Search results for "Carbene"

showing 10 items of 152 documents

Comparative biological evaluation and G-quadruplex interaction studies of two new families of organometallic gold(I) complexes featuring N-heterocycl…

2020

Experimental organometallic gold(I) compounds hold promise for anticancer therapy. This study reports the synthesis of two novel families of gold(I) complexes, including N1-substituted bis-N-heterocyclic carbene (NHC) complexes of general formula [Au(N1-TBM) 2]BF 4 (N1-TBM = N1-substituted 9-methyltheobromin-8-ylidene) and mixed gold(I) NHC-alkynyl complexes, [Au(N1-TBM)alkynyl]. The compounds were fully characterised for their structure and stability in aqueous environment and in the presence of N-acetyl cysteine by nuclear magnetic resonance (NMR) spectroscopy. The structures of bis(1-ethyl-3,7,9-trimethylxanthin-8-ylidene)gold(I), (4-ethynylpyridine)(1,9-dimethyltheobromine-8-ylidene)gol…

Circular dichroismStereochemistryAntineoplastic Agents010402 general chemistryG-quadruplexLigands01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundNeoplasmsMoietyGold(I) organometallicsHumansN-heterocyclic carbenesCancer010405 organic chemistryChemistryFluorescenceG-quadruplexes0104 chemical sciencesFörster resonance energy transferMCF-7 CellsBODIPYDrug Screening Assays AntitumorSelectivityCarbeneAlkynyl ligandsMethaneOrganogold Compounds
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Metal NHC Complexes with Naphthalimide Ligands as DNA-Interacting Antiproliferative Agents

2017

Naphthalimide-based N-heterocyclic carbene (NHC) complexes of the type [(1,5-cyclooctadiene)(NHC)RhCl)] (4 a-c), [(p-cymene)(NHC)RuCl2 )] (5 a-c), and [(NHC)CuBr] (6 a-c) were synthesized and investigated as antiproliferative agents that target DNA. The cytotoxic effects were largely driven by the naphthalimide structure, which is a DNA-intercalating moiety. Regarding the metal center, the highest activities were observed with the rhodium complexes, and cytotoxic activity was significantly lower for the ruthenium derivatives. The stable coordination of the NHC ligands of selected complexes 4 b and 5 b in solution was confirmed, and their DNA binding properties were studied by UV/Vis spectro…

Circular dichroismStereochemistryIntercalation (chemistry)Molecular Conformationchemistry.chemical_elementApoptosisCrystallography X-RayLigands010402 general chemistry01 natural sciencesBiochemistryRhodiumMetalchemistry.chemical_compoundDrug StabilityCoordination ComplexesDrug DiscoveryHumansMoietyGeneral Pharmacology Toxicology and PharmaceuticsrutheniumCell ProliferationPharmacology010405 organic chemistryChemistryCircular DichroismOrganic ChemistryDNAnaphthalimideIntercalating Agentsanticancer agent0104 chemical sciencesRutheniumcarbeneNaphthalimidesSettore CHIM/03 - Chimica Generale E Inorganicacoppervisual_artrhodiumMCF-7 CellsMonoterpenesvisual_art.visual_art_mediumCymenesMolecular MedicineSpectrophotometry UltravioletHT29 CellsMethaneCarbeneDNAChemMedChem
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Complexes de métaux de transition avec des ligands carbènes N-hétérocycliques : synthèses et réactivité

2015

The purpose of this work is the synthesis of complexes containing imine-functionalized protic NHC ligands in order to further develop synthetic methodologies giving access to pNHC, C-bound ‘anionic’ imidazolide, and homo- and heterodinuclear complexes. In the case of imidazoles without functional group, deprotonation with n-butyl lithium afforded (1-aryl-1H-imidazol-2-yl)lithium in good yield. Reaction of (1-aryl-1H-imidazol-2-yl)lithium with [Ir(cod)(μ-Cl)]2 or [Rh(cod)(μ-Cl)]2 yielded a doubly C2,N3-bridged dinuclear complex. In the case of imine-functionalized imidazole, the Ir(I) N-bound imidazole complex can tautomerize to Ir(I) imine-functionalized pNHC complex chloride abstraction at…

