0000000001299249

AUTHOR

Oleg V. Levin

showing 14 related works from this author

Supramolecular Assembly of Metal Complexes by (Aryl)I⋯dz2[PtII] Halogen Bond

2020

The theoretical data for the half‐lantern complexes [Pt(C^N)(μ‐S^N)] 2 ( 1 – 3 ; С^N is cyclometalated 2‐Ph‐benzothiazole; S^N is 2‐SH‐pyridine 1 , 2‐SH‐benzoxazole 2 , 2‐SH‐tetrafluorobenzothiazole 3 ) indicate that the Pt···Pt orbital interaction leads to an increment of the nucleophilicity of the outer d z 2 ‐orbitals to provide assembly with electrophilic species. 1 – 3 were co‐crystallized with bifunctional halogen bond (XB) donors to give adducts ( 1 – 3 ) 2 ∙(1,4‐diiodotetrafluorobenzene) and infinite polymeric [ 1 ·1,1’‐diiodoperfluorodiphenyl] n . X‐ray crystallography revealed that the supramolecular assembly is achieved via (Aryl)I∙∙∙ d z 2 [Pt II ] XB between iodine σ‐holes and …

platinakemialliset sidoksetcyclometalated complexhalogen bondingsupramolekulaarinen kemiaplatinumkompleksiyhdisteetsupramolecular chemistrytheoretical calculations
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Halogen Bonding Involving Palladium(II) as an XB Acceptor

2020

The half-lantern PdII2 complexes trans-(O,C)-[Pd(ppz)(μ-O∩N)]2 (1) and trans-(E,N)-[Pd(ppz)(μ-E∩N)]2 (E∩N is a deprotonated 2-substituted pyridine; E = S (2), Se (3); Hppz = 1-phenylpyrazole) were ...

Halogen bond010405 organic chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesMedicinal chemistryAcceptor0104 chemical scienceschemistry.chemical_compoundDeprotonationchemistryPyridineGeneral Materials SciencePalladiumCrystal Growth & Design
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Supramolecular Assembly of Metal Complexes by (Aryl)I⋅⋅⋅d[PtII] Halogen Bonds

2020

The theoretical data for the half-lantern complexes [{Pt( CN^ )(μ- SN^ )}2 ] [1-3; CN^ is cyclometalated 2-Ph-benzothiazole; SN^ is 2-SH-pyridine (1), 2-SH-benzoxazole (2), 2-SH-tetrafluorobenzothiazole (3)] indicate that the Pt⋅⋅⋅Pt orbital interaction increases the nucleophilicity of the outer d z2 orbitals to provide assembly with electrophilic species. Complexes 1-3 were co-crystallized with bifunctional halogen bonding (XB) donors to give adducts (1-3)2 ⋅(1,4-diiodotetrafluorobenzene) and infinite polymeric [1⋅1,1'-diiodoperfluorodiphenyl]n . X-ray crystallography revealed that the supramolecular assembly is achieved through (Aryl)I⋅⋅⋅d z2 [PtII ] XBs between iodine σ-holes and lone pa…

chemistry.chemical_classificationHalogen bond010405 organic chemistryArylOrganic ChemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSupramolecular assemblychemistry.chemical_compoundCrystallographychemistryElectrophileNon-covalent interactionsBifunctionalLone pairChemistry – A European Journal
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CCDC 1982282: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Matti Haukka, Oleg V. Levin, Antonio Frontera, Vadim Yu. Kukushkin|2020|Chem.-Eur.J.|26|7692|doi:10.1002/chem.202001196

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-pyridine-2-thiolato)-bis(2-(13-benzothiazol-2-yl)phenyl)-di-platinum hemikis(2356-tetrafluoro-14-di-iodobenzene) dichloromethane solvateExperimental 3D Coordinates
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CCDC 1982285: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Matti Haukka, Oleg V. Levin, Antonio Frontera, Vadim Yu. Kukushkin|2020|Chem.-Eur.J.|26|7692|doi:10.1002/chem.202001196

