0000000001302113

AUTHOR

Helmar Görls

showing 13 related works from this author

Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n (n=1-4; m=3-7)

2020

The Te…Te secondary bonding interactions (SBI) in solid heterocyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2)m]n (n = 1‐4; m = 3‐7) species. The SBIs in 1,7‐Te2(CH2)10, 1,8‐Te2(CH2)12, 1,5,9‐Te3(CH2)9, 1,8,15‐Te3(CH2)18, 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)28 led to the tubular packing of the molecules, as has been observed previously for related thio‐ and selenoether rings. The nature of the intermolecular interactions was explored by solid‐state PBE0‐D3/pob‐TZVP calculations involving periodic boundary conditions. The packing of molecules in 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)…

eetteritheterocyclesnoncovalent interactionskemialliset sidoksettelluuritelluriumdensity functional calculationssolid-state structurestiheysfunktionaaliteoriaorganometalliyhdisteet
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Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n(n=1–4;m=3–7)

2020

The Te⋅⋅⋅Te secondary bonding interactions (SBIs) in solid cyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2 )m ]n (n=1-4; m=3-7) species. The SBIs in 1,7-Te2 (CH2 )10 , 1,8-Te2 (CH2 )12 , 1,5,9-Te3 (CH2 )9 , 1,8,15-Te3 (CH2 )18 , 1,7,13,19-Te4 (CH2 )20 , 1,8,15,22-Te4 (CH2 )24 and 1,9,17,25-Te4 (CH2 )28 lead to tubular packing of the molecules, as has been observed previously for related thio- and selenoether rings. The nature of the intermolecular interactions was explored by solid-state PBE0-D3/pob-TZVP calculations involving periodic boundary conditions. The molecular packing in 1,7,13,19-Te4 (CH2 )20 , 1,8,15,22-Te4 (CH2 )24 and 1,9,17,…

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryIntermolecular forcechemistry.chemical_elementThio-General ChemistryOrbital overlap010402 general chemistry01 natural sciencesBond orderCatalysis0104 chemical sciencesChalcogenCrystallographychemistryMoleculeNon-covalent interactionsTelluriumChemistry – A European Journal
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Lanthanoid Complexes with[(dad)Li] Ligands—New Starting Materials for Organolanthanoid Chemistry

1995

LanthanideChemistryOrganic chemistryGeneral MedicineGeneral ChemistryCatalysisAngewandte Chemie International Edition in English
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Abyssomicin E, a highly functionalized polycyclic metabolite from Streptomyces species.

2007

Abyssomicin E (1), a new polycyclic metabolite with a C19 skeleton, was isolated from Streptomyces sp. (HKI0381). Its chemical structure was determined by comprehensive NMR and MS spectroscopic analyses. For the first time in this recently discovered class of compounds, the absolute stereochemistry was directly established by subsequent single-crystal X-ray diffraction study using anomalous dispersion with copper radiation.

Models MolecularbiologyMolecular StructureChemistryStereochemistryChemical structureMetaboliteOrganic ChemistryGeneral MedicineAbyssomicin Ebiology.organism_classificationBridged Bicyclo Compounds HeterocyclicBiochemistryStreptomycesStreptomyces speciesStreptomyceschemistry.chemical_compoundOrganic chemistryPhysical and Theoretical ChemistryOrganic letters
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Lanthanoidkomplexe mit [(dad)Li]-Liganden – neue Ausgangsverbindungen in der Organolanthanoidchemie

1995

ChemistryGeneral MedicineAngewandte Chemie
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Front Cover: Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH 2 ) m ] n ( n= 1–4; m= 3–7) (Chem. Eur. J. 61/2020)

2020

chemistry.chemical_classificationCrystallographyChalcogenFront coverchemistryOrganic Chemistrychemistry.chemical_elementNon-covalent interactionsGeneral ChemistryTelluriumCatalysisChemistry – A European Journal
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CCDC 1986246: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters17-ditelluracyclododecaneExperimental 3D Coordinates
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CCDC 1986247: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

Space GroupCrystallographyCrystal System18-ditelluracyclotetradecaneCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1986249: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

1815-tritelluracyclohenicosaneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1986248: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

Space GroupCrystallographyCrystal System159-tritelluracyclododecaneCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1986251: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters181522-tetratelluracyclooctacosane unknown solvateExperimental 3D Coordinates
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CCDC 1986252: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

Space GroupCrystallographyCrystal SystemCrystal Structure191725-tetratelluracyclodotriacontane unknown solvateCell ParametersExperimental 3D Coordinates
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CCDC 1986250: Experimental Crystal Structure Determination

2020

Related Article: Marko Rodewald, J. Mikko Rautiainen, Tobias Niksch, Helmar Görls, Raija Oilunkaniemi, Wolfgang Weigand, Risto S. Laitinen|2020|Chem.-Eur.J.|26|13806|doi:10.1002/chem.202002510

Space GroupCrystallographyCrystal SystemCrystal Structure171319-tetratelluracyclotetracosane unknown solvateCell ParametersExperimental 3D Coordinates
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