Search results for "Mechanochemistry"

showing 3 items of 13 documents

Solvent-free ball-milling subcomponent synthesis of metallosupramolecular complexes.

2015

Subcomponent self-assembly from components A, B, C, D, and Fe(2+) under solvent-free conditions by self-sorting leads to the construction of three structurally different metallosupramolecular iron(II) complexes. Under carefully selected ball-milling conditions, tetranuclear [Fe4 (AD2 )6 ](4-) 22-component cage 1, dinuclear [Fe2 (BD2 )3 ](2-) 11-component helicate 2, and 5-component mononuclear [Fe(CD3 )](2+) complex 3 were prepared simultaneously in a one-pot reaction from 38 components. Through subcomponent substitution reaction by adding subcomponent B, the [Fe4 (AD2 )6 ](4-) cage converts quantitatively to the [Fe2 (BD2 )3 ](2-) helicate, which, in turn, upon addition of subcomponent C, …

Substitution reactionSolvent freeChemistryStereochemistryOrganic ChemistrySupramolecular chemistryGeneral ChemistryCatalysisball millself-sortingsupramolecular chemistryTurn (biochemistry)CrystallographySelf sortingMechanochemistrymulticomponent synthesisdynamic imine chemistryChemical stabilitymechanochemistryBall millta116Chemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Divalent metal phosphonates – new aspects for syntheses, in situ characterization and structure solution

2016

Abstract Divalent metal phosphonates are promising hybrid materials with a broad field of application. The rich coordination chemistry of the phosphonate linkers enables the formation of structures with different dimensionalities ranging from isolated complexes and layered structures to porous frameworks incorporating various functionalities through the choice of the building blocks. In brief, metal phosphonates offer an interesting opportunity for the design of multifunctional materials. Here, we provide a short review on the class of divalent metal phosphonates discussing their syntheses, structures, and applications. We present the advantages of the recently introduced mechanochemical pa…

chemistry.chemical_classificationIn situMaterials science010405 organic chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesPhosphonateCombinatorial chemistry0104 chemical sciencesCharacterization (materials science)Coordination complexDivalentInorganic ChemistryMetalchemistry.chemical_compoundchemistryMechanochemistryvisual_artvisual_art.visual_art_mediumOrganic chemistryGeneral Materials ScienceHybrid materialZeitschrift für Kristallographie - Crystalline Materials
researchProduct

Force Distribution Analysis of Mechanochemically Reactive Dimethylcyclobutene

2013

Internal molecular forces can guide chemical reactions, yet are not straightforwardly accessible within a quantum mechanical description of the reacting molecules. Here, we present a force-matching force distribution analysis (FM-FDA) to analyze internal forces in molecules. We simulated the ring opening of trans-3,4-dimethylcyclobutene (tDCB) with on-the-fly semiempirical molecular dynamics. The self-consistent density functional tight binding (SCC-DFTB) method accurately described the force-dependent ring-opening kinetics of tDCB, showing quantitative agreement with both experimental and computational data at higher levels. Mechanical force was applied in two different ways, namely, exter…

ta114CyclobuteneChemistryMolecular ConformationMolecular Dynamics SimulationRing (chemistry)Atomic and Molecular Physics and Optics:Science::Biological sciences::Biophysics [DRNTU]chemistry.chemical_compoundMolecular dynamicsAccelerationTight bindingIsomerismComputational chemistryChemical physicsMechanochemistryQuantum TheoryMoleculeReactivity (chemistry)Physical and Theoretical Chemistryta116CyclobutanesChemPhysChem
researchProduct