0000000000465444

AUTHOR

Sandro Keller

0000-0001-5469-8772

showing 5 related works from this author

Oxoanion binding to a cyclic pseudopeptide containing 1,4-disubstituted 1,2,3-triazole moieties

2016

A macrocyclic pseudopeptide 3 is described featuring three amide groups and three 1,4-disubstituted 1,2,3-triazole units along the ring. This pseudopeptide was designed such that the amide NH groups and the triazole CH groups converge toward the cavity, thus creating an environment well suited for anion recognition. Conformational studies in solution combined with X-ray crystallography confirmed this preorganisation. Solubility of 3 restricted binding studies to organic media such as 5 vol% DMSO/acetone or DMSO/water mixtures with a water content up to 5 vol%. These binding studies demonstrated that 3 binds to a variety of inorganic anions in DMSO/acetone including chloride, nitrate, sulfat…

010405 organic chemistryChemistryStereochemistryDimerOrganic ChemistryTriazoleoxoanion bindings010402 general chemistry01 natural sciencesBiochemistryChlorideMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundpseudopeptidesStability constants of complexesAmidemedicineMoleculePhysical and Theoretical ChemistrySulfateSolubilityta116medicine.drugOrganic & Biomolecular Chemistry
researchProduct

Carbon’s Three-Center-Four-Electron Tetrel Bond, Treated Experimentally

2018

Tetrel bonding is the noncovalent interaction of group IV elements with electron donors. It is a weak, directional interaction that resembles hydrogen and halogen bonding yet remains barely explored. Herein, we present an experimental investigation of the carbon-centered, three-center, four-electron tetrel bond, [N−C− N]+ , formed by capturing a carbenium ion with a bidentate Lewis base. NMRspectroscopic, titration-calorimetric, and reaction-kinetic evidence for the existence and structure of this species is reported. The studied interaction is by far the strongest tetrel bond reported so far and is discussed in comparison with the analogous halogen bond. The necessity of the involvement of…

Lewis basehalogeenitionithiilielektronittetrel bonding
researchProduct

CCDC 1581474: Experimental Crystal Structure Determination

2018

Related Article: Alavi Karim, Nils Schulz, Hanna Andersson, Bijan Nekoueishahraki, Anna-Carin C. Carlsson, Daniel Sarabi, Arto Valkonen, Kari Rissanen, Jürgen Gräfenstein, Sandro Keller, Máté Erdélyi|2018|J.Am.Chem.Soc.|140|17571|doi:10.1021/jacs.8b09367

Space GroupCrystallographyCrystal System1-(triphenylmethyl)pyridin-1-ium tetrafluoroborateCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1505706: Experimental Crystal Structure Determination

2016

Related Article: Disha Mungalpara, Harald Kelm, Arto Valkonen, Kari Rissanen, Sandro Keller, Stefan Kubik|2017|Org.Biomol.Chem.|15|102|doi:10.1039/C6OB02172G

Space GroupCrystallography(RRR)-61830-trimethyl-34581516172027282932373941-pentadeca-azaheptacyclo[31.3.1.125.1913.11417.12125.12629]dotetraconta-1(37)2(42)39(41)101214(40)1521(39)222426(38)273335-pentadecaene-71931-trione dimethyl sulfoxide solvate hydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1504361: Experimental Crystal Structure Determination

2016

Related Article: Disha Mungalpara, Harald Kelm, Arto Valkonen, Kari Rissanen, Sandro Keller, Stefan Kubik|2017|Org.Biomol.Chem.|15|102|doi:10.1039/C6OB02172G

Space GroupCrystallographyCrystal Systemtris(tetra-n-butylammonium) bis(61830-trimethyl-34581516172027282932373941-pentadecaazaheptacyclo[31.3.1.125.1913.11417.12125.12629]dotetraconta-1(37)2(42)39(41)101214(40)1521(39)222426(38)273335-pentadecaene-71931-trione) tris(dihydrogen phosphate) dimethyl sulfoxide solvate hydrateCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct