Search results for "Conformational isomerism"

showing 10 items of 163 documents

Ambident PCN Heterocycles: N- and P-Phosphanylation of Lithium 1,3-Benzazaphospholides

2009

Synthetic and structural aspects of the phosphanylation of 1,3-benzazaphospholides 1(Li), ambident benzofused azaphosphacyclopentadienides, are presented. The unusual properties of phospholyl-1,3,2-diazaphospholes inspired us to study the coupling of 1(Li) with chlorodiazaphospholene 2, which led to the N-substituted product 3. Reaction of 1(Li) with chlorodiphenyl- and chlorodicyclohexylphosphane likewise gave N-phosphanylbenzazaphospholes 4 and 5, whereas with the more bulky di-tert-butyl- and di-1-adamantylchlorophosphanes, the diphosphanes 6 and 7 are obtained; in the case of 7 they are isolated as a dimeric LiCl(THF) adduct. Structural information was provided by single-crystal X-ray d…

Models MolecularSteric effectsMagnetic Resonance SpectroscopyChemistryStereochemistryOrganic Chemistrychemistry.chemical_elementStereoisomerismGeneral ChemistryNuclear magnetic resonance spectroscopyLithiumCrystallography X-RayRing (chemistry)Quantum chemistryCatalysisAdductCrystallographyOrganophosphorus CompoundsHeterocyclic CompoundsThermodynamicsLithiumConformational isomerismTwo-dimensional nuclear magnetic resonance spectroscopyChemistry - A European Journal
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Multiple Decay Mechanisms and 2D-UV Spectroscopic Fingerprints of Singlet Excited Solvated Adenine-Uracil Monophosphate

2016

The decay channels of singlet excited adenine uracil monophosphate (ApU) in water are studied with CASPT2//CASSCF:MM potential energy calculations and simulation of the 2D-UV spectroscopic fingerprints with the aim of elucidating the role of the different electronic states of the stacked conformer in the excited state dynamics. The adenine 1La state can decay without a barrier to a conical intersection with the ground state. In contrast, the adenine 1Lb and uracil S(U) states have minima that are separated from the intersections by sizeable barriers. Depending on the backbone conformation, the CT state can undergo inter-base hydrogen transfer and decay to the ground state through a conical …

Models Molecularmolecular electronicsChemistry MultidisciplinaryMolecular electronicsphotophysic2-DIMENSIONAL ELECTRONIC SPECTROSCOPYSTATE DYNAMICSBASE-STACKINGPhotochemistry01 natural sciences[CHIM] Chemical SciencesNUCLEIC-ACIDSQuímica quànticaEspectrofotometriaConformational isomerismComputingMilieux_MISCELLANEOUSphotophysics010304 chemical physicsFull PaperHydrogen bondChemistryChemistry (all)Full PapersMolecular spectroscopy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryChemistryFOURIER-TRANSFORM SPECTROSCOPYSpectrophotometryExcited statePhysical Sciences1ST-PRINCIPLES SIMULATION03 Chemical SciencesGround stateUridine MonophosphateQuantum chemistryEspectroscòpia molecularmolecular electronic010402 general chemistryMolecular physicsCatalysisUltraviolet visible spectroscopy0103 physical sciencesPhotophysics | Hot Paper[CHIM]Chemical SciencesSinglet stateUV/Vis spectroscopyULTRAFAST INTERNAL-CONVERSIONSpectroscopyLIGHT-HARVESTING COMPLEXab initio calculationScience & Technologyab initio calculationsOrganic ChemistryGeneral ChemistryDNAConical intersectionDNA FingerprintingAdenosine Monophosphate0104 chemical sciences[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryAB-INITIO SIMULATIONSElectrònica molecularMOLECULAR-DYNAMICSSpectrophotometry Ultraviolet
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United Atom Force Field for Molecular Dynamics Simulations of 1,4-Polybutadiene Based on Quantum Chemistry Calculations on Model Molecules

1998

We present a united atom force field for simulations of 1,4-polybutadiene based on ab initio quantum chemistry calculations on model molecules. The geometries and energies of conformers and rotational energy barriers in model alkenes and dienes have been determined from high-level quantum chemistry calculations. A rotational isomeric state (RIS) model for 1,4-polybutadiene based on the conformer geometries and energies of the model molecules has been derived. The characteristic ratio and its temperature dependence for cis-1,4-polybutadiene and trans-1,4-polybutadiene, and the characteristic ratio of a random copolymer of cis and trans units, as predicted by the RIS model, are in good agreem…

Molecular dynamicsChemistryPhysics::Atomic and Molecular ClustersAb initioMoleculePhysical and Theoretical ChemistryAtomic physicsQuantum chemistryConformational isomerismCis–trans isomerismForce field (chemistry)Rotational energyThe Journal of Physical Chemistry A
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Pressure induced changes in the Raman spectra of liquidn-alkanes and perfluoro-n-alkanes

1982

The main effect of pressures up to 6 kbar on the Raman spectra of liquidn-alkanes and perfluoro-n-alkanes is a reduction of line widths indicative for a slowing-down of rotational motions about the long axes. There is no evidence for a change in the conformer populations.

N alkanessymbols.namesakeColloid and Surface ChemistryPolymers and PlasticsChemistryMaterials ChemistryAnalytical chemistrysymbolsPhysical and Theoretical ChemistryRaman spectroscopyConformational isomerismLine (formation)Colloid and Polymer Science
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Structure Determination of Photoproducts of Anthracenes with (Arylmethoxymethyl) Sidechains

2007

Irradiation of 9-(arylmethoxymethyl)anthracenes 3 leads either to a cyclomer and cyclodimer mixture (3a  4a,5a), to selectively formed dimers (3b  5b), or a selectively formed cyclomer (3c  4c). The [4π+4π]cyclodimerization is under the conditions used a regioselective head-to-tail process. In the crystals of the dimers 5a,b, the sidechains are attached in an antiperiplanar position related to the CC bonds generated in the dimerization. In solutions, however, the structures consist of three rotamers the equilibration of which was studied by temperature-dependent NMR spectra. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

NMR spectra databaseCrystallographyChemistryStereochemistryOrganic ChemistryAlkane stereochemistryRegioselectivityPhysical and Theoretical ChemistryConformational isomerismEuropean Journal of Organic Chemistry
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Experimental and theoretical studies into the structural perturbations between neutral, oxidised and reduced forms of 1,4-dithiinoquinoxaline derivat…

2000

The syntheses and electrochemistry of thieno[3',4'r5,6][1,4]dithiino[2,3-b]quinoxaline (9), 2,3-bis(methylsulfanyl)[1,4]dithiino[2,3-b]quinoxaline (16) and 2,3-ethylenedisulfanyl[1,4]dithiino[2,3-b]quinoxaline (17) are reported, together with the X-ray crystal structures of 9, 16 and the charge-transfer complex 9.TCNQ. In the thieno derivative 9, the molecular structure undergoes a significant change from a boat conformer to a planar system, upon oxidation with TCNQ. Theoretical calculations show that oxidation leads to planarisation of the molecular structure due to the aromatisation of the dithiine moiety. The study of the oxidised/reduced species helps to rationalise the electrochemical …

NitrileChemistryStereochemistryGeneral ChemistryCrystal structureCharge-transfer complexElectrochemistrychemistry.chemical_compoundCrystallographyQuinoxalineMaterials ChemistryMoietyMoleculeConformational isomerismJournal of Materials Chemistry
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The Right Answer for the Right Electrostatics: Force Field Methods Are Able to Describe Relative Energies of DNA Guanine Quadruplexes

2014

Different force fields and approximate density functional theory were applied in order to study the rotamer space of the telomeric G-quadruplex DNA. While some force fields show an erratic behavior when it comes to the reproduction of the higher-order DNA conformer space, OPLS and MMFF implementations are able to reproduce the experimentally known energy order. The stabilizing effect of the AA (anti−anti) versus SA (syn−anti) conformer is analyzed applying mechanical bond strength descriptors (compliance constants). The fact that we observe the correct energy order using appropriate force fields is in contrast with results previously reported, which suggested the general inappropriateness o…

