Search results for "supramolecular chemistry"

showing 10 items of 721 documents

Binding motif of ebselen in solution: Chalcogen and hydrogen bonds team up

2020

Ebselen (2-phenyl-1,2-benzoselenazol-3(2H)one), a glutathione peroxidase mimic, is active against several RNA viruses, among others the retrovirus responsible for the COVID-19 pandemic. In this paper 77Se and 1H NMR studies of ebselen are reported and they identify the chalcogen bond (ChB) and hydrogen bond (HB) that are central in the landscape of interactions formed by the compound in solution. The selenium atom and the hydrogen atom at the C7 carbon act as ChB and HB donors and the O and N atoms of neutral molecules function as acceptors. The ChB and HB give rise to a bifurcated supramolecular synthon, which fastens the interaction acceptor opposite to the N–Se covalent bond of the selen…

chemistry.chemical_classificationStereochemistryEbselenHydrogen bondSynthonSupramolecular chemistryGeneral ChemistryCatalysisdrugssupramolecular chemistrychemistry.chemical_compoundChalcogenchemistrycovid-19Covalent bondMaterials ChemistryThiolMoleculeselenium drugs covid-19 chalcogen bond supramolecular chemistryseleniumchalcogen bond
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Tri- and tetraurea piperazine cyclophanes: synthesis and complexation studies of preorganized and folded receptor molecules.

2010

A series of symmetrical tri- and tetrameric N-ethyl- and N-phenylurea-functionalized cyclophanes have been prepared in nearly quantitative yields (86-99 %) from the corresponding tri- and tetraamino-functionalized piperazine cyclophanes and ethyl or phenyl isocyanates. Their conformational and complexation properties have been studied by single-crystal X-ray diffraction, variable-temperature NMR spectroscopy, and ESI-MS analysis. The rigid 27-membered trimeric cyclophane skeleton assisted by a seam of intramolecular hydrogen bonds results in a preorganized ditopic recognition site with an all-syn conformation of the urea moieties that, complemented by a lipophilic cavity of the cyclophane, …

chemistry.chemical_classificationStereochemistryHydrogen bondOrganic ChemistryIodideSupramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisCrystallographychemistry.chemical_compoundPiperazinechemistryIntramolecular forceMoleculeCyclophaneChemistry (Weinheim an der Bergstrasse, Germany)
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Controlling Multivalent Interactions in Triply-Threaded Two-Component Superbundles

2003

We have investigated the (1)H NMR spectra, the absorption spectra, the fluorescence spectra and decays, and the electrochemical properties of i). a tritopic receptor in which three benzo[24]crown-8 macrorings are fused onto a triphenylene core, ii). a trifurcated trication wherein three dibenzylammonium ions are linked 1,3,5 to a central benzenoid core, and iii). their 1:1 adduct which constitutes a triply-threaded, two-component supramolecular bundle. X-Ray crystallography has established the precise geometry of this paucivalent recognition motif in the solid state. In addition to [N(+)-H...O] hydrogen bonding and [C-H...O] interactions between the NH(2) (+) centers on the three dibenzylam…

chemistry.chemical_classificationStereochemistryHydrogen bondOrganic ChemistryStackingSupramolecular chemistryTriphenyleneGeneral ChemistryCatalysisAdductCrystallographychemistry.chemical_compoundMolecular recognitionchemistryProton NMRCrown etherChemistry - A European Journal
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Recognition-Directed Supramolecular Assemblies of Metal Complexes of Terpyridine Derived Ligands with Self-Complementary Hydrogen Bonding Sites

2000

The synthesis and X-ray structures of three metal complexes with terpyridine-derived ligands that contain amino-pyrimidine and amino-pyrazine moieties are presented. They have been designed in view of directing their self-assembly into specific supramolecular arrays through molecular recognition interactions. The solid-state structures indeed reveal extensive hydrogen-bonded networks. The Co complex 4a with PF6- counterions builds a two-dimensional infinite interwoven grid through strong double hydrogen bonds (d(N-H-N) =2.918-3.018 A) between the amino groups and the N atoms of the rings, with all H-bonding sites saturated. Changing the anions to BF4- in 4b leads to a similar infinite but p…

chemistry.chemical_classificationStereochemistryHydrogen bondOrganic ChemistrySupramolecular chemistryGeneral ChemistryCrystal engineeringCatalysisCoordination complexSupramolecular assemblySupramolecular polymerschemistry.chemical_compoundCrystallographyMolecular recognitionchemistryTerpyridineChemistry
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Generation of [2×2] Grid Metallosupramolecular Architectures from Preformed Ditopic Bis(acylhydrazone) Ligands and through Component Self‐Assembly

2007

Ditopic bis(acylhydrazone) ligands, derived from the reactions of carbohydrazides with 2-phenylpyrimidine-4,6-dicarbaldehyde and designed for grid formation with octahedrally coordinating transition-metal ions, exhibit a varied coordination chemistry depending upon the degree of their deprotonation. The neutral acylhydrazones are relatively poor ligands and are seemingly involved in multiple, labile complexation equilibria varying with the solvent and the particular metal salt in solution; nevertheless, grid complexes of different forms can be isolated in the solid state. Although only limited study has been made of the singly deprotonated ligands, grid species appear to be much more readil…

chemistry.chemical_classificationStereochemistrySupramolecular chemistrySalt (chemistry)Crystal structureCoordination complexInorganic ChemistryMetalSolventCrystallographyDeprotonationchemistryvisual_artvisual_art.visual_art_mediumSelf-assemblyEuropean Journal of Inorganic Chemistry
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Efficient Self-Assembly of Di-, Tri-, Tetra-, and Hexavalent Hosts with Predefined Geometries for the Investigation of Multivalency

