Search results for "CELL"

showing 10 items of 65972 documents

Triorganotin( iv ) cation-promoted dimethyl carbonate synthesis from CO 2 and methanol: solution and solid-state characterization of an unexpected di…

2018

Two novel C,N-chelated organotin(IV) complexes bearing weakly coordinating carborane moieties were prepared by the reaction of the corresponding C,N-chelated organotin(IV) chloride (i.e. LCNR2SnCl, R = n-Bu (1) and Ph (2); LCN = 2-(N,N-dimethylaminomethyl)phenyl)) with monocarba-closo-dodecaborate silver salt (AgCB11H12; Ag·3). Both products of the metathesis, [LCN(n-Bu)2Sn]+[CB11H12]− (4) and [LCNPh2Sn]+ [CB11H12]− (5), respectively, were characterized by both multinuclear NMR spectroscopy and elemental analysis. The instability of 4 and 5 towards water is discussed. The solid-state structure of LCN(n-Bu)2SnOH·B(C6F5)3 (4a) as a model compound with a Sn–O(H)⋯B linkage is also reported. The…

010405 organic chemistryInfrared spectroscopyGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistryMetathesis01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryMaterials ChemistryCarborane[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryMethanolDimethyl carbonateStoichiometryComputingMilieux_MISCELLANEOUS
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Insights into the crystal packing of phosphorylporphyrins based on the topology of their intermolecular interaction energies

2014

Four metal complexes of 5,15-bis(diethoxyphosphoryl)-10,20-diphenylporphyrin 1M (M = Cd(II), Ni(II), Pd(II), and Pt(II)) were synthesized and crystallographically characterized. The crystal organization patterns were analyzed using DFT (B97-D3/def2-SVP) calculations of the intermolecular interaction energies between complexes in the crystals. For the systematic analysis of crystal packing, the calculations were extended to previously reported compounds 1M (M = H2, Cu(II), and Zn(II)). Quantitative analysis of the interaction energies shows the essential role of weak intermolecular interactions, such as C-H⋯O, C-H⋯π and M⋯π, in the formation of basic structural motifs and their organization …

010405 organic chemistryIntermolecular forceGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesPorphyrin0104 chemical sciencesCrystalMetalchemistry.chemical_compoundCrystallographychemistryPolymorphism (materials science)Intermolecular interactionvisual_artvisual_art.visual_art_medium[CHIM]Chemical SciencesGeneral Materials ScienceComputingMilieux_MISCELLANEOUS
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Synthesis of 1,3-bis(trimethylcyclam) and 1,3-bis(trimethylcyclen) substituted benzenes

2009

Pd-catalyzed amination of 1,3-dibromobenzene with N,N',N''-trimethylcyclam and N,N',N''-trimethylcyclen provided corresponding 1,3-bis(tetraazamacrocyclic) derivatives of benzene in 25-32% yields. The dependence of the products yields on the phosphine ligand applied (BINAP, DavePHOS) as well as on the stoichiometry of starting compounds was established. Scope and limitations for the synthesis of N-phenyl and N-(3-bromophenyl) derivatives of trimethylcyclam and trimethylcyclen were demonstrated.

010405 organic chemistryLigandPd catalysis[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistryamination[CHIM.ORGA] Chemical Sciences/Organic chemistry010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical Chemistryaryl halideschemistry.chemical_compoundchemistrytetraazamacrocycles[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistryBenzenePhosphineStoichiometryAminationComputingMilieux_MISCELLANEOUSBINAP
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The Cu(II) complex of a C-lipophilized 13aneN4 macrocycle with an additional protonable amino group as micellar anion receptor.

2009

Three 13aneN4 macrocyclic ligands have been prepared bearing a -CH(2)NHR side arm (R = H, n-C(5)H(11), n-C(10)H(21)) on a carbon atom. When Cu(2+) is complexed in the macrocyclic ring, the amino group of the side arm undergoes an acid-base protonation equilibrium but it is not able to coordinate apically the metal cation even when it is deprotonated. The Cu(2+) complex with the ligand bearing the longest appended aliphatic chain is fully confined inside Triton X-100 micelles, and its ability to bind and sequestrate a series of anions inside micelles has been studied at two different pH values, i.e. both with protonated and neutral side-arm amino group. The favourable role played by the prot…

010405 organic chemistryLigandStereochemistryChemistryProtonation010402 general chemistryRing (chemistry)01 natural sciencesMicelle0104 chemical sciencesInorganic ChemistryMetalDeprotonationGroup (periodic table)visual_artvisual_art.visual_art_mediumAnion receptorDalton transactions (Cambridge, England : 2003)
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Mononuclear and One-Dimensional Cobalt(II) Complexes with the 3,6-Bis(picolylamino)-1,2,4,5-tetrazine Ligand

2018

International audience

010405 organic chemistryLigandchemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciences3. Good healthInorganic ChemistryTetrazinechemistry.chemical_compoundchemistryPolymer chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltComputingMilieux_MISCELLANEOUS
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A robust viologen and Mn-based porous coordination polymer with two types of Lewis acid sites providing high affinity for H 2 O, CO 2 and NH 3

2017

A novel porous coordination polymer [Mn(pc3)(H2O)2]·xH2O (3 < x < 4) is synthesized in water at pH = 7 using the anionic viologen-carboxylate ligand 4,4′-bipyridinium,1,1′-bis-(2,4-dicarboxyphenyl) (pc32−). Dehydration of the material results in the formation of open pores containing two types of accessible Lewis acid sites: exposed Mn2+ cations and N+ atoms of viologen units. Due to this property the PCP shows high affinity and capacity in the adsorption of H2O, CO2 and NH3. Despite the presence of strong adsorption sites this material is stable in liquid water and in gaseous NH3.

