Search results for "kemialliset sidokset"

showing 10 items of 71 documents

Theoretical and experimental studies of some main group compounds : from closed shell interactions to singlet diradicals and stable radicals

2012

Acquiring knowledge of different interactions within and between molecules is a fascinating undertaking as it not only deepens our understanding of chemical bonding but also offers insight into electronic structures, molecular properties and the connections between these two. This dissertation combines together three main group chemistry related topics within the aforementioned theme. Research presented in the first third of this dissertation describes wave function and density functional theory studies of weak inter- and intramolecular interactions in pnictogen-based dimers X3Pn···PnX3 (Pn = N-Bi; X = F-I), dithallenes RTlTlR (R = H, Me, tBu, Ph) and octachalcogen dications Ch82+ (Ch = S, …

atomitkemialliset sidoksetstable radicalssynthesisintermolecular interactionskemiatheoretical and computational chemistrysinglet diradical characterintramolecular interactionsmolekyylitsynteesimain group chemistryclosed shell interactions
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Definition of the chalcogen bond (IUPAC Recommendations 2019)

2019

Abstract This recommendation proposes a definition for the term “chalcogen bond”; it is recommended the term is used to designate the specific subset of inter- and intramolecular interactions formed by chalcogen atoms wherein the Group 16 element is the electrophilic site.

chalcogen bond; IUPAC Organic and Biomolecular Chemistry Division; IUPAC Physical and Biophysical Chemistry Division; nomenclature; noncovalent interactions; self-assembly; supramolecular chemistryGeneral Chemical EngineeringChemical nomenclature010402 general chemistrynoncovalent interaction01 natural sciencessupramolecular chemistrykemialliset sidoksetnoncovalent interactionsChalcogenGroup (periodic table)supramolekulaarinen kemiaNon-covalent interactionsIUPAC Organic and Biomolecular Chemistry DivisionIUPAC Physical and Biophysical Chemistry Divisionchalcogen bondchemistry.chemical_classification010405 organic chemistryChemistryBondSolid State & Structural Chemistry Unitself-assemblyGeneral Chemistry0104 chemical sciencesTerm (time)ChemistryCrystallographyIntramolecular forcenimikkeistötnomenclaturePure and Applied Chemistry
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Studies of Nature of Uncommon Bifurcated I–I···(I–M) Metal-Involving Noncovalent Interaction in Palladium(II) and Platinum(II) Isocyanide Cocrystals

2021

Two isostructural trans-[MI2(CNXyl)2]·I2 (M = Pd or Pt; CNXyl = 2,6-dimethylphenyl isocyanide) metallopolymeric cocrystals containing uncommon bifurcated iodine···(metal–iodide) contact were obtained. In addition to classical halogen bonding, single-crystal X-ray diffraction analysis revealed a rare type of metal-involved stabilizing contact in both cocrystals. The nature of the noncovalent contact was studied computationally (via DFT, electrostatic surface potential, electron localization function, quantum theory of atoms in molecules, and noncovalent interactions plot methods). Studies confirmed that the I···I halogen bond is the strongest noncovalent interaction in the systems, followed …

chemistry.chemical_classificationplatinaHalogen bondhalogeenit010405 organic chemistryChemistryIsocyanideAtoms in moleculeskompleksiyhdisteet010402 general chemistrypalladium01 natural sciencesCocrystalElectron localization function0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographykemialliset sidoksetNucleophileNon-covalent interactionsPhysical and Theoretical ChemistryIsostructuralmetallit
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Uranium( iv ) cyclobutadienyl sandwich compounds: synthesis, structure and chemical bonding

2019

The 1 : 1 reactions of uranium(IV) tetrakis(borohydride) with the sodium and potassium salts of the cyclobutadienyl anion [C4(SiMe3)4]2− (Cb′′′′) produce the half-sandwich complexes [Na(12-crown-4)2][U(η4-Cb′′′′)(BH4)3] and [U(η4-Cb′′′′)(μ-BH4)3{K(THF)2}]2. In the 1 : 2 reaction of U(BH4)4 with Na2Cb′′′′, formation of [U(η4-Cb′′′′)(η3-C4H(SiMe3)3-κ-(CH2SiMe2)(BH4))]− reveals that a Cb′′′′ ligand undergoes an intramolecular deprotonation, resulting in an allyl/tuck-in bonding mode. A computational study reveals that the uranium–Cb′′′′ bonding has an appreciable covalent component with contributions from the uranium 5f and 6d orbitals. peerReviewed

chemistry.chemical_element010402 general chemistryBorohydride01 natural sciencesMedicinal chemistryCatalysisIonkemialliset sidoksetchemistry.chemical_compoundDeprotonationMaterials Chemistrykemiallinen synteesi010405 organic chemistryLigandChemistryMetals and AlloyskompleksiyhdisteetGeneral ChemistryUranium3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsuraaniChemical bondCovalent bondIntramolecular forceCeramics and CompositesChemical Communications
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Single crystal X-ray structural dataset of 1,2,4-dithiazolium tetrafluoroborate

2022

Herein, we present the crystallographic dataset of 1,2,4-dithiazolium tetrafluoroborate. Single crystal X-ray structural analysis evidences that the 1,2,4-dithiazolium ring is almost planar. The 1,2,4-dithiazolium and tetrafluoroborate ions contribute in hydrogen bonding wherein the N-H·N hydrogen bonding in 1,2,4-dithiazolium dimer forms an eight-membered pseudo ring with the R22(8) Etter's graph set. The information provided in this data contributes to the understanding of structural chemistry and hydrogen bonding interactions in dithiazole derivatives.

