Search results for "ATOMS"

showing 10 items of 208 documents

A Combined Experimental and Theoretical Charge Density Study of the Chemical Bonding and Magnetism in 3-Amino-propanolato Cu(II) Complexes Containing…

2008

The experimental (100 K) and theoretical charge densities in the binuclear complexes [Cu2(ap)2(L)2] (ap = 3-aminopropanolate) 1 (L = nitrite), 2 (L = nitrate), and 3 (L = formate) have been examined. These complexes contain the same centrosymmetric alkoxy-bridged motif, where each strongly Jahn-Teller distorted Cu(II) ion is ligated to three O atoms and one N atom in a square-planar arrangement. This primary coordination sphere is augmented by a long contact with the O atom of a pendant L anion from an adjacent molecule in the crystal lattice. Topological analyses of the experimental and theoretical densities according to the quantum theory of atoms in molecules (QTAIM) are in excellent agr…

Delocalized electronCrystallographyCoordination sphereChemical bondChemistryComputational chemistryAtoms in moleculesCharge densityMoleculeCrystal structurePhysical and Theoretical ChemistryIonThe Journal of Physical Chemistry A
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Synthesis, structure and in vitro anticancer activity of Pd(II) complexes of mono- and bis-pyrazolyl-s-triazine ligands

2020

Abstract The square planar complexes [Pd(MPT)Cl2] (1) and [Pd(BPT)Cl]ClO4 (2) were synthesized by the reaction of the 4,4′-(6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine-2,4-diyl)dimorpholine (MPT) and N-methyl-N-phenyl-4,6-di(1H-pyrazol-1-yl)-1,3,5-triazin-2-amine (BPT) ligands with PdCl2 (1:1) in acetone under thermal conditions, respectively. In complex 1, the Pd(II) ion is coordinated with the MPT ligand as a bidentate NN-chelate, augmented with two chloride ligands in cis positions. In complex 2, the Pd(II) ion is coordinated with the BPT ligand as a tridentate N-chelate in a pincer fashion, together with one chloride ligand. Hirshfeld analysis indicated that complex 1 is packed with…

Denticity010405 organic chemistryChemistryHydrogen bondLigandAtoms in moleculesStacking010402 general chemistry01 natural sciencesMedicinal chemistryChloride0104 chemical sciencesPincer movementInorganic Chemistrychemistry.chemical_compoundMaterials ChemistrymedicinePhysical and Theoretical Chemistrymedicine.drugTriazinePolyhedron
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Molecular and supramolecular structures of self-assembled Cu(II) and Co(II) complexes with 4,4’-[6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine-2,4-…

2020

Abstract The molecular and supramolecular structures of [Cu(PTM)Cl2]∗0.75MeOH (1), [Co(PTM)Cl2]; (2A) and [Co(PTM)Cl2(EtOH)]; (2B) complexes, where PTM is 4,4’-[6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazine-2,4-diyl]dimorpholine, were presented. In complexes 1 and 2A, the Cu(II) and Co(II) are tetra-coordinated with a distorted tetrahedral coordination environment. In case of complex 2B, an additional ethanol molecule is found coordinated with Co(II) leading to a highly distorted penta-coordinated Co(II) complex. In all cases, the PTM ligand is acting as a bidentate NN-chelate. Hirshfeld surface analysis indicated the importance of H⋯H (49.0–55.1%), Cl⋯H (18.8–20.5%) and O⋯H (8.3–9.9%) co…

Denticity010405 organic chemistryLigandChemistryOrganic ChemistryAtoms in moleculesSupramolecular chemistry010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystallographyCovalent bondMoleculeOpen shellSpectroscopyNatural bond orbitalJournal of Molecular Structure
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[1,2,3]Triazolo[1,5-a]pyridines. A theoretical (DFT) study of the ring-chain isomerization

2008

The ring opening isomerization of [1,2,3]triazolo[1,5-a]pyridines to the corresponding 2-pyridyl derivatives has been studied by means of DFT calculations at the B3LYP/6-31+G(d,p) computational level. The effect of the substitution as well as those of protonation, deprotonation, and lithiation on different positions has been studied. The electronic characteristics of the optimized structures have been analyzed by means of the Atoms In Molecules (AIM), Electron Localization Function (ELF), Molecular Electrostatic Potential (MEP), and Natural Bond Orbital (NBO) methodologies. © 2008 Elsevier Ltd. All rights reserved.

DeprotonationComputational chemistryChemistryOrganic ChemistryDrug DiscoveryAtoms in moleculesTriazolopyridineProtonationRing (chemistry)BiochemistryIsomerizationElectron localization functionNatural bond orbital
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Biofabrication of biosilica-glass by living organisms

2008

Biosilicification is an evolutionarily old and widespread type of biomineralization both in unicellular and multicellular organisms, including sponges, diatoms, radiolarians, choanoflagellates, and higher plants. In the last few years combined efforts in molecular biology, cell biology, and inorganic and analytical chemistry have allowed the first insight into the molecular mechanisms by which these organisms form an astonishing variety of siliceous structures that cannot be achieved by chemical methods. Here we report about the present stage of knowledge on structure, biochemical composition, and mechanisms of biosilica formation, focusing our attention particularly on sponges because of t…

DiatomsModels MolecularSequence Homology Amino AcidProtein ConformationMolecular Sequence DataOrganic ChemistryBiologySilicon DioxideCathepsinsBiochemistryPoriferaMulticellular organismSequence homologyEvolutionary biologyDrug DiscoveryBiochemical compositionAnimalsGlassBiomineralizationBiofabricationNatural Product Reports
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The importance of a highly active and DeltapH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cyc…

