Search results for "supramolecular chemistry"

showing 10 items of 721 documents

Spontaneous Resolution of an Electron‐Deficient Tetrahedral Fe4L4cage

2015

A highly electron-deficient C3-symmetric tris(bipyridyl) ligand was prepared in four steps and used for the coordination of Fe(OTf)2, thereby resulting in the homochiral assembly of a new family of robust tetrahedral M4L4 cages. This homochiral T-symmetric cage containing a relatively large cavity of 330 A(3) is capable of encapsulating an anionic guest, as was determined by mass spectrometry, (19)F NMR spectroscopy, and finally shown from its crystal structure. Moreover, crystallization of the cage from CH3CN led to crystals containing both (ΔΔΔΔ and ΛΛΛΛ) enantiomers, while crystallization from CH3 OH resulted in crystals containing only the right-handed (ΔΔΔΔ) cage. The difference in the…

crystallization010405 organic chemistryChemistryLigandelectron-deficient tetrahedral Fe4L4Supramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCrystal structureGeneral Medicine010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceslaw.inventionCrystalCrystallographylawX-ray crystallographyCrystallizationChirality (chemistry)ta116Angewandte Chemie
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Efficient photoinduced electron transfer in a porphyrin tripod-fullerene supramolecular complex via pi-pi interactions in nonpolar media.

2010

A novel porphyrin tripod (TPZn(3)) was synthesized via "click chemistry". Three porphyrin moieties of TPZn(3) are geometrically close and linked by a flexible linker. The electron-transfer oxidation of TPZn(3) results in intramolecular pi-dimer formation between porphyrin moieties as indicated by electrochemical, vis-NIR, and ESR measurements. The cyclic voltammogram of TPZn(3) exhibited stepwise one-electron oxidation processes of three porphyrin moieties in the range from 0.58 to 0.73 V (vs SCE in CH(2)Cl(2)). When TPZn(3) was oxidized by tris(2,2'-bipyridyl)-ruthenium(III) ([Ru(bpy)(3)](3+)), the oxidized species (TPZn(3))(n+) (0n/= 3) exhibited a charge resonance band in the NIR region …

dyadFullerenePorphyrinsMacromolecular SubstancesPhotochemistrySupramolecular chemistrycharge-separated state010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisPhotoinduced electron transferchemistry.chemical_compoundColloid and Surface Chemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryMoleculeComputingMilieux_MISCELLANEOUSMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryTripod (photography)reaction center mimicryGeneral ChemistryPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryZincchemistryIntramolecular forceclick chemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryClick chemistryQuantum TheoryFullerenesporphyrinOxidation-ReductionJournal of the American Chemical Society
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Strategies for Exploring Functions from Dynamic Combinatorial Libraries

2020

Dynamic combinatorial chemistry (DCC) is a powerful approach for creating complex chemical systems, giving access to the studies of complexity and exploration of functionality in synthetic systems. However, compared with more advanced living systems, the man‐made chemical systems are still less functional, due to their limited complexity and insufficient kinetic control. Here we start by introducing strategies to enrich the complexity of dynamic combinatorial libraries (DCLs) for exploiting unexpected functions by increasing the species of building blocks and/or templates used. Then, we discuss how dynamic isomerization of photo‐switchable molecules help DCLs increase and alter the systemic…

dynamic combinatorial chemistrynoncovalent interactionskemiallinen synteesisupramolekulaarinen kemiakinetic controlchemical complexitykompleksisuussupramolecular chemistry
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Supramolecular Hydro- and Ionogels: A Study of Their Properties and Antibacterial Activity.

