Search results for "Dithiolane"

showing 5 items of 5 documents

Naphthyridine Derivatives as a Model System for Potential Lithium-Sulfur Energy-Storage Applications

2015

Naphthyridines have been identified as structural elements in sulfurized polyacrylonitrile, which is a common electrode material in lithium–sulfur batteries. Some dibenzonaphthyridine derivatives with a fused dithiolo moiety were prepared as model compounds for battery studies. These heterocyclic systems were prepared via the corresponding diphenyldicarbamide intermediate. Followed by naphthyridione formation, stepwise installation of the dithiolane subunit occurred in a straightforward manner. In the solid state, the heteroaromatic system is completely planar and was thoroughly characterized. Initial battery cycling tests indicated a potential use of such structural motifs in sulfur–lithiu…

Battery (electricity)Organic ChemistryPolyacrylonitrilechemistry.chemical_elementElectrochemistryCombinatorial chemistrySulfurEnergy storageDithiolanechemistry.chemical_compoundchemistryMoietyOrganic chemistryLithiumPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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The effect of tether groups on the spin states of iron(ii)/bis[2,6-di(pyrazol-1-yl)pyridine] complexes

2021

The synthesis of six 2,6-di(pyrazol-1-yl)pyridine derivatives bearing dithiolane or carboxylic acid tether groups is described: [2,6-di(pyrazol-1-yl)pyrid-4-yl]methyl (R)-lipoate (L1), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]ethyl (R)-lipoate (L2), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxy]ethyl (R)-lipoate (L3), N-([2,6-di(pyrazol-1-yl)pyrid-4-ylsulfanyl]-2-aminoethyl (R)-lipoamide (L4), 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]acetic acid (L5) and 2-[(2,6-di(pyrazol-1-yl)pyridine)-4-carboxamido]propionic acid (L6). The iron(ii) perchlorate complexes of all the new ligands exhibit gradual thermal spin-crossover (SCO) in the solid state above room temperature, except L4 who…

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundAcetic acidPerchloratechemistrySpin statesCarboxylic acidPyridineFunctional groupRing (chemistry)Medicinal chemistryDithiolaneDalton Transactions
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Long-range electronic connection in picket-fence like ferrocene–porphyrin derivatives

2012

The effects of a direct connection between ferrocene and porphyrin units have been thoroughly investigated by electrochemical and spectroscopic methods. These data not only reveal that substitution of the porphyrin macrocycle by one, two, three or four ferrocenyl groups strongly affects the electronic properties of the porphyrin and ferrocenyl moieties, they also clearly demonstrate that the metallocene centres are "connected" through the porphyrin-based electronic network. The dynamic properties of selected ferrocene-porphyrin conjugates have been investigated by VT NMR and metadynamic calculations. 1,3-Dithiolanyl protecting groups have been introduced on the upper rings of the ferrocene …

010405 organic chemistrySupramolecular chemistryCrystal structure010402 general chemistryPhotochemistryElectrochemistry01 natural sciencesPorphyrin0104 chemical sciencesDithiolaneInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryFerrocene[CHIM]Chemical SciencesMetalloceneComputingMilieux_MISCELLANEOUS
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CCDC 2012973: Experimental Crystal Structure Determination

2021

Related Article: Alejandro Torres, Alba Collado, Mar Go��mez-Gallego, Carmen Rami��rez de Arellano, Miguel A. Sierra|2021|ACS Org. Inorg. Au|2|23|doi:10.1021/acsorginorgau.1c00011

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(mu-2-[10-(2H-13-dithiol-2-ylidene)anthracen-9(10H)-ylidene]-13-dithiolane-45-dithiolato)-hexacarbonyl-di-ironExperimental 3D Coordinates
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CCDC 1866690: Experimental Crystal Structure Determination

2018

Related Article: Valentina M. Breising, Tile Gieshoff, Anton Kehl, Vincent Kilian, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Org.Lett.|20|6785|doi:10.1021/acs.orglett.8b02904

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters44-dimethyl-N3N5-bis(4-methylphenyl)-12-dithiolane-35-diimineExperimental 3D Coordinates
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