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-4567-tetrafluoro-13-benzothiazole-2-thiolato)-bis(2-(13-benzothiazol-2-yl)phenyl)-di-platinum hemikis(2356-tetrafluoro-14-di-iodobenzene) benzene solvateExperimental 3D Coordinates
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CCDC 2040618: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Anton V. Rozhkov, Oleg V. Levin, Matti Haukka, Maxim L. Kuznetsov, Vadim Yu. Kukushkin|2021|Cryst.Growth Des.|21|1159|doi:10.1021/acs.cgd.0c01474

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-pyridin-2-olato)-bis[2-(1H-pyrazol-1-yl)phenyl]-di-palladium(ii) 1245-tetrafluoro-36-diiodobenzene unknown solvateExperimental 3D Coordinates
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CCDC 1982284: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Matti Haukka, Oleg V. Levin, Antonio Frontera, Vadim Yu. Kukushkin|2020|Chem.-Eur.J.|26|7692|doi:10.1002/chem.202001196

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatesbis(mu-13-benzoxazole-2-thiolato)-bis(2-(benzothiazol-2-yl)phenyl)-di-platinum hemikis(2356-tetrafluoro-14-di-iodobenzene)
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CCDC 2040622: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Anton V. Rozhkov, Oleg V. Levin, Matti Haukka, Maxim L. Kuznetsov, Vadim Yu. Kukushkin|2021|Cryst.Growth Des.|21|1159|doi:10.1021/acs.cgd.0c01474

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-pyridine-2-selenolato)-bis[2-(1H-pyrazol-1-yl)phenyl]-di-palladium(ii)Experimental 3D Coordinates
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CCDC 2040620: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Anton V. Rozhkov, Oleg V. Levin, Matti Haukka, Maxim L. Kuznetsov, Vadim Yu. Kukushkin|2021|Cryst.Growth Des.|21|1159|doi:10.1021/acs.cgd.0c01474

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatesbis(mu-pyridine-2-thiolato)-bis[2-(1H-pyrazol-1-yl)phenyl]-di-palladium(ii) dichloromethane solvate
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CCDC 1982286: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Matti Haukka, Oleg V. Levin, Antonio Frontera, Vadim Yu. Kukushkin|2020|Chem.-Eur.J.|26|7692|doi:10.1002/chem.202001196

Space GroupCrystallographybis(mu-4567-tetrafluoro-13-benzothiazole-2-thiolato)-bis[2-(13-benzothiazol-2-yl)phenyl]-di-platinumCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2040617: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Anton V. Rozhkov, Oleg V. Levin, Matti Haukka, Maxim L. Kuznetsov, Vadim Yu. Kukushkin|2021|Cryst.Growth Des.|21|1159|doi:10.1021/acs.cgd.0c01474

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-pyridin-2-olato)-bis[2-(1H-pyrazol-1-yl)phenyl]-di-palladium(ii) unknown solvateExperimental 3D Coordinates
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CCDC 1982283: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Matti Haukka, Oleg V. Levin, Antonio Frontera, Vadim Yu. Kukushkin|2020|Chem.-Eur.J.|26|7692|doi:10.1002/chem.202001196

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatesbis(mu-pyridine-2-thiolato)-bis(2-phenyl-13-benzothiazole)-di-platinum 22'33'55'66'-octafluoro-44'-di-iodo-11'-biphenyl unknown solvate
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CCDC 2040619: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Anton V. Rozhkov, Oleg V. Levin, Matti Haukka, Maxim L. Kuznetsov, Vadim Yu. Kukushkin|2021|Cryst.Growth Des.|21|1159|doi:10.1021/acs.cgd.0c01474

Space GroupCrystallographybis(mu-pyridine-2-thiolato)-bis[2-(1H-pyrazol-1-yl)phenyl]-di-palladium(ii) bis(1245-tetrafluoro-36-diiodobenzene)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2040621: Experimental Crystal Structure Determination

2020

Related Article: Eugene A. Katlenok, Anton V. Rozhkov, Oleg V. Levin, Matti Haukka, Maxim L. Kuznetsov, Vadim Yu. Kukushkin|2021|Cryst.Growth Des.|21|1159|doi:10.1021/acs.cgd.0c01474

Space GroupCrystallographybis(mu-pyridine-2-selenolato)-bis[2-(1H-pyrazol-1-yl)phenyl]-di-palladium(ii) bis(1245-tetrafluoro-36-diiodobenzene)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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