2017

Diimidazolium-based organic salts, bearing peptides or amino acids as anions have been synthesised and tested for their gelling ability in biocompatible solvents. These low molecular weight salts were successfully used as gelators in phosphate buffered saline (PBS) solution and ionic liquids. Then, the properties of the obtained soft materials were analysed in terms of melting temperature and gel strength as accounted for by rheological investigations. The gel-phase formation was studied by using UV/Vis and resonance light scattering measurements, whereas the morphology of the soft materials was analysed by using polarised optical microscopy and scanning electron microscopy. To get informat…

gelantibacterial activity; gels; hydrogels; ionic liquids; ionogels; Chemistry (all)Scanning electron microscopeSupramolecular chemistryIonic Liquids02 engineering and technologyMicrobial Sensitivity Tests010402 general chemistryGram-Positive Bacteria01 natural sciencesCatalysischemistry.chemical_compoundRheologyantibacterial activityX-Ray DiffractionPhase (matter)Gram-Negative BacteriaOrganic chemistryThermal stabilityhydrogelsionic liquidOrganic ChemistryChemistry (all)ImidazolesGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesAnti-Bacterial AgentsionogelchemistryChemical engineeringionogelsSelf-healing hydrogelsIonic liquidMicroscopy Electron ScanningSolventshydrogel0210 nano-technologyAntibacterial activityRheologyGelsChemistry (Weinheim an der Bergstrasse, Germany)
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Communication between iron(II) building blocks in cooperative spin transition phenomena

2003

[EN] In the present article we discuss the cooperative nature of the spin crossover phenomenon in iron(II) complexes, providing a perspective of the state of the art in this area. The first aspect we discuss is the role of the intermolecular interactions, more precisely the ¿-interactions, in mononuclear complexes. We show that by playing with the nature of the ligands, aliphatic, aromatic, or extended aromatic, it is possible to create stronger cohesive forces and receive a more cooperative response from the compound. In the next step the singular family of bipyrimidine-bridged iron(II) dinuclear compounds is presented as the simplest example of polynuclear spin crossover complexes exhibit…

genetic structuresStereochemistryChemistryIntermolecular forceSupramolecular chemistrySpin transitionSpin transitionIron(II) complexesInorganic ChemistryChemical physicsSpin crossoverFISICA APLICADAIntramolecular forceMaterials ChemistryMolecular magnetismPhysical and Theoretical ChemistrySupramolecular chemistryTopology (chemistry)Curse of dimensionalityCoordination Chemistry Reviews
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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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Recognition of alkali metal halide contact ion pairs by uranyl-salophen receptors bearing aromatic sidearms. The role of cation-pi interactions.

2005

Hard anions have long been known to bind strongly to the uranium of uranyl-salophen complexes. Upon functionalization of the salophen framework with one or two benzyloxy substituents, efficient ditopic receptors for alkali metal ions are obtained. The solid-state structures of complexes formed by the two-armed receptor 1 with CsF and with the chlorides of K+, Rb+, and Cs+ reported here reveal the existence of dimeric supramolecular assemblies in which two receptor units assemble into capsules fully enclosing (MX)2 ion quartets. In addition to the strong coordinative binding of the anion to the uranyl center and to electrostatic cation-anion interactions, stabilizing interactions arise from …

host-guest recognitionStereochemistrySupramolecular chemistryGeneral ChemistryCrystal structureAlkali metalUranylBiochemistrysupramolecular chemistryCatalysisIonchemistry.chemical_compoundCrystallographyalkaly metal ions. ditopic receptorsColloid and Surface ChemistrychemistryAlkali metal halideX-ray crystallographyReceptorJournal of the American Chemical Society
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Self-assembly of 2,8,14,20-tetraisobutyl-5,11,17,23-tetrahydroxyresorc[4]arene

1999

We report herein the observation of a hexameric structure of a hydroxyresorc[4]arene in the solid state, enclosing a large interior space. This artificial molecular container is stabilized only by hydrogen bonds. The tendency to form aggregates in solution is demonstrated mainly by means of ESI-MS methods.

hydroxyresorc[4]arenesChemistryHydrogen bondOrganic ChemistrySupramolecular chemistrySolid-stateself-assemblyContainer (type theory)supramolecular chemistryCrystallographyhexameric structurehydrogen bondsSelf-assemblyInterior spacePhysical and Theoretical Chemistry
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Organogel formed by imidazolium salts: molecular recognition processes

imidazolium salts organogel supramolecular chemistrySettore CHIM/06 - Chimica Organica
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