Search results for "supramolecular"

showing 10 items of 830 documents

Organoplatinum(II) Complexes Self-Assemble and Recognize AT-Rich Duplex DNA Sequences

2021

The specific recognition of AT-rich DNA sequences opens up the door to promising diagnostic and/or therapeutic strategies against gene-related diseases. Here, we demonstrate that amphiphilic PtII complexes of the type [Pt(dmba)(N∧N)]NO3 (dmba = N,N-dimethylbenzylamine-κN, κC; N∧N = dpq (3), dppz (4), and dppn (5)) recognize AT-rich oligonucleotides over other types of DNA, RNA, and model proteins. The crystal structure of 4 shows the presence of significant π-stacking interactions and a distorted coordination sphere of the d8 PtII atom. Complex 5, containing the largest π-conjugated ligand, forms supramolecular assemblies at high concentrations under aqueous environment. However, its aggreg…

Coordination sphereOrganoplatinum CompoundsStereochemistrySupramolecular chemistryDMBAElectrophoretic Mobility Shift Assay010402 general chemistryCrystallography X-RayLigands01 natural sciencesArticleInorganic Chemistrychemistry.chemical_compoundCoordination ComplexesHumansPhysical and Theoretical ChemistryDNA • light-switch • platinum • pseudo-tetrahedral • antitumor agent • DFTOrganoplatinumGel electrophoresisMolecular Structure010405 organic chemistryChemistryOligonucleotideLigandSpectrum AnalysisStereoisomerismDNAIntercalating Agents0104 chemical sciencesA549 CellsSettore CHIM/03 - Chimica Generale E InorganicaDNA
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Molecular, Supramolecular Structures Combined with Hirshfeld and DFT Studies of Centrosymmetric M(II)-azido {M=Ni(II), Fe(II) or Zn(II)} Complexes of…

2021

The supramolecular structures of the three metal (II) azido complexes [Fe(4bzpy)4(N3)2]

Coordination spherePhysics and Astronomy (miscellaneous)Coordination polymerGeneral MathematicsSupramolecular chemistryCentrosymmetryazidoMetalchemistry.chemical_compoundComputer Science (miscellaneous)supramolekulaarinen kemiaQA1-939AIM4-benoylpyridinecentrosymmetryAtoms in moleculeskompleksiyhdisteetself-assemblyCrystallographyOctahedronchemistryChemistry (miscellaneous)visual_artvisual_art.visual_art_mediumAzidesupramolecular structuresMathematicsSymmetry
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Syntheses and Structural Study of Novel Tetranuclear Bis(phenoxido)‐Bridged Cu II Metal–Organic Macrocycles

2012

Six new tetranuclear copper(II) complexes were prepared exploiting novel ditopic alkylenediamine-N,N,N′,N′-tetraphenolate ligands. The geometrical parameters of the compounds can be varied by introducing different solvents of crystallization into the lattice. The structures of all six complexes were determined from single-crystal X-ray diffraction analyses and the magnetic properties of the complexes were estimated by computational DFT calculations. The relationship between the magnetic exchange coupling constant (J) and the Cu–O–Cu angle (θ) in these bis(phenoxido)-bridged complexes was investigated and a magnetostructural correlation was established between J and the θ angle. All studied …

Coupling constantDiffractionSupramolecular chemistrychemistry.chemical_elementCopperMagnetic exchangelaw.inventionInorganic ChemistryMetalCrystallographychemistrylawvisual_artvisual_art.visual_art_mediumAntiferromagnetismCrystallizationta116European Journal of Inorganic Chemistry
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Functionalization of Graphene with Molecules and/or Nanoparticles for Advanced Applications

2019

Graphene is considered the material of the third millennium, due to its extraordinary electronic and mechanical properties, and due to the possibility to modulate its conductivity, flexibility, elasticity, transparency, and biocompatibility by bottom-up approach. The possibility to gather the proper- ties of graphene and graphene oxide with those of functional moieties or nanoparticles is herein reviewed. The synthetic approaches proposed, either covalent or noncovalent, are aimed to tune appropriately graphene’s properties for the realization of materials for advanced uses, such as bio- medical applications, sensors, catalysis, and energy devices. In particular, methods based on covalent l…

Covalent functionalizationMaterials scienceCovalent functionalizationsupramolecular functionalizationgraphene oxidecomposite materials biomedical applications sensors catalysis energy devicesGraphenelawSurface modificationNanoparticleMoleculeNanotechnologySettore CHIM/06 - Chimica Organicalaw.inventionCatalysisHandbook of Graphene
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Self-assembled hydrogen-bonded coordination networks in two copper(II) carboxylates with 4-pyridylmethanol

