Search results for "405"

showing 10 items of 3208 documents

High affinity of "arbor" iron porphyrins for dioxygen

1998

International audience; The equilibrium rates of dioxygen and carbon monoxide binding have been measured for a series of capped iron porphyrins called "arbor". The affinity for dioxygen of these models is 100-fold higher than the highest previously reported values.

inorganic chemicals010405 organic chemistryChemistryMaterials Chemistry[CHIM]Chemical SciencesCarbon monoxide bindingGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistry[ CHIM ] Chemical SciencesCatalysis0104 chemical sciences
researchProduct

On the physicochemical properties of pyridohelicenes.

2014

A comprehensive study on the physicochemical properties of a series of mono- and diaza[5]helicenes as well as mono- and diaza[6]helicenes is reported. Through the use of both computational and experimental methods, these helically chiral pyridohelicenes with the nitrogen atom(s) in various positions are characterised according to their inversion barriers, protonation constants and redox potentials. By using DFT calculations, kinetic measurements, UV/Vis titrations, cyclic voltammetry and EPR spectroscopy, a self-contained picture of their behaviour under conventional treatment by heat, acids and oxidising/reducing agents is provided.

inorganic chemicals010405 organic chemistryChemistryReducing agent[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryProtonationGeneral Chemistry010402 general chemistryKinetic energy01 natural sciencesRedoxCatalysis0104 chemical scienceslaw.invention[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrylawComputational chemistryOrganic chemistryTitrationCyclic voltammetryElectron paramagnetic resonanceChirality (chemistry)ComputingMilieux_MISCELLANEOUSChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Acidic Co-Catalysts in Cationic Gold Catalysis.

2016

A systematic study on the effects of Lewis or Bronsted acid co-catalysts in gold-catalyzed reactions was undertaken using representative reactions (O-, N-, and C-nucleophilic additions to alkynes). Through these reactions, it was demonstrated that an acidic co-catalyst can increase the catalyst turnover significantly, enabling practical reaction rates at competitive catalyst loadings (<1 mol %). Further investigation is currently underway to improve the understanding of the subtle principles underlying these experimental observations.

inorganic chemicals010405 organic chemistryChemistryorganic chemicalsOrganic ChemistryCationic polymerizationGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysisReaction rateTransition metalOrganic chemistryheterocyclic compoundsLewis acids and basesBrønsted–Lowry acid–base theoryChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Equilibrium and structural studies of complexes with a hexadentate ligand containing amide, amine and pyridyl nitrogen donors. Crystal structures of …

2002

A novel potentially hexadentate ligand, 1,8-bis(2-pyridylcarbamoyl)-3,6-diazaoctane (pyctrien) has been synthesised as its tetrahydrochloride salt; its protonation constants and the stability constants of the copper(II) and nickel(II) chelates have been determined by potentiometry. Amide group deprotonation permits the formation of [MLH−1]+ and [MLH−2] species in all cases, whereas the detection of the neutral or the protonated species depends on the nature of the metal ions. The solid complexes of copper, nickel and cobalt with the neutral and the deprotonated ligand have been synthesised and characterised by IR and UV–VIS spectroscopy. The amidic groups are coordinated through the oxygen …

inorganic chemicals010405 organic chemistryLigandInorganic chemistrychemistry.chemical_elementProtonationGeneral Chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesSquare pyramidal molecular geometry0104 chemical scienceschemistry.chemical_compoundNickelCrystallographyDeprotonationchemistryAmidePyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltComputingMilieux_MISCELLANEOUS
researchProduct

Uncapping the N-terminus of a ubiquitous His-tag peptide enhances its Cu2+ binding affinity

2019

Metal complexes with an N-terminally free and N-terminally acetylated polyhistidine region of Echis ocellatus venom, with an interesting His-rich motif present in numerous metal binding proteins from all kingdoms of life (DHDHDHHHHHHPGSSV-NH2 and Ac-DHDHDHHHHHHPGSSV-NH2) show the role of the free amino group in the thermodynamic enhancement of Cu2+, Ni2+ and Zn2+ binding. In the studied sequences, Cu2+ can be coordinated by different sets of imidazole rings, and a 3–10 helix is detected in close proximity of Cu2+ binding sites. The complexes are more stable than those with a typical His6-tag, despite a similar copper(II) coordination mode in both cases.

inorganic chemicals010405 organic chemistryStereochemistryChemistryPeptide sequence tagVenom010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalN-terminuschemistry.chemical_compoundAcetylationvisual_artvisual_art.visual_art_mediumImidazoleBinding siteUncappingDalton Transactions
researchProduct

Monoamide Derivatives of EDTA Incorporating Pendent Carboxylates or Pyridyls: Synthesis, Metal Binding, and Crystal Structure of a Dinuclear Ca2+ Com…

