Search results for "Carbocation"

showing 10 items of 17 documents

Monoradicals and Diradicals of Dibenzofluoreno[3,2-b]fluorene Isomers: Mechanisms of Electronic Delocalization

2020

The preparation of a series of dibenzo- and tetrabenzo-fused fluoreno[3,2-b]fluorenes is disclosed, and the diradicaloid properties of these molecules are compared with those of a similar, previously reported series of anthracene-based diradicaloids. Insights on the diradical mode of delocalization tuning by constitutional isomerism of the external naphthalenes has been explored by means of the physical approach (dissection of the electronic properties in terms of electronic repulsion and transfer integral) of diradicals. This study has also been extended to the redox species of the two series of compounds and found that the radical cations have the same stabilization mode by delocalization…

AnthraceneDiradicalGeneral ChemistryFluoreneCarbocation010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundDelocalized electronColloid and Surface ChemistrychemistryComputational chemistryStructural isomerMoleculeCarbanionJournal of the American Chemical Society
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Silicon guided rearrangement of epoxydecalines to spirocyclic compounds. Synthesis of gleenol and axenol from carvone

2005

Abstract The synthesis of the spirocyclic sesquiterpenes (−)-gleenol and (−)-axenol in enantiomerically pure form has been achieved starting from R-(−)-carvone. The key step is the silicon guided acid-promoted rearrangement of a 9-trimethylsilyl-5,6-epoxy-noreudesmane prepared from 3-trimethylsilyldihydrocarvone in several steps involving Robinson annulation, enone deconjugation and epoxidation. Acid treatment of the epoxy-noreudesmane gave a norspiroaxane as the main product, which was used as intermediate for the synthesis of two naturally occurring sesquiterpenes gleenol and axenol.

CarvoneSiliconStereochemistryOrganic Chemistrychemistry.chemical_elementCarbocationBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryRobinson annulationOrganic chemistryAcid treatmentEnoneTetrahedron
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ChemInform Abstract: Methylium Ions with OPV Chains - New NIR Dyes.

2010

Carbinols, which contain three OPV chains, were generated in convergent syntheses. The extension of the conjugation leads to a bathochromic effect that shifts the absorption from the UV into the visible region. The carbinol series has a convergence limit of the absorption at λmax = 415 nm. The corresponding carbenium ions exhibit a stronger bathochromic shift with the increasing number of repeating units in each chain. Thus, NIR dyes were obtained which show a convergence limit at λmax = 879 nm. The charge distribution in the ground state of the carbocations is discussed on the basis of 13C NMR spectroscopic data.

ChemistryBathochromic shiftCharge densityGeneral MedicineCarbon-13 NMRCarbocationAbsorption (chemistry)Ground statePhotochemistryIonChemInform
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Aryl carbinols as nerve agent probes. Influence of the conjugation on the sensing properties

2012

Two new aryl carbinols (1 and 3) have been synthesised and characterised and their ability as OFF-ON probes for the chromogenic detection of the nerve agent simulant in acetonitrile has been tested. In addition compound 2 has been also studied. The carbinols suffered a phosphorylation reaction followed by an elimination process giving rise to the corresponding carbocations. This transformation of the carbinol into the carbocation is responsible for a significant color change. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.

ChemistryChromogenicChemical warfare agentArylQUIMICA INORGANICAGeneral ChemistryCarbocationPhotochemistryCombinatorial chemistryChemical reactionCatalysisElimination reactionchemistry.chemical_compoundQUIMICA ORGANICAMethanol derivativeMaterials ChemistrymedicineElimination reactionAcetonitrilePhosphorylationAcetonitrileChemical reactionMolecular probeNerve agentmedicine.drug
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Methylium Ions with OPV Chains − New NIR Dyes

2001

Carbinols, which contain three OPV chains, were generated in convergent syntheses. The extension of the conjugation leads to a bathochromic effect that shifts the absorption from the UV into the visible region. The carbinol series has a convergence limit of the absorption at λmax = 415 nm. The corresponding carbenium ions exhibit a stronger bathochromic shift with the increasing number of repeating units in each chain. Thus, NIR dyes were obtained which show a convergence limit at λmax = 879 nm. The charge distribution in the ground state of the carbocations is discussed on the basis of 13C NMR spectroscopic data.

