sameAs
Gas-phase fragmentation of deprotonated p-hydroxyphenacyl derivatives.Probing isomers of the benzene dication in a low-temperature trap.Two-color infrared predissociation spectroscopy of C₆H₆²⁺ isomers using helium tagging.Generation, Spectroscopic, and Chemical Characterization of an Octahedral Iron(V)-Nitrido Species with a Neutral Ligand Platform.Spectroscopic Characterization and Reactivity of Triplet and Quintet Iron(IV) Oxo Complexes in the Gas Phase.Chiral superbases: the proton affinities of 1- and 2-aza[6]helicene in the gas phase.Comparison of 2,2'-bipyridine and 2,2'-bipyridyl-N,N'-dioxide as ligands in zinc complexes.Ligand effects on the [Cu(PhO)(PhOH)]+ redox active complex.Naphthol coupling monitored by infrared spectroscopy in the gas phase.The interaction of zinc(II) and hydroxamic acids and a metal-triggered Lossen rearrangement.Large effect of a small substitution: competition of dehydration with charge retention and coulomb explosion in gaseous [(bipy(R))Au(mu-O)2Au(bipy(R))]2+ dications.Growth of doubly ionized C,H,N compounds in the presence of methane.N,O-diacylhydroxylamines-structures in crystals and solutions.Can electrospray mass spectrometry quantitatively probe speciation? Hydrolysis of uranyl nitrate studied by gas-phase methods.Decomposition of neutral, singly and doubly protonated benzoquinone in the gas phase.The diatomic dication PO2+.The role of trinuclear species in a palladium acetate/trifluoroacetic acid catalytic system.Generation and dissociation pathways of singly and doubly protonated bisguanidines in the gas phase.A CuI/CuIII prototypical organometallic mechanism for the deactivation of an active pincer-like CuI catalyst in Ullmann-type couplings.Ionization and fragmentation of monochloro-isomers of 3-hydroxy-2-phenyl-4(1H)-quinolinone.Generation of the elusive meta-benzoquinone in the gas phase.Revision of the second ionization energy of toluene.Formation of Oxazoles from Elusive Gold(I) α-Oxocarbenes: A Mechanistic Study.Competitive complexation of gaseous Mn(II) by 1,10-phenanthroline, 2,2'-bipyridine, and 4,5-diazafluorene.Gas-phase study on the C-C coupling of naphthol catalyzed by Cu IITMEDA: evidence for the key role of binuclear clusters.Role of gold(I) α-oxo carbenes in the oxidation reactions of alkynes catalyzed by gold(I) complexes.Gaseous iron(II) and iron(III) complexes with BINOLate ligands.Gas-phase models for catalysis: alkane activation and olefin epoxidation by the triatomic cation Ag2O+.Structural aspects of long-lived C7H8(2+) dications generated by the electron ionization of toluene.Detection of Indistinct Fe-N Stretching Bands in Iron(V) Nitrides by Photodissociation Spectroscopy.A Comparative IRMPD and DFT Study of Fe3+ and UO22+ Complexation with N-Methylacetohydroxamic Acid.Why can a gold salt react as a base?Reactivity of Copper(III)-Oxo Complexes in the Gas Phase.Aurophilic Interactions in [(L)AuCl]...[(L')AuCl] Dimers: Calibration by Experiment and Theory.Chasing the Evasive Fe═O Stretch and the Spin State of the Iron(IV)-Oxo Complexes by Photodissociation Spectroscopy.Synthesis of Nucleosides through Direct Glycosylation of Nucleobases with 5-O-Monoprotected or 5-Modified Ribose: Improved Protocol, Scope, and Mechanism.Spin-State-Controlled Photodissociation of Iron(III) Azide to an Iron(V) Nitride Complex.Infrared Multiphoton Dissociation Spectroscopy with Free-Electron Lasers: On the Road from Small Molecules to Biomolecules.Unexpected gas-phase reactivity of the CH3OH adduct of Michler's hydrol blue: proton-shuttle catalysis and stepwise radical expulsions.Organocatalytic preparation of substituted cyclopentanes: a mechanistic study.
