Search results for "ylid"

showing 10 items of 1155 documents

CCDC 248542: Experimental Crystal Structure Determination

2004

Related Article: C.Boskovic, A.Sieber, G.Chaboussant, H.U.Gudel, J.Ensling, W.Wernsdorfer, A.Neels, G.Labat, H.Stoeckli-Evans, S.Janssen|2004|Inorg.Chem.|43|5053|doi:10.1021/ic049600f

Space GroupCrystallographytris((mu~2~-2-(alpha-phenylsalicylidenealdiminato)ethanolato)-(mu~2~-acetato)-iron(iii)) dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1948965: Experimental Crystal Structure Determination

2019

Related Article: Guang Zhang, Felix Hermerschmidt, Anup Pramanik, Dieter Schollmeyer, Martin Baumgarten, Pranab Sarkar, Emil J. W. List-Kratochvil, Klaus Müllen|2019|J.Mater.Chem.C|7|15252|doi:10.1039/C9TC04748D

Space GroupCrystallographytris(13-bis(4-((tri-isopropylsilyl)ethynyl)phenyl)-13-dihydro-2H-benzimidazol-2-ylidene)-iridium dichloromethane unknown solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 984545: Experimental Crystal Structure Determination

2014

Related Article: Samia Benmansour, Eugenio Coronado, Carlos Giménez-Saiz, Carlos J. Gómez-García, Carola Rößer|2014|Eur.J.Inorg.Chem.||3949|doi:10.1002/ejic.201402023

Space GroupCrystallographytris(36-dichloro-45-dioxy-12-benzoquinone)-iron hexakis(2-(56-dihydro[13]dithiolo[45-b][14]dithiin-2-ylidene)-56-dihydro[13]dithiolo[45-b][14]dithiine) dichloromethane solvate sesquihydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1579780: Experimental Crystal Structure Determination

2018

Related Article: Lorena Martínez, Livia Arizaga, Donatella Armentano, Francesc Lloret, Ricardo González, Carlos Kremer, Raúl Chiozzone|2018|J.Coord.Chem.|71|748|doi:10.1080/00958972.2018.1441405

Space GroupCrystallographytris(mu-{[1-(pyridin-2-yl)ethylidene]amino}oxido)-diaqua-(nitrato)-di-iron nitrate dihydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1048422: Experimental Crystal Structure Determination

2015

Related Article: Suraj Mondal, Shuvankar Mandal, Luca Carrella, Arpita Jana, Michel Fleck, Andreas Köhn, Eva Rentschler, and Sasankasekhar Mohanta|2015|Inorg.Chem.|54|117|doi:10.1021/ic501900d

Space GroupCrystallographytris(mu2-22'-(Butane-14-diylbis(nitrilomethylylidene))diphenolato)-tetra-copper(ii) diperchlorate acetonitrile solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1828644: Experimental Crystal Structure Determination

2018

Related Article: Joaquín Viqueira, María L. Durán, José A. García-Vázquez, Jesús Castro, Carlos Platas-Iglesias, David Esteban-Gómez, Gloria Alzuet-Piña, Angeles Moldes, Otaciro R. Nascimento|2018|New J.Chem.|42|15170|doi:10.1039/C8NJ03292K

Space GroupCrystallography{N-[2-({[3-ethoxy-2-oxyphenyl]methylidene}amino)phenyl]-4-methylbenzene-1-sulfonamidato}-(110-phenanthroline)-copper(ii) acetonitrile solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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A mechanistic study of the participation of azomethine ylides and carbonyl ylides in [3+2] cycloaddition reactions

2015

The participation of azomethine ylides (AYs) and carbonyl ylides (CYs) in [3+2] cycloaddition (32CA) reactions has been analysed at the DFT B3LYP/6-31G(d) level. The asymmetric substitution breaks the pseudodiradical character of the simplest three-atom-components (TACs), modifying their electrophilic and nucleophilic behaviours. These TACs react quickly towards electrophilic nitroethylene. However, while the reaction with AY takes place via a zw-type mechanism, the reaction with CY appears to take place via a pr-type mechanism. A different behaviour is found in the reactivity towards the nucleophilic methyl vinyl ether. While AY presents a high activation energy, CY presents a high reactiv…

StereochemistryChemistryOrganic ChemistryAzomethine ylideRegioselectivityMethyl vinyl etherBiochemistryCycloadditionchemistry.chemical_compoundNucleophileNitroethyleneDrug DiscoveryElectrophileReactivity (chemistry)Tetrahedron
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Straightforward Regio- and Diastereoselective Synthesis, Molecular Structure, Intermolecular Interactions and Mechanistic Study of Spirooxindole-Engr…

