0000000000033719

AUTHOR

Oleg V. Shishkin

showing 12 related works from this author

Columnar supramolecular architecture of crystals of 2-(4-Iodophenyl)-1,10-phenanthroline derived from values of intermolecular interaction energy

2011

Using results of X-ray diffraction study supramolecular architecture of crystals of 2-(4-iodophenyl)-1,10-phenanthroline has been analyzed on the basis of quantum-chemical calculations of intermolecular interactions energy. It is demonstrated that these crystals have three levels of organization. Molecules form stacked dimers with the highest binding energy (first level). These dimers represent basic unit of infinite columns stabilized by stacking interactions between dimers (second level). The energy of intermolecular interactions between neighbouring stacked columns is very close. This does not allow to figure out any layers in the crystal. Therefore crystals of this compound have columna…

DiffractionChemistryPhenanthrolineIntermolecular forceBinding energyStackingSupramolecular chemistryGeneral ChemistryCondensed Matter PhysicsCrystalCrystallographychemistry.chemical_compoundMoleculeGeneral Materials ScienceCrystEngComm
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Synthesis and Tautomerization of 6,7-Dihydro-(1,2,3)-triazolo[1,5-a]pyrimidines.

2007

The condensation of 5-amino-4-phenyl-1,2,3-triazole (1) with chalcones 2a-e or 3-dimethylamino-propiophenone (4f) leads to the 6,7-dihydro-(1,2,3)-triazolo[1,5-a]pyrimidines 3a-f. The equilibrium of 3 and the tautomeric 4,7-dihydro-(1,2,3)-triazolo[1,5-a]pyrimidines 3′ is described.

ChemistryStereochemistryOrganic ChemistryCondensationGeneral MedicineTautomerMedicinal chemistryChemInform
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Tautomerism of Diazepines Fused with Pyrimidine Rings.

2003

The tautomerism of 1,4-diazepines fused with pyrimidine rings was studied by means of nmr spec-troscopy, X-ray analysis and quantum chemical calculations. It was found that in the case of 6,8-diphenyl-pyrimido[4,5-b][1,4]diazepin-4-ols (7a - e) the enamine form is more stable than the diimine form. This result is rationalized with the electron-withdrawing effect of the 4-hydroxypyrimidine ring and with the formation of intermolecular hydrogen bonds. In contrast to 7a - e, the 6,8-diaryl-2,3,4,7-tetrahydro-1,3-dimethyl-1H-pyrimido[4,5-b][1,4]diazepine-2,4-diones (9a, c, f) exist in the diimine form.

Quantum chemicalPyrimidineStereochemistryHydrogen bondOrganic ChemistryIntermolecular forceGeneral MedicineRing (chemistry)TautomerEnaminechemistry.chemical_compoundCrystallographychemistryDiimineChemInform
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Reactions of 4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidines with α,β-unsaturated carbonyl compounds

2004

The reaction of 5,7-diphenyl-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidine (1) with α,β-unsaturated carbonyl compounds 2a-f led to the formation of the alkylated heterocycles 3a-f (Figure 1). However, the reaction of 5-methyl-7-phenyl-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidine (5) with 2a-c yielded under the same conditions the triazolo[5,1-b]quinazolines 6a-c (Figure 3). In this case, the alkylation is followed by a cyclocondensation. The structure elucidation of the products is based on ir, ms, 1H and 13C nmr measurements and on an X-ray diffraction study.

chemistry.chemical_compoundPyrimidineStereochemistryChemistryOrganic ChemistryTriazole derivativesGeneral MedicineCarbon-13 NMRAlkylationMedicinal chemistryJournal of Heterocyclic Chemistry
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Supramolecular diversity and magnetic properties of novel heterometallic Cu(II)/Cr(III) complexes prepared from copper powder, Reineckes salt and eth…

2009

Abstract Three novel heterometallic complexes [Cu(en) 2 Cr(NCS) 4 (NH 3 ) 2 ][Cr(NCS) 4 (NH 3 ) 2 ] · 6dmf ( 1 ), [Cu(en) 2 Cr(NCS) 4 (NH 3 ) 2 ](OAc) ( 2 ) and [{Cu(en) 2 } 3 {Cr(NCS) 4 (NH 3 ) 2 } 2 (NCS) 2 ](NCS) 2 ( 3 ) have been synthesized in a one-pot reaction from copper powder, Reineckes salt, NH 4 X [X −  = OAc − ( 2 ), NCS − ( 3 )] in a dmf ( 1 ) or CH 3 CN ( 2 , 3 ) solution of ethylenediamine (en). X-ray studies showed that 1 and 2 consist of cationic polymeric chains, formed by Cu ( en ) 2 2 + and Cr ( NCS ) 4 ( NH 3 ) 2 - building blocks that bridged through thiocyanate anions. In both complexes, distinct hydrogen bonds are present and serve to increase the dimensionality of …

ThiocyanateHydrogen bondChemistryStereochemistrySupramolecular chemistryCationic polymerizationchemistry.chemical_elementEthylenediamineCopperSupramolecular assemblyInorganic ChemistryCrystallographychemistry.chemical_compoundChromiumMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Structural and magnetic studies of tetranuclear heterometallic M/Cr (M = Co, Mn) complexes self-assembled from zerovalent cobalt or manganese, Reinec…

