Search results for "Theoretical"

showing 10 items of 11439 documents

Synthesis and structural characterization of well-defined bis(oxamato)palladate(II) precatalysts for Suzuki and Heck reactions

2018

Abstract A family of tetra-n-butylammonium salts of bis(oxamato)palladate(II) complexes of formula (n-Bu4N)2[Pd(Lm)2]·pH2O [m = 1–9; L1 = N-phenyloxamate (pma) and p = 2 (1), L2 = N-2-methylphenyloxamate (2-Mepma) and p = 4 (2), L3 = N-4-methylphenyloxamate (4-Mepma) and p = 2 (3), L4 = N-2,3-dimethylphenyloxamate (2,3-Me2pma) and p = 3 (4), L5 = N-2,4-dimethylphenyloxamate (Me2pma) and p = 4 (5), L6 = N-2,5-dimethylphenyloxamate (2,5-Me2pma) and p = 7 (6), L7 = N-3,4-dimethylphenyloxamate (3,4-Me2pma) and p = 6 (7), L8 = N-3,5-dimethylphenyloxamate (3,5-Me2pma) and p = 5 (8)] have been prepared and characterized by spectroscopic methods. The crystal structure of 1 that has been solved by s…

010405 organic chemistryLigandArylCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistryBond lengthchemistry.chemical_compoundDeprotonationchemistrySuzuki reactionHeck reactionMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
researchProduct

Scalable and Selective Preparation of 3,3′,5,5′-Tetramethyl-2,2′-biphenol

2016

Biphenols are indispensable building blocks in ligand systems for organic catalysis. 3,3′5,5′-Tetramethyl-2,2′-biphenol is a particular versatile motif in different catalytic systems. We developed an easy to perform and scalable process to give access to large quantities of this important building block by the use of selenium dioxide, a common and readily available oxidizer.

010405 organic chemistryLigandChemistryOrganic ChemistryScalabilityOrganic chemistryPhysical and Theoretical Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysisBlock (data storage)Organic Process Research & Development
researchProduct

Rational Synthesis of Chiral Metal-Organic Frameworks from Preformed Rodlike Secondary Building Units.

2017

The lack of rational design methodologies to obtain chiral rod-based MOFs is a current synthetic limitation that hampers further expansion of MOF chemistry. Here we report a metalloligand design strategy consisting of the use, for the first time, of preformed 1D rodlike SBUs (1) for the rational preparation of a chiral 3D MOF (2) exhibiting a rare eta net topology. The encoded chiral information on the enantiopure ligand is efficiently transmitted first to the preformed helical 1D building block and, in a second stage, to the resulting chiral 3D MOF. These results open new routes for the rational design of chiral rod-based MOFs, expanding the scope of these unique porous materials.

010405 organic chemistryLigandChemistryRational designNanotechnology010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesInorganic ChemistryEnantiopure drugMetal-organic frameworkSBusPhysical and Theoretical ChemistryTopology (chemistry)Inorganic chemistry
researchProduct

Modulation of the ordering temperature in anilato-based magnets

2019

Abstract Four new 2D honeycomb anilato-based ferrimagnets with Mn(II) and Cr(III) have been prepared and characterized. These compounds, formulated as (NBu4)[MnCr(C6O4X2)3(PhCHO)]·PhY (X/Y = Cl/H (1), Br/H (2), Cl/CHO (3) and Br/CHO (4) show that it is possible to include benzaldehyde as a co-ligand coordinated to the Mn(II) metal atom in these 2D ferrimagnets. This inclusion increases the coordination number of Mn(II) to seven resulting in a change in the ordering temperatures of these 2D ferrimagnets (from ca. 10–11 K to ca. 7 K). Here we show the role played by the additional benzaldehyde ligand and by the crystallization solvent molecules (benzene in 1 and 2 and benzaldehyde in 3 and 4)…

010405 organic chemistryLigandCoordination number010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistrySolventBenzaldehydeMetalchemistry.chemical_compoundCrystallographychemistrylawvisual_artMaterials Chemistryvisual_art.visual_art_mediumMoleculePhysical and Theoretical ChemistryCrystallizationBenzenePolyhedron
researchProduct

Ligand Noninnocence in Cobalt Dipyrrin–Bisphenols: Spectroscopic, Electrochemical, and Theoretical Insights Indicating an Emerging Analogy with Corro…

2019

Three cobalt dipyrrin-bisphenol (DPPCo) complexes with different meso-aryl groups (pentafluorophenyl, phenyl, and mesityl) were synthesized and characterized based on their electrochemistry and spectroscopic properties in nonaqueous media. Each DPPCo undergoes multiple oxidations and reductions with the potentials, reversibility, and number of processes depending on the specific solution conditions, the specific macrocyclic substituents, and the type and number of axially coordinated ligands on the central cobalt ion. Theoretical calculations of the compounds with different coordination numbers are given in the current study in order to elucidate the cobalt-ion oxidation state and the innoc…

010405 organic chemistryLigandCoordination numberchemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistryMetalchemistryOxidation statelawComputational chemistryvisual_artvisual_art.visual_art_mediumMacrocyclic ligandPhysical and Theoretical ChemistryElectron paramagnetic resonanceCobaltInorganic Chemistry
researchProduct

