about
Metal-free binding and coupling of carbon monoxide at a boron-boron triple bond.Ring Expansions of Boroles with Diazo Compounds: Steric Control of C or N Insertion and Aromatic/Nonaromatic Products.O,N,B-Containing eight-membered heterocycles by ring expansion of boroles with nitrones.Heteroleptic [n]chromoarenophanes: ansa complexes derived from [Cr(η(5)-C5H5)(η(6)-C6H6)].Neutral and cationic main group element cages of germanium(II) with pyrazolyl ligands: solid state structures, DFT calculations and advanced solution NMR investigations.Syntheses, structures and electronic properties of zwitterionic iron(II) and cobalt(II) complexes featuring ambidentate tris(pyrazolyl)methanide ligands.Preparation, Properties, and Structures of the Radical Anions and Dianions of Azapentacenes.From Borane to Borylene without Reduction: Ambiphilic Behavior of a Monovalent Silylisonitrile Boron Species.Main-Group Metallomimetics: Transition Metal-like Photolytic CO Substitution at Boron.Generation of Dicoordinate Boron(I) Units by Fragmentation of a Tetra-Boron(I) Molecular Square.Boryl-functionalized σ-alkynyl and vinylidene rhodium complexes: synthesis and electronic properties.Neutral Diboron Analogues of Archetypal Aromatic Species by Spontaneous Cycloaddition.A Binuclear 1,1'-Bis(boratabenzene) Complex: Unprecedented Intramolecular Metal-Metal Communication through a B-B Bond.Syntheses, reactivity and DFT studies of group 2 and group 12 metal complexes of tris(pyrazolyl)methanides featuring "free" pyramidal carbanions.Boron as a powerful reductant: synthesis of a stable boron-centered radical-anion radical-cation pair.Isolation of a neutral boron-containing radical stabilized by a cyclic (alkyl)(amino)carbene.Diborabutatriene: an electron-deficient cumulene.Boron radical cations from the facile oxidation of electron-rich diborenes.Pyrene Molecular Orbital Shuffle-Controlling Excited State and Redox Properties by Changing the Nature of the Frontier Orbitals.Half-Sandwich Complexes of an Extremely Electron-Donating, Redox-Active η6-Diborabenzene Ligand.Dibora[2]ferrocenophane: A Carbene-Stabilized Diborene in a Strained cis-Configuration.Synthesis and Trapping of Iminoboranes by M=B/C=N Bond Metathesis.Engineering a Small HOMO-LUMO Gap and Intramolecular C-H Borylation by Diborene/Anthracene Orbital Intercalation.Boryl- and Silyl-Substituted Mixed Sandwich Compounds of Scandium.Scope of the Thermal Ring-Expansion Reaction of Boroles with Organoazides.Abnormal Tin-Boron Exchange in the Attempted Synthesis of a Borylated Borole.Hole Transfer Processes in meta- and para-Conjugated Mixed Valence Compounds: Unforeseen Effects of Bridge Substituents and Solvent Dynamics.Stable Organic (Bi)Radicals by Delocalization of Spin Density into the Electron-Poor Chromophore Core of Isoindigo.Nitrogen fixation and reduction at boron.DFT Studies on the reactions of boroles with alkynes.Ansa-Complexes of [Mn(η(5) -C5 H5 )(η(6) -C6 H6 )]: Preparation, Characterization, and Reactivity of [n]Manganoarenophanes (n=1, 2, 3).Correlations and Contrasts in Homo- and Heteroleptic Cyclic (Alkyl)(amino)carbene-Containing Pt(0) Complexes.The Radical Anion and Dianion of Tetraazapentacene.Ansa-bridged bis(benzene) titanium complexes.Formation of a stable radical by oxidation of a tetraorganoborate.Multiple reduction of 2,5-bis(borolyl)thiophene: isolation of a negative bipolaron by comproportionation.Isolation of diborenes and their 90°-twisted diradical congeners.Neutral zero-valent s-block complexes with strong multiple bondingAn Isolable Radical Anion Based on the Borole FrameworkAminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation
P50
Q33460036-7E26416A-4722-4B7C-BEEF-79C0A39280C5Q40414732-C94D18D9-AD84-4AD5-A97A-6E41451EA2CBQ40636478-78FD3976-00B9-47DC-901F-AC93B412783DQ43712158-53DA904D-25B8-4205-8CDE-7E150D0ED625Q45947076-AE16C6F9-36E1-4AF0-8D34-899BBCA40B68Q46106617-3E57F0B4-48F9-4E56-950D-C317A001F032Q46291779-9ACF605C-C81F-49BB-A173-4094B23D6F69Q46346149-E01F17B9-056B-4E3A-A886-65DE2DC0580EQ46430671-BC749EA2-EE58-4A27-9135-F91D22326B66Q46464678-4F934AD0-1C76-4B31-BAEA-107E5D3A9F5FQ46523131-9B3CECFB-8B9A-49F2-85D9-5A7C3F340441Q46523774-CC99869B-4CCF-4CF1-86D3-43B965EF0BBFQ46540554-F81D9F8F-E624-46F0-9A88-D52CF345720BQ46586567-4DF9776B-8B07-4C16-A1A8-1F3B363C2A34Q46815400-9DCE7222-AFD5-4F88-9B6F-6BA76ECB32EEQ46881189-813468B4-8CFA-4180-B599-DAFA777B5B2EQ46889601-5BE922FC-4B35-4835-93C5-B7C19188E613Q46908479-107981E7-3AA5-457C-BB6A-8EC2EEC4C3B1Q48108895-0BD386BB-A594-4433-9535-48805E9E8D8AQ48110269-FB60D685-E5FE-4336-B6D0-DEFB0518C2BDQ48135956-9DE957D3-1AEA-40F4-8B6B-77C6F9B44D79Q48139322-44589BE4-2F0D-4423-A1DB-6208F933D34BQ48158682-672F23CC-CED6-4921-9B84-E3DF4078A371Q48178568-536F35A3-EE23-447A-A069-5B49A15DB75EQ48248369-7D6A2667-2E20-49A4-9A0B-897302268C1BQ48271875-152CF07A-A295-4258-BD9A-49F9AD768D78Q48285338-C1793B01-3838-4A9F-AAA3-924071F81EB8Q49610063-84FCE6DF-3D50-428D-AF99-6DFAC93FBDC8Q51748682-471084FF-3B86-4AD3-94D6-7158EBC92F7FQ52567831-7CE6C01B-58A1-44D0-B4B5-3C34EA19039EQ53344578-AB08DB73-FA59-4270-952D-ED0068FCA039Q53395744-484A91AB-01AC-415B-8F23-529FEA0B2499Q53589500-43794BAC-3335-49C1-8C52-E5635C719F57Q53641955-FC958830-FB50-4F46-AB36-F28A359A5F9DQ53760881-8D82D83D-4EA0-473F-965C-AF7210A7F389Q54765318-CFDFF74B-DEE6-42EF-B4D0-EA4E7B68AD27Q54946221-B72F492E-0D73-4657-9183-537D68A4DEADQ55887427-73C6C312-F206-417F-B9B3-0E8DE894C80EQ57654009-5226D129-A698-4559-95FC-95A5911BD931Q57903813-7E4B963E-19E6-4C5C-A0D8-667230762028
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Ivo Krummenacher
@en
Ivo Krummenacher
@nl
type
label
Ivo Krummenacher
@en
Ivo Krummenacher
@nl
prefLabel
Ivo Krummenacher
@en
Ivo Krummenacher
@nl
P31
P496
0000-0001-9537-1506