2005

The present study focuses on the regulation of diatoxanthin (Dtx) epoxidation in the diadinoxanthin (Ddx) cycle containing algae Phaeodactylum tricornutum, Thalassiosira pseudonana, Cyclotella meneghiniana and Prymnesium parvum and its significance for the control of the photosystem II (PS II) antenna function. Our data show that Dtx epoxidase can exhibit extremely high activities when algal cells are transferred from high light (HL) to low light (LL). Under HL conditions, Dtx epoxidation is strongly inhibited by the light-driven proton gradient. Uncoupling of the cells during HL illumination restores the high epoxidation rates observed during LL. In Ddx cycle containing algae, non-photoche…

DiatomsPhotosystem IIbiologyLightPhysiologyZeaxanthin epoxidaseAlgal ProteinsDiadinoxanthinDiatoxanthinEukaryotaPhotosystem II Protein ComplexPlant ScienceHydrogen-Ion ConcentrationXanthophyllsPhotochemistrychemistry.chemical_compoundchemistryPhotoprotectionbiology.proteinElectrochemical gradientChlorella vulgarisOxidoreductasesAgronomy and Crop ScienceChlorophyll fluorescenceViolaxanthinJournal of plant physiology
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Innovative and Applied Research in Biology: Proceedings

2022

The collection contains SCIENTIFIC articles on the topics of the LU 80 conference reports. The main focus is on innovative and applied research in biology and interdisciplinary fields.

DiatomsRed beetroot juiceLow frequency electromagnetic radiationEU habitatsRare and threatened speciesArtificial lightCloudberry:NATURAL SCIENCES::Biology [Research Subject Categories]Pest controlYellow sticky trapsSpecially protected whorl snails (Vertigo spp.)Aquatic pollutionPoint mutationsBioindicatorsGlutathione peroxidaseGreenhouse whitefliesDuckweed Lemna minorThe Daugava RiverPro/antioxidative actionChlorophyll fluorescenceNature protectionSpecific Pollution Sensitivity Index (IPS)
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QTAIM View of Metal-Metal Bonding in Di- and Trinuclear Disulfido Carbonyl Clusters

2012

The experimental and theoretical charge densities in the sulfido-bridged cluster compounds Fe2(μ-S2)(CO)6 (1), Fe3(μ3-S)2(CO)9 (2), Mn2(μ-S2)(μ-CO)(CO)6 (3), and Fe2(μ-S2)(CO)5(PPh3) (4) have been studied using the quantum theory of atoms in molecules (QTAIM) methodology. High-resolution X-ray diffraction data have been measured for compounds 2–4 at 100 K. The topological analyses show that only in compounds 1 and 4 is there any evidence for metal–metal bonding in terms of the presence of a bond path. For compound 1, the topology of the Fe2S2 cage is highly dependent on the Fe–Fe separation, and the deformation along this vector is an extremely soft mode. The experimentally observed topolog…

DiffractionChemistryOrganic ChemistryAtoms in moleculesCharge (physics)Soft modesDecompositionInorganic ChemistryCrystallographyDelocalized electronComputational chemistryCluster (physics)Physical and Theoretical Chemistryta116Topology (chemistry)Organometallics
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Revisiting the charge density analysis of 2,5-dichloro-1,4-benzoquinone at 20 K

2017

A high-resolution X-ray diffraction measurement of 2,5-dichloro-1,4-benzoquinone (DCBQ) at 20 K was carried out. The experimental charge density was modeled using the Hansen–Coppens multipolar expansion and the topology of the electron density was analyzed in terms of the quantum theory of atoms in molecules (QTAIM). Two different multipole models, predominantly differentiated by the treatment of the chlorine atom, were obtained. The experimental results have been compared to theoretical results in the form of a multipolar refinement against theoretical structure factors and through direct topological analysis of the electron density obtained from the optimized periodic wavefunction. The si…

DiffractionElectron density202 engineering and technology010402 general chemistry01 natural sciencesMolecular physics14-Benzoquinonechemistry.chemical_compound5-di­chloro-1Materials Chemistryelectron densityWave functionIntermolecular forceAtoms in moleculesMetals and AlloysCharge density021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsQTAIMchemistry4-benzo­quinonemultipole models0210 nano-technologyMultipole expansionActa Crystallographica Section B Structural Science, Crystal Engineering and Materials
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Magic numbers, excitation levels, and other properties of small neutral math clusters (N < 50)

2006

The ground-state energies and the radial and pair distribution functions of neutral math clusters are systematically calculated by the diffusion Monte Carlo method in steps of one math atom from 3 to 50 atoms. In addition the chemical potential and the low-lying excitation levels of each cluster are determined with high precision. These calculations reveal that the “magic numbers” observed in experimental math cluster size distributions, measured for free jet gas expansions by nondestructive matter-wave diffraction, are not caused by enhanced stabilities. Instead they are explained in terms of an enhanced growth due to sharp peaks in the equilibrium concentrations in the early part of the e…

DiffusionHelium neutral atoms ; Atomic clusters ; Ground states ; Excited states ; Chemical potential ; Diffusion ; Monte Carlo methods ; Molecular configurationsHelium neutral atomsAtomic clustersExcited statesMonte Carlo methods:FÍSICA::Química física [UNESCO]Chemical potentialMolecular configurationsGround statesUNESCO::FÍSICA::Química física
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