0000000000026541

AUTHOR

Ian S. Morgan

showing 26 related works from this author

Effect of a Rigid Sulfonamide Bond on Molecular Folding: A Case Study

2015

A disulfonamide compound with bulky aromatic side chains was prepared, and its properties as a potential building block for foldamers were evaluated. Two different solvate crystal forms of the compound were identified and compared to the structures of an analogous oligoamide and related disulfonamides. The disulfonamide is unfolded in one of the solvates, whereas in the other one, a loosely folded conformer stabilized by an intramolecular hydrogen bond is found. Density functional calculations indicated that the loosely folded conformer is slightly more stable than its unfolded isomer. The calculations also identified a third, more tightly folded and more extensively hydrogen bonded, confor…

HydrogenStereochemistrychemistry.chemical_elementmolecular foldingkonformeeritorgaaninen synteesiCrystalSide chainmolecular conformersGeneral Materials Sciencemolekyylien laskostuminenta116sulfonamidisidosConformational isomerismX-ray crystallographychemistry.chemical_classificationHydrogen bondsulfonamide bondGeneral Chemistryorganic synthesisCondensed Matter PhysicsSulfonamideFolding (chemistry)chemistryIntramolecular forceröntgenkristallografiaCrystal Growth & Design
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Synthesis of a labile sulfur-centred ligand, [S(H)C(PPh2S)2]−: structural diversity in lithium(i), zinc(ii) and nickel(ii) complexes

2016

A high-yield synthesis of [Li{S(H)C(PPh2S)2}]2 [Li2·(3)2] was developed and this reagent was used in metathesis with ZnCl2 and NiCl2 to produce homoleptic complexes 4 and 5b in 85 and 93% yields, respectively. The solid-state structure of the octahedral complex [Zn{S(H)C(PPh2S)2}2] (4) reveals notable inequivalence between the Zn-S(C) and Zn-S(P) contacts (2.274(1) Å vs. 2.842(1) and 2.884(1) Å, respectively). Two structural isomers of the homoleptic complex [Ni{S(H)C(PPh2S)2}2] were isolated after prolonged crystallization processes. The octahedral green Ni(ii) isomer 5a exhibits the two monoprotonated ligands bonded in a tridentate (S,S',S'') mode to the Ni(ii) centre with three distinctl…

Stereochemistrychemistry.chemical_elementmetal complexes010402 general chemistry01 natural sciencesisomerizationelectronic structuresInorganic Chemistrychemistry.chemical_compoundelektronirakenteetrikkipohjaiset liganditStructural isomerSinglet stateTriplet stateHomolepticta116010405 organic chemistryLigandsulphur-centered ligands0104 chemical sciencesBond lengthNickelCrystallographyOctahedronchemistryisomerisaatiometallikompleksitDalton Transactions
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Synthesis and characterisation of p-block complexes of biquinoline at different ligand charge states

2017

The first examples of p-block coordination complexes of biquinoline, namely [(biq)BCl2]Cl and [(biq)BCl2]˙, were synthesized and structurally characterized. The acquired data allowed the estimation of the ligand charge state based on its metrical parameters. The subsequent use of this protocol, augmented with theoretical calculations, revealed ambiguities in the published data for transition metal complexes of biquinoline. peerReviewed

Inorganic ChemistryCrystallographyTransition metal010405 organic chemistryChemistryLigandCharge (physics)p-block complexes010402 general chemistryBlock (periodic table)01 natural sciencesta1160104 chemical sciencesDalton Transactions
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Coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization in the first lanthanide complex of a 1,2,4-benzotriazinyl …

2017

The first lanthanide complex of a 1,2,4-benzotriazinyl radical (1), Dy(1)(tbacac)3 (2, tbacac = 2,2,6,6-tetramethyl-3,5-heptane-dionato), was synthesised and found to have an antiferromagnetically ordered ground state with a metamagnetic phase diagram and a critical field of 0.91 T at 1.85 K. The application of a small dc field revealed the single-molecule magnet behaviour of 2, illustrating the coexistence of long-range antiferromagnetic order and slow relaxation of the magnetization. peerReviewed

LanthanideCondensed matter physics010405 organic chemistryChemistryRelaxation (NMR)[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetharvinaiset maametallit010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryMagnetizationMagnetmagnetismAntiferromagnetismcoordination complexesmagnetismiGround staterare earth metalsCritical fieldta116ComputingMilieux_MISCELLANEOUSPhase diagram
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Comment on “Crystallographic Snapshot of an Arrested Intermediate in the Biomimetic Activation of CO2”

