Search results for "Molecular chemistry"

showing 10 items of 1103 documents

Heteropolymetallic Supramolecular Solid-State Architectures Constructed from [Cr(AA)(C2O4)2]- Tectons, and Sustained by Coordinative, Hydrogen Bond a…

2004

The paper reports on four novel solid-state architectures constructed by using tectons having the general formula:  [Cr(AA)(C2O4)2]- [AA = 2,2‘-bipyridine (bipy) and 1,10-phenanthroline (phen)]. These building blocks are involved in various intermolecular interactions:  coordinative, hydrogen bonds, and π−π contacts. Two new crystallohydrates in the Ba[Cr(AA)(C2O4)2]2·nH2O family have been characterized:  [BaCr2(bipy)2(C2O4)4(H2O)2]·4H2O (1) and [BaCr2(phen)2(C2O4)4(H2O)2] (2). Because of the different numbers of water molecules, their crystal structures are completely different from those of two others previously reported, [BaCr2(bipy)2(C2O4)4(H2O)]·H2O and [BaCr2(phen)2(C2O4)4(H2O)2]·4H2O…

DenticityChemistryHydrogen bondPhenanthrolineStackingSupramolecular chemistryGeneral ChemistryCrystal structureCondensed Matter Physics22'-Bipyridinechemistry.chemical_compoundCrystallographyMoleculeGeneral Materials ScienceCrystal Growth & Design
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Cu(II) and Cu(I) complexes with 1,2-dithiosquarate as a ligand; from molecular compounds to supramolecular network structures

2008

Abstract Four new complexes of copper(II) and/or copper(I) with 1,2-dtsq as a ligand have been synthesized and characterized by single crystal X-ray diffraction methods, [CuII(terpy)(1,2-dtsq)] (1), [CuII(dmen)(1,2-dtsq)]n (2), {[CuII(dmen)2][CuI(1,2-dtsq)]2}n·2nH2O(3) and {[CuII(men)2][CuI (1,2-dtsq)]2}n·nH2O (4) (1,2-dtsq = 1,2-dithiosquarate, dianion of 3,4-dimercapto-1-cyclobutene-1,2-dione; dmen = N,N-dimethylethylenediamine; men = N-methylethylenediamine, terpy = 2,2′:6,2″-terpyridine). Compound 1 consists of neutral [CuII(terpy)(1,2-dtsq)] mononuclear units which are held together by O⋯H–C and van der Waals interactions. Compound 2 is built of neutral [CuII(dmen)(1,2-dtsq)] entities …

DenticityCoordination sphereChemistryLigandOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementCrystal structureCopperAnalytical ChemistryInorganic Chemistrysymbols.namesakeCrystallographysymbolsvan der Waals forceSingle crystalSpectroscopyJournal of Molecular Structure
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Manganese(II) complexes with croconate and 2-(2-pyridyl)imidazole ligands: Syntheses, X-ray structures and magnetic properties

2009

Abstract The mixed-ligand complexes of manganese(II) of formula [Mn(pyim)2(C5O5)] (1) and [Mn(pyim)(H2O)(C5O5)]n · 2.5nH2O (2) [pyim = 2-(2-pyridyl)imidazole and C 5 O 5 2 -  = croconate (dianion of 4,5-dihydroxy-4-cyclopentene-1,2,3-trione)] have been prepared and their structures determined by X-ray crystallographic methods. Compound 1 is a tris-chelated mononuclear complex where the manganese atom is six-coordinate: four nitrogen atoms from two pyim molecules and two oxygen atoms from a croconate group build a somewhat distorted octahedral surrounding around the metal atom. The resulting neutral mononuclear units are linked to each other through double bridges which are constituted by th…

DenticityLigandInorganic chemistrySupramolecular chemistrychemistry.chemical_elementCrystal structureManganeseInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronMaterials ChemistryMoleculeImidazolePhysical and Theoretical ChemistryInorganica Chimica Acta
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Study of the complex formation between the [Cu(bpca)]+ secondary building unit and the aromatic N donors 2,3,5,6-tetra(2-pyridyl)pyrazine (tppz) and …

2017

Two new complexes of the formula [{Cu(bpca)}2(μ-tppz)](NO3)2·5H2O (1) and [Cu(bpca)(H2O)(ClO4)(μ-bpp)Cu(bpca)(H2O)2]ClO4·H2O (2) [tppz = 2,3,5,6-tetra(2-pyridyl)pyrazine and bpp = 1,3-bis(4-pyridyl)propane] have been prepared by the reaction of the [Cu(bpca)]+ [Hbpca = bis(2-pyridylcarbonyl)imide] building block and the tppz and bpp N donors. An unusual coordination mode of the tppz ligand was observed in 1, which functions as a bis(bidentate) ligand to two copper(II) atoms each coordinated to a nitrogen atom of the pyrazine moiety and a pyridyl nitrogen atom. This compound presents a layered structure of alternating anionic (ca. 1.6 A) and cationic (ca. 10 A) slices, providing the opportun…

