Search results for "rikki"

showing 10 items of 36 documents

1,2‐Benzothiazine Derivatives from Sulfonimidamides by Metal‐Catalyzed Annulation Reactions in Solution and under Solvent‐Free Mechanochemical Condit…

2021

Advanced synthesis & catalysis (2021). doi:10.1002/adsc.202001505 special issue: "Hot Topic: C-H Activation"

Annulationkemiallinen synteesiSolvent free660iridium catalysisChemistrysulfonimidamideGeneral ChemistryBenzothiazine12-benzothiazineC−H activationCatalysisMetalchemistry.chemical_compoundMechanochemistryvisual_artkatalyysirikkiyhdisteetddc:660visual_art.visual_art_mediumrhodium catalysisOrganic chemistrymechanochemistryorgaaniset yhdisteet
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A study on the fragmentation of sulfuric acid and dimethylamine clusters inside an atmospheric pressure interface time-of-flight mass spectrometer

2022

Abstract. Sulfuric acid and dimethylamine vapours in the atmosphere can form molecular clusters, which participate in new particle formation events. In this work, we have produced, measured, and identified clusters of sulfuric acid and dimethylamine using an electrospray ionizer coupled with a planar-differential mobility analyser, connected to an atmospheric pressure interface time-of-flight mass spectrometer (ESI–DMA–APi-TOF MS). This set-up is suitable for evaluating the extent of fragmentation of the charged clusters inside the instrument. We evaluated the fragmentation of 11 negatively charged clusters both experimentally and using a statistical model based on quantum chemical data. Th…

Atmospheric Sciencedimethylamine clustersilmanpaine010504 meteorology & atmospheric sciencesamiinitrikkihapposulfuric acidTA715-787Environmental engineeringTA170-171pienhiukkaset010402 general chemistry01 natural sciences114 Physical sciencesAMINE0104 chemical sciencesilmakemiaklusteritatmospheric pressureEarthwork. Foundationsfragmentationhajoaminen (kemia)PARTICLE FORMATION0105 earth and related environmental sciencesNUCLEATION
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Non-Innocent Base Properties of 3- and 4-Pyridyl-dithia- and Diselenadiazolyl Radicals : The Effect of N-Methylation

2018

International audience; Condensation of persilylated nicotinimideamide and isonicotinimideamide with sulfur monochloride affords double salts of the 3-, 4-pyridyl-substituted 1,2,3,5-dithiadiazolylium DTDA cations of the general formula [3-, 4-pyDTDA][Cl][HCl] in which the pyridyl nitrogen serves as a noninnocent base. Reduction of these salts with triphenylantimony followed by deprotonation of the intermediate-protonated radical affords the free base radicals [3-, 4-pyDTDA], the crystal structures of which, along with those of their diselenadiazolyl analogues [3-, 4-pyDSDA], have been characterized by powder or single-crystal X-ray diffraction. The crystal structures consist of “pancake” π…

Base (chemistry)Radicalsuolat (yhdisteet)free radicals02 engineering and technologyCrystal structure010402 general chemistryMetathesistriflate saltsvapaat radikaalit01 natural sciencesMedicinal chemistryChlorideInorganic ChemistrydimersDeprotonationrikkiyhdisteetmedicinePhysical and Theoretical Chemistryta116dithiadiazoleschemistry.chemical_classificationIntermolecular forceFree base[CHIM.MATE]Chemical Sciences/Material chemistryN-methylation021001 nanoscience & nanotechnology0104 chemical sciencesoligomeerichemistry0210 nano-technologymedicine.drug
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Thiourea Organocatalysts as Emerging Chiral Pollutants: En Route to Porphyrin-Based (Chir)Optical Sensing

2021

Environmental pollution with chiral organic compounds is an emerging problem requiring innovative sensing methods. Amino-functionalized thioureas, such as 2-(dimethylamino)cyclohexyl-(3,5-bis(trifluoromethyl)phenyl)thiourea (Takemoto’s catalyst), are widely used organocatalysts with virtually unknown environmental safety data. Ecotoxicity studies based on the Vibrio fischeri luminescence inhibition test reveal significant toxicity of Takemoto’s catalyst (EC50 = 7.9 mg/L) and its NH2-substituted analog (EC50 = 7.2–7.4 mg/L). The observed toxic effect was pronounced by the influence of the trifluoromethyl moiety. En route to the porphyrin-based chemosensing of Takemoto-type thioureas, their s…