2021

Straightforward regio- and diastereoselective synthesis of bi-spirooxindole-engrafted rhodanine analogs 5a–d were achieved by one-pot multicomponent [3 + 2] cycloaddition (32CA) reaction of stabilized azomethine ylide (AYs 3a–d) generated in situ by condensation of L-thioproline and 6-chloro-isatin with (E)-2-(5-(4-chlorobenzylidene)-2,4-dioxothiazolidin-3-yl)-N-(2-morpholinoethyl)acetamide. The bi-spirooxindole-engrafted rhodanine analogs were constructed with excellent diastereo- and regioselectivity along with high chemical yield. X-ray crystallographic investigations for hybrid 5a revealed the presence of four contiguous stereocenters related to C11, C12, C19 and C22 of the spiro struct…

StereochemistryHirshfeld DFTPharmaceutical ScienceAzomethine ylideOrganic chemistryArticleAnalytical ChemistryStereocenterchemistry.chemical_compoundQD241-441spirooxindole; rhodanine; azomethine ylides; [3 + 2] cycloaddition (32CA) reactions; hydrogen bonding; Hirshfeld DFT; supernucleophilesNucleophileDrug DiscoveryrhodanineReactivity (chemistry)Physical and Theoretical Chemistryheterosykliset yhdisteetsupernucleophilesvetysidoksettiheysfunktionaaliteoriaRegioselectivityazomethine ylidesspirooxindolehydrogen bondingCycloaddition[3 + 2] cycloaddition (32CA) reactionsRhodaninechemistryChemistry (miscellaneous)Molecular MedicineDerivative (chemistry)Molecules; Volume 26; Issue 23; Pages: 7276
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Synthesis and Reactivity toward Isonitriles of (2-Aminoaryl)palladium(II) Complexes

2001

Mixtures of “Pd(dba)2” (dba = dibenzylideneacetone) and 2,2‘-bipyridine (bpy; 1:2) or N,N,N‘,N‘-tetramethylethylenediamine (tmeda; 1:1) react with 2-bromo-4-nitroaniline to give [Pd{C6H3NH2-2-NO2-5}Br(N−N)] (N−N = bpy (1b), tmeda (1b‘)). Reactions of 2-iodoaniline with mixtures of “Pd(dba)2” and isonitriles RNC (R = C6H3Me2-2,6 (Xy), 2:1:2 molar ratios; R = tBu, 2.9:1:2 molar ratios) result in the formation of the complexes [Pd{κ2C,N-C(NXy)C6H4NH2-2}I(CNXy)] (2a) and trans-[Pd{C(NtBu)C6H4NH2-2}I(CNtBu)2] (3a*). The reactions of [Pd{C6H4NH2-2}I(bpy)] and 1b‘ with RNC give the complexes trans-[Pd{C(NR)C6H3NH2-2-Y-5}}X(CNR)2] (Y = H, X = I, R = Xy (3a), tBu (3a*); Y = NO2, X = Br, R = Xy (3b),…

StereochemistryLigandOrganic ChemistryCationic polymerizationchemistry.chemical_elementDecompositionMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryDibenzylideneacetoneReactivity (chemistry)Physical and Theoretical ChemistryPalladiumOrganometallics
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Diorganotin(IV) Complexes of Methyl 2-{[(E)-8-Oxo-5, 8-dihydroquinolin-5-ylidene]hydrazino}benzoate

2012

Three cis-bis{5-[(E)-2-(2-carbomethoxyphenyl)-1- diazenyl]quinolinolato}-diorganotin(IV), R2Sn(L)2, complexes [R = Me (1), Ph (2) and Bz (3)] were synthesized and characterized by 1H-, 13C-, 119Sn- NMR, IR, and 119Sn Mössbauer spectroscopic techniques in combination with elemental analysis. The structure of diphenyltin(IV) complex Ph2Sn(L)2 (2) was determined by single-crystal X-ray crystallography as its tri-benzene solvate. Each complex was found to adopt a distorted cis-R2 octahedral arrangement around the tin atom with the quinolinolato ligands being N,O-chelating; the oxygen atoms are trans to each other. The complexes retain their solid- state structure in non-coordinating solvents as…

StereochemistryStructure elucidationchemistry.chemical_elementNuclear magnetic resonance spectroscopyMedicinal chemistryInorganic ChemistryNMR spectroscopyOxygen atomchemistryOctahedronTinSettore CHIM/03 - Chimica Generale E InorganicaMössbauer spectroscopyMethyl 2-{[(E)-8-oxo-58-dihydroquinolin-5-ylidene]hydrazino}benzoateSpectroscopyTin119Sn Mössbauer spectroscopyZeitschrift für anorganische und allgemeine Chemie
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