2015

Out of focus: A recent Communication published in this journal describes the synthesis of [nBu4 N]HCO3 . The authors performed a single-crystal X-ray study that revealed a putative species described as an incipient hydroxide ion engaging in a long, and presumably weak, interaction with CO2 . Our recent exploration of the coordination chemistry of CO2 with small ions leads us to believe that such an exceptional bonding situation is unlikely. Instead, we argue that the crystal structure is that of [nBu4 N]O2 CCH3 and therefore not representative of the bulk powder from the synthesis.

hiilidioksidichemistry.chemical_classificationMolecular StructureGeneral ChemistryCrystal structureCarbon Dioxidelaskennallinen kemiaCrystallography X-Raycomputational chemistryCatalysisstructure elucidation: X-ray crystallographyCoordination complexchemistry.chemical_compoundCrystallographychemistryBiomimeticsX-ray crystallographyHydroxideMoleculekiderakenteen ratkaisuta116röntgenkristallografiaAngewandte Chemie International Edition
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1‑Phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl: The First "Blatter Radical" for Coordination Chemistry

2014

A neutral air- and moisture-stable N,N′-chelating radical ligand, 1-phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl (1) was synthesized and characterized by electron paramagnetic resonance spectroscopy, X-ray crystallography, and magnetic measurements. Subsequent reaction of 1 with Cu(hfac)2·2H2O (hfac = hexafluoroacetylacetonate) under ambient conditions afforded the coordination complex Cu(1)(hfac)2 in which the radical binds to the metal in a bidentate fashion. Magnetic susceptibility data collected from 1.8 to 300 K indicate a strong ferromagnetic metal-radical interaction in the complex and weak antiferromagnetic radical···radical interactions between the Cu(1)(hfac)2 units. Detailed com…

chemistry.chemical_classificationDenticityStereochemistryLigandpysyvät radikaalitRadicalmetal complexes[CHIM.INOR]Chemical Sciences/Inorganic chemistryMedicinal chemistryMagnetic susceptibilityCoordination complexInorganic ChemistryMetalParamagnetismCoordination Chemistrystable radicalschemistryBlatter radikaalivisual_artvisual_art.visual_art_mediumAntiferromagnetismBlatter radicalPhysical and Theoretical Chemistryta116metallikompleksit
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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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CCDC 1424396: Experimental Crystal Structure Determination

2016

Related Article: Ramalingam Thirumoorthi, Tristram Chivers, Susanna Häggman, Akseli Mansikkamäki, Ian S. Morgan, Heikki M. Tuononen, Manu Lahtinen, Jari Konu|2016|Dalton Trans.|45|12691|doi:10.1039/C6DT02565J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(bis(diphenylphosphorothioyl)methanethiolato)-nickel(ii)Experimental 3D Coordinates
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CCDC 1424395: Experimental Crystal Structure Determination

2016

Related Article: Ramalingam Thirumoorthi, Tristram Chivers, Susanna Häggman, Akseli Mansikkamäki, Ian S. Morgan, Heikki M. Tuononen, Manu Lahtinen, Jari Konu|2016|Dalton Trans.|45|12691|doi:10.1039/C6DT02565J

bis(bis(diphenylphosphorothioyl)methanethiolato)-nickel(ii) toluene solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1057508: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal SystemCrystal Structurebis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-cobalt(ii)Cell ParametersExperimental 3D Coordinates
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CCDC 1022891: Experimental Crystal Structure Determination

2015

Related Article: Aku Suhonen, Ian S. Morgan, Elisa Nauha, Kaisa Helttunen, Heikki M. Tuononen, Maija Nissinen|2015|Cryst.Growth Des.|15|2602|doi:10.1021/acs.cgd.5b00424

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersNN'-(13-Phenylenebis(sulfonylimino-21-phenylene))dibenzamide 12-dichloroethane solvateExperimental 3D Coordinates
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CCDC 1057512: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal System1-Phenyl-3-(pyridin-2-yl)-14-dihydro-124-benzotriazineCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1022892: Experimental Crystal Structure Determination

2015

Related Article: Aku Suhonen, Ian S. Morgan, Elisa Nauha, Kaisa Helttunen, Heikki M. Tuononen, Maija Nissinen|2015|Cryst.Growth Des.|15|2602|doi:10.1021/acs.cgd.5b00424

Space GroupCrystallographyCrystal SystemNN'-(13-Phenylenebis(sulfonylimino-21-phenylene))dibenzamide tetrahydrofuran solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1518784: Experimental Crystal Structure Determination