2010

Abstract Four novel heterometallic complexes [Co2Cr2(NCS)4(HDea)2(Dea)2]·4dmf (1), [Co2Cr2(NCS)4(HDea)2(Dea)2]·4dmso (2), [Mn2Cr2(NCS)4(HDea)2(Dea)2(dmf)2]·2dmf (3) and [Mn2Cr2(NCS)4(HDea)2(Dea)2(dmso)2]·4dmso (4) have been prepared using zerovalent cobalt (1, 2) or manganese (3, 4), Reineckes salt, ammonium thiocyanate and a non-aqueous solution of diethanolamine (H2Dea) in air. The single X-ray analysis reveals that all compounds have similar centrosymmetric crystal structures based on a tetranuclear {M2Cr2(μ3-O)2(μ-O)4} (M = Co, Mn) core. Variable-temperature magnetic susceptibility measurements of 1, 2 and 4 show antiferromagnetic coupling between the magnetic centers, while 3 exhibits …

chemistry.chemical_classificationDiethanolamineMagnetismInorganic chemistrychemistry.chemical_elementSalt (chemistry)ManganeseCrystal structureMagnetic susceptibilityInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryMaterials ChemistryAmmonium thiocyanatePhysical and Theoretical ChemistryCobaltPolyhedron
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Cyclecondensation of 3-amino-1,2,4-triazole with substituted methyl cinnamates

1999

The reaction of 3-amino-1,2,4-triazole (1) with substituted methyl cinnamates 2a-h leads selectively to the formation of 7-aryl-6,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-ones 3a-h. The structure eluci dation of the products is based on ir, 1H and 13C nmr measurements and X-ray diffraction.

chemistry.chemical_compoundchemistryOrganic ChemistryCinnamates3-Amino-124-triazoleCarbon-13 NMRMedicinal chemistryJournal of Heterocyclic Chemistry
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OH–π and halogen–π interactions as driving forces in the crystal organisations of tri-bromo and tri-iodo trityl alcohols

2008

The trityl alcohols bearing three bromine or three iodine atoms at the para-positions of the aromatic units, have been known for more than a hundred years. In our case these compounds have been synthesized in one-pot sequence starting from the 1,4-dihalogenobenzenes via mono-lithiation and the successive reaction with diethylcarbonate. The compounds have been crystallized from different solvent mixtures leading to one structure of bromo- (A) and three structures of iodo trityl alcohols (B–D). The inclusion of dichloromethane (C) or benzene (D) in the crystalline lattices has been observed. In all cases the OH–π and halogen–π (and in one case the halogen-halogen and CH-O weak) contacts play …

BromineStereochemistryIntermolecular forcechemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsSolventCrystalchemistry.chemical_compoundCrystallographychemistryHalogenMoleculeGeneral Materials ScienceBenzeneDichloromethaneCrystEngComm
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CCDC 998788: Experimental Crystal Structure Determination

2014

Related Article: Roman I. Zubatyuk, Anna A. Sinelshchikova, Yulia Y. Enakieva, Yulia G. Gorbunova, Aslan Y. Tsivadze, Sergey E. Nefedov, Alla Bessmertnykh-Lemeune, Roger Guilard, Oleg V. Shishkin|2014|CrystEngComm|16|10428|doi:10.1039/C4CE01623H

Space GroupCrystallography(tetraethyl (1020-diphenylporphyrin-515-diyl)bis(phosphonatato))-nickel(ii) hexane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 998789: Experimental Crystal Structure Determination

2014

Related Article: Roman I. Zubatyuk, Anna A. Sinelshchikova, Yulia Y. Enakieva, Yulia G. Gorbunova, Aslan Y. Tsivadze, Sergey E. Nefedov, Alla Bessmertnykh-Lemeune, Roger Guilard, Oleg V. Shishkin|2014|CrystEngComm|16|10428|doi:10.1039/C4CE01623H

Space GroupCrystallographyCrystal SystemCrystal Structure(tetraethyl (1020-diphenylporphyrin-515-diyl)bis(phosphonatato))-palladium(ii)Cell ParametersExperimental 3D Coordinates
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CCDC 998787: Experimental Crystal Structure Determination

2014

Related Article: Roman I. Zubatyuk, Anna A. Sinelshchikova, Yulia Y. Enakieva, Yulia G. Gorbunova, Aslan Y. Tsivadze, Sergey E. Nefedov, Alla Bessmertnykh-Lemeune, Roger Guilard, Oleg V. Shishkin|2014|CrystEngComm|16|10428|doi:10.1039/C4CE01623H

(tetraethyl (1020-diphenylporphyrin-515-diyl)bis(phosphonatato))-platinum(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 998790: Experimental Crystal Structure Determination

2014

Related Article: Roman I. Zubatyuk, Anna A. Sinelshchikova, Yulia Y. Enakieva, Yulia G. Gorbunova, Aslan Y. Tsivadze, Sergey E. Nefedov, Alla Bessmertnykh-Lemeune, Roger Guilard, Oleg V. Shishkin|2014|CrystEngComm|16|10428|doi:10.1039/C4CE01623H

Space GroupCrystallographyCrystal SystemCrystal Structurecatena-[(mu-tetraethyl (1020-diphenylporphyrin-515-diyl)bis(phosphonatato))-cadmium]Cell ParametersExperimental 3D Coordinates
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