2017

EDTA is a powerful, cheap and widely-used chelating unit for a large range of metal ions. To link it covalently to other molecules, the formation of an amide bond using one of the carboxylates is an attractive and simple approach, even though it may compromise metal ion binding as one of the four carboxylate donors is lost. Here we undertake a quantitative study of the metal ion binding of two new mono-amide derivatives of EDTA, namely AmGly1 and AmPy1, featuring an additional coordinating carboxylate or pyridyl group in the amide, respectively. The compounds are conveniently synthesised through alkylation of the tris-t-butyl ester of ethylenediamine-triacetic acid with the appropriate α-ch…

inorganic chemicalsAqueous solution010405 organic chemistryStereochemistryChemistryMetal ions in aqueous solutionGeneral ChemistryCrystal structure010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAmidePolymer chemistryMoleculeChelationCarboxylateCoordination geometryChemistrySelect
researchProduct

Dynamic Refolding of Ion-Pair Catalysts in Response to Different Anions.

2019

Four distinct folding patterns were identified in two foldamer-type urea-thiourea catalysts bearing a basic dimethylamino unit by a combination of X-ray crystallography, solution NMR studies, and computational studies (DFT). These patterns are characterized by different intramolecular hydrogen bonding schemes that arise largely from different thiourea conformers. The free base forms of the catalysts are characterized by folds where the intramolecular hydrogen bonds between the urea and the thiourea units remain intact. In contrast, the catalytically relevant salt forms of the catalyst, where the catalyst forms an ion pair with the substrate or substrate analogues, appear in two entirely dif…

inorganic chemicalsBearing (mechanical)anionitcatalysis010405 organic chemistryChemistryorganic chemicalsOrganic Chemistryfolding anion bindingIon pairs010402 general chemistrykidetiede01 natural sciences0104 chemical sciencesCatalysislaw.inventionFolding (chemistry)X-rayCrystallographyconformational changelawkatalyysisolution structuresröntgenkristallografiaThe Journal of organic chemistry
researchProduct

A solvent-free regioselective iodination route of ortho-carboranes.

2006

Tetraiodo-ortho-carborane based X-ray contrast agents can be readily prepared in a high yield, fast, clean, regioselective fashion by a solvent-free reaction of ortho-carboranes with iodine in sealed tubes.

inorganic chemicalsBoron Compoundschemistry.chemical_elementContrast MediaOrganic-reactions010402 general chemistryIodine01 natural sciencesChemical synthesisInorganic ChemistryQUIMICA ANALITICAOrganic chemistryheterocyclic compoundsSolvent freeintegumentary system010405 organic chemistryChemistryorganic chemicalsRegioselectivityHalogenationCombinatorial chemistry0104 chemical sciencesRadiographyChemical-synthesisOrganic reactionYield (chemistry)SolventsbacteriaDerivativesIodineDalton transactions (Cambridge, England : 2003)
researchProduct

The reduction of molecular oxygen by iron porphyrins

2002

Abstract Molecular assemblies have been synthesised to reproduce the structure of the cytochrome c oxidase (C c O) active site and to explore the roles played by its different features. It was discovered that a single iron porphyrin, adsorbed at the surface of a graphite electrode, is a selective catalyst for the four-electron reduction of dioxygen to water, at pH 7. To cite this article: D. Ricard et al., C. R. Chimie 5 (2002) 33–36

inorganic chemicalsCytochromebiology010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryActive sitechemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistryElectrocatalyst01 natural sciencesPorphyrinOxygen[ CHIM ] Chemical Sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistry[CHIM] Chemical Sciencesbiology.proteinCytochrome c oxidase[CHIM]Chemical SciencesGraphite
researchProduct

Substituent Effects on the [N-I-N](+) Halogen Bond

2016

We have investigated the influence of electron density on the three-center [N-I-N](+) halogen bond. A series of [bis(pyri din e) io dine](+) and [1,2-bis ( (pyridin e-2-71 ethynyl)b e nze n e)io dine](+) BF4- complexes substituted with electron withdrawing and donating functionalities in the para-position of their pyridine nitrogen were synthesized and studied by spectroscopic and computational methods. The systematic change of electron density of the pyridine nitrogens upon alteration of the para-substituent (NO2, CF3, H, F, Me, OMe, NMe2) was confirmed by N-15 NMR and by computation of the natural atomic population and the pi electron population of the nitrogen atoms. Formation of the [N-…

inorganic chemicalsElectron densityPopulationInorganic chemistryhalogen bondsSubstituent010402 general chemistry01 natural sciencesBiochemistryCatalysisArticlechemistry.chemical_compoundColloid and Surface ChemistryPyridineeducationBenzeneta116education.field_of_studyHalogen bond010405 organic chemistryChemical shiftGeneral ChemistryKemi0104 chemical sciencesCrystallographychemistryChemical SciencesPolar effect
researchProduct