Search results for "macrocycle"

showing 10 items of 50 documents

Synthèse et étude physico-chimique de ligands macrocycliques, macrobicycliques et macrotricycliques dérivés du 5,12-dioxocyclame

2002

The synthesis and the physico-chemical studies of macropolycyclic ligands based on 5,12-dioxocyclam L1 are presented. The first part of this dissertation presents the structural and physico-chemical properties of L1 and its N-substituted derivatives L2 and L3. A potentiometric study reveald a cooperative protonation of the two macrocyclic ligands L1 and L2 whereas the study of the macrotricycle L3 in a methanol-water mixture revealed a sequential cooperative diprotonation of the four tertiary amines. The square planar nickel and copper complexes were synthesized and characterized using infrared, UV-vis and ESR spectgroscopy. The spectroscopic studies showed the presence of intermolecular hy…

conformationnickelcoordinationcuivrecopperprotonation[CHIM] Chemical Sciencestétraazamacrocycles[CHIM]Chemical Sciencescyclamstructurecyclame[ CHIM ] Chemical Sciences
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One‐pot synthesis of [2+2]‐helicate‐like macrocycle and 2+4‐μ4‐oxo tetranuclear open frame complexes : Chiroptical properties and asymmetric oxidativ…

2020

Synthesis of binuclear Cu(II) terminally closed [2+2]‐ double‐stranded helicate‐like macrocycles 1, 1′,1″, 2, 2′, 2″ and 2+4‐μ4‐oxo tetranuclear open frame complexes 3, 3′, 3″, 4, 4′, 4″ are established. Adapting one‐pot self‐assembly technique from simple three components systems: 1,1′‐binaphthyl‐2,2′‐diamine, 4‐methyl‐2,6‐diformyl phenol and cupric salts, the helicate‐like [2+2]‐ macrocyclic complexes 1–1″, 2–2″ and 2+4‐μ4‐oxo tetranuclear complexes 3–3″, 4–4″ were obtained by appropriately altering the reaction condition such as temperature and subcomponent ratio. Density Functional Theory (DFT) calculations were carried out for understanding the structural geometries, intermediates invo…

helicatemetal templateself‐assemblyBINOLmacrocycle
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Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

2018

Molecular recognition of aromatic hydrocarbons by four endo-functionalized molecular tubes has been studied by 1H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅π interactions. peerReviewed

hydrogen bondmacrocyclesvetyhost-guest chemistryaromatic hydrocarbonmolekyylidynamiikkamolecular recognitionhiilivedyt
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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
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An Off-On-Off Fluorescent Sensor for pH Windows Based on the 13aneN4-Zn 2+ System

2016

International audience; The new ligand L was prepared and features a 13-membered tetraaza macrocyclic ring with a 1,8-naphthalimide fluorophore appended to a C atom of its backbone. The protonation constants of L as well as its complexation constants with Zn2+ ions were determined in 1:1 water/methanol solutions by potentiometric titrations. Fluorimetric pH titrations were performed with L alone and L in the presence of Zn2+ ions (1:1), and the species distributions (%) versus pH were compared. A window-shaped fluorescence trend was observed with pH for the L/Zn2+ system, which behaves as an off-on-off pH sensor. The on window is centred in the 6.5-7.5 pH range, in correspondence with the f…

inorganic chemicalsFluorophorePotentiometric titrationInorganic chemistryProtonationYeast cellsSensors; Fluorescence; Zinc; Yeast cells; Macrocyclic ligands010402 general chemistry01 natural sciencesMicelleFluorescenceInorganic Chemistrychemistry.chemical_compoundMacrocyclic ligandsCyclamLipophilicity[SDV.IDA]Life Sciences [q-bio]/Food engineeringEquilibriaMicellesIonsChemosensors010405 organic chemistryLigandSensorsChelation-enhanced fluorescencezinc[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringMetal-complexesFluorescence0104 chemical scienceschemistryCyclamTitrationMacrocycles
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Large Azobenzene Macrocycles : Formation and Detection by NMR and MS Methods

2023

Azobenzene macrocycles are widely investigated as potential drug delivery systems and as part of molecular machines due to their photo-responsive properties. Herein, we detect the formation of a series of new azobenzene macrocycles that feature up to eight switchable repeating units. High-resolution mass spectrometry and ion mobility (IM) mass spectrometry experiments and 1H and diffusion-ordered spectroscopy (DOSY) NMR are used to detect the presence of the macrocycles that contain 10 to 40 aromatic rings in the gas phase and solution, respectively. The responsiveness of the Z-to-E photo-switching of the smallest of the macrocycles, exhibiting two azobenzene units and in total 10 aromatic …

large azobenzene-containing macrocyclesresponsive moleculesmassaspektrometriaspektroskopiaatsobentseeniphotoisomerizationmolekyylitmakrosyklitESI-MS and IM detection
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Chiral hemicucurbit[8]uril as an anion receptor: selectivity to size, shape and charge distribution

2017

A novel eight-membered macrocycle of the hemicucurbit[n]uril family, chiral (all-R)-cyclohexanohemicucurbit[8]uril (cycHC[8]) binds anions in a purely protic solvent with remarkable selectivity. The cycHC[8] portals open and close to fully encapsulate anions in a 1 : 1 ratio, resembling a molecular Pac-Man™. Comprehensive gas, solution and solid phase studies prove that the binding is governed by the size, shape and charge distribution of the bound anion. Gas phase studies show an order of SbF6− ≈ PF6− > ReO4− > ClO4− > SCN− > BF4− > HSO4− > CF3SO3− for anion complexation strength. An extensive crystallographic study reveals the preferred orientations of the anions within the octahedral cav…

macrocyclesanion receptorsvalikoivuushemicucurbituril
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CCDC 1524101: Experimental Crystal Structure Determination

2017

UCUZOK : 6,12,18,24-tetramethoxy-2,8,14,20-tetranonyl-4,10,16,22-tetrahydroxycalix[4]arene propan-2-ol solvate Space Group: P-1, Cell: a 12.27090(10)Å b 13.96500(10)Å c 19.53620(10)Å, α 83.2880(1)° β 89.0250(1)° γ 84.9650(1)° Work published 2017 via Cambridge Crystallographic Data Centre.

resorcinarenesolvatecalixarenemacrocyclesupramolecular chemistry
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CCDC 264161: Experimental Crystal Structure Determination

2017

WEJVOZ : New structure undergoing enhancement. Space Group: P21/c, Cell: a 18.5217(4)Å b 23.2973(6)Å c 21.1118(3)Å, α 90.00° β 96.591(1)° γ 90.00°. Work published 2017 via Cambridge Crystallographic Data Centre.

resorcinarenesolvateoctapodandcalixarenemacrocyclesupramolecular chemistry
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The Scope of Application of Macrocyclic Polyamines Beyond Metal Chelation

2019

International audience; Recent advances in the use of radiometals for both imaging and therapy has spurred on the development of an original chemistry that endows radionuclide-chelating molecular cages with ever sharper physicochemical properties. Macrocyclic polyamines (MPAs) such as cyclen and DOTA are among the most frequently encountered cages for the design of new radiotracers, owing to their versatile chemistry that makes them customizable molecular tools. The idea of using MPAs for alternative purposes has recently emerged, with an eye towards benefiting from their unique topology, versatility, symmetry and water-solubility. This review summarizes strategies that have been recently i…

theranosticsbioactive compounds[CHIM.ORGA]Chemical Sciences/Organic chemistrymolecular platform[CHIM.THER]Chemical Sciences/Medicinal ChemistrymultivalencypolyazamacrocyclesEuropean Journal of Organic Chemistry
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