2015

Coordination-driven self-assembly of differently shaped di- to hexavalent crown-ether host molecules is described. A series of [21]crown-7- and [24]crown-8-substituted bipyridine and terpyridine ligands was synthetized in a "toolbox" approach. Subsequent coordination to 3d transition metal and ruthenium(II) ions provides an easy and fast access to host assemblies with variable valency and pre-defined orientations of the crown-ether moieties. Preliminary isothermal calorimetry (ITC) titrations provided promising results, which indicated the host complexes under study to be suitable for the future investigation of multivalent and cooperative binding. The hosts described herein will also be su…

chemistry.chemical_classificationStereochemistrycrown ethersOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementIsothermal titration calorimetryGeneral ChemistrymultivalencyCombinatorial chemistrysupramolecular chemistryCatalysisRutheniumCoordination complexBipyridinechemistry.chemical_compoundstomatognathic systemchemistrycoordination chemistryMoleculeSelf-assemblyTerpyridineta116pseudorotaxanesChemistry - A European Journal
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Impact of Molecular Size and Shape on the Supramolecular Co‐Assembly of Chiral Tricarboxamides: A Comparative Study

2020

We report herein a comparative investigation of the chiral amplification features of a series of three families of C 3 -symmetric tricarboxamides: 1,3,5-triphenylbenzenetricarboxamides (TPBAs), benzenetricarboxamides (BTAs) and oligo(phenylene ethynylene) tricarboxamides (OPE-TAs). As previously observed for BTAs and OPE-TAs, a similar dichroic response is obtained for TPBAs decorated with three, two or only one chiral side chain bearing stereogenic centers, thus confirming the efficient transfer of point chirality to the supramolecular helical aggregates. Unlike BTAs and OPE-TAs, the chiral amplification ability of TPBAs in majority rules experiments shows a negligible dependence on the nu…

chemistry.chemical_classificationSteric effects010405 organic chemistryChemistryOrganic ChemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesStereocenterSupramolecular polymersCrystallographyPhenyleneSide chainMoleculeChirality (chemistry)Chemistry – A European Journal
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Self-Assembly, Characterisation, and Crystal Structure of Multinuclear Metal Complexes of the [2×3] and [3×3] Grid-Type

2002

The self-assembly of new multimetallic complexes of grid-type architecture is described. The binding of a set of tris-terdentate ligands, 1 a-1 d, based on terpyridine-like subunits, with different octahedrally coordinated metal ions leads to the formation of species whose structure depends strongly on the ligand, the metal ion, the counterion, the solvent, and the reaction conditions. Under suitable conditions, the [3 x 3] grid was obtained from the reaction of ligand 1 a with zinc tetrafluoroborate and from ligand 1 b with mercury triflate. The other ligands led to the formation of mainly one compound of composition [M(6)L(5)](12+), which has the structure of an incomplete [2 x 3] grid. T…

chemistry.chemical_classificationSteric effectsStereochemistryLigandOrganic ChemistrySupramolecular chemistryGeneral ChemistryCrystal structureCatalysisNon-innocent ligandCoordination complexCrystallographychemistryCounterionTrifluoromethanesulfonateChemistry - A European Journal
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Decoding the Consequences of Increasing the Size of Self-Assembling Tricarboxamides on Chiral Amplification

2019

A complete series of experimental and theoretical investigations on the supramolecular polymerization of chiral (1 and 2) and achiral (3) oligo(phenylene ethynylene) tricarboxamides (OPE-TAs) is reported. The performance of seargents-and-soldiers (SaS) and majority rules (MR) experiments has allowed deriving a full set of thermodynamic parameters, including the helix reversal penalty (HRP) and the mismatch penalty (MMP). The results described illustrate the influence exerted by the number of stereogenic centers per monomeric unit and the temperature on the chiral amplification phenomenon. While the HRP decreases upon decreasing the number of chiral side chains, the MMP follows an opposite t…

chemistry.chemical_classificationSteric effectsSupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesStereocenterSupramolecular polymersCrystallographyColloid and Surface ChemistrychemistryPhenyleneHelixSide chainChirality (chemistry)Journal of the American Chemical Society
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Kinetically Controlled Sequential Growth of Surface-Grafted Chiral Supramolecular Copolymers.

2016

We report a facile strategy to grow supramolecular copolymers on Au surfaces by successively exposing a surface-anchored monomer to solutions of oppositely charged peptide comonomers. Charge regulation on the active chain end of the polymer sufficiently slows down the kinetics of the self-assembly process to produce kinetically trapped copolymers at near-neutral pH. We thereby achieve architectural control at three levels: The β-sheet sequences direct the polymerization away from the surface, the height of the supramolecular copolymer brushes is well-controlled by the stepwise nature of the alternating copolymer growth, and 2D spatial resolution is realized by using micropatterned initiatin…

chemistry.chemical_classificationSurface (mathematics)Materials science010405 organic chemistryKineticsSupramolecular chemistryNanotechnologyGeneral ChemistryPolymer010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationCopolymerSelf-assemblyAngewandte Chemie (International ed. in English)
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