Complexes du rhodiumIridium complexesFonctionnalité-imine[CHIM.OTHE] Chemical Sciences/OtherProtic N-heterocyclic carbenesRhodium complexesCarbènes N-hétérocyclique protiqueImine-functionalizationsComplexes de l'iridiumC-H activationActivation C-H
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Bidentate pyridyl‐NHC ligands: synthesis, ground and excited state properties of their iron(II) complexes and role of the fac/mer isomerism

2021

International audience; Iron complexes are promising candidates for the development of sustainable molecular photoactive materials as an alternative to those based on precious metals such as Ir, Pt or Ru. These compounds possess metal-ligand charge transfer (MLCT) transitions potentially of high interest for energy conversion or photocatalysis applications if the ultrafast deactivation via lower-lying metal-centred (MC) states can be impeded. Following an introduction describing the main design strategies used so far to increase the MLCT lifetimes, we review some of our latest contributions to the field regarding bidentate Fe(II) complexes comprising N-heterocyclic carbene ligands. The disc…

Computational chemistryDenticity010405 organic chemistryChemistryIronBidentate ligands[CHIM.COOR] Chemical Sciences/Coordination chemistry010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryExcited state[CHIM.COOR]Chemical Sciences/Coordination chemistryCarbene ligandsUltrafast spectroscopy
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Ammonia Activation by a Nickel NCN-Pincer Complex featuring a Non-Innocent N-Heterocyclic Carbene: Ammine and Amido Complexes in Equilibrium

2015

A Ni0-NCN pincer complex featuring a six-membered N-heterocyclic carbene (NHC) central platform and amidine pendant arms was synthesized by deprotonation of its NiII precursor. It retained chloride in the square-planar coordination sphere of nickel and was expected to be highly susceptible to oxidative addition reactions. The Ni0 complex rapidly activated ammonia at room temperature, in a ligand-assisted process where the carbene carbon atom played the unprecedented role of proton acceptor. For the first time, the coordinated (ammine) and activated (amido) species were observed together in solution, in a solvent-dependent equilibrium. A structural analysis of the Ni complexes provided insig…

Coordination spheretyppiliganditN-heterosykliset karbeenitammoniakkiPhotochemistryammoniaCatalysisAmidinenikkelikomopleksichemistry.chemical_compoundDeprotonationPolymer chemistrypincer ligandsN-heterocyclic carbenesta116bond activationChemistryLigandTransition metal carbene complexnickel complexGeneral ChemistryGeneral Medicinesidoksen aktivointiOxidative additionPincer movementCarbeneAngewandte Chemie
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Azolium and acetate ions in DMF: Formation of free N-heterocyclic carbene. A voltammetric analysis

2016

In order to reveal the possible formation of free N-heterocyclic carbene (NHC) in DMF-azolium and acetate solutions, the proton exchange equilibrium between azolium cations and CH3COO− was investigated (by cyclic voltammetry) by adding CH3COOH or tetrabutylammonium acetate to DMF solutions of imidazolium or thiazolium salts of different acidity.The voltammetric analysis confirms that the deprotonation of the azolium cation by CH3COO− (with the formation of free NHC) is significant in the case of the more acidic thiazolium cations, while it is not effective with the less acidic imidazolium ones.Accordingly, the NHC-catalyzed benzoin condensation was carried out in DMF solutions of azolium sa…

Cyclic voltammetryNHCInorganic chemistryTetrabutylammonium acetate010402 general chemistryAcetic acid01 natural sciencesMedicinal chemistryIonlcsh:ChemistryBenzaldehydeAcetic acidchemistry.chemical_compoundDeprotonationBenzoinElectrochemistryBenzoin condensationBenzoin condensation010405 organic chemistryChemistry0104 chemical sciencesAzolium saltslcsh:Industrial electrochemistrylcsh:QD1-999Acetic acid; Azolium salts; Benzoin condensation; Cyclic voltammetry; NHC; Tetrabutylammonium acetate; ElectrochemistryAzolium saltCyclic voltammetryCarbenelcsh:TP250-261
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Highly Enantioselective Kinetic Resolution of Michael Adducts through N-Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes

2018

Ahighly efficient strategy for the kinetic resolu-tion of Michael adductswas realized using achiral N-het-erocyclic carbene catalyst.The kinetic resolution providesanew convenientroute to single diastereomers of cyclo-hexenes and Michael adducts in good yields with highenantiomeric excesses (up to 99 % ee with aselectivityfactor of up to 458). This “two flies with one swat” con-cept allows the synthesis of these two synthetically valua-ble compound classes at the same time by asingle trans-formation. peerReviewed

