Search results for "kemiallinen synteesi"

showing 10 items of 92 documents

Synthesis of Enaminones-Based Benzo[d]imidazole Scaffold: Characterization and Molecular Insight Structure

2020

(E)-1-(1H-Benzo[d]imidazol-2-yl)-3-(dimethylamino)prop-2-en-1-one 2 was synthesized by one-pot synthesis protocol of 2-acetyl benzo[d]imidazole with dimethylformamide dimethylacetal (DMF-DMA) in xylene at 140 &deg

General Chemical EngineeringAcetylacetoneChemical structure010402 general chemistry01 natural sciencesDFTInorganic Chemistrychemistry.chemical_compound<i>β</i>-enaminonelcsh:QD901-999ImidazoleMoleculeGeneral Materials ScienceReactivity (chemistry)β-enaminoneorgaaniset yhdisteetkemiallinen synteesi010405 organic chemistrytiheysfunktionaaliteoriabenzo[<i>d</i>]imidazoleHirshfeld analysiskiteetCondensed Matter Physics0104 chemical sciencesCrystallographyDMF-DMAchemistrybenzo[d]imidazoleOrthorhombic crystal systemlcsh:CrystallographyDerivative (chemistry)Monoclinic crystal systemCrystals
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Synthesis, X-ray Structure, Conformational Analysis, and DFT Studies of a Giant s-Triazine bis-Schiff Base

2021

The current work involves the synthesis of 2,2′-(6-(piperidin-1-yl)-1,3,5-triazine-2,4-diyl)bis(hydrazin-2-yl-1-ylidene))bis(methanylylidene))diphenol 4, characterization, and the DFT studies of the reported compound. The crystal unit cell parameters of 4 are a = 8.1139(2) Å, b = 11.2637(2) Å, c = 45.7836(8) Å. The unit cell volume is 4184.28(15) Å3 and Z = 4. It crystallized in the orthorhombic crystal system and Pbca space group. The O…H, N…H, C…H, H…H and C…C intermolecular contacts which affect the crystal stability were quantitatively analyzed using Hirshfeld calculations. Their percentages were calculated to be 9.8, 15.8, 23.7, 46.4, and 1.6% from the whole contacts occurred in the cr…

General Chemical EngineeringInorganic ChemistryCrystalchemistry.chemical_compounds-triazineNBOGeneral Materials Sciencebis-Schiff basetyppiyhdisteetheterosykliset yhdisteetConformational isomerismkemiallinen synteesiSchiff baseCrystallography<i>s</i>-triazineChemistryHydrogen bondtiheysfunktionaaliteoriaIntermolecular forceconformational analysisHirshfeld analysiskiteetCondensed Matter Physics<i>bis</i>-Schiff baseCrystallographyQD901-999Intramolecular forceOrthorhombic crystal systemröntgenkristallografiaNatural bond orbitalCrystals
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Synthesis, and Molecular Structure Investigations of a New s-Triazine Derivatives Incorporating Pyrazole/Piperidine/Aniline Moieties

2021

In this work, we synthesized two new s-triazine incorporates pyrazole/piperidine/aniline moieties. Molecular structure investigations in the light of X-ray crystallography combined with Hirshfeld and DFT calculations were presented. Intermolecular interactions controlling the molecular packing of 4-(3,5-dimethyl-1H-pyrazol-1-yl)-N-phenyl-6-(piperidin-1-yl)-1,3,5-triazin-2-amine; 5a and N-(4-bromophenyl)-4-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)-1,3,5-triazin-2-amine; 5b were analyzed using Hirshfeld calculations. The most dominant interactions are the H...H, N...H and H...C contacts in both compounds. The N...H and H...C interactions in 5a and the N...H, Br...H and H...H interacti…

General Chemical EngineeringPyrazoleInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeAnilines-triazinehydrazino-s-triazineComputational chemistry<i>s</i>-triazine; pyrazole; hydrazino-<i>s</i>-triazine; Hirshfeld calculationsMoleculeHirshfeld calculationsGeneral Materials Scienceheterosykliset yhdisteetDebyeTriazinekemiallinen synteesiCrystallography<i>s</i>-triazineChemical shiftIntermolecular forceCondensed Matter Physicspyrazolechemistryhydrazino-<i>s</i>-triazineQD901-999symbolsPiperidineCrystals
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Synthesis and X-ray Crystal Structure of New Substituted 3-4′-Bipyrazole Derivatives. Hirshfeld Analysis, DFT and NBO Studies

