Search results for "iva"

showing 10 items of 25115 documents

A family of layered chiral porous magnets exhibiting tunable ordering temperatures.

2013

A simple change of the substituents in the bridging ligand allows tuning of the ordering temperatures, Tc, in the new family of layered chiral magnets A[M(II)M(III)(X2An)3]·G (A = [(H3O)(phz)3](+) (phz = phenazine) or NBu4(+); X2An(2-) = C6O4X2(2-) = 2,5-dihydroxy-1,4-benzoquinone derivative dianion, with M(III) = Cr, Fe; M(II) = Mn, Fe, Co, etc.; X = Cl, Br, I, H; G = water or acetone). Depending on the nature of X, an increase in Tc from ca. 5.5 to 6.3, 8.2, and 11.0 K (for X = Cl, Br, I, and H, respectively) is observed in the MnCr derivative. Furthermore, the presence of the chiral cation [(H3O)(phz)3](+), formed by the association of a hydronium ion with three phenazine molecules, lead…

010405 organic chemistryHexagonal crystal systemInorganic chemistryPhenazineBridging ligand010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMagnetAcetone[CHIM]Chemical SciencesMoleculePhysical and Theoretical ChemistryPorosityComputingMilieux_MISCELLANEOUSDerivative (chemistry)Inorganic chemistry
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Reversible O–H bond activation by an intramolecular frustrated Lewis pair

2019

The interactions of the O-H bonds in alcohols, water and phenol with dimethylxanthene-derived frustrated Lewis pairs (FLPs) have been probed. Within the constraints of this backbone framework, the preference for adduct formation or O-H bond cleavage to give the corresponding zwitterion is largely determined by pKa considerations. In the case of the PPh2/B(C6F5)2 system and p-tBuC6H4OH, an equilibrium is established between the two isomeric forms which allows the thermodynamic parameters associated with zwitterion formation via O-H bond cleavage to be probed.

010405 organic chemistryHydrogen bondintramolecular frustrated Lewis pair010402 general chemistry01 natural sciencesFrustrated Lewis pair0104 chemical sciencesAdductInorganic Chemistrykemialliset sidoksetCrystallographychemistry.chemical_compoundchemistryreversible O-H bond activationZwitterionIntramolecular forceta116Bond cleavageDalton Transactions
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Acylchalcogenourea Complexes of Silver(I)

2016

Acylthio- or acylselenoureas react with silver(I) oxide to form tetranuclear silver(I) complexes containing the deprotonated acylchalcogenourea ligands bound to the silver atoms through the chalcogen and oxygen atoms. These tetrasilver(I) species react with either 4 or 8 equiv. of a phosphine to afford either dinuclear silver(I) phosphine complexes or tetrahedral silver diphosphine complexes. In these compounds, the acylchalcogenourea ligands form six-membered rings by coordinating to the metal atom through the chalcogen and oxygen atoms. In one case, we observed a very rare example of an acylthiourea ligand coordinated through the nitrogen and sulfur atoms to form a four-membered ring. A s…

010405 organic chemistryLigand010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundChalcogenDeprotonationchemistryvisual_artPolymer chemistryvisual_art.visual_art_mediumsilver complexesta116CarbeneDerivative (chemistry)PhosphineEuropean Journal of Inorganic Chemistry
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Design of bimetallic magnetic chains based on oxalate complexes: towards single chain magnets

2009

We describe the synthesis, structure and magnetic characterization of several oxalate-based bimetallic 1D systems. We will exemplify how by suitable choice of the molecular building blocks and strict control of their arrangement in the solid state, the magnetic properties of these low-dimensional materials can be tuned to finally obtain bimetallic oxalate chains behaving as single-chain magnets (SCM). First, we will focus on compounds [K(18-crown-6)][MII(bpy)Cr(ox)3] (1, 2; MII = Mn, Co; bpy = C10N2H8). The MnCr derivative behaves as a 1D ferromagnet down to 2 K, the lowest investigated temperature. The lack of magnetic ordering in this chain prompted us to prepare the more anisotropic MnCo…

010405 organic chemistryLigandRelaxation (NMR)Supramolecular chemistryGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryFerromagnetismMagnetGeneral Materials ScienceBimetallic stripDerivative (chemistry)CrystEngComm
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Preparative-Scale Synthesis of Vedejs Chiral DMAP Catalysts

2018

A scalable synthesis of chiral Vedejs-type DMAP catalysts is reported. The key step of the synthesis is amination of the enantiomerically pure 4-chloropyridine derivative using well-defined ZnCl2(amine)2 complexes. A series of Zn(II)–amine complexes have been synthesized to explore the scope of the ZnCl2-mediated amination of 4-halopyridines. Mechanistic studies support a Zn(II)-facilitated nucleophilic aromatic substitution as a plausible mechanism for the chlorine-to-amine exchange.

010405 organic chemistryOrganic Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryNucleophilic aromatic substitutionpolycyclic compoundsAmine gas treatingDerivative (chemistry)AminationThe Journal of Organic Chemistry
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A Phenylene-Bridged Cyclohexa-meta-phenylene as Hexa-peri-hexabenzocoronene Precursor.

