0000000001302111

AUTHOR

Marko Rodewald

showing 10 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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct