Search results for "substituent effect"

showing 10 items of 20 documents

Synthesis and Structural Characterization of Substituted 2-Phenacylbenzoxazoles

2013

1 H and 13C NMR spectra of eleven 2-phenacylbenzoxazoles (ketimine form) show that their CDCl3-solutions contains also (Z)-2-(benzo[d]oxazol-2-yl)-1-phenylethenols (enolimine form). Intramolecular hydrogen bonding in the latter tautomer was found to be significantly weaker than that one in respective (Z)-2-(2-hydroxy-2-phenylvinyl)pyridines. Integrals of the 1 H NMR signals were used to evaluate the molar ratio of the tautomers. Strong electron-donating substituents were found to stabilize the ketimine tautomer. pKT (negative logarithm of the equilibrium constant, KT = [ketimine]/[enolimine]) was found to be linearly dependent on the Hammett substituent constant σ. The results of the MP2 ab…

Stereochemistry2-phenyacylbenzoxazoleSubstituent2-fenasyylibentsoksatsoli010402 general chemistry01 natural sciencesArticleCatalysisInorganic Chemistrylcsh:Chemistryresonance interactionchemistry.chemical_compoundAb initio quantum chemistry methods2-phenacylbenzoxazolePhysical and Theoretical Chemistryta116Molecular Biologylcsh:QH301-705.5SpectroscopyEquilibrium constanthydrogen bond010405 organic chemistryHydrogen bondOrganic Chemistryquantum-chemical calculationsGeneral MedicineCarbon-13 NMRTautomerNMR0104 chemical sciencesComputer Science ApplicationsCrystallographytautomerismchemistrylcsh:Biology (General)lcsh:QD1-999Intramolecular forceProton NMRsubstituent effect
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Dual Substituent Parameter Modeling of Theoretical, NMR and IR Spectral Data of 5-Substituted Indole-2,3-diones

2002

Correlations of AM1 and PM3 theoretical data, 13C-NMR substituent chemical shifts (13C-SCS) and IR carbonyl group wave numbers [ν(C3â•ÂO)] were studied using dual substituent parameter (DSP) models for 5-substituted indole-2,3-diones. For the C7 atom a reverse substituent effect attributed to extended À-polarization was observed. On the other hand, the DSP approaches for the C3 atom showed normal substituent effects with some contribution of reverse effect supported strongly by 13C-SCS correlations. In the ν(C3â•ÂO) and p(C3â•ÂO) DSP correlations the field effect contribution predominates over the resonance effect, which justifies the using of earlier suggested vibrational cou…

StereochemistrySubstituentPharmaceutical ScienceField effectArticleAnalytical Chemistry3-dioneslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistry5-Substituted indole-23-dionesDrug DiscoveryAtomAM1 and PM3 theoretical dataπ-polarizationWavenumberPhysical and Theoretical ChemistrySpectral dataIndole testreverse substituent effectChemistryChemical shiftOrganic ChemistryIR and NMR data DSP correlationsChemistry (miscellaneous)5-Substituted indole-2Molecular MedicinePhysical chemistryÀ-polarizationRotational–vibrational couplingMolecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
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13C-NMR Based Evaluation of the Electronic and Steric Interactions in Aromatic Amines

2005

Abstract: Chemical shifts of the para carbon atoms, δ(13C-4), in a series of aromatic amines were used to calculate the Ãp, ÃR and ÃOR substituent constants for different amino groups. 1-Pyrrolidino, N,N-di-n-butylamino and N,N-diethylamino groups were found to be the most strong electron-donors. ortho-Substitution decreases the donor properties of the amino group. The amino groups in 2,6-di-i-propylaniline and N,N-2,6-tetramethylaniline have very weak electron-donor properties. The nitrogen atom in benzoquinuclidine and N,N-dimethyl-2,6-di-i-propylaniline have an electron-acceptor character. The calculated substituent constants of the amino groups studied are consistent with the s…

Steric effectsAmino groups; substituent effects; steric inhibition to resonance; 13C- and 15N-NMR; aromatic aminesStereochemistryaromatic aminesSubstituentsteric inhibition to resonanceMedicinal chemistryCatalysisInorganic Chemistrylcsh:Chemistrychemistry.chemical_compoundGroup (periodic table)AtomElectronic effectReactivity (chemistry)Physical and Theoretical ChemistryMolecular Biologylcsh:QH301-705.5SpectroscopyAmino groupssubstituent effectsChemistryChemical shiftOrganic Chemistry13C- and 15N-NMRGeneral MedicineCarbon-13 NMRComputer Science Applicationslcsh:Biology (General)lcsh:QD1-999International Journal of Molecular Sciences
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Ethylene oligomerization with 2-hydroxymethyl-5,6,7-trihydroquinolinyl-8-ylideneamine-Ni(II) chlorides

