Search results for "RHENIUM"

showing 10 items of 244 documents

CCDC 1550276: Experimental Crystal Structure Determination

2017

Related Article: Anders H. Pedersen, Miguel Julve, José Martínez-Lillo, Joan Cano, Euan K. Brechin|2017|Dalton Trans.|46|16025|doi:10.1039/C7DT02216F

Space GroupCrystallographytetrakis(1-butyl-1H-imidazole)-copper hexachloro-rheniumCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1550274: Experimental Crystal Structure Determination

2017

Related Article: Anders H. Pedersen, Miguel Julve, José Martínez-Lillo, Joan Cano, Euan K. Brechin|2017|Dalton Trans.|46|16025|doi:10.1039/C7DT02216F

Space GroupCrystallographytetrakis(1H-imidazole)-copper hexachloro-rhenium isopropanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 982641: Experimental Crystal Structure Determination

2014

Related Article: Samia Benmansour, Eugenio Coronado, Carlos Giménez-Saiz, Carlos J. Gómez-García, Carola Rößer|2014|Eur.J.Inorg.Chem.||3949|doi:10.1002/ejic.201402023

Space GroupCrystallographytetrakis(2-(56-dihydro[13]dithiolo[45-b][14]dithiin-2-ylidene)-56-dihydro[13]dithiolo[45-b][14]dithiine) tetrachloro-(oxalato)-rhenium benzonitrile solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Rhenium(I) and platinum(II) complexes with diimine ligands bearing acidic phenol substituents: hydrogen-bonding, acid-base chemistry and optical prop…

2010

Tricarbonylchloro-rhenium(i) (1-4) and catecholato-platinum(ii) complexes (6, 7) of diimine ligands bearing phenol and O-protected phenol substituents have been prepared and fully characterised including single crystal structure analyses of 1, 4 and 7. The redox behaviour of the catecholato platinum(ii) complexes 6 and 7 has been probed by cyclic voltammetry, preparative oxidation and EPR spectroscopy (6˙(+), 7˙(+)). Reversible deprotonation of the hydroxy substituted complexes 1, 3 and 6 to 1(-), 3(-) and 6(-) resulted in significant changes in their electronic spectra. The luminescence properties of the diamagnetic complexes have been investigated using emission spectroscopy. DFT and TD-D…

Spectrophotometry InfraredMolecular Conformationchemistry.chemical_elementPhotochemistryCrystallography X-RayLigandsRedoxlaw.inventionInorganic ChemistryDeprotonationlawCoordination ComplexesPolymer chemistryElectron paramagnetic resonanceDiiminePlatinumPhenolHydrogen bondHydrogen BondingRheniumRheniumchemistryQuantum TheorySpectrophotometry UltravioletIminesCyclic voltammetryPlatinumDalton transactions (Cambridge, England : 2003)
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Self-Assembled One- and Two-Dimensional Networks Based on NH2Me2[ReX5(DMF)] (X = Cl and Br) Species: Polymorphism and Supramolecular Isomerism in Re(…

2011

Three mononuclear rhenium(IV) compounds of general formula NH 2 Me 2 [ReX 5 (DMF)] [NH 2 Me 2 + = dimethylammonium cation, DMF = N,N-dimethylformamide, and X = Cl (1 and 2) and Br (3)] have been prepared and characterized. In all three cases, the rhenium atom is six-coordinated by five chloro (1 and 2) or bromo (3) atoms and one oxygen atom from a DMF molecule (1―3) building a somewhat distorted octahedral surrounding. Short Re IV ―X · · · X―Re IV contacts and H-bonds occur in the crystal lattice generating novel supramolecular Re(IV) architectures. 1 and 2 are polymorphs and supramolecular isomers that exhibit supramolecular ladder-like ( 1 ) and rectangular two-dimensional grids (2), the …

StereochemistrySupramolecular chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureRheniumCondensed Matter PhysicsMagnetic susceptibilitylaw.inventionCrystallographychemistryOctahedronlawMoleculeAntiferromagnetismGeneral Materials ScienceCrystallizationCrystal Growth & Design
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Mono- and di-nuclear 2,3-diazabutadiene and 2-azabutadiene complexes of Rhenium(I): Syntheses, luminescence spectra and X-ray structures

2008

Abstract Treatment of [Re(CO)3(THF)(μ-Br)]2 with 4,4-dichloro-1,1-diphenyl-2-azabuta-1,3-diene [Cl2C C(H)–N CPh2] (1a) yields the di-nuclear benzophenone azine-bridged compound [(OC)3Re(μ-Ph2C N–N CPh2)(μ-Br)2Re(CO)3] (2a), albeit in low yield. Alternatively, compounds [(OC)3Re(μ-Ph2C N–N CPh2)(μ-X)2Re(CO)3] (2a,b) (X = Br, Cl) are obtained in high yields by direct reaction of [Re(CO)3(THF)(μ-Br)]2 or [Re(CO)5Cl] with benzophenone azine. Nucleophilic attack of NaSPh on 1a affords the 2-azabutadiene derivative [(PhS)(Cl)C C(H)–N CPh2] (1b), which upon reaction with [Re(CO)3(THF)(μ-Br)]2 forms the S,N-chelate complex fac-[(OC)3ReBr{(PhS)(Cl)C C(H)–N CPh2}] (3). The crystal structures of 1b, 2…