2011

AbstractThe crystal and molecular structure of [Cu(nif)2(4-PM)2]·CH3OH (1) and [Cu(2-Clbz)2(4-PM)2(H2O)] (2), (where nif = niflumate anion, 2-Clbz = 2-chlorobenzoate anion and 4-PM is the 4-pyridylmethanol), have been determinated by X-ray crystallography. The Cu2+ cation in (1), is coordinated by two pairs of oxygen atoms from asymmetric bidentate niflumate anions and by a pair of pyridine nitrogen atoms from monodentate 4-pyridylmethanol ligands in trans position forming an extremely elongated bipyramid. The Cu2+ cation in (2), is coordinated by a pair of oxygen atoms from monodentate 2-chlorobenzoate anions, further by a pair of pyridine nitrogen atoms from monodentate 4-pyridylmethanol …

CrystallographyBipyramidchemistry.chemical_compoundDenticityHydrogen bondChemistryPyridineMaterials ChemistrySupramolecular chemistryStackingMoleculeGeneral ChemistryCrystal structureOpen Chemistry
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Supramolecular order of stilbenoid dendrons: importance of weak interactions

2006

Stilbenoid dendrons with various donor and acceptor groups on the focal unit were synthesised by a Wittig–Horner reaction, starting from an aldehyde functionalised dendron and various substituted phosphonic acid esters. The target molecules are composed of meta-branched arms, two of them with extended conjugation (distyrylbenzene) and three flexible dodecyloxy chains; the focal group consists of a donor or acceptor substituted styryl unit. The cross-conjugation of the arms prevents the strong electronic influence of substituents on the two extended oligophenylenevinylene chromophores. However, intermolecular interactions mediated by the focal unit allow control of the supramolecular stackin…

CrystallographyChemistryHydrogen bondLiquid crystalDendrimerMaterials ChemistryStackingSupramolecular chemistryMoleculeMesophaseGeneral ChemistryPhotochemistryAcceptorJ. Mater. Chem.
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2-(Benzotriazol-1-ylmethyl)-1-phenyl-3-pyrazolidinone: two weak hydrogen bonds combine to form molecular ladders

2002

In the supramolecular structure of C16H15N5O, weak C—H⋯O and C—H⋯N bonds combine to form molecular ladders, the former bonds acting as the rungs and the latter as the uprights.

CrystallographyChemistryHydrogen bondSupramolecular chemistryGeneral Materials ScienceGeneral ChemistryCondensed Matter PhysicsActa Crystallographica Section E Structure Reports Online
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A C(π-hole)⋯Cl-Zn tetrel interaction driving a metal-organic supramolecular assembly

2020

A brominated pyrimidinyl triazolopyridine ligand (bptpy) forms a C(π-hole)⋯Cl-Zn tetrel interaction that plays a determining role in the formation of supramolecular layers through chain assembly in 18 membered metallacycle [(ZnCl2)2(μ-bptpy)2] crystals. Supramolecular chains are formed through C-H⋯X interactions. The observed interactions are supported by DFT calculations using model dimers. This journal is

CrystallographyChemistryLigandSupramolecular chemistryGeneral Materials ScienceTriazolopyridineGeneral ChemistryMetallacycleCondensed Matter PhysicsSupramolecular assemblyCrystEngComm 22: 6979-6982 (2020)
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ChemInform Abstract: Halogen-Bonded Supramolecular Complexes and Networks

2009

In spite of some controversy of the true nature of the interaction between polarized halogen atoms and neutral or charged Lewis bases, termed “halogen bonding”, as a primary interaction, it is a very useful new tool/way to construct supramolecular complexes and networks. This is especially true in solid state supramolecular chemistry where utilization of weak intermolecular interactions such as halogen bonding opens up new insights to materials design and supramolecular synthesis.

CrystallographyHalogen bondChemistryIntermolecular forceHalogenSupramolecular chemistrySolid-stateGeneral MedicineLewis acids and basesMaterials designChemInform
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Alternative Motifs for Halogen Bonding (Eur. J. Org. Chem. 9/2013)

2013

CrystallographyHalogen bondChemistryOrganic ChemistryIntermolecular forceX-ray crystallographySupramolecular chemistryOrganic chemistryPhysical and Theoretical ChemistryCrystal engineeringEuropean Journal of Organic Chemistry
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