Search results for "Trifluoromethanesulfonate"

showing 6 items of 276 documents

Homoleptic Pnictogen-Chalcogen Coordination Complexes

2012

The synthesis and structural characterization of dicationic selenium and tellurium analogues of the carbodiphosphorane and triphosphenium families of compounds are reported. These complexes, [Ch(dppe)][OTf](2) [Ch = Se, Te; dppe = 1,2-bis(diphenylphosphino)ethane; OTf = trifluoromethanesulfonate], are formed using [Ch](2+) reagents via a ligand-exchange protocol and represent extremely rare examples of homoleptic pnictogen → chalcogen coordination complexes. The corresponding arsenic compounds were also prepared, [Ch(dpAse)][OTf](2) [Ch = Se, Te; dpAse = 1,2-bis(diphenylarsino)ethane], exhibiting the first instance of an arsenic → chalcogen dative bond. The electronic structures of these un…

chemistry.chemical_elementPhotochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundChalcogenchemistryReagentPhysical and Theoretical ChemistryHomolepticTelluriumPnictogenTrifluoromethanesulfonateta116SeleniumArsenicInorganic Chemistry
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Crystal structure of diaqua[5,10,15,20-tetrakis(4-methoxyphenyl)porphyrinato-κ4N]iron(III) diaqua(18-crown-6)potassium bis(trifluoromethanesulfonate)…

2015

In the title compound, [FeIII(C48H36N4O2)(H2O)2][K(C12H24O6)(H2O)2](SO3CF3)2·2C12H24O6, the FeIIIatom is situated on an inversion centre and is octahedrally coordinated by four pyrrole N atoms of the deprotenated 5,10,15,20-tetrakis(4-methoxyphenyl)porphyrinate ligand and two water molecules. The average equatorial Fe—N(pyrrole) bond length [2.043 (6) Å] is consistent with a high-spin (S= 5/2) iron(III) metalloporphyrin derivative. The K+cation, which also lies on an inversion centre, is chelated by the six O atoms of one 18-crown-6 molecule and is additionally coordinated by two water molecules in a distorted hexagonal–bipyramidal geometry. In the crystal, the cations, anions and one non-c…

crystal structureCrystallographytrifluoromethanesulfonateHydrogen bondStereochemistryLigand18-Crown-6Methane sulfonateGeneral ChemistryCrystal structureCondensed Matter PhysicsMedicinal chemistryPorphyrinData ReportsBond lengthiron(III) complex saltchemistry.chemical_compoundchemistryQD901-999General Materials Sciencetri­fluoro­methane­sulfonateporphyrinPyrroleActa Crystallographica Section E Crystallographic Communications
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Crystal structure of bis-(azido-κN)bis[2,5-bis(pyridin-2-yl)-1,3,4-thia-diazole-κ(2) N (2),N (3)]cobalt(II).

2015

The structure of the title compound is isotypic with that of the analogous nickel(II) complex, in which the CoN6 core shows an axially weakly compressed octa­hedral geometry as opposed to the almost regular geometry exhibited by the NiN6 octa­hedron.

crystal structureDenticityStereochemistryπ–π inter­actionsCrystal structuretransition metalResearch Communicationslcsh:Chemistrychemistry.chemical_compoundazide compounds25-bis­(pyridin-2-yl)-134-thia­diazole ligandPyridineGeneral Materials ScienceChemistryLigandGeneral ChemistryCondensed Matter Physicshydrogen bondingCrystallographylcsh:QD1-99925-bis(pyridin-2-yl)-134-thiadiazole ligandπ–π interactionsDiazoleSodium azideAzideTrifluoromethanesulfonateActa crystallographica. Section E, Crystallographic communications
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CCDC 976053: Experimental Crystal Structure Determination

2015

Related Article: L. Ben Haj Hassen, Z. Denden, Y. Rousselin, H. Nasri|2015|Acta Crystallogr.,Sect.E:Cryst.Commun.|71|m215|doi:10.1107/S2056989015021039

diaqua-(5101520-tetrakis(4-methoxyphenyl)porphyrinato)-iron(iii) (18-crown-6)-diaqua-potassium(i) bis(trifluoromethanesulfonate) bis(18-crown-6)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Synthesis of new hybrid 1,4-thiazinyl-1,2,3-dithiazolyl radicals via Smiles rearrangement

2017

The condensation reaction of 2-aminobenzenethiols and 3-aminopyrazinethiols with 2-amino-6-fluoro-N-methylpyridinium triflate afforded thioether derivatives that were found to undergo Smiles rearrangement and cyclocondensation with sulphur monochloride to yield new hybrid 1,4-thiazine-1,2,3-dithiazolylium cations. The synthesized cations were readily reduced to the corresponding stable neutral radicals with spin densities delocalized over both 1,4-thiazinyl and 1,2,3-dithiazolyl moieties. peerReviewed

synthesis010405 organic chemistryChemistryRadical12010402 general chemistryPhotochemistryCondensation reaction01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundDelocalized electron14-thiazinyl-123-dithiazolyl radicalsThioether4-thiazinyl-1Smiles rearrangementYield (chemistry)Polymer chemistrysynteesiSmiles rearrangementTrifluoromethanesulfonateta1163-dithiazolyl radicalsDalton Transactions
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CCDC 1873815: Experimental Crystal Structure Determination

2019

Related Article: Kristina S. Kisel, Alexei S. Melnikov, Elena V. Grachova, Antti J. Karttunen, Antonio Doménech-Carbó, Kirill Yu. Monakhov, Valentin G. Semenov, Sergey P. Tunik, Igor O. Koshevoy|2019|Inorg.Chem.|58|1988|doi:10.1021/acs.inorgchem.8b02974

tetrakis(mu-cyano)-tetrakis(22'-bipyridine)-dodecacarbonyl-platinum-tetra-rhenium bis(trifluoromethanesulfonate) unknown solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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