ChemistryOrganic ChemistryBathochromic shiftAnalytical chemistryCharge densityPhysical and Theoretical ChemistryCarbon-13 NMRCarbocationAbsorption (chemistry)PhotochemistryGround stateIonEuropean Journal of Organic Chemistry
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Rearrangement of 4,5-epoxy-9-trimethylsilyldecalines. Application to the synthesis of the natural eremophilane (-)-aristolochene.

2006

Several 4,5-epoxy-9-trimethylsilyl-eudesmanes and 15-nor-eudesmanes, having different relative stereochemistry and substitution at the oxirane ring, have been prepared starting from (-)-carvone and subjected to acid-promoted rearrangement. The presence of the silicon at C9 favors two different main reaction pathways involving C14-methyl or C1-methylene migration through the stabilization of a C10 carbocation intermediate. Selective 1,2-migration of the bridgehead methyl group takes place with trisubstituted beta-epoxide and tetrasubstituted alpha-epoxide, yielding 4-hydroxy-eremophilane and 15-nor-eremophilane compounds, while the trisubstituted alpha-epoxide suffers successive rearrangemen…

ChemistryStereochemistryMonoterpeneOrganic ChemistryMolecular ConformationEpoxideStereoisomerismCarbocationNaphthalenesRing (chemistry)SesquiterpeneChemical synthesischemistry.chemical_compoundOrganic chemistrySelectivityAristolocheneSesquiterpenesThe Journal of organic chemistry
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MINDO/3 Study of the Rearrangement of 1-Methylcyclohexyl Cation to 1,2-Dimethylcyclopentyl Cation

1986

The rearrangement of the 1-methylcyclohexyl cation to the 1,2-dimethylcyclopentyl cation has been studied by MINDO/3 calculations, as an application of the branching mechanism model for cycloalkanes. Possible intermediates and transition states have been characterized by diagonalization of their Hessian matrixes. Two nonequivalent pathways, α and β scissions, are relatively close in energy. The calculated transition states are almost equivalent in energy to those found for cyclohexyl cation. Hence, the energy barriers are higher for the rearrangement of the 1-methyl than for cyclohexyl cation, because the former is less stable than the latter.

Computational MathematicsAcid catalysisCycloalkanechemistry.chemical_compoundchemistryComputational chemistryGeneral ChemistryReaction intermediateCarbocationBranching (polymer chemistry)IsomerizationMINDOTransition stateJournal of Computational Chemistry
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Supercritical Carbon Dioxide: A Promoter of Carbon-Halogen Bond Heterolysis

2013

as the leaving groupdeparts from the carbon atom prior to the entrance of thenucleophile. Polar protic solvents with high dielectric con-stants promote polar bond heterolysis by providing effectiveH-bonding and electron-pair donation interactions to theleaving group and the incipient carbocation, respectively.Then, the solvent captures the carbocation intermediate togive the corresponding S

Halogen bondSupercritical carbon dioxideChemistrychemistry.chemical_elementGeneral ChemistryGeneral MedicineCarbocationPhotochemistryHeterolysisCatalysisSupercritical fluidSolventSolvent effectsCarbonAngewandte Chemie
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Synthesis of Sesquiterpenes via silicon-guided rearrangement of epoxydecalins

2008

A survey of the rearrangement of methyldecalins via C-5 carbocation intermediates, with special attention to the silicon-guided rearrangement of epoxydecalins is provided. A TMS group properly positioned on either C-1 or C-9 promotes the acidic rearrangement of 10-methyl-4,5-epoxydecalins and 10-methyl-5,6-epoxydecalins with exclusive migration toward C-5 of the methyl or methylene groups linked directly to C-10. The application of this biomimetic approach to the synthesis of a number of spirocyclic and eremophilane sesquiterpenes is reported.

PharmacologyComplementary and alternative medicineSiliconchemistryGroup (periodic table)StereochemistryDrug Discoverychemistry.chemical_elementPlant ScienceGeneral MedicineCarbocation
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ChemInform Abstract: Synthesis of Sesquiterpenes via Silicon-Guided Rearrangement of Epoxydecalins

2009

A survey of the rearrangement of methyldecalins via C-5 carbocation intermediates, with special attention to the silicon-guided rearrangement of epoxydecalins is provided. A TMS group properly posi...

TerpeneSiliconChemistryStereochemistryGroup (periodic table)chemistry.chemical_elementGeneral MedicineCarbocationChemInform
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