0000000000267451

AUTHOR

Christian Köhler

showing 6 related works from this author

Functionalized phosphonates as building units for multi-dimensional homo- and heterometallic 3d-4f inorganic-organic hybrid-materials.

2016

Using the multifunctional ligand H4L (2,2'-bipyridinyl-5,5'-diphosphonic acid), a new family of inorganic-organic hybrid-materials was prepared. The ligand shows a very high flexibility regarding the coordination mode, leading to a large structural diversity. The compounds 1a, 1b ([M(H2L)(H2O)4]·2.5H2O; M = Co(2+) (a), Ni(2+) (b)), 2 ([Gd2(H2H'L)2(H2H'2L)(H2O)6]Cl4·14H2O), 3a, 3b, 3c ([MCo(iii)(H2L)3(H2O)2]·6.5H2O; M = Gd(3+) (a), Dy(3+) (b) and Tb(3+) (c)), and 4 ([GdNi(ii)(H2L)3(H2O)3]NaCl·6H2O) were isolated and characterized with single crystal X-ray diffraction. Depending on the used metal ions and on the stoichiometry, either discrete entities (0D), extended 2D layers or 3D frameworks…

010405 organic chemistryLigandStereochemistryMetal ions in aqueous solution010402 general chemistry01 natural sciencesPhosphonate0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMulti dimensionalHydrothermal synthesisHybrid materialSingle crystalStoichiometryDalton transactions (Cambridge, England : 2003)
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The First 1,3,4‐Oxadiazole Based Dinuclear Iron(II) Complexes Showing Spin Crossover Behavior with Hysteresis

2015

Three new dinuclear complexes [FeII2(μ-L)2]X4 (L is the bis-tridentate ligand 2,5-bis{[(2-pyridylmethyl)amino]methyl}-1,3,4-oxadiazole and X = ClO4–, BF4– and CF3SO3–) have been synthesized and fully characterized by single-crystal X-ray diffraction, Mossbauer spectroscopy and magnetic susceptibility measurements. Upon cooling, a trapped [high-spin–low-spin] state of the iron(II) centres is detected. Depending on the counterion, a pronounced thermal hysteresis is found. In one case, it was possible to observe a space group change that accompanies the spin transition. This is the first system showing spin crossover based on an oxadiazole ligand.

chemistry.chemical_classification010405 organic chemistryLigandInorganic chemistrySpin transitionOxadiazole010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryHysteresischemistry.chemical_compoundCrystallographychemistrySpin crossoverMössbauer spectroscopyCounterionEuropean Journal of Inorganic Chemistry
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CCDC 1434704: Experimental Crystal Structure Determination

2016

Related Article: Christian Köhler and Eva Rentschler|2016|Eur.J.Inorg.Chem.||1955|doi:10.1002/ejic.201501278

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-NN'-(134-oxadiazole-25-diylbis(methylene))bis(1-(pyridin-2-yl)methanamine))-di-iron(ii) tetrakis(trifluoromethanesulfonate) acetonitrile solvateExperimental 3D Coordinates
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CCDC 1434702: Experimental Crystal Structure Determination

2016

Related Article: Christian Köhler and Eva Rentschler|2016|Eur.J.Inorg.Chem.||1955|doi:10.1002/ejic.201501278

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-NN'-(134-oxadiazole-25-diylbis(methylene))bis(1-(pyridin-2-yl)methanamine))-di-iron(ii) tetraperchlorate acetonitrile solvateExperimental 3D Coordinates
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CCDC 1434703: Experimental Crystal Structure Determination

2016

Related Article: Christian Köhler and Eva Rentschler|2016|Eur.J.Inorg.Chem.||1955|doi:10.1002/ejic.201501278

bis(mu-NN'-(134-oxadiazole-25-diylbis(methylene))bis(1-(pyridin-2-yl)methanamine))-di-iron(ii) tetrakis(tetrafluoroborate) acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1434701: Experimental Crystal Structure Determination

2016

Related Article: Christian Köhler and Eva Rentschler|2016|Eur.J.Inorg.Chem.||1955|doi:10.1002/ejic.201501278

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-NN'-(134-oxadiazole-25-diylbis(methylene))bis(1-(pyridin-2-yl)methanamine))-di-iron(ii) tetraperchlorate acetonitrile solvateExperimental 3D Coordinates
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