259–64. http://dx.doi.org/10.2298/jsc0703259s.

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Anew series of two types of acyclic binuclear Schiff base complexes, prepared by the template condensation of N-aminopyrimidine and 2,3-butandion in the presence of Cu(II), Ni(II), Co(II) and Zn(II) in n-BuOH solution, were analyzed and characterized by elemental analyses, IR and electronic spectroscopy, conductivity and magnetic measurements. From the conductivity measurements, it is concluded that the complex of NiII is a 1:1 type of electrolyte. All the complexes have sub-normal magnetic moments in accordance with their binuclear nature. The thermal behaviour of the complexes was studied by
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35

Romanova, Kseniya A., and Yuriy G. Galyametdinov. "Quantum-Chemical Approaches to Creation of Mesogenic Binuclear Europium(III) Complexes with Intensive Luminescence." Liquid Crystals and their Application 23, no. 4 (2023): 19–30. http://dx.doi.org/10.18083/lcappl.2023.4.19.

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This article contains data on the application of quantum-chemical methods for simulation of mesogenic binuclear complexes of europium(III) (Eu(III)) with substituted β-diketones and Lewis bases along with the possibility of prediction of their liquid crystalline (LC) properties. The relationships between geometric parameters of the complexes' molecules, the structural features of their coordination polyhedra and the probability of mesophase behavior were considered. According to the calculated parameters of Voronoi-Dirichlet polyhedra, the structural features of the first coordination sphere o
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Srivastava, Abhay, Netra Singh, and Chandra Shriwastaw. "Synthesis and characterization of bioactive binuclear transition metal complexes of Schiff base ligand derived from 4-amino-pyrimidine-2-one, diacetyl and glycine." Journal of the Serbian Chemical Society 79, no. 4 (2014): 421–33. http://dx.doi.org/10.2298/jsc130123148s.

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A series of novel binuclear transition metal complexes was synthesized by reaction of a Schiff base ligand (1-Methyl-2-(2-oxo-1,2-dihydro-pyrimidin-4-ylimino)-propylideneamino-acetic acid) (LaH) derived from 4-amino-pyrimidine-2-one, diacetyl, glycine and corresponding chloride salt of Cu(II), Ni(II), Co(II) and Zn(II) metals in 1:1 (metal : ligand) molar ratio. The compounds were characterized by elemental analyses, molar conductance measurement, magnetic moment measurement and various spectral studies viz. IR, UV-visible, 1H-NMR, 13C-NMR, EPR and ESI-MS. Molar conductance measurement data re
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37

Ram, N. Patel, P. Patel Ayodhya, and B. Pandeya Krishna. "Synthesis, magnetic and spectral properties of binuclear imidazolate bridged copper(II)-copper(II) and copper(II)-zinc(II) complexes." Journal of Indian Chemical Society Vol. 78, Jan 2001 (2001): 6–8. https://doi.org/10.5281/zenodo.5846016.

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Department of Chemistry, A P. S. University, Rewa-486 003, India <em>Manuscript received 1 November 1999, revised 17 April 2000. accepted 26 August 2000</em> Two new binuclear imidazolate bridged complexes, [(PAN)Cu(im)Cu(PAN)] (ClO<sub>4</sub>)<sub>2</sub>&nbsp;and&nbsp;[(PAN)Cu(im)Zn(PAN)](ClO<sub>4</sub>)<sub>2</sub> (PAN =1. (2-pyridylazo)-2-naphthol, im = imidazolate) have been prepared. Room temperature magnetic susceptibility of [(PAN)Cu(im)Cu(PAN)] (ClO<sub>4</sub>)<sub>2</sub>&nbsp;(reveals the presence of intramolecular antiferromagnetic interactions through the imidazolate bridge. X
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38

Sun, Xia-Xing, Juan Du, Jie-Jie Tan, and Shu-Zhong Zhan. "A mono-oxo-bridged binuclear iron(iii) complex with a Fe–O–Fe angle of 180.0° and its catalytic activity for hydrogen evolution." New Journal of Chemistry 46, no. 8 (2022): 3794–99. http://dx.doi.org/10.1039/d1nj05904a.

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39

A., K. BANERJEE, C. VERMA A., SATYA PRAKASH SHEO, and K. ROY S. "Metal Complex as Ligand : Binuclear Alkali and Alkaline Earth Metal Complexes with Magnesium Bis-8-hydroxyquinolinate." Journal of Indian Chemical Society Vol. 71, Sep 1994 (1994): 569–70. https://doi.org/10.5281/zenodo.5896324.

