Search results for "FORCE"

showing 10 items of 3423 documents

Planar Benzo[1,2-b:4,5-b′]dithiophene Derivatives Decorated with Nitronyl and Imino Nitroxides

2018

Four weakly antiferromagnetic interacting biradicals of benzo[1,2- b:4,5- b']dithiophene (BDT) and BDT extended with two thiophenes (BDTTh2) linked with nitronyl and imino nitroxides (NN and IN) as BDT-NN, BDT-IN, BDTTh2-NN, and BDTTh2-IN were designed, synthesized, and characterized. Short intermolecular π-π distances were found (3.42 A) for BDT-NN, whereas larger ones were found for BDT-IN (3.54 A) and BDTTh2-NN (3.67 A), respectively. Intramolecular magnetic interaction ( Jintra,exp/ kB) of BDT-NN (-26 K) is much larger than for BDT-IN (-5.3 K), while it is reduced for the dithiophene-extended molecule BDTTh2-NN (-2.3 K). Intermolecular interactions ( zJinter,exp/ kB) of BDT-NN (-6.5 K) …

010405 organic chemistryChemistryOrganic ChemistryCrystalline materialsIntermolecular force010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographyPlanarIntramolecular forceAntiferromagnetismMoleculeMagnetic interactionSpin (physics)The Journal of Organic Chemistry
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Synthesis of substituted piperidines by enantioselective desymmetrizing intramolecular aza-Michael reactions.

2018

An organocatalytic enantioselective intramolecular aza-Michael reaction has been described for the first time in a desymmetrization process employing substrates different from cyclohexadienones. By using 9-amino-9-deoxy-epi-hydroquinine as the catalyst and trifluoroacetic acid as a co-catalyst, a series of enantiomerically enriched 2,5-and 2,6-disubstituted piperidines have been obtained in good yields and with moderate diastereoselectivity. Depending on the catalyst/co-catalyst loading ratio, either the major or the minor diastereoisomer of the final piperidine products was achieved with high levels of enantioselectivity. Finally, some mechanistic insights have been considered by means of …

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisDiastereomer010402 general chemistry01 natural sciencesBiochemistryDesymmetrization0104 chemical sciencesCatalysischemistry.chemical_compoundLoading ratioIntramolecular forceTrifluoroacetic acidOrganic chemistryPiperidinePhysical and Theoretical ChemistryOrganicbiomolecular chemistry
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Vinyl Fluorides: Competent Olefinic Counterparts in the Intramolecular Pauson–Khand Reaction

2019

Despite the great advances achieved in the Pauson-Khand reaction and the ever-increasing demand for fluorinated compounds, the use of vinyl fluorides as olefinic counterparts in the above-mentioned transformation had been completely overlooked. Herein, we describe, for the first time, the intramolecular Pauson-Khand reaction of enynes containing a vinyl fluoride moiety.

010405 organic chemistryChemistryPauson–Khand reactionOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundIntramolecular forcePolymer chemistryMoietyPhysical and Theoretical ChemistryVinyl fluorideOrganic Letters
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Oxotris(oxalate)niobate(V): An oxalate delivery agent in the design of building blocks

2018

This work concerns the oxalate delivery process that occurs when using (NH4)3[NbO(C2O4)3]·6H2O as a suitable oxalate source in the synthesis of two compounds, [Cu(dmphen)(C2O4)(H2O)] (1) and [{Cu(dmphen)(CH3OH)}2(μ-C2O4)](ClO4)2 (2) (dmphen = 2,9-dimethyl-1,10-phenanthroline). {[Fe{HB(pz)3}(CN)2(μ-CN)]2[{Cu(dmphen)}2(μ-C2O4)]}∙xCH3OH (3) (2.0 ≤ x ≤ 2.4) was obtained by reacting 2 and PPh4[Fe{HB(pz)3}(CN)3]∙H2O [ = tetraphenylphosphonium and = tris(pyrazolyl)borate]. Crystal structures of 1–3 have been determined by single-crystal X-ray diffraction experiments: 1 is a mononuclear trigonal bipyramidal copper(II) species, 2 is a centrosymmetric oxalato-bridged dicopper(II) complex, and 3 consi…

010405 organic chemistryChemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopperOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographyTrigonal bipyramidal molecular geometryIntramolecular forceMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryBoronNatural bond orbital
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A novel two-dimensional organostannoxane coordination network promoted by phenazine: Synthesis, characterization and X-ray structure of

