About: Karl Kirchner

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Karl Kirchner (en) Karl Kirchner (es) Karl Kirchner (nl) Karl Kirchner (sl) Karl Kirchner (ast)
skos:prefLabel	Karl Kirchner (en) Karl Kirchner (es) Karl Kirchner (nl) Karl Kirchner (sl) Karl Kirchner (ast)
name	Karl Kirchner (en) Karl Kirchner (es) Karl Kirchner (nl) Karl Kirchner (sl) Karl Kirchner (ast)
Scopus author ID	wds:Q41186517-28937E06-D3C0-4650-A36B-356C539A7A77 wds:Q41186517-B1A6C03B-3643-4596-A7A9-4EA3974AF104
Scopus author ID	57200501377
given name	wds:Q41186517-7CB5C2B4-7137-4021-BCEE-648D07C1330E
given name	Karl
instance of	wds:Q41186517-4320AB5C-1242-4910-A482-46CDD3B9C378
instance of	Homo sapiens
occupation	wds:Q41186517-DCEE16E5-53E2-435D-97B3-47CC9E2DE994
employer	wds:Q41186517-3DE12AE1-A396-4B68-B76C-36BC90F651CA
sex or gender	wds:Q41186517-A638817B-9AA6-4D8E-8881-77371A4466CA
ISNI	wds:Q41186517-C9DBE1FE-0C8C-409A-8F1D-17A469633351
VIAF ID	wds:Q41186517-C1823057-5D2B-4C1F-8790-CE790DEC1572
GND ID	wds:Q41186517-0dde42f6-018d-4139-9eb1-8e6320c8bd5e
IdRef ID	wds:Q41186517-4AAFCA85-A056-4129-98B0-2EB2590358A9
family name	wds:Q41186517-28644359-26F2-42BC-B3E5-B1DDD79CFD30
National Library of Israel J9U ID	wds:Q41186517-38491EC8-7ECC-4206-8EB0-A8C24C240F51
VIAF ID	http://viaf.org/viaf/314886282
GND ID	https://d-nb.info/gnd/136202187
IdRef ID	http://www.idref.fr/199570671/id
occupation	researcher
employer	TU Wien
sex or gender	male
ISNI	0000000419182254
VIAF ID	314886282
GND ID	136202187
IdRef ID	199570671
family name	Kirchner
National Library of Israel J9U ID	987007357812405171
ORCID iD	wds:Q41186517-4176A552-29E6-4A3D-91E6-9F20758B9079
ORCID iD	https://orcid.org/0000-0003-0872-6159
ORCID iD	0000-0003-0872-6159
ResearcherID	wds:Q41186517-27BDCDC1-F7E7-4CFC-8800-CD19A9F3B4B3 wds:Q41186517-2B8FC05D-1B46-4159-B9B7-B12BBB01E1E0
Publons author ID	wds:Q41186517-e15379a3-e005-4bb7-894b-83b203700c04
ResearcherID	L-9555-2016 P-1268-2018
Publons author ID	2228563
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q41186517
is author of	A critique of Stewart's approach: the chemical mechanism of dilutional acidosis Modularly designed transition metal PNP and PCP pincer complexes based on aminophosphines: synthesis and catalytic applications. Mechanism for the cyclotrimerization of alkynes and related reactions catalyzed by CpRuCl Facile migratory insertion of a N-heterocyclic carbene into a ruthenium-carbon double bond: a new type of reaction of a NHC ligand Mechanistic investigations and substrate scope evaluation of ruthenium-catalyzed direct sp3 arylation of benzylic positions directed by 3-substituted pyridines Efficient Hydrogenation of Ketones and Aldehydes Catalyzed by Well-Defined Iron(II) PNP Pincer Complexes: Evidence for an Insertion Mechanism. Iron(ii) complexes featuring κ3- and κ2-bound PNP pincer ligands – the significance of sterics High-spin iron(II) complexes with mono-phosphorylated 2,6-diaminopyridine ligands Synthesis and reactivity of TADDOL-based chiral Fe(ii) PNP pincer complexes-solution equilibria between κ2P,N- and κ3P,N,P-bound PNP pincer ligands Reactivity of coordinatively unsaturated iron complexes towards carbon monoxide: to bind or not to bind? Non-precious metal complexes with an anionic PCP pincer architecture Heterolytic Cleavage of Dihydrogen by an Iron(II) PNP Pincer Complex via Metal-Ligand Cooperation Synthesis and Characterization of Hydrido Carbonyl Molybdenum and Tungsten PNP Pincer Complexes Stereospecific and reversible CO binding at iron pincer complexes (η-Cyclo-penta-dien-yl)(η-mesitylamine)ruthenium(II) hexa-fluorido-phosphate Synthesis and reactivity of BINEPINE-based chiral Fe(II) PNP pincer complexes Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity Carbon dioxide hydrogenation catalysed by well-defined Mn(i) PNP pincer hydride complexes. Manganese-Catalyzed Aminomethylation of Aromatic Compounds with Methanol as a Sustainable C1 Building Block. Divergent Coupling of Alcohols and Amines Catalyzed by Isoelectronic Hydride Mn(I) and Fe(II) PNP Pincer Complexes. Sustainable Synthesis of Quinolines and Pyrimidines Catalyzed by Manganese PNP Pincer Complexes. Synthesis and reactivity of coordinatively unsaturated halocarbonyl molybdenum PNP pincer complexes Selective Hydrogenation of Aldehydes Using a Well-Defined Fe(II) PNP Pincer Complex in Biphasic Medium Ruthenium-mediated cyclotrimerization of alkynes utilizing the cationic complex [RuCp(CH3CN)3]PF6 Iron PCP Pincer Complexes in Three Oxidation States: Reversible Ligand Protonation To Afford an Fe(0) Complex with an Agostic C–H Arene Bond Stable, Yet Highly Reactive Nonclassical Iron(II) Polyhydride Pincer Complexes: Z-Selective Dimerization and Hydroboration of Terminal Alkynes. Hydrogenation of Nitriles and Ketones Catalyzed by an Air-Stable Bisphosphine Mn(I) Complex Isoelectronic Manganese and Iron Hydrogenation/Dehydrogenation Catalysts: Similarities and Divergences. Well-defined bifunctional iron catalysts for the hydrogenation of ketones: iron, the new ruthenium A complete series of halocarbonyl molybdenum PNP pincer complexes - Unexpected differences between NH and NMe spacers

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