2018

A phenylene-bridged cyclohexa-meta-phenylene was synthesized via intramolecular Yamamoto coupling of an appropriate p-quinquephenyl derivative carrying four m-chlorophenyl substituents. The structural proof could be obtained by single-crystal X-ray diffraction analysis, which also revealed a slightly strained structure with an internal phenylene bridge. Notably, this cyclo-meta-phenylene served as a novel precursor for hexa-peri-hexabenzocoronene (HBC). The cyclodehydrogenation proceeded smoothly, providing the corresponding HBC derivative as confirmed by MALDI-TOF-MS, and UV/Vis spectroscopy.

010405 organic chemistryOrganic ChemistryHexa-peri-hexabenzocoroneneGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryPhenyleneIntramolecular forcePolymer chemistrySpectroscopyDerivative (chemistry)Chemistry (Weinheim an der Bergstrasse, Germany)
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Corrosion inhibition performance of a structurally well-defined 1,2,3-triazole derivative on mild steel-hydrochloric acid interface

2021

Abstract In the present work, a new 1,4-disubstituted-1,2,3-triazole product, named 4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-morpholine (MPTM) was successfully synthesized under click chemistry regime. The structure of the new compound that has a rigid triazole moiety and a flexible morpholine ligand has been characterized using 1H NMR, 13C NMR, HRMS, and FTIR spectroscopy. Its inhibition performance for mild steel in acidic medium 1 M HCl has been studied by utilizing a combination of experimental, spectroscopic and computational methods. The electrochemical characterization was carried out by a gravimetric study, electrochemical impedance spectroscopy (EIS), and potentiodynam…

010405 organic chemistryOrganic ChemistryLangmuir adsorption modelCarbon-13 NMR010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryDielectric spectroscopyInorganic Chemistrysymbols.namesakechemistry.chemical_compoundAdsorptionchemistryMorpholinesymbolsProton NMRFourier transform infrared spectroscopySpectroscopyDerivative (chemistry)Nuclear chemistryJournal of Molecular Structure
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Combining Amines and 3-(2-Pyridyl)-[1,2,3]Triazolo[1,5-a]pyridine: An Easy Access to New Functional Polynitrogenated Ligands

2019

Triazolopyridine-pyridine amine ligands are easily obtained by means of either thermal- or copper(II)-mediated reactions. Starting from a readily accessible iodo derivative of triazolopyridine-pyridine and different amines, this new family of compounds combines aromatic and aliphatic nitrogen atoms with promising coordinating properties. Furthermore, chemical derivatization of a new triazolopyridine-pyridine diamine compound, N1-[6-([1,2,3]triazolo[1,5-a]pyridin-3-yl)pyridin-2-yl]ethan-1,2-diamine, allows the preparation of several remote-pyridine-containing ligands.

010405 organic chemistryOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesNitrogenCopperCombinatorial chemistryCatalysisAmine ligands0104 chemical scienceschemistry.chemical_compoundchemistryDiaminePyridineDerivatizationDerivative (chemistry)Synthesis
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Substitution of the laser borane anti-B18H22 with pyridine: a structural and photophysical study of some unusually structured macropolyhedral boron h…

2018

Reaction of anti-B18H221 with pyridine in neutral solvents gives sparingly soluble B16H18-3',8'-Py23a as the major product (ca. 53%) and B18H20-6',9'-Py22 (ca. 15%) as the minor product, with small quantities of B18H20-8'-Py 4 (ca. 1%) also being formed. The three new compounds 2, 3a and 4 are characterized by single-crystal X-ray diffraction analyses and by multinuclear multiple-resonance NMR spectroscopy. Compound 2 is of ten-vertex nido:ten-vertex arachno two-atoms-in-common architecture, long postulated for a species with borons-only cluster constitution, but previously elusive. Compound 3a is of unprecedented ten-vertex nido:eight-vertex arachno two-atoms-in-common architecture. The si…

010405 organic chemistryQuantum yieldNuclear magnetic resonance spectroscopyBorane010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographysymbols.namesakechemistryPyridinesymbolsPicolinevan der Waals forcePhosphorescenceDerivative (chemistry)Dalton Transactions
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Effect of Iodination on the Photophysics of the Laser Borane anti-B18H22: Generation of Efficient Photosensitizers of Oxygen

2019

Treatment of the laser borane anti-B18H22 (compound 1) with iodine in ethanol gives the monoiodinated derivative 7-I-anti-B18H21 (compound 2) in 67% yield, or, by reaction with iodine or ICl in the presence of AlCl3 in dichloromethane, the diiodinated derivative 4,4'-I2-anti-B18H20 (compound 3) in 85% yield. On excitation with 360 nm light, both compounds 2 and 3 give strong green phosphorescent emissions (λmax = 525 nm, ΦL = 0.41 and λmax = 545 nm, ΦL = 0.71 respectively) that are quenched by dioxygen to produce O2(1Δg) singlet oxygen with quantum yields of ΦΔ = 0.52 and 0.36 respectively. Similarly strong emissions can be stimulated via the nonlinear process of two-photon absorption when …

010405 organic chemistrySinglet oxygenNuclear magnetic resonance spectroscopyBorane010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryYield (chemistry)Physical and Theoretical ChemistrySpectroscopyPhosphorescenceDerivative (chemistry)DichloromethaneInorganic Chemistry
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