Enhanced Interplay between Host–Guest and Spin-Crossover Properties through the Introduction of an N Heteroatom in 2D Hofmann Clathrates

2021

Controlled modulation of the spin-crossover (SCO) behavior through the sorption-desorption of invited molecules is an extensively exploited topic because of its potential applications in molecular sensing. For this purpose, understanding the mechanisms by which the spin-switching properties are altered by guest molecules is of paramount importance. Here, we show an experimental approach revealing a direct probe of how the interplay between SCO and host-guest chemistry is noticeably activated by chemically tuning the host structure. Thus, the axial ligand 4-phenylpyridine (4-PhPy) in the 2D Hofmann clathrates {Fe(4-PhPy)2[M(CN)4]} (PhPyM; M = Pt, Pd) is replaced by 2,4-bipyridine (2,4-Bipy),…

010405 organic chemistryLigandHeteroatomSubstituent010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyAdsorptionchemistrySpin crossoverMoleculeMethanolPhysical and Theoretical ChemistryChemical compositionInorganic Chemistry
researchProduct

Combination of magnetic susceptibility and electron paramagnetic resonance to monitor the 1D to 2D solid state transformation in flexible metal-organ…

2012

Two families of coordination polymers, {[M(btix)(2)(OH(2))(2)]·2NO(3)·2H(2)O}(n) [M = Co (1), Zn (2), Co-Zn (3); btix = 1,4-bis(triazol-1-ylmethyl)benzene] and {[M(btix)(2)(NO(3))(2)]}(n) [M = Co (4), Zn (5), Co-Zn (6)], have been synthesized and characterized. The two conformations of the ligand, syn and anti, lead to one-dimensional (1D) cationic chains or two-dimensional (2D) neutral grids. Extrusion of the water molecules of the 1D compounds results in an irreversible transformation into the 2D compounds, which involves a change in conformation of the btix ligands and a rearrangement in the metal environment with cleavage and reformation of covalent bonds. This structural transformation…

010405 organic chemistryLigandInorganic chemistry010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical scienceslaw.inventionInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryCovalent bondlawvisual_artvisual_art.visual_art_mediumMoleculeMetal-organic frameworkPhysical and Theoretical ChemistryElectron paramagnetic resonanceBenzeneInorganic chemistry
researchProduct

Selective Metal–Ligand Bond-Breaking Driven by Weak Intermolecular Interactions: From Metamagnetic Mn(III)-Monomer to Hexacyanoferrate(II)-Bridged Me…

2020

Metal–ligand coordination interactions are usually much stronger than weak intermolecular interactions. Nevertheless, here, we show experimental evidence and theoretical confirmation of a very rare...

010405 organic chemistryLigandIntermolecular forceHexacyanoferrate IITrimerBond breaking010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographyMonomerchemistryvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryInorganic Chemistry
researchProduct

Hexanuclear manganese(III) single-molecule magnets based on oxime and azole-type ligands

2019

Abstract Two novel hexanuclear manganese(III) complexes belonging to the Mn6 family of single-molecule magnets (SMMs), of formulae [Mn6(μ3-O)2(H2N-sao)6(bta)2(EtOH)6]·2EtOH·4H2O (1) and [Mn6(μ3-O)2(H2N-sao)6(pta)2(EtOH)6]·4EtOH (2) [H2N-saoH2 = salicylamidoxime, bta = 1,2,3-benzotriazolate anion, pta = 5-phenyl-tetrazolate anion], have been synthesized and characterized structurally and magnetically. Both compounds crystallize in the triclinic system with space group P 1 ¯ (1 and 2). In their crystal packing, adjacent Mn6 complexes are connected through non-coordinating solvent molecules, which are H-bonded to N atoms of azole rings and –NH2 groups of salicylamidoxime ligand. The study of t…

010405 organic chemistryLigandMetal ions in aqueous solutionRelaxation (NMR)chemistry.chemical_elementManganeseTriclinic crystal system010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographyMagnetizationchemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryPolyhedron
researchProduct

A P-chirogenic β-aminophosphine synthesis by diastereoselective reaction of the α-metallated PAMP–borane complex with benzaldimine

2004

International audience; The diastereoselective synthesis of a P-chirogenic β-aminophosphine ligand with carbon–carbon bond formation of the ethano bridge in a 3:1 ratio via reaction of an α-metallated P-chirogenic phosphine borane with a benzaldimine is described. The diastereoselectivity is attributed to a transition state where the lithium cation chelates the phosphine borane carbanion and the nitrogen of the imine and the attack of the C@N occurs on the face opposite to the P–B bond, due to its interaction with the antibonding P–B bond. The major diastereoisomeric β-aminophosphine borane was then separated and decomplexed into the corresponding β-aminophosphine under neutral conditions a…

010405 organic chemistryLigandOrganic ChemistryImineEnantioselective synthesisAsymmetric synthesisBoranesAminophosphineBoraneChiral phosphorous010402 general chemistryAntibonding molecular orbital01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryBoraneOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryPhosphineCarbanionTetrahedron: Asymmetry
researchProduct