2021

Abstract A series of Ni complexes of the general formula [2-(MeOH)-8-{N(Ar)}C9H8N]NiCl2, where Ar = 2,6-Me2C6H3 in Ni1; 2,6-Et2C6H3 in Ni2; 2,6-i-Pr2C6H3 in Ni3; 2,4,6-Me3C6H2 in Ni4; 2,6-Et2-4-MeC6H2 in Ni5 and 2,4,6-t-Bu3C6H2 in Ni6 has been synthesized and characterized by elemental analysis and IR spectroscopy. On activation with MMAO or Et2AlCl, these complexes showed high activity in ethylene oligomerization, reaching 2.23 × 106 g·mol–1 (Ni) h–1 at 30 °C with the Al/Ni ratio of 5500 and 9.11 × 105 g·mol–1 (Ni) h–1 with the Al/Ni of 800, respectively. Moreover, the content of α-C4 indicated high selectivity exceeding 99% in the Ni/Et2AlCl system. Comparing with the previous report by o…

Steric effectsEthyleneSubstituentInfrared spectroscopy010402 general chemistryCo-catalyst01 natural sciencesBiochemistryMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundSubstituent effectEthylene oligomerizationMaterials ChemistryHydroxymethylSelectivityPhysical and Theoretical ChemistryNickel complexes010405 organic chemistryChemistryLigandOrganic Chemistry0104 chemical sciencesActivityElemental analysisvisual_artvisual_art.visual_art_mediumJournal of Organometallic Chemistry
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On the relations between aromaticity and substituent effect

2019

Aromaticity/aromatic and substituent/substituent effects belong to the most commonly used terms in organic chemistry and related fields. The quantitative description of aromaticity is based on energetic, geometric (e.g., HOMA), magnetic (e.g., NICS) and reactivity criteria, as well as the properties of the electronic structure (e.g., FLU). The substituent effect can be described using either traditional Hammett-type substituent constants or characteristics based on quantum-chemistry. For this purpose, the energies of properly designed homodesmotic reactions and electron density distribution are used. In the first case, a descriptor named SESE (energy stabilizing the substituent effect) is o…

chemistry.chemical_classificationElectronic structure010405 organic chemistrySubstituentMolecular modelingAromaticityElectronic structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundSubstituent effectCharge of the substituent active regionchemistryComputational chemistryIntramolecular forceSubstituent effect stabilization energyReactivity (chemistry)Physical and Theoretical ChemistryBenzeneAromatic hydrocarbonStructural Chemistry
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Substituent effects of nitro group in cyclic compounds

2020

AbstractNumerous studies on nitro group properties are associated with its high electron-withdrawing ability, by means of both resonance and inductive effect. The substituent effect of the nitro group may be well described using either traditional substituent constants or characteristics based on quantum chemistry, i.e., cSAR, SESE, and pEDA/sEDA models. Interestingly, the cSAR descriptor allows to describe the electron-attracting properties of the nitro group regardless of the position and the type of system. Analysis of classical and reverse substituent effects of the nitro group in various systems indicates strong pi-electron interactions with electron-donating substituents due to the re…

education.field_of_study010405 organic chemistryPopulationSubstituentMolecular modeling010402 general chemistryCondensed Matter PhysicsRing (chemistry)Resonance (chemistry)01 natural sciencesMedicinal chemistryQuantum chemistry0104 chemical sciencesNitro groupchemistry.chemical_compoundDelocalized electronCharge of the substituent active regionchemistrySigma and pi electron structureSubstituent effectsNitroSubstituent effect stabilization energyPhysical and Theoretical ChemistryeducationInductive effectStructural Chemistry
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Non-covalent interactions of N-phenyl-1,5-dimethyl-1H-imidazole-4-carboxamide 3-oxide derivatives—a case of intramolecular N-oxide hydrogen bonds