crystal structurehydrogen bondkemialliset sidoksetMultidisciplinaryvetysidoksetdata124-Dithiazoliumheterosykliset yhdisteetheterocycle
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Photoactive Yellow Protein Chromophore Photoisomerizes around a Single Bond if the Double Bond Is Locked

2020

Photoactivation in the Photoactive Yellow Protein, a bacterial blue light photoreceptor, proceeds via photo-isomerization of the double C=C bond in the covalently attached chromophore. Quantum chemistry calculations, however, have suggested that in addition to double bond photo-isomerization, the isolated chromophore and many of its analogues, can isomerize around a single C-C bond as well. Whereas double bond photo-isomerization has been observed with x-ray crystallography, experimental evidence for single bond photo-isomerization is currently lacking. Therefore, we have synthesized a chromophore analogue, in which the formal double bond is covalently locked in a cyclopentenone ring and ca…

double bond0301 basic medicinephotoactive yellow proteinLetterDouble bondPhotoisomerizationisomeriaPhotochemistryConjugated systemsingle bond010402 general chemistryRing (chemistry)Photochemistry01 natural scienceskemialliset sidokset03 medical and health sciencesSingle bondHumansGeneral Materials ScienceBisphenol A-Glycidyl MethacrylatePhysical and Theoretical Chemistrychemistry.chemical_classificationMolecular switchProteinsChromophore0104 chemical sciences030104 developmental biologychemistryphotoactivationCovalent bondvalokemiaproteiinitphoto-isomerizationThe Journal of Physical Chemistry Letters
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Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n (n=1-4; m=3-7)

2020

The Te…Te secondary bonding interactions (SBI) in solid heterocyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2)m]n (n = 1‐4; m = 3‐7) species. The SBIs in 1,7‐Te2(CH2)10, 1,8‐Te2(CH2)12, 1,5,9‐Te3(CH2)9, 1,8,15‐Te3(CH2)18, 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)28 led to the tubular packing of the molecules, as has been observed previously for related thio‐ and selenoether rings. The nature of the intermolecular interactions was explored by solid‐state PBE0‐D3/pob‐TZVP calculations involving periodic boundary conditions. The packing of molecules in 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)…

eetteritheterocyclesnoncovalent interactionskemialliset sidoksettelluuritelluriumdensity functional calculationssolid-state structurestiheysfunktionaaliteoriaorganometalliyhdisteet
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Molecular Complexes Featuring Unsupported Dispersion-Enhanced Aluminum–Copper and Gallium–Copper Bonds

2020

The reaction of the copper(I) β-diketiminate copper complex {(Cu(BDIMes))2(μ-C6H6)} (BDIMes = N,N′-bis(2,4,6-trimethylphenyl)pentane-2,4-diiminate) with the low-valent group 13 metal β-diketiminates M(BDIDip) (M = Al or Ga; BDIDip = N,N′-bis(2,6-diisopropylphenyl)pentane-2,4-diiminate) in toluene afforded the complexes {(BDIMes)CuAl(BDIDip)} and {(BDIMes)CuGa(BDIDip)}. These feature unsupported copper–aluminum or copper–gallium bonds with short metal–metal distances, Cu–Al = 2.3010(6) Å and Cu–Ga = 2.2916(5) Å. Density functional theory (DFT) calculations showed that approximately half of the calculated association enthalpies can be attributed to London dispersion forces. peerReviewed

galliumkemialliset sidoksetligandsenthalpycoppermetalskuparikompleksiyhdisteetelectron densityalumiiniJournal of the American Chemical Society
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Iodine(I) and Silver(I) Complexes of Benzoimidazole and Pyridylcarbazole Derivatives

2021

The synthesis of iodine(I) complexes with either benzoimidazole or carbazole-derived sp 2 N -containing Lewis bases is described, as well as their corresponding silver(I) complexes. The addition of elemental iodine to the linear two-coordinate Ag(I) complexes produces iodine(I) complexes with a three-center four-electron (3c-4e) [N — I — N] + bond. The 1 H and 1 H- 15 N HMBC NMR studies unambiguously confirm the formation of the complexes in all cases via the [N — Ag — N] + → [N — I — N] + cation exchange, with the 15 N NMR chemical shift change between 94 to 111 ppm when compared to the free ligand. The single crystal X-ray crystallographic studies on four I + complexes revealed highly sym…

halogeenitLigandChemical shiftOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyhalogen(I)kompleksiyhdisteetIodineCatalysissupramolecular chemistryNMRCrystallographykemialliset sidoksetchemistryX-ray crystallographysupramolekulaarinen kemiahalogen bondLewis acids and basesNMR-spektroskopiaSingle crystalröntgenkristallografiaX-ray crystallography
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Design and construction of halogen-bonded capsules and cages

2017

This thesis describes the design, synthesis and characterization of supramolecular halogen-bonded capsules and cages from multivalent ligands. In the first part of the thesis, an overview to halogen bonding is provided. After discussing the general features of the halogen bonding, the most frequently used halogen bond donors are introduced and examples of their utilization in halogen-bonded systems are discussed. The chapter also presents recent advances made in the field of halogen-bonded supramolecular capsules. The first part of the thesis also includes a review of halogen-bonded complexes involving halonium ions, and a brief introduction to [N···X+···N] halogen bonds is provided along w…

halogeenitcation exchangemolekyylitkompleksiyhdisteetself-assemblycavitandssupramolecular chemistrykavitanditkemialliset sidoksetsupramolekyylikemiahalogen-bonded capsuleshalogen bondhalogeenisidoshalonium ionsmolekyylikapselitröntgenkristallografiaX-ray crystallography
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