P50
Q34727900-D9506147-1749-42A9-973F-BE7A60FCB312Q35094372-2E9DAB8B-03CE-440E-8DCF-4DEB78F926A9Q35428174-AE39D1F9-0916-4634-89A6-805027CA25A3Q38734219-AC5FFB82-D86F-4C9F-B300-FE19902D1EBFQ38779917-60F740DC-3803-48C7-B631-771B663FBAE9Q40188141-93D88C3E-513B-4ED7-9F2B-48C74D9303F1Q42921405-588A9C68-85BB-4D29-BE63-22F7BD143A95Q42931248-111C4679-9015-468C-9A5A-ACFDDF7547D5Q43232097-761C1EB7-C9B0-455C-A0D6-64116B741F46Q43235936-3FCB926C-8F2F-495A-A0BE-1142185772F8Q43286453-F8D935AB-8990-4CE9-BF1B-5D4E2A54A4D7Q43288138-C475A713-C7B3-48A0-875E-3BD39DE38C1EQ45014275-97F60F3D-0494-4898-B902-12A6066A1727Q45027151-6B65C488-8CDC-4915-9965-76AA7C48C4DCQ45172701-46E46C77-A348-4CE1-9C7F-AB149A5E5747Q45928139-AB18E35D-70C3-4C33-8AD2-03B4E149E1E2Q46261283-576F88F8-0C1A-4CC0-B435-B596CA54796FQ46265577-0DFB8BDC-A79C-4F3A-A7A5-623CB8FD9A89Q46332783-A3CAAC89-E157-4CAA-B12F-0A619145B791Q46393879-A7451A68-FDA2-4EE4-B98B-2819080E82FDQ46435806-31E26E20-58E3-4CB4-84FF-06C0466631FCQ46442144-8C016B01-F0F0-4F38-9715-A0FA24C15548Q46535874-72B8E45E-3315-4C47-BACB-A925D0E6F5A0Q46583912-FE3E66EB-9429-475B-85A6-735DD4C1119FQ46818394-24251376-CBA9-40E0-994D-7BAFD8CE7A27Q46860238-640548E1-5FCE-4896-A23B-AC0EC6CCC500Q46863126-AACD7BEF-3413-40F3-925E-E9B86A283110Q46895173-150EE75A-B980-4AA5-A481-BD658463F992Q46970038-EA5FC3AC-C4D5-4936-AADE-A6E394511952Q47191317-3EDC90A2-6581-4AA8-90B7-AB066116ED64Q47714868-3CC1DC9A-ECC9-4545-ADD3-79A4E6AC1F42Q47896873-281D3222-7B5E-4827-869F-F29D61EEB967Q48028520-FD22E986-284F-4B78-B48A-649D9EE0E3EEQ48042947-720C5972-2EF8-45D4-8077-8AB5222DEE81Q48308542-AEBC8B40-DBB5-427C-892F-D1B960F380BDQ48323988-59E8D40E-F595-45ED-8B27-7B658B2A8265Q48360803-7182AEE3-4A4C-48BD-B98E-84A81AE2EC62Q50124111-AA96B912-8992-4181-B3D5-A6EC04C140C7Q50465731-D7F0D0EE-22B3-48AB-A8DA-026AE4F94ECFQ51120469-3889A076-35DD-4BAD-A5C6-F59E16C0590E
P50
description
Czech chemist
@en
Czech chemist
@en-ca
Czech chemist
@en-gb
Tšehhi keemik
@et
ceimiceoir Seiceach
@ga
chimiste tchèque
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chimistă cehă
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kimiste çeke
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pedagoga checa
@ast
pedagogoe uit Tsjechië
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name
Jana Roithova
@sq
Jana Roithová
@ast
Jana Roithová
@cs
Jana Roithová
@en
Jana Roithová
@es
Jana Roithová
@fr
Jana Roithová
@ga
Jana Roithová
@nl
Jana Roithová
@sl
type
label
Jana Roithova
@sq
Jana Roithová
@ast
Jana Roithová
@cs
Jana Roithová
@en
Jana Roithová
@es
Jana Roithová
@fr
Jana Roithová
@ga
Jana Roithová
@nl
Jana Roithová
@sl
altLabel
J. Roithova
@nl
J. Roithová
@nl
Jana Roithova
@ast
Jana Roithova
@en
Jana Roithova
@es
Jana Roithova
@nl
prefLabel
Jana Roithova
@sq
Jana Roithová
@ast
Jana Roithová
@cs
Jana Roithová
@en
Jana Roithová
@es
Jana Roithová
@fr
Jana Roithová
@ga
Jana Roithová
@nl
Jana Roithová
@sl
P106
P69
P214
P2080
P21
P214
P31
P496
0000-0001-5144-0688
P569
1974-11-12T00:00:00Z
P69
P691
uk2013766801
P735
P7449
PRS1340069