2017

The crystal structures of new N-phenyl-1,5-dimethyl-1H-imidazole-4-carboxamide 3-oxide derivatives are reported. The results of X-ray diffraction showed the existence of intramolecular hydrogen bonding between carboxamide nitrogen donors and N-oxide oxygen acceptors. The use of Quantum Theory of Atoms in Molecules allowed its classification as a strong interaction, with energy about 10 kcal/mol, and of intermediate character between closed shell and shared bonds. Comparison of experimental data and quantum theoretical calculations indicated that a substituent attached to the phenyl ring in the para position influences the strength and geometry of the title hydrogen bonding. Stronger π-elect…

medicine.drug_classLow-barrier hydrogen bondintramolecular hydrogen bondSubstituentCarboxamideN-oxide group010402 general chemistry01 natural scienceschemistry.chemical_compoundComputational chemistrymedicineNon-covalent interactionsHirshfeld surface analysisPhysical and Theoretical Chemistrychemistry.chemical_classification010405 organic chemistryHydrogen bondIntermolecular forceAtoms in moleculesCondensed Matter Physicshydrogen bonding0104 chemical sciencesCrystallographychemistryQTAIMIntramolecular forcesubstituent effectStructural Chemistry
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Chemoselective, Substrate-directed Fluorination of Functionalized Cyclopentane β-Amino Acids

2016

This work describes a substrate-directed fluorination of some highly functionalized cyclopentane derivatives. The cyclic products incorporating CH2 F or CHF2 moieties in their structure have been synthesized from diexo- or diendo-norbornene β-amino acids following a stereocontrolled strategy. The synthetic study was based on an oxidative transformation of the ring carbon-carbon double bond of the norbornene β-amino acids, followed by transformation of the resulted "all cis" and "trans" diformyl intermediates by fluorination with "chemodifferentiation".

molecular diversitycyclizationDouble bondHalogenationHydrocarbons FluorinatedStereochemistryMolecular Conformationchemistry.chemical_elementCyclopentanes010402 general chemistryRing (chemistry)Crystallography X-Ray01 natural sciencesBiochemistrychemistry.chemical_compoundfluorineCyclopentaneta116Norbornenechemistry.chemical_classificationamino acidssubstituent effects010405 organic chemistryOrganic ChemistrySubstrate (chemistry)StereoisomerismGeneral Chemistry0104 chemical sciencesAmino acidchemistryFluorineOxidation-ReductionChemistry: An Asian Journal
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Studies in organic mass spectrometry. Part 23. Role of the aroyl group on the competitive fragmentation reactions of the molecular ion of aroylanilid…

1999

The 70 eV and mass-analysed ion kinetic energy (MIKE) spectra of some thiophenecarboxanilides and benzoylanilides (1–10) have been compared in order to investigate the role of the aroyl (or heteroaroyl) moiety on the abundance of the competitive fragmentation reactions occurring in their molecular ions (amide–bond cleavage and phenol radical ion formation). It has been shown that the electron ionisation induced decompositions with high (70 eV) and low (MIKE) internal energy excess are qualitatively similar, but remarkable quantitative differences have been observed that can be accounted for in terms of the different effectiveness in the transmission of electronic effects of substituents in …

substituent effectsChemistryrearrangement processesPolyatomic ionAnalytical chemistryaroylanilidesMass spectrometryPhotochemistryelectron ionisation; positive ions; ion chemistry; aroylanilides; substituent effects; rearrangement processesIonchemistry.chemical_compoundRadical ionFragmentation (mass spectrometry)positive ionsThiopheneElectronic effectMoietyion chemistryelectron ionisationSpectroscopy
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Classical and reverse substituent effects in meta- and para-substituted nitrobenzene derivatives

2017

Electron-accepting properties of the nitro group were studied in a series of meta- and para-X-substituted nitrobenzene derivatives (X = NMe2, NH2, OH, OMe, CH3, H, F, Cl, CF3, CN, CHO, COMe, CONH2, COOH, COCl, NO2, NO). For this purpose Hammett-like approaches were applied based on quantum chemistry modeling; the B3LYP/6-311++ G(d,p) method was used. The substituent effect (SE) was characterized by the mutually interrelated descriptors: the charge of the substituent active region, cSAR(X), and substituent effect stabilization energy, SESE, as well as substituent constants, σ. Classical SE is realized by dependences of the structural parameters of the nitro group (ONO angle and NO bond lengt…

substituent effectsMolecular modelmolecular modeling010405 organic chemistryDinitrobenzeneStereochemistrySubstituentelectronic structure010402 general chemistryCondensed Matter Physics01 natural sciencesQuantum chemistry0104 chemical sciencesNitroanilineBond lengthNitrobenzenechemistry.chemical_compoundchemistrysubstituent effect stabilization energyNitroPhysical and Theoretical Chemistrycharge of the substituent active regionStructural Chemistry
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