Search Results - "Ballmann, Gerd"
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Heavy Alkali Metal Manganate Complexes: Synthesis, Structures and Solvent‐Induced Dissociation Effects
Published in Chemistry : a European journal (04-10-2022)“…Rare examples of heavier alkali metal manganates [{(AM)Mn(CH2SiMe3)(N‘Ar)2}∞] (AM=K, Rb, or Cs) [N‘Ar=N(SiMe3)(Dipp), where Dipp=2,6‐iPr2‐C6H3] have been…”
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2
Simple Access to the Heaviest Alkaline Earth Metal Hydride: A Strongly Reducing Hydrocarbon‐Soluble Barium Hydride Cluster
Published in Angewandte Chemie International Edition (22-12-2017)“…Reaction of Ba[N(SiMe3)2]2 with PhSiH3 in toluene gave simple access to the unique Ba hydride cluster Ba7H7[N(SiMe3)2]7 that can be described as a square…”
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3
Stabilization of Calcium Hydride Complexes by Fine Tuning of Amidinate Ligands
Published in Organometallics (10-10-2016)“…A range of symmetric amidinate ligands RAmAr (R is backbone substituent, Ar is N substituent) have been investigated for their ability to stabilize calcium…”
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4
Application of Bis(amido)alkyl Magnesiates toward the Synthesis of Molecular Rubidium and Cesium Hydrido-magnesiates
Published in Organometallics (24-06-2024)“…Rubidium and cesium are the least studied naturally occurring s-block metals in organometallic chemistry but are in plentiful supply from a sustainability…”
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5
Three Oxidative Addition Routes of Alkali Metal Aluminyls to Dihydridoaluminates and Reactivity with CO2
Published in Chemistry : a European journal (09-10-2023)“…Three distinct routes are reported to the soluble, dihydridoaluminate compounds, AM[Al(NONDipp)(H)2] (AM=Li, Na, K, Rb, Cs; [NONDipp]2−=[O(SiMe2NDipp)2]2−;…”
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Synthesis, Characterization, and Structural Analysis of AM[Al(NONDipp)(H)(SiH2Ph)] (AM = Li, Na, K, Rb, Cs) Compounds, Made Via Oxidative Addition of Phenylsilane to Alkali Metal Aluminyls
Published in Inorganic chemistry (12-12-2022)“…We report the oxidative addition of phenylsilane to the complete series of alkali metal (AM) aluminyls [AM{Al(NONDipp)}]2 (AM = Li, Na, K, Rb, and Cs)…”
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A combined gas-phase dissociative ionization, dissociative electron attachment and deposition study on the potential FEBID precursor [Au(CH 3 ) 2 Cl] 2
Published in Beilstein journal of nanotechnology (06-12-2023)“…Motivated by the potential of focused-electron-beam-induced deposition (FEBID) in the fabrication of functional gold nanostructures for application in…”
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On the Electron-Induced Reactions of (CH 3 )AuP(CH 3 ) 3 : A Combined UHV Surface Science and Gas-Phase Study
Published in Nanomaterials (Basel, Switzerland) (08-08-2022)“…Focused-electron-beam-induced deposition (FEBID) is a powerful nanopatterning technique where electrons trigger the local dissociation of precursor molecules,…”
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9
LiAlH4: From Stoichiometric Reduction to Imine Hydrogenation Catalysis
Published in Angewandte Chemie International Edition (11-06-2018)“…Imine‐to‐amine conversion with catalytic instead of stoichiometric quantities of LiAlH4 is demonstrated (85 °C, catalyst loading≥2.5 mol %, pressure≥1 bar)…”
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10
Magnesium Cyanide or Isocyanide?
Published in Angewandte Chemie International Edition (28-10-2019)“…Preference for the binding mode of the CN− ligand to Mg (Mg−CN vs. Mg−NC) is investigated. A monomeric Mg complex with a terminal CN ligand was prepared using…”
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11
Insights into LiAlH4 Catalyzed Imine Hydrogenation
Published in Chemistry : a European journal (04-01-2021)“…Commercial LiAlH4 can be used in catalytic quantities in the hydrogenation of imines to amines with H2. Combined experimental and theoretical investigations…”
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12
Low Valent Magnesium Chemistry with a Super Bulky β‐Diketiminate Ligand
Published in Angewandte Chemie International Edition (08-01-2019)“…The steric bulk of the well‐known DIPPBDI ligand (CH[C(CH3)N‐DIPP]2, DIPP=2,6‐diisopropylphenyl) was increased by replacing isopropyl for isopentyl groups…”
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13
Dipyrromethene and β‑Diketiminate Zinc Hydride Complexes: Resemblances and Differences
Published in Organometallics (22-07-2019)“…A new dipyrromethene (DPM) ligand with bulky DIPP-substituents is introduced (DIPP = 2,6-diisopropylphenyl). The ligand, abbreviated as DIPPDPM, was…”
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Stabilization of Heteroleptic Heavier Alkaline Earth Metal Complexes with an Encapsulating Dipyrromethene Ligand
Published in European journal of inorganic chemistry (31-08-2019)“…A new dipyrromethene ligand with 9‐anthracenyl substituents for steric shielding of the metal has been introduced. The ligand, AnthDPM‐H (3), was directly…”
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15
Insights into LiAlH 4 Catalyzed Imine Hydrogenation
Published in Chemistry : a European journal (04-01-2021)“…Commercial LiAlH can be used in catalytic quantities in the hydrogenation of imines to amines with H . Combined experimental and theoretical investigations…”
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16
A Simple Route to Calcium and Strontium Hydride Clusters
Published in Angewandte Chemie International Edition (18-09-2017)“…The first strontium hydride complex has been obtained by simply treating Sr[N(SiMe3)2]2 with PhSiH3 in the presence of PMDTA. The Sr complex…”
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Low‐Coordinate Monomeric Zinc Hydride Complexes with Encapsulating Dipyrromethene Ligands and Reactivity with B(C6F5)3
Published in Zeitschrift für anorganische und allgemeine Chemie (1950) (15-07-2020)“…The dipyrromethene (DPM) ligand is the key to isolation of monomeric Zn hydride complexes with tricoordinate zinc centers. A range of RDPM ligands with various…”
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18
LiAlH 4 : From Stoichiometric Reduction to Imine Hydrogenation Catalysis
Published in Angewandte Chemie International Edition (11-06-2018)“…Imine-to-amine conversion with catalytic instead of stoichiometric quantities of LiAlH is demonstrated (85 °C, catalyst loading≥2.5 mol %, pressure≥1 bar). The…”
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19
Three Oxidative Addition Routes of Alkali Metal Aluminyls to Dihydridoaluminates and Reactivity with CO 2
Published in Chemistry : a European journal (09-10-2023)“…Abstract Three distinct routes are reported to the soluble, dihydridoaluminate compounds, AM[Al(NON Dipp )(H) 2 ] (AM=Li, Na, K, Rb, Cs; [NON Dipp ] 2−…”
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20
Imine hydrogenation with simple alkaline earth metal catalysts
Published in Nature catalysis (01-01-2018)“…Hydrogenation of unsaturated bonds is dominated by transition metal catalysis. Compared with transition metals, the use of other metals is less explored,…”
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