Circular dichroismSupramolecular chemistrychiralitymonitorointiEnvironmental pollutionchiral amineVibrio fischeriQD415-436010402 general chemistryBiochemistry01 natural sciencesMedicinal chemistrysupramolecular chemistrybakteeritAnalytical Chemistry<i>Vibrio</i> <i>fischeri</i>chemistry.chemical_compoundkatalyytitrikkiyhdisteetsupramolekulaarinen kemiaMoiety[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrythioureaorgaaniset yhdisteetchiral pollutantsTrifluoromethyl010405 organic chemistrytoxicityhost–guest bindingPorphyrin0104 chemical sciencesTakemoto’s catalystcircular dichroismekotoksikologiachemistryThiourea13. Climate action[SDV.TOX.ECO]Life Sciences [q-bio]/Toxicology/Ecotoxicology[SDE.BE]Environmental Sciences/Biodiversity and EcologyChirality (chemistry)porphyrinorganocatalyst
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Synthesis of a labile sulfur-centred ligand, [S(H)C(PPh2S)2]−: structural diversity in lithium(i), zinc(ii) and nickel(ii) complexes

2016

A high-yield synthesis of [Li{S(H)C(PPh2S)2}]2 [Li2·(3)2] was developed and this reagent was used in metathesis with ZnCl2 and NiCl2 to produce homoleptic complexes 4 and 5b in 85 and 93% yields, respectively. The solid-state structure of the octahedral complex [Zn{S(H)C(PPh2S)2}2] (4) reveals notable inequivalence between the Zn-S(C) and Zn-S(P) contacts (2.274(1) Å vs. 2.842(1) and 2.884(1) Å, respectively). Two structural isomers of the homoleptic complex [Ni{S(H)C(PPh2S)2}2] were isolated after prolonged crystallization processes. The octahedral green Ni(ii) isomer 5a exhibits the two monoprotonated ligands bonded in a tridentate (S,S',S'') mode to the Ni(ii) centre with three distinctl…

Stereochemistrychemistry.chemical_elementmetal complexes010402 general chemistry01 natural sciencesisomerizationelectronic structuresInorganic Chemistrychemistry.chemical_compoundelektronirakenteetrikkipohjaiset liganditStructural isomerSinglet stateTriplet stateHomolepticta116010405 organic chemistryLigandsulphur-centered ligands0104 chemical sciencesBond lengthNickelCrystallographyOctahedronchemistryisomerisaatiometallikompleksitDalton Transactions
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Microscopic Insights Into the Formation of Methanesulfonic Acid–Methylamine–Ammonia Particles Under Acid-Rich Conditions

2022

Understanding the microscopic mechanisms of new particle formation under acid-rich conditions is of significance in atmospheric science. Using quantum chemistry calculations, we investigated the microscopic formation mechanism of methanesulfonic acid (MSA)–methylamine (MA)–ammonia (NH3) clusters. We focused on the binary (MSA)2n-(MA)n and ternary (MSA)3n-(MA)n-(NH3)n, (n = 1–4) systems which contain more acid than base molecules. We found that the lowest-energy isomers in each system possess considerable thermodynamic and dynamic stabilities. In studied cluster structures, all bases are protonated, and they form stable ion pairs with MSA, which contribute to the charge transfer and the stab…

aerosolitbase ratio [acid]proton transferEcologyammoniakkipienhiukkasetilmakemiahappamuusklusteritnew particle formationrikkiyhdisteetacid-rich conditiontyppiyhdisteetmethanesulfonic acid–methylamine–ammonia particlesEcology Evolution Behavior and SystematicsFrontiers in Ecology and Evolution
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Molecular properties affecting the hydration of acid-base clusters