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Chemistry Department, Patna University, Patna-800 005 <em>Manuscript received 11 May 1992, accepted 28 July 1993</em> Metal Complex as Ligand : Binuclear Alkali and Alkaline Earth Metal Complexes with Magnesium Bis-8-hydroxyquinolinate.
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40

Gong, Gehui, Wenji Wang, and Weihong Du. "Binuclear ruthenium complexes inhibit the fibril formation of human islet amyloid polypeptide." RSC Advances 7, no. 30 (2017): 18512–22. http://dx.doi.org/10.1039/c6ra28107a.

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41

Wen-Jwuwang та Cheu-Pyeng Chen. "Binuclear Complexes. II. Electron Paramagnetic Resonance Study of Binuclear Copper Complexes with α-Diimine Ligand". Journal of the Chinese Chemical Society 37, № 6 (1990): 541–45. http://dx.doi.org/10.1002/jccs.199000074.

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42

Andruh, Marius. "Binuclear complexes as tectons in designing supramolecular solid-state architectures." Pure and Applied Chemistry 77, no. 10 (2005): 1685–706. http://dx.doi.org/10.1351/pac200577101685.

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Oligonuclear complexes as well as coordination polymers with various network topologies can be obtained by using homo- or heterobinuclear complexes as starting materials. These building blocks are stable complexes, where the metal ions are held together by compartmental ligands, or alkoxo-bridged Cu(II) species. The binuclear nodes can be connected through appropriate exo-dentate ligands, or through metal-containing anions (e.g., [M(CN)6]3-, M = CrIII, FeIII, CoIII). A rich variety of 3d-3d and 3d-4f heterometallic complexes, with interesting architectures and topologies of the spin carriers,
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43

Ashoo, Pezhman, Reza Yousefi, Syed M. Nabavizadeh, et al. "Three Pt-Pt Complexes with Donor-acceptor Feature: Anticancer Activity, DNA Binding Studies and Molecular Docking Simulation." Anti-Cancer Agents in Medicinal Chemistry 19, no. 14 (2019): 1762–74. http://dx.doi.org/10.2174/1871520619666190702114211.

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Background: Due to their unique properties and potential applications in variety of areas, recently, a special attention is given to the binuclear platinum (II) complexes. They reveal a highly tunable features upon the modification of their cyclometallating and bridging ligands. Objective: The aim of this study was to evaluate the anticancer activity and DNA binding affinity of three binuclear platinum (II) complexes, including ht-[(p-FC6H4)Pt(µ-PN)(µ-NP)PtMe2](CF3CO2)(1), ht-[(p- MeC6H4)Pt(µ-PN)(μ-NP)Pt(p MeC6H4) Me] (CF3CO2)(2) and ht-[Pt2Me3(µ-PN)2](CF3CO2) (3). Methods: MTT assay was perfo
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44

Koch, Felix, Hartmut Schubert, Peter Sirsch, and Andreas Berkefeld. "Binuclear complexes of Ni(i) from 4-terphenyldithiophenol." Dalton Transactions 44, no. 29 (2015): 13315–24. http://dx.doi.org/10.1039/c5dt01178g.

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45

R., K. GARG, and M. SHARMA L. "Binuclear Copper(II) Complexes with the Schiff Base derived from Furan-2-aldehyde and Dapsone." Journal of Indian Chemical Society 69, Nov 1992 (1992): 703–5. https://doi.org/10.5281/zenodo.6034391.

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Department of Chemistry, N. A. S. College, Meerut-250 001 <em>Manuscript received 1 April 1992, accepted 31 July 1992</em> Binuclear Cu<sup>ll</sup> complexes of M<sub>2</sub>L<sub>3</sub>X<sub>4</sub>&nbsp;type, where L=4,4&#39;-di(furan-2-formylimIno)diphenyl&nbsp;sulphone (FD) ; X= Cl<sup>-</sup>, NO\(_3^-\)&nbsp;and CH<sub>3</sub>COO<sup>-</sup>, having octahedral environment around metal ions, are reported. Characterisation of the complexes has been done on the basis of elemental analysis, conductivity, magnetic, ir, uv and esr spectral measurements.
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46

Begum, M. S., M. B. H. Howlader, M. C. Sheikh, R. Miyatake та E. Zangrando. "Crystal structure of bis[μ-S-hexyl 3-(2-oxidobenzylidene)dithiocarbazato-κ4O,N3,S:O]dicopper(II)". Acta Crystallographica Section E Crystallographic Communications 71, № 12 (2015): m249—m250. http://dx.doi.org/10.1107/s2056989015022914.