Cyclohexenesasymmetric synthesis010402 general chemistry01 natural sciencesCatalysisCatalysisKinetic resolutionMichael adductschemistry.chemical_compoundkinetic resolutionN-heterocyclic carbenesta116orgaaniset yhdisteetkemiallinen synteesi010405 organic chemistryOrganic ChemistryDiastereomerEnantioselective synthesisGeneral ChemistryCombinatorial chemistry0104 chemical scienceschemistrycyclohexenesEnantiomerSelectivityCarbeneChemistry - A European Journal
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Structural and Luminescent Properties of Homoleptic Silver(I), Gold(I), and Palladium(II) Complexes with nNHC-tzNHC Heteroditopic Carbene Ligands

2019

Novel silver(I), gold(I), and palladium(II) complexes were synthesized with bidentate heteroditopic carbene ligands that combine an imidazol-2-ylidene (nNHC) with a 1,2,3-triazol-5-ylidene (tzNHC) connected by a propylene bridge. The silver(I) and gold(I) complexes were dinuclear species, [M-2(nNHC-tzNHC)(2)](PF6)(2) (M = Ag or Au), with the two bidentate ligands bridging the metal centers, whereas in the palladium(II) complex [Pd(nNHC-tzNHC)(2)]-(PF6)(2), the two ligands were chelated on the same metal center. Because of the presence of two different carbene units, isomers were observed for the gold(I) and palladium(II) complexes. The molecular structures of the head-to-tail isomer for gol…

Denticity010405 organic chemistryGeneral Chemical EngineeringINTEGRATION SCHEMEchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesArticleREACTIVITY0104 chemical scienceslcsh:ChemistryELECTRONIC-PROPERTIESchemistry.chemical_compoundchemistrylcsh:QD1-999Polymer chemistrySTATISTICAL AVERAGEMETAL-COMPLEXESHomolepticLuminescenceCarbenePalladiumAPPROXIMATION
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Charged Bis-Cyclometalated Iridium(III) Complexes with Carbene-Based Ancillary Ligands

2013

Charged cydometalated (CN) iridium(III) complexes with carbene-based ancillary ligands are a promising family of deep-blue phosphorescent compounds. Their emission properties are controlled primarily by the main CN ligands, in contrast to the classical design of charged complexes where NN ancillary ligands with low-energy pi* orbitals, such as 2,2'-bipyridine, are generally used for this purpose. Herein we report two series of charged iridium complexes with various carbene-based ancillary ligands. In the first series the CAN ligand is 2-phenylpyridine, whereas in the second one it is 2-(2,4-difluorophenyl)-pyridine. One biscarbene (:CC:) and four different pyridine carbene (NC:) chelators a…

DenticityLigandchemistry.chemical_elementCrystal structurePhotochemistryElectrochemistryEMITTING ELECTROCHEMICAL-CELLS; ELECTROLUMINESCENT DEVICES; IR(III) COMPLEXES; QUANTUM YIELDS; SOLID-STATE; BLUE PHOSPHORESCENCE; METAL-COMPLEXES; EXCITED-STATES; GREEN; COLORInorganic Chemistrychemistry.chemical_compoundchemistryPyridinePolymer chemistryIridiumPhysical and Theoretical ChemistryPhosphorescenceCarbene
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Development of trackable metal-based drugs: new generation of therapeutic agents

2016

International audience; In medicinal chemistry, the aim is not only to conceive ever more efficient molecules, but also to understand their mechanism of action. In very recent years, a new promising strategy was developed to tackle this issue: the conception of trackable therapeutic agents. Metal-based drugs are ideal to exploit this expanding area of research.

Diagnostic ImagingExploitTheranostic NanomedicineComputer scienceNanotechnologyphosphine-porphyrinpotential anticancer agents[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesin-vivo[ CHIM ] Chemical SciencesTheranostic NanomedicineInorganic Chemistrytheranostic agentsplatinum(ii) complexesorganometallic compoundsAnimals[CHIM]Chemical Sciences010405 organic chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry0104 chemical sciences3. Good healthcancer-cellsRisk analysis (engineering)photodynamic therapycytotoxic propertiesDrug Designheterocyclic carbene complexes
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