2021

In the atmosphere, water in all phases is ubiquitous and plays important roles in catalyzing atmospheric chemical reactions, participating in cluster formation and affecting the composition of aerosol particles. Direct measurements of water-containing clusters are limited because water is likely to evaporate before detection, and therefore, theoretical tools are needed to study hydration in the atmosphere. We have studied thermodynamics and population dynamics of the hydration of different atmospherically relevant base monomers as well as sulfuric acid–base pairs. The hydration ability of a base seems to follow in the order of gas-phase base strength whereas hydration ability of acid–base p…

aerosolitmolekyylifysiikkarikkihappotermodynamiikkavesipienhiukkaset
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Computational investigations of 18-electron triatomic sulfur–nitrogen anions

2018

MRCI-SD/def2-QZVP and PBE0/def2-QZVP calculations have been employed for the analysis of geometries, stabilities, and bonding of isomers of the 18-electron anions N2S2−, NS2−, and NSO−. Isomers of the isoelectronic neutral molecules SO2, S2O, S3, and O3 are included for comparison. The sulfur-centered acyclic NSN2−, NSS−, and NSO− anions are the most stable isomers of their respective molecular compositions. However, the nitrogen-centered isomers SNS− and SNO− lie close enough in energy to their more stable counterparts to allow their occurrence. The experimental structural information, where available, is in good agreement with the optimized bond parameters. The bonding in all investigate…

anionit010405 organic chemistryisomeriaTriatomic moleculeOrganic Chemistrychemistry.chemical_elementGeneral ChemistryElectron010402 general chemistrylaskennallinen kemia01 natural sciencesSulfurNitrogenCatalysis0104 chemical scienceselectronic structureschemistry18-electron triatomicssulfur–nitrogen anionsrikkiyhdisteetPhysical chemistryisomerstyppiyhdisteettheoretical calculations
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Design, Construction, and Characterization of a New Regioisomer and Diastereomer Material Based on the Spirooxindole Scaffold Incorporating a Sulphon…

2020

The 1,3-dipolar cycloaddition reaction is one of the most rapid, and efficient protocols to access, and construct highly divergent heterocycle chiral auxiliaries. Free catalyst synthesis of spirooxindole scaffold incorporating sulphone moiety via one pot&ndash

aromaattiset yhdisteetPhysics and Astronomy (miscellaneous)isomeriaGeneral Mathematics13-dipolar cycloaddition reaction010402 general chemistry01 natural sciencesdiastereomerComputational chemistrysulphonerikkiyhdisteetComputer Science (miscellaneous)MoietyReactivity (chemistry)Molecular orbitalHOMO/LUMOorgaaniset yhdisteet010405 organic chemistryChemistrylcsh:MathematicsChemical shiftDiastereomerspirooxindoleHirshfeld analysislcsh:QA1-939Cycloaddition0104 chemical sciencesregioisomerChemistry (miscellaneous)Natural bond orbitalSymmetry
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X-Ray structure, Hirshfeld analysis and DFT studies of two new hits of triazolyl-indole bearing alkylsulfanyl moieties

2021

Two new hits of triazolyl-indole containing two different alkylsulfanyl analogues named tert-butyl 2-((4-amino-5-(1H-indol-2-yl)-4H-1,2,4-triazol-3-yl)thio)acetate 2, and ethyl 2-((4-amino-5-(1H-indol-2-yl)-4H-1,2,4-triazol-3-yl)thio)acetate 3 were synthesized via reaction of 4-amino-5-(1H-indol-2-yl)-1,2,4-triazol-3(2H)-thione 1 with tert-butyl bromoacetate and ethyl chloroacetate in the presence of base (Et3N). The molecular structure of 2, and 3 was confirmed by single-crystal X-ray diffraction and 1H/13C- NMR spectroscopic techniques. In compound 2, the molecular packing depends on significant O...H (9.3%), N...H (12.4%) and S...H (3.1%) as well as relatively weak C...H (14.1%), S...C (…

aromaattiset yhdisteettriazolyl-indolereactivity descriptorsThio-Uv-Vis010402 general chemistry01 natural sciencesDFTAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundrikkiyhdisteetNBOMoleculeHirshfeld surface analysisReactivity (chemistry)Ethyl chloroacetateSpectroscopyIndole testkemiallinen synteesi010405 organic chemistryChemistryHydrogen bondChemical polarityOrganic Chemistry0104 chemical sciencesCrystallographyNatural bond orbital
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