Search results for "ion chemistry"

showing 4 items of 254 documents

.Single-Ion Magnetic Behaviour in an Iron(III) Porphyrin Complex: A Dichotomy Between High Spin and 5/2-3/2 Spin Admixture

2020

International audience; A mononuclear iron(III) porphyrin compound exhibiting unexpectedly slow magnetic relaxation, which is a characteristic of single-ion magnet behaviour, is reported. This behaviour originates from the close proximity (approximate to 550 cm(-1)) of the intermediate-spinS=3/2 excited states to the high-spinS=5/2 ground state. More quantitatively, although the ground state is mostlyS=5/2, a spin-admixture model evidences a sizable contribution (approximate to 15 %) ofS=3/2 to the ground state, which as a consequence experiences large and positive axial anisotropy (D=+19.2 cm(-1)). Frequency-domain EPR spectroscopy allowed them(S)= |+/- 1/2⟩->|+/- 3/2&Rig…

porphyrinoids010402 general chemistry[MATH.MATH-FA]Mathematics [math]/Functional Analysis [math.FA]01 natural sciencesMolecular physicsCatalysislaw.inventionMagnetizationchemistry.chemical_compoundiron[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]lawMössbauer spectroscopy[CHIM.COOR]Chemical Sciences/Coordination chemistryAnisotropyElectron paramagnetic resonanceSpin (physics)010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryExcited statesingle-ion magnetsdensity functional calculationsmagnetic propertiesGround state
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Studies in organic mass spectrometry. Part 23. Role of the aroyl group on the competitive fragmentation reactions of the molecular ion of aroylanilid…

1999

The 70 eV and mass-analysed ion kinetic energy (MIKE) spectra of some thiophenecarboxanilides and benzoylanilides (1–10) have been compared in order to investigate the role of the aroyl (or heteroaroyl) moiety on the abundance of the competitive fragmentation reactions occurring in their molecular ions (amide–bond cleavage and phenol radical ion formation). It has been shown that the electron ionisation induced decompositions with high (70 eV) and low (MIKE) internal energy excess are qualitatively similar, but remarkable quantitative differences have been observed that can be accounted for in terms of the different effectiveness in the transmission of electronic effects of substituents in …

substituent effectsChemistryrearrangement processesPolyatomic ionAnalytical chemistryaroylanilidesMass spectrometryPhotochemistryelectron ionisation; positive ions; ion chemistry; aroylanilides; substituent effects; rearrangement processesIonchemistry.chemical_compoundRadical ionFragmentation (mass spectrometry)positive ionsThiopheneElectronic effectMoietyion chemistryelectron ionisationSpectroscopy
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The Synthesis of Quinoline‐based Tin Complexes with Pendant Schiff Bases

2019

Whilst pursuing the synthetic utility of quinoline‐based tin complexes, Me2Sn(Quin‐NO2)2 (1) and Ph2Sn(Quin‐NO2)2 (2) (Quin‐NO2 = 5‐nitroquinolino‐8‐oate) were synthesized bearing coordinatively inert nitro groups. Conventional reduction methodologies successfully converted 1 to Me2Sn(Quin‐NH2)2 (3) and 2 to Ph2Sn(Quin‐NH2)2 (4) (Quin‐NH2 = 5‐aminoquinolino‐8‐oate). The synthetically useful amine groups proved difficult to exploit in the presence of the central tin atom, however, a complete Schiff base functionalized Sn complex of the dimethyltin pro‐ligand Me2Sn(Quin‐py)2 (6) was successfully synthesized from 5‐[(pyridin‐2‐ylmethylene)amino]quinolin‐8‐ol (HQuin‐py; 5) in good yield via an …

tinquinolinecoordination chemistrySchiff basestinakompleksiyhdisteetmain group elements
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Neorganisko jonu ietekme uz jonu apmaiņas ekstrahentu adsorbciju uz fāžu robežvirsmām starp ūdens un organiskiem šķīdumiem

2000

Šķīdumi (Ķīmija):NATURAL SCIENCES::Chemistry::Physical chemistry [Research Subject Categories]Virsmu ķīmijaAdsorbcijaFāžu robežvirsmasFizikālā ķīmijaLiquidsColloidsAdsorptionSolution chemistrySurface chemistry
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