Stereochemistrychemistry.chemical_elementCrystal structureRheniumMedicinal chemistryInorganic ChemistryAzinechemistry.chemical_compoundchemistryNucleophileThioetherMaterials ChemistryBenzophenonePhysical and Theoretical ChemistryLuminescenceDerivative (chemistry)Inorganic Chemistry Communications
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(2,2‐Dibromovinyl)ferrocene as a Building Block for the Assembly of Heterodinuclear Complexes – Preparation of an σ‐Alkenylpalladium Complex and Dime…

2007

The oxidative addition of (2,2-dibromovinyl)ferrocene [Br2C=C(H)–Fc] (1) to [Pd(PPh3)4] yields the heterodinuclear σ-alkenyl complex trans-[{Pd(Br)(PPh3)2}–C(Br)=C(H)–Fc] (2). Nucleophilic attack of sodium thiolates on 1 unexpectedly affords the vinyl thioether derivatives (Z)-[(RS)(H)C=C(H)–Fc] (4a: R = Ph; 4b: R = tBu; 4c: R = Et). Complexes 4a and 4c can also be prepared by addition of NaSR across the triple bond of Fc–C≡C–H (3). Addition of an excess of NaSR to 1 affords the dithioether derivatives (Z)-[(RS)(H)C=C(SR)–Fc] (5a: R = Ph; 5b: R = p-tolyl; 5c: R = Et). An addition/elimination sequence is suggested to account for this surprising result. The yield of 5c is very low due to a co…

Stereochemistrychemistry.chemical_elementRheniumMetathesisTriple bondMedicinal chemistryOxidative additionInorganic Chemistrychemistry.chemical_compoundFerrocenechemistryThioetherNucleophilePalladiumEuropean Journal of Inorganic Chemistry
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Ligand substitution reactions of the [ReX6]2− (X=Cl, Br) anions. Synthesis and crystal structure of novel oxalato complexes of rhenium(IV)

2006

Abstract The reaction of K2[ReX6] (X = Cl, Br) with oxalic acid and triethylamine in dimethylformamide solution yields the substituted complexes [ReX4(ox)]2− and cis-[ReX2(ox)2]2−, which can be obtained separately depending on the amount of added amine. The crystal structures of (PPh4)2[ReBr4(ox)], cis-(PPh4)2[ReBr2(ox)2] and cis-(AsPh4)2[ReCl2(ox)2] have been determined by single-crystal X-ray diffraction. The anionic complexes are octahedral with only slight distortions. The direct isolation of the pure complexes as well as the formation of only the cis isomers – without the presence of trans isomers and/or [Re(ox)3]2− – is probably due to the kinetic inertness of Re(IV)–X bonds, which in…

Substitution reactionChemistryStereochemistryLigandchemistry.chemical_elementCrystal structureRheniumMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryDimethylformamideAmine gas treatingPhysical and Theoretical ChemistryTriethylamineCis–trans isomerismInorganica Chimica Acta
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CCDC 644916: Experimental Crystal Structure Determination

2008

Related Article: F.Durola, L.Russo, J.-P.Sauvage, K.Rissanen, O.S.Wenger|2007|Chem.-Eur.J.|13|8749|doi:10.1002/chem.200700684

Tricarbonyl-pyridine-(88'-bis(4-methoxyphenyl)-33'-biisoquinoline-NN')-rhenium(i) hexafluorophosphateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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A high-temperature x-ray absorption spectroscopy study of

1996

We present for the first time a high-temperature x-ray absorption spectroscopy study of at the edge. The analysis both of the XANES and of the EXAFS regions shows that, in , a progressive localization of the 5d states following the temperature rise is accompanied at T > 350 K by a distortion of the octahedra, which increases up to the decomposition temperature . The distortion leads to the lowering of the rhenium site symmetry from and is due to the electron - phonon coupling of the 5d electrons with the and phonons and to the Jahn - Teller effect caused by the rhenium electron which becomes localized at high temperature.

X-ray absorption spectroscopyCondensed matter physicsAbsorption spectroscopyExtended X-ray absorption fine structureJahn–Teller effectchemistry.chemical_elementElectronRheniumCondensed Matter PhysicsMolecular physicsXANESElectron localization functionCondensed Matter::Materials SciencechemistryCondensed Matter::SuperconductivityCondensed Matter::Strongly Correlated ElectronsGeneral Materials ScienceJournal of Physics: Condensed Matter
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