Search results for "Pram"

showing 10 items of 1064 documents

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
researchProduct

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
researchProduct

Expansion and Compression of a Helicate with Central Diol-Units as Stereocontrolling Moieties

2022

The dicatechol ester ligand 2-H4 forms the compressed helicate Li4[(2)3Ti2] which upon removal of the internally bound lithium cations expands. In the compressed form, the chiral diol units control the stereochemistry of the complex which is lost upon expansion of the system. peerReviewed

helicatelitiumstereochemistrykationitsupramolekulaarinen kemiamolekyylitnanotekniikkaself-assemblykompleksiyhdisteetmetallitmolecular switch
researchProduct

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
researchProduct

Selective gas adsorption by calixarene-based porous octahedral M32 coordination cages

2022

Giant octahedral M32 coordination cages were prepared via self-assembly of sulfonylcalix[4]arene-supported tetranuclear M(II) clusters (M = Co, Ni) with hybrid linker based on tris(dipyrrinato)cobalt(III) complexes appended with peripherical carboxylic groups. Due to intrinsic and extrinsic porosity, the obtained solid-state supramolecular architectures demonstrated good performance as adsorbents for the separation of industrially important gases mixtures. peerReviewed

huokoisuuskaasutkarboksyylihapotsupramolekulaarinen kemiakompleksiyhdisteetkobolttiadsorptio
researchProduct

Fluorescent supramolecular hydrogels for biomedical applications

2019

hydrogels imidazolium salts supramolecular gels bioimaging anticancer activity
researchProduct

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
researchProduct

Organogel formed by imidazolium salts: molecular recognition processes

imidazolium salts organogel supramolecular chemistrySettore CHIM/06 - Chimica Organica
researchProduct

Asymmetric [N–I–N]+halonium complexes in solution?

2020

Assessment of the solution equilibria of [bis(pyridine)iodine(I)]+ complexes by ESI-MS and NMR reveals the preference of iodine(I) to form complexes with a more basic pyridine. Mixtures of symmetric [bis(pyridine)iodine(I)]+ complexes undergo statistical ligand exchange, with a predominant entropic driving force favoring asymmetric systems. The influence of ligand basicity, concentration, temperature, and ligand composition is evaluated. Our findings are expected to facilitate the investigations, and the supramolecular and synthetic applications of halonium ions’ halogen bonds. peerReviewed

inorganic chemicals2019-20 coronavirus outbreakliuoksetLigandMetals and AlloysSupramolecular chemistrychemistry.chemical_elementliganditkompleksiyhdisteetGeneral ChemistryIodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonjodichemistry.chemical_compoundchemistryPyridineHalogenMaterials ChemistryCeramics and CompositesHalonium ionChemical Communications
researchProduct

Azonia spiro polyaza macrocycles containing biphenyl subunits as anion and cation receptors

2011

Abstract The reaction of N-Boc triprotected cyclam with bis(chloromethyl)biphenyl followed by the corresponding deprotection of the nitrogen atoms allows the preparation of receptor 3 containing an azonia spiro subunit. This receptor shows slightly increased basicity than cyclam, in particular for the formation of the appropriate triply charged species as a consequence of the reduced capacity of the structure present in 3 to stabilize the species with lower protonation degrees through the formation of intramolecular hydrogen bonds. The properties of 3 as a receptor for Cu2+ and Zn2+ and the anions derived from PO 4 3 − ( Pi ) , P 2 O 7 4 − ( PPi ) , P 3 O 10 5 − ( TPP ) and ATP have been st…

inorganic chemicalsBiphenylAqueous solutionHydrogen bondStereochemistryChemistryOrganic ChemistrySupramolecular chemistryStackingProtonationBiochemistryMedicinal chemistryAnion recognitionchemistry.chemical_compoundMetal complexesIntramolecular forceDrug DiscoveryCyclamPolyaza cyclophanesSupramolecular chemistryMacrocyclesTetrahedron
researchProduct