OPLSMechanical bondChemistrycomputer.software_genreElectrostaticsForce field (chemistry)Computer Science Applicationschemistry.chemical_compoundClassical mechanicsSettore CHIM/03 - Chimica Generale E InorganicaDFT calculations Molecular mechanics calculations G-quadruplex DNADensity functional theoryData miningPhysical and Theoretical ChemistryGuanine-QuadruplexescomputerConformational isomerismDNAJournal of Chemical Theory and Computation
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Tetramethyl-Bis(ethylenedithio)-Tetrathiafulvalene (TM-BEDT-TTF) Revisited: Crystal Structures, Chiroptical Properties, Theoretical Calculations, and…

2013

The (S,S,S,S) and (R,R,R,R) enantiomers of tetramethyl-bis(ethylenedithio)-tetrathiafulvalene (TM-BEDT-TTF) show equatorial conformation for the four methyl groups in the solid state, according to the single-crystal X-ray analyses. Theoretical calculations at the Density Functional Theory (DFT) and time-dependent (TD) DFT levels indicate higher gas phase stability for the axial conformer than the equatorial one by 1.25kcal center dot mole-1 and allow the assignment of the UV-vis and circular dichroism transitions. A complete series of radical cation salts of 1:1 stoichiometry with the triiodide anion I3- was obtained by electrocrystallization of both enantiopure and racemic forms of the don…

Pharmacology010405 organic chemistryOrganic ChemistryCrystal structure010402 general chemistry01 natural sciencesCatalysis3. Good health0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundCrystallographyEnantiopure drugchemistryRadical ionComputational chemistryDrug DiscoveryDensity functional theoryTriiodideChirality (chemistry)Conformational isomerismSpectroscopyTetrathiafulvaleneChirality
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Conformational properties of the residues connected by ester and methylated amide bonds: theoretical and solid state conformational studies

2010

Peptides produced by bacteria and fungi often contain an ester bond in the main chain. Some of them have both an ester and methylated amide bond at the same residue. A broad spectrum of biological activities makes these depsipeptides potential drug precursors. To investigate the conformational properties of such modified residues, a systematic theoretical analysis was performed on N-acetyl-L-alanine N′-methylamide (Ac-Ala-NHMe) and the analogues with the ester bond on the C-terminus (Ac-Ala-OMe), N-terminus (Ac-[psi](COO)-Ala-NHMe) as well as the analogues methylated on the N-terminus (Ac-(Me)Ala-OMe) and C-terminus (Ac-[psi](COO)-Ala-NMe2). The ϕ, ψ potential energy surfaces and the confor…

PharmacologyDepsipeptidechemistry.chemical_classificationChloroformChemistryStereochemistryOrganic ChemistryPeptideGeneral MedicineBiochemistrySolventchemistry.chemical_compoundResidue (chemistry)Structural BiologyAmideDrug DiscoveryMolecular MedicinePeptide bondMolecular BiologyConformational isomerismJournal of Peptide Science
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The conformational properties of dehydrobutyrine and dehydrovaline: theoretical and solid-state conformational studies

2010

Dehydrobutyrine is the most naturally occurring dehydroamino acid. It is also the simplest dehydroamino acid having the geometrical isomers E/Z. To investigate its conformational properties, a theoretical analysis was performed on N-acetyl-α,β-dehydrobutyrine N′-methylamides, Ac-(E)-ΔAbu-NHMe and Ac-(Z)-ΔAbu-NHMe, as well as the dehydrovaline derivative Ac-ΔVal-NHMe. The ϕ, ψ potential energy surfaces and the localised conformers were calculated at the B3LYP/6-311 + + G(d,p) level of theory both in vacuo and with inclusion of the solvent (chloroform, water) effect (SCRF method). The X-ray crystal structures of Ac-(Z)-ΔAbu-NHMe and Ac-ΔVal-NHMe were determined at 85 and 100 K, respectively. …

Pharmacologychemistry.chemical_classificationAlanineDouble bondStereochemistryOrganic ChemistryPeptideGeneral MedicineCrystal structureBiochemistrychemistry.chemical_compoundCrystallographychemistryStructural BiologyDrug DiscoverySide chainMolecular MedicineMolecular BiologyConformational isomerismCis–trans isomerismDerivative (chemistry)Journal of Peptide Science
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