010405 organic chemistryLiquid waterCoordination polymerLigandInorganic chemistryViologen010402 general chemistrymedicine.disease01 natural sciences0104 chemical sciencesInorganic Chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAdsorptionchemistrymedicine[CHIM]Chemical SciencesLewis acids and basesDehydrationPorosityComputingMilieux_MISCELLANEOUSmedicine.drug
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First titanium-catalyzed 1,4-hydrophosphination of 1,3-dienes

2010

International audience

010405 organic chemistryOrganic Chemistrychemistry.chemical_elementHomogeneous catalysisGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistry01 natural scienceshomogeneous catalysisCatalysis0104 chemical sciencesCatalysis[ CHIM.CATA ] Chemical Sciences/CatalysisphosphineschemistryhydrophosphinationdienesOrganic chemistryHydrophosphinationtitaniumComputingMilieux_MISCELLANEOUSTitanium
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Iron( ii ) and cobalt( ii ) complexes based on anionic phenanthroline-imidazolate ligands: reversible single-crystal-to-single-crystal transformations

2018

A series of low-spin FeII and CoII complexes based on phenanthroline-imidazolate (PIMP) ligands are reported. The FeII complex (H9O4)[Fe(PIMP)3]·(C4H10O)2(H2O) (1a) shows reversible crystalline phase transformations to afford two new phases (H9O4)[Fe(PIMP)3]·(H2O) (1b) and (H9O4)[Fe(PIMP)3]·(C8H18O)(C4H10O)(H2O) (1c) by release of diethyl ether and absorption of diethyl/dibutyl ether, respectively. This reversible uptake/release of solvent molecules is a clear example of single-crystal-to-single-crystal transformation involving a discrete metal complex. On the other hand, the corresponding CoII complex (H9O4)[Co(PIMP)3]·(C4H10O)2(H2O)2 (2) does not exhibit similar phase transformations. In …

010405 organic chemistryPhenanthrolinechemistry.chemical_elementGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciences3. Good health0104 chemical sciencesSolventDibutyl etherMetalchemistry.chemical_compoundCrystallographyDeprotonationchemistryvisual_artImidazolatevisual_art.visual_art_medium[CHIM]Chemical SciencesGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryDiethyl etherCobaltComputingMilieux_MISCELLANEOUS
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Hierarchical Beta zeolites obtained in concentrated reaction mixtures as catalysts in tetrahydropyranylation of alcohols

2020

Abstract Hierarchical zeolites consisting of Beta nanoparticles (15–40 nm) were obtained via hydrothermal treatment of a concentrated zeolite gel-precursor (H2O/Si = 2.5–14) without utilization of complex SDAs. The proposed approach is based on the formation of a large number of zeolite nuclei under particular crystallization conditions, followed by their agglomeration resulting in the dense packing of the particles preventing their further growth. The micelles of cetyltrimethylammonium bromide (CTAB) can be used to additionally limit the growth of zeolite nanoparticles during hydrothermal treatment of concentrated reaction mixtures. Such deceleration of crystallization promotes the formati…

010405 organic chemistryProcess Chemistry and TechnologyNanoparticle010402 general chemistry01 natural sciencesMicelleCatalysis0104 chemical sciencesCatalysislaw.inventionAmorphous solid[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundChemical engineeringchemistrylawAluminosilicateBromideCrystallizationZeoliteComputingMilieux_MISCELLANEOUS
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Highly Anisotropic Rhenium(IV) Complexes: New Examples of Mononuclear Single-Molecule Magnets

2013

The rhenium(IV) complex (NBu4)2[ReBr4(ox)] (1) (ox = oxalate and NBu4(+) = tetra-n-butylammonium cation) has been prepared and its crystal structure determined by X-ray diffraction. The structure is made up of discrete [ReBr4(ox)](2-) anions and bulky NBu4(+) cations. Each [ReBr4(ox)](2-) anion is surrounded by six NBu4(+) cations, which preclude any significant intermolecular contact between the anionic entities, the shortest rhenium···rhenium distance being 9.373(1) Å. Variable temperature dc and ac magnetic susceptibility measurements and field-dependent magnetization experiments on polycrystalline samples of 1 reveal the occurrence of highly anisotropic magnetically isolated Re(IV) cent…

010405 organic chemistryRelaxation (NMR)Inorganic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureRhenium010402 general chemistry01 natural sciencesBiochemistryMagnetic susceptibilityCatalysisOxalate3. Good health0104 chemical sciencesMagnetizationchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryMolecule[PHYS.COND.CM-SCE]Physics [physics]/Condensed Matter [cond-mat]/Strongly Correlated Electrons [cond-mat.str-el]IsostructuralComputingMilieux_MISCELLANEOUSJournal of the American Chemical Society
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