DenticityPyrazine010405 organic chemistryInorganic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundPerchlorateCrystallographychemistryElectronic effectMoleculeMoietyGeneral Materials ScienceImideCrystEngComm
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Hydrogen and Halogen Bond Mediated Coordination Polymers of Chloro-Substituted Pyrazin-2-Amine Copper(I) Bromide Complexes

2020

A new class of six mono- (1

DenticityPyrazineDimer116 Chemical sciencesSubstituentSupramolecular chemistry010402 general chemistry01 natural scienceskemialliset sidoksetchemistry.chemical_compoundcopper halidehydrogen bondvetysidoksetHalogen bondhalogeenit010405 organic chemistryHydrogen bondCopper(I) bromideGeneral Medicine3. Good health0104 chemical sciencesCrystallographychemistryhalogeenisidoksetchloropyrazinechloropyrazin-2-aminepyrazinehalogen bondChemistry
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Bio-metal-organic frameworks for molecular recognition and sorbent extraction of hydrophilic vitamins followed by their determination using HPLC-UV

2020

A bio-metal-organic framework (bio-MOF) derived from the amino acid L-serine has been prepared in bulk form and evaluated as sorbent for the molecular recognition and extraction of B-vitamins. The functional pores of bio-MOF exhibit high amounts of hydroxyl groups jointly directing other supramolecular host-guest interactions thus providing the recognition of B-vitamins in fruit juices and energy drinks. Single-crystal X-ray diffraction studies reveal the specific B-vitamin binding sites and the existence of multiple hydrogen bonds between these target molecules and the framework. It offered unique snapshots to accomplish an efficient capture of these solutes in complex aqueous matrices. Fo…

Detection limitVitaminesSorbentChromatographySurface PropertiesUltraviolet RaysElutionChemistryHydrophilic interaction chromatography010401 analytical chemistryExtraction (chemistry)Supramolecular chemistryQuímica analítica010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryBegudesMolecular recognitionVitamin B ComplexAdsorptionSolid phase extractionParticle SizeHydrophobic and Hydrophilic InteractionsMetal-Organic FrameworksMicrochimica Acta
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ChemInform Abstract: “Supramolecular” Solid-State Chemistry: Interpenetrating Diamond-Type Frameworks of U4+ Ions Linked by S,S′-Bidentate P2S2-6 Mol…

2010

Diamond typeSolid-state chemistryCrystallographyDenticityChemistrySupramolecular chemistryGeneral MedicineRodIonChemInform
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Deprotonation of resorcinarenes by mono- and diamine bases: complexation and intermolecular interactions in the solid state

2014

The deprotonation of resorcinarenes by mono- and dibasic amines, viz. triethylamine (TEA) and its dibasic analogue, N,N′-dimethylpiperazine (DMPip), was studied and the resulting supramolecular complexes were analysed in the solid state, in solution and in the gas phase. In the solid state, 1:1 (2TEAH+·(ethyl-resorcinarene)2−·MeOH), 3:2 [DMPip·2DMPipH+·2(ethyl-resorcinarene−)] and 3:2 [2DMPip·DMPipH22+@(2methyl-ethyl-resorcinarene−)2·2MeOH] solid state complexes and interesting resorcinarene−⋯resorcinarene− supramolecular networks formed via enhanced hydrogen bonds involving the hydroxyl groups and the deprotonated hydroxyl groups of the resorcinarenes were observed. The host–guest complexe…

Dibasic acidHydrogen bondInorganic chemistrySupramolecular chemistryGeneral ChemistryResorcinareneCondensed Matter Physicschemistry.chemical_compoundDeprotonationchemistryDiaminePolymer chemistryGeneral Materials ScienceTitrationTriethylamineta116CrystEngComm
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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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Three‐Component Self‐Assembly Changes its Course: A Leap from Simple Polymers to 3D Networks of Spherical Host–Guest Assemblies

2021

Angewandte Chemie / International edition 60(21), 12132 - 12142 (2021). doi:10.1002/anie.202103178

DiffractionMaterials science010402 general chemistryMass spectrometry01 natural sciencesCatalysisSelf‐AssemblyMetalcoordination networksResearch Articleschemistry.chemical_classification010405 organic chemistrypentaphosphaferroceneflexible linkersGeneral ChemistryNuclear magnetic resonance spectroscopyPolymermetallosupramolecular chemistry5400104 chemical sciencesCrystallographychemistryTransmission electron microscopyvisual_artYield (chemistry)ddc:540visual_art.visual_art_mediumSelf-assemblysupramoleculesResearch Article
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