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The title compound, [Cu2(C14H18N2OS2)2], is a binuclear copper(II) complex of an oxybenzylidenedithiocarbazate ligand. The ligand coordinates in a tridentate manner through N-, S- and O-donor atoms. Each O atom also bridges to a second CuIIion to form the binuclear species. It has a central Cu2O2rhomboid moiety and a metal-to-metal separation of 2.9923 (6) Å. In the crystal, the binuclear complexes stack along theaaxis with all the hexyl chains located side-by-side, forming a hydrophobic region. The complexes are linkedviaC—H...N hydrogen bonds, forming chains along thec-axis direction. One Cu
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47

Preuss, Fritz, Monika Vogel, Uwe Fischbeck, et al. "Amido-tert-butylimido-vanadium(V)-Verbindungen. Darstellung, Reaktionen und 51V-NMR-spektroskopische Untersuchungen / Amido-tert-butylimidovanadium(V) Compounds. Synthesis, Reactions and 51V NMR Spectroscopic Studies." Zeitschrift für Naturforschung B 56, no. 11 (2001): 1100–1108. http://dx.doi.org/10.1515/znb-2001-1102.

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The reactions of tBuN = VCl2 · DME with LiX (X = NHtBu, NR2, OSiPh3, SR, Alkyl, Cp) have been studied. LiNHtBu and LiCH3 furnish the binuclear diamagnetic tert-butylimido-vanadium( IV) compounds [(μ-NtBu)2V2X4]; in all other cases only the vanadium(V) compounds tBuN=VX3 and tBuN=VCpCl2 formed by disproportionation reactions of vanadium(IV) can be isolated. The syntheses of various mononuclear amido tert-butylimido-vanadium(V) complexes as well as of the binuclear complexes [μ-NtBu)2V2(NtBu)2Cl2] and [(μ-0)V2(NtBu)2Cp2Cl2] are also described. All compounds obtained have been characterized by 51
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48

Mohamed Kasim, Mohamed Subarkhan, Saranya Sundar, and Ramesh Rengan. "Synthesis and structure of new binuclear ruthenium(ii) arene benzil bis(benzoylhydrazone) complexes: investigation on antiproliferative activity and apoptosis induction." Inorganic Chemistry Frontiers 5, no. 3 (2018): 585–96. http://dx.doi.org/10.1039/c7qi00761b.

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New binuclear Ru(ii) arene benzil bis(benzoylhydrazone) complexes show excellent cytotoxicity against human cancer cell lines. The results of biochemical assays demonstrated that complexes are able to induce apoptosis.
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49

Shmelev, M. A., G. A. Razgonyaeva, D. S. Yambulatov, A. G. Starikov, A. A. Sidorov, and I. L. Eremenko. "Effect of Substituents in the Pentafluorobenzoate and 2,3,4,5- and 2,3,5,6-Tetrafluorobenzoate Anions on the Structure of Cadmium Complexes." Координационная химия 50, no. 4 (2024): 231–50. http://dx.doi.org/10.31857/s0132344x24040022.

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New cadmium 2,3,4,5-tetrafluorobenzoate (6HTfb) and 2,3,5,6-tetrafluorobenzoate (4Htfb) complexes, [Cd(6HTfb)(H2O)3]n·(6HTfb)·2nH2O (I), [Cd3(Phen)2(6HTfb)6] (II, Phen = 1,10-phenanthroline), [Cd2(Phen)2(4Htfb)4]n·2nH2O (III), and [Cd(Phen)2(4Htfb)2] (IV), were synthesized. Analysis of the obtained results and published data demonstrated that a decrease in the number of fluorine substituents is unfavorable for the formation of coordination polymers comprising stacked alternating fluorinated and nonfluorinated aromatic moieties. In the case of 2,4,5-trifluorobenzoate complex, a typical trivial
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50

Popov, Roman A., Alexander S. Novikov, Vitalii V. Suslonov, and Vadim P. Boyarskiy. "Molecular Switching through Chalcogen-Bond-Induced Isomerization of Binuclear (Diaminocarbene)PdII Complexes." Inorganics 11, no. 6 (2023): 255. http://dx.doi.org/10.3390/inorganics11060255.

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Binuclear diaminocarbene complexes, which form as a regioisomer mixture in the reaction between isocyanide–palladium(II) complex cis-[PdCl2(CNXyl)2] and 1,3-thiazol-2-amine, are able to exchange an anionic chloride ligand with other halides, such as Br or I. This process also affords binuclear complexes as mixtures of kinetically and thermodynamically controlled regioisomers. In CDCl3 solutions, we observed interconversion of kinetically and thermodynamically controlled regioisomers. The results of the DFT calculations revealed that in CHCl3 solution, each pair of the isomers exhibited two dif
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