2021

A new compounds named 3-4′-bipyrazoles 2 and 3 were synthesized in high chemical yield from a reaction of pyran-2,4-diketone 1 with aryl hydrazines under thermal conditions in MeOH. Compound 2 was unambiguously confirmed by single-crystal X-ray analysis. It crystalizes in a triclinic crystal system and space group P-1. Its crystal structure was found to be in good agreement with the spectral characterizations. With the aid of Hirshfeld calculations, the H…H (54.8–55.3%) and H…C (28.3–29.2%) intermolecular contacts are the most dominant, while the O…H (5.8–6.5%), N…H (3.8–4.6%) and C…C (3.0–4.9%) are less dominant. The compound has a polar nature with a net dipole moment of 6.388 Debye. The …

General Chemical Engineeringpyran-24-dioneCrystal structureTriclinic crystal systemDFTInorganic Chemistrychemistry.chemical_compoundkemialliset sidoksetNBOGeneral Materials Scienceorgaaniset yhdisteetkemiallinen synteesiCrystallographyArylIntermolecular forcetiheysfunktionaaliteoriaHirshfeld analysisCondensed Matter PhysicskiteetbipyrazoleDipoleCrystallographychemistryQD901-999Intramolecular forceYield (chemistry)röntgenkristallografiaNatural bond orbitalCrystals
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X-ray Single Crystal Structure, Tautomerism Aspect, DFT, NBO, and Hirshfeld Surface Analysis of a New Schiff Bases Based on 4-Amino-5-Indol-2-yl-1,2,…

2021

Four different new Schiff basses tethered indolyl-triazole-3-thione hybrid were designed and synthesized. X-ray single crystal structure, tautomerism, DFT, NBO and Hirshfeld analysis were explored. X-ray crystallographic investigations with the aid of Hirshfeld calculations were used to analyze the molecular packing of the studied systems. The H···H, H···C, S···H, Br···C, O···H, C···C and N···H interactions are the most important in the molecular packing of 3. In case of 4, the S···H, N···H, S···C and C···C contacts are the most significant. The results obtained from the DFT calculations indicated that the thione tautomer is energetically lower than the thiol one by 13.9545 and 13.7464 kcal…

General Chemical Engineeringtautomerism aspectInorganic Chemistrysymbols.namesakeGeneral Materials SciencetyppiyhdisteetDebyechemistry.chemical_classificationkemiallinen synteesiCrystallographyX-rayCondensed Matter Physicsindolyl-triazole-3-thioneTautomerSchiff bases; indolyl-triazole-3-thione; tautomerism aspect; Hirshfeld Surface AnalysisCrystallographyDipolechemistryQD901-999Thiolsymbols1 2 4 triazole 3 thioneSchiff basesHirshfeld Surface AnalysisSingle crystaltautomeriaNatural bond orbitalCrystals; Volume 11; Issue 9; Pages: 1041
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Deoxygenative Divergent Synthesis : En Route to Quinic Acid Chirons

2020

The installation of vicinal mesylate and silyl ether groups in a quinic acid derivative generates a system prone for stereoselective borane-catalyzed hydrosilylation through a siloxonium intermediate. The diversification of the reaction conditions allowed the construction of different defunctionalized fragments foreseen as useful synthetic fragments. The selectivity of the hydrosilylation was rationalized on the basis of deuteration experiments and computational studies. peerReviewed

Hydrosilylation010402 general chemistry01 natural sciencesBiochemistrySilyl etherchemistry.chemical_compoundredox reactionsPhysical and Theoretical Chemistryhapetus-pelkistysreaktioorgaaniset yhdisteeteetteritkemiallinen synteesi010405 organic chemistryreaction productsOrganic ChemistryhydrosilylationQuinic acidCombinatorial chemistry0104 chemical sciencesbond cleavageetherschemistryStereoselectivitySelectivityDivergent synthesisDerivative (chemistry)Vicinal
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Chemoselective heterogeneous iridium catalyzed hydrogenation of cinnamalaniline