2009

Abstract Reaction of the dimeric hydroxo di-n-butylstannane trifluoromethanesulfonato complex [n-Bu2Sn(μ-OH)(H2O)0.5(η1-O3SCF3)]2 (1) with phenazine (C12H8N2, Phz) (2) in dichloromethane at room temperature in a 1:3 molar ratio yielded the novel two-dimensional organometallic coordination polymer 2 ∞ { [ n - Bu 2 ( μ -OH ) SnOSn ( μ - η 2 - O 3 SCF 3 ) n - Bu 2 ] 2 [ n - Bu 2 ( μ -OH ) SnOSn ( η 1 - O 3 SCF 3 ) n - Bu 2 ] 2 } (3), together with the phenazinium trifluoromethanesulfonate salt [C12H9N2]+ [CF3SO3]−, crystallographically isolated in two different structural arrangements, free 4 and in π–π aromatic stacking interaction with independent intercalated non-protonated phenazine molecu…

010405 organic chemistryCoordination polymerOrganic ChemistryIntermolecular forcePhenazineSupramolecular chemistryStacking010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryTrifluoromethanesulfonateDichloromethaneJournal of Organometallic Chemistry
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Synthesis, crystal structures and magnetic properties of picolinate-bridged copper(II) chains

2018

The paper reports the synthesis, crystal structures, and magnetic properties of two copper(II) coordination polymers, Cu2(L1)4 (1) and Cu3(L2)6 (2), based on rigid ethynylene-bridged ditopic ligands containing one picolinate subunit (L1 = 5-(pyridin-3-ylethynyl)picolinate anion; L2 = 5-((4-(methoxycarbonyl)phenyl)ethynyl)picolinate anion). Both 1 and 2 have a chain structure. In 1, the repeating unit in the chain is a doubly bridged picolinate dicopper(II) complex, whereas 2 is built upon trimeric units where the Cu2+ ions are also connected by double picolinate bridges. Both compounds exhibit antiferromagnetic interactions in the solid state. The magnetic properties of 1 and 2 were analyze…

010405 organic chemistryDimerIntermolecular forcechemistry.chemical_elementTrimerCrystal structure010402 general chemistry01 natural sciencesCopper0104 chemical sciencesIonchemistry.chemical_compoundCrystallographychemistryMaterials ChemistryAntiferromagnetismMetal-organic frameworkPhysical and Theoretical Chemistry
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Dicopper(II) pyrazolenophanes: Ligand effects on their structures and magnetic properties

2016

Abstract The use of simple pyrazolate anions and related polychelating acyclic or macrocyclic pyrazolate derivatives as bridging ligands, and occasionally additional blocking ligands, has led to the stereospecific Cu II -mediated self-assembly of both homo- and heteroleptic di-μ-pyrazolatodicopper(II) complexes of the metallacyclophane type, so-called dicopper(II) pyrazolenophanes. Besides their unique molecular conformation features and binding abilities toward both neutral molecules and charged anionic species, which have illustrated the putative role of weak intramolecular π–π stacking, hydrogen bonding, and coordinative interactions in the self-assembling process, dicopper(II) pyrazolen…

010405 organic chemistryHydrogen bondStereochemistryChemistryLigandStacking010402 general chemistry01 natural sciencesInductive couplingPlanarity testing0104 chemical sciencesInorganic ChemistryMetalvisual_artIntramolecular forceMaterials Chemistryvisual_art.visual_art_mediumMoleculePhysical and Theoretical ChemistryCoordination Chemistry Reviews
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Solution Conformation and Self‐Assembly of Ferrocenyl(thio)ureas

2016

Conformations and (dis)assembly processes of ureas and thioureas are of fundamental importance in supramolecular chemistry, anion binding, or crystal engineering, both in solution and in the solid state. For sensing and switching processes a redox-active unit, such as the ferrocene/ferrocenium couple, is especially suitable. Here, self-assembly processes of redox-active ferrocenyl(thio)ureas FcNHC(X)NHR [X = O, R = Fc (1), Ph (2), 1-naphthyl (3), Me (4), Et (5); X = S, R = Fc (6), 1-anthracenyl (7)] through hydrogen bonds – both in the solid state and in THF and CH2Cl2 solution – are reported. Special emphasis is placed on the impact of nonclassical intramolecular NH···Fe hydrogen bonds in …

010405 organic chemistryHydrogen bondStereochemistrySupramolecular chemistryThio-010402 general chemistryCrystal engineering01 natural sciencesRedox0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyFerrocenechemistryIntramolecular forceAnion bindingEuropean Journal of 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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Lewis Base Catalyzed Intramolecular Reduction of Salicylaldehydes by Pinacol-Derived Chlorohydrosilane

2018

010405 organic chemistryHydrosilylationPinacolOrganic ChemistryHomogeneous catalysis010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisReduction (complexity)chemistry.chemical_compoundchemistryIntramolecular forceLewis acids and basesPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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