2017

Related Article: Juha Hurmalainen, Akseli Mansikkamäki, Ian S. Morgan, Anssi Peuronen, Heikki M. Tuononen|2017|Dalton Trans.|46|1377|doi:10.1039/C6DT04504A

Space GroupCrystallographyCrystal SystemCrystal Structure1414-dichloro-14lambda5-quinolino[1'2':34][132]diazaborolo[15-a]quinoline radicalCell ParametersExperimental 3D Coordinates
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CCDC 1022889: Experimental Crystal Structure Determination

2015

Related Article: Aku Suhonen, Ian S. Morgan, Elisa Nauha, Kaisa Helttunen, Heikki M. Tuononen, Maija Nissinen|2015|Cryst.Growth Des.|15|2602|doi:10.1021/acs.cgd.5b00424

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersNN'-(13-Phenylenebis(sulfonylimino-21-phenylene))dibenzamide unknown solvateExperimental 3D Coordinates
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CCDC 1022890: Experimental Crystal Structure Determination

2015

Related Article: Aku Suhonen, Ian S. Morgan, Elisa Nauha, Kaisa Helttunen, Heikki M. Tuononen, Maija Nissinen|2015|Cryst.Growth Des.|15|2602|doi:10.1021/acs.cgd.5b00424

Space GroupCrystallographyCrystal SystemCrystal StructureNN'-(13-Phenylenebis(sulfonylimino-21-phenylene))dibenzamide acetonitrile solvateCell ParametersExperimental 3D Coordinates
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CCDC 1057511: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersNN'-Diphenylpyridine-2-carbohydrazonamideExperimental 3D Coordinates
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CCDC 1057510: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal SystemCrystal StructureN-Phenylpyridine-2-carbothioamideCell ParametersExperimental 3D Coordinates
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CCDC 1486829: Experimental Crystal Structure Determination

2016

Related Article: Ramalingam Thirumoorthi, Tristram Chivers, Susanna Häggman, Akseli Mansikkamäki, Ian S. Morgan, Heikki M. Tuononen, Manu Lahtinen, Jari Konu|2016|Dalton Trans.|45|12691|doi:10.1039/C6DT02565J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(bis(diphenylphosphorothioyl)methanethiolato)-zinc(ii)Experimental 3D Coordinates
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CCDC 1057507: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

bis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-iron(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1036823: Experimental Crystal Structure Determination

2015

Related Article: Juha Hurmalainen, Michael A. Land, Katherine N. Robertson, Christopher J. Roberts, Ian S. Morgan, Heikki M. Tuononen and Jason A. C. Clyburne|2015|Angew.Chem.,Int.Ed.|54|7484|doi:10.1002/anie.201411654

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersTetra-n-butylammonium acetateExperimental 3D Coordinates
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CCDC 1424394: Experimental Crystal Structure Determination

2016

Related Article: Ramalingam Thirumoorthi, Tristram Chivers, Susanna Häggman, Akseli Mansikkamäki, Ian S. Morgan, Heikki M. Tuononen, Manu Lahtinen, Jari Konu|2016|Dalton Trans.|45|12691|doi:10.1039/C6DT02565J

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-bis(diphenylphosphorothioyl)methanethiolato)-di-lithiumExperimental 3D Coordinates
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CCDC 1057506: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

bis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-manganese(ii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1563199: Experimental Crystal Structure Determination

2017

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Mathieu Rouzières, Rodolphe Clérac, Heikki M. Tuononen|2017|Dalton Trans.|46|12790|doi:10.1039/C7DT02766D

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterstris(acetylacetonato)-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-dysprosium(iii)Experimental 3D Coordinates
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CCDC 1057509: Experimental Crystal Structure Determination

2015

Related Article: Ian S. Morgan, Akseli Mansikkamäki, Georgia A. Zissimou, Panayiotis A. Koutentis, Mathieu Rouzières, Rodolphe Clérac and Heikki M. Tuononen|2015|Chem.-Eur.J.|21|15843|doi:10.1002/chem.201501343

Space GroupCrystallographyCrystal Systembis(111555-Hexafluoroacetylacetonato-OO')-(1-phenyl-3-(pyridin-2-yl)-124-benzotriazin-4(1H)-yl radical)-nickel(ii)Crystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1518783: Experimental Crystal Structure Determination

2017

Related Article: Juha Hurmalainen, Akseli Mansikkamäki, Ian S. Morgan, Anssi Peuronen, Heikki M. Tuononen|2017|Dalton Trans.|46|1377|doi:10.1039/C6DT04504A

Space GroupCrystallography1414-dichloroquinolino[1'2':34][132]diazaborolo[15-a]quinolinium chlorideCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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