2020

International audience; Selective hydrogenation of unsaturated imines over heterogeneous catalysts is an ecologically feasible and effective way to produce commercially valuable saturated imines and unsaturated amines under mild conditions, avoiding the utilization of toxic halides. The liquid-phase hydrogenation of a model imine, cinnamalaniline, over Ir, Ru, Pd and Au catalysts was studied in polar protic (methanol, 2-propanol), polar aprotic (methyl tert-butyl ether) and non-polar aprotic (toluene) solvents at 40-80°C under atmospheric hydrogen pressure. Different metal oxides (Al 2 O 3 , ZrO 2 , SiO 2) and carbon composites based on carbon nitrides synthesized by pyrolysis of ethylenedi…

Iminechemistry.chemical_elementEthylenediamineplatinametallit010402 general chemistry01 natural sciences7. Clean energyCatalysisCatalysischemistry.chemical_compoundkatalyytitOrganic chemistryIridiumtyppiyhdisteetChemoselectivityhydrausorgaaniset yhdisteetkemiallinen synteesi010405 organic chemistry0104 chemical sciencesSolvent[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry13. Climate actionkatalyysiAmine gas treatingMethanol
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Straightforward One-Pot Synthesis of New 4-Phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one Derivatives: X-ray Single Crystal Structure and Hirshfeld Ana…

2022

A straightforward one-pot route for the synthesis of a new 4-phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one is reported form the direct hydrazinolysis of triketo ester and hydrazine hydrate in ethanol. 4-Phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one was subjected to aza-Michael addition and N-alkylation on reaction with a set of alkylating agents in the presence of K2CO3. Hydrazinolysis of 4-phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one ester to hydrazide and conversion of hydrazide to thiosemicarbazide were successful. X-Ray single crystals analysis and 1H, 13C NMR were used for unambiguous structure confirmation. The O&hellip;H, N&hellip;H, C&hellip;N and C&hellip;C in 2, and the N&hellip;H, …

Inorganic ChemistryHirshfeld Analysesaromaattiset yhdisteetkemiallinen synteesipolycyclic aromatic heterocyclesfluoranthenes; polycyclic aromatic heterocycles; <i>aza</i>-Michael addition; <i>N</i>-alkylation; Hirshfeld AnalysesGeneral Chemical EngineeringfluoranthenesGeneral Materials Scienceaza-Michael additionN-alkylationheterosykliset yhdisteetCondensed Matter PhysicsCrystals; Volume 12; Issue 2; Pages: 262
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The Difficult Marriage of Triarylcorroles with Zinc and Nickel Ions.

2022

The coordination chemistry of corrole has witnessed a great improvement in the past few years and its Periodic Table has been widened to be so large that it is compared with that of porphyrins. However, Ni and Zn ions, commonly used with porphyrins for both synthetic and theoretical purposes, are sparsely reported in the case of corroles. Here, we report synthetic protocols for preparing Ni and Zn triarylcorrole complexes. In the case of Zn, the preliminary oxidation of the free base corrole in DMSO to the neutral corrole radical is a necessary step to obtain the coordination of the metal ion, because the direct reaction led to the formation of an open-chain tetrapyrrole. The Ni complex cou…

Inorganic ChemistryIonskemiallinen synteesiaromaattiset yhdisteetZincsinkki (metallit)PorphyrinsNickelSettore CHIM/07Dimethyl SulfoxidekompleksiyhdisteetPhysical and Theoretical ChemistrynikkeliInorganic chemistry
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Utility of Three-Coordinate Silver Complexes Toward the Formation of Iodonium Ions

2021

The work herein describes the synthesis of five three-coordinate silver(I) complexes comprising a bidentate ligand L1, either bpy (2,2′-bipyridyl) or bpyMe2 (4,4′-dimethyl-2,2′-dipyridyl), and a monodentate ligand L2, either mtz (1-methyl-1H-1,2,3-triazole), 4-Etpy (4-ethylpyridine), or 4-DMAP (N,N-dimethylpyridin-4-amine). Upon reaction of the three-coordinate silver(I) complexes with 0.5 equiv of I2, the reactions quantitatively produce a 1:1 pair of complexes of a four-coordinate silver(I) complex [Ag(L1)2]PF6 and a two-coordinate iodonium complex [I(L2)2]PF6. The combination of [Ag(bpyMe2)2]PF6 and [I(4-DMAP)2]PF6 gave rise to an I+···Ag+ interaction where the I+ acts as a nucleophile, …

Inorganic Chemistrykemiallinen synteesiDenticityNucleophilekemialliset yhdisteetChemistryhopealiganditkompleksiyhdisteetPhysical and Theoretical ChemistryMedicinal chemistryArticleIon
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