about
Essential dynamics for the study of microstructures in liquids.A density functional theory (DFT) study on gas-phase proton transfer reactions of derivatized and underivatized peptide ions generated by matrix-assisted laser desorption ionization.Imaging molecular structure through femtosecond photoelectron diffraction on aligned and oriented gas-phase molecules.Au38(SPh)24: Au38 Protected with Aromatic Thiolate Ligands.Optical properties of nanoalloys.Au21S(SAdm)15: An Anisotropic Gold Nanomolecule. Optical and Photoluminescence Spectroscopy and First-Principles Theoretical Analysis.Off-resonance photoemission dynamics studied by recoil frame F1s and C1s photoelectron angular distributions of CH3F.Electronic properties of the boroxine-gold interface: evidence of ultra-fast charge delocalization.Conformational effects in photoelectron circular dichroism of alaninol.Density functional study on the circular dichroism of photoelectron angular distribution from chiral derivatives of oxirane.Recoil frame photoelectron angular distributions of BF3: a sensitive probe of the shape resonance in the F 1s continuum.Angle-resolved photoelectron spectroscopy of randomly oriented 3-hydroxytetrahydrofuran enantiomers.Valence photoionization dynamics in circular dichroism of chiral free molecules: the methyl-oxirane.Conformational sensitivity in photoelectron circular dichroism of 3-methylcyclopentanone.Transformation of Au144(SCH2CH2Ph)60 to Au133(SPh-tBu)52 Nanomolecules: Theoretical and Experimental Study.Self-assembled metallacycles with pyrazine edges: a new example in which the unexpected molecular triangle prevails over the expected molecular square.2-amino-1-propanol versus 1-amino-2-propanol: valence band and C 1s core-level photoelectron spectra.Theoretical study of sulfur L-edge XANES of thiol protected gold nanoparticles.S2p core level spectroscopy of short chain oligothiophenes.Study of the electronic structure of short chain oligothiophenes.Erratum: "Intense fluorescence of Au20" [J. Chem. Phys. 147, 074301 (2017)].Intense fluorescence of Au20.Strong oscillations in molecular valence photoemission intensities.A new time dependent density functional algorithm for large systems and plasmons in metal clusters.The valence electronic structure and conformational flexibility of epichlorohydrin.Time dependent density functional study of the photoionization dynamics of SF6.Vibrationally resolved NEXAFS at C and N K-edges of pyridine, 2-fluoropyridine and 2,6-difluoropyridine: A combined experimental and theoretical assessment.Femtosecond x-ray photoelectron diffraction on gas-phase dibromobenzene moleculesLong-Lived Palladium Catalysts for CO/Vinyl Arene Polyketones Synthesis: A Solution to Deactivation ProblemsPalladium Complexes with 3-Alkyl-Substituted-1,10-Phenanthrolines: Effect of the Remote Alkyl Substituent on the CO/Olefin Copolymerization ReactionsTime-dependent density-functional study of the photoabsorption spectrum of Au25 (SC2 H4 C6 H5 )18 anion: Validation of the computational protocolIndividual Component Map of Rotatory Strength and Rotatory Strength Density Plots As Analysis Tools of Circular Dichroism Spectra of Complex SystemsTheoretical study of ultrafast x-ray photoelectron diffraction from molecules undergoing photodissociationPrinciples of Optical Spectroscopy of Aromatic Alloy Nanomolecules: Au36–xAgx(SPh-tBu)24Au279(SR)84: The Smallest Gold Thiolate Nanocrystal That Is Metallic and the Birth of PlasmonPd doping, conformational, and charge effects on the dichroic response of a monolayer protected Au38(SR)24 nanoclusterAu21S(SAdm)15: Crystal Structure, Mass Spectrometry, Optical Spectroscopy, and First-Principles Theoretical AnalysisLigand-Enhanced Optical Response of Gold Nanomolecules and Its Fragment Projection Analysis: The Case of Au30(SR)18Optical Properties of Metal Nanoclusters—TheoryPhotoelectron circular dichroism of isopropanolamine
P50
Q30881757-C935F688-37C9-4928-8D5E-A8FE7FC97CF8Q33431082-C3BDED13-890D-4631-89B1-CC59937CDDAFQ35308728-B84DE676-EF6C-456C-AF7E-E698420CE388Q36316201-B8460292-8D17-4C71-B8BF-E444BEF0A957Q39017945-F3C5E7EB-0876-4ACE-ABB3-5428A8E7070FQ39043371-1082DCC4-6C11-4BB4-B34D-082F425F6C45Q41452925-887E1A61-5E6D-44E3-A086-D77FE739662BQ41826216-763CBB98-C1CC-464F-A741-B33316F70330Q44942844-D25DC59C-823A-42C3-8E33-ED055E06FB94Q44989152-3BE37465-010C-4AFF-ACDD-A1BA90E5DC1BQ45915274-B1787945-4320-43C9-A138-6BA3094C0C31Q46536066-749462DD-8F65-4F4E-BDBB-460765EAA594Q46612035-522BF307-07AB-4DA1-B312-C25409F94316Q46657322-F1CF0653-40C4-4A18-A949-96A31404FF24Q46685466-3932ADEF-7F65-4196-B62C-C514A844AF9BQ46906143-6535153E-8EA7-4261-85C8-51A256F77119Q46951945-E79CBD22-9687-4310-B97C-4D78C217B934Q46984481-963F9C9B-9D9A-45BE-9BC4-00F98CD97545Q48045130-AA03FC3E-679E-409F-A538-61F69A7EDC06Q48047760-3DB74D09-B1DF-48BB-9108-071519D7C2B3Q48101284-1F86CDE2-46FF-4DDC-B108-6248EEB897D9Q48201347-8F5239DF-34DF-4ACB-A465-4E86985D8C25Q50738435-88B3FF15-6A18-4151-963D-A29F6508FE18Q50882423-E7AEBF8F-A260-45DE-B27A-6C236C9A0163Q51558912-2B215535-0768-43E8-AE84-DCEDCA5AF1BBQ51945277-4FE65297-5A46-45B9-8A9E-F1AB020E6B27Q53182836-6A271A82-FAE3-4479-A9D2-341B6F0A0EB5Q56045991-AC9FA883-F695-40C0-AEE5-E7F332D7F65DQ57499226-71D150CE-18BB-42C8-8466-DF55CE6CE9FAQ57499245-B710F537-436C-45C2-B49F-0C48DC5C1488Q57526174-B4DA53AB-AD37-4A77-B4E3-1D0EBE9AAD01Q57526175-898A1F0F-BE67-442B-B44C-16CDB778F864Q57526179-85B7C499-3CA6-498D-AC8A-811A31CD8CADQ57526180-905E7B55-99E5-4CAD-9E84-232AC77EE25AQ57526181-A2BA8441-4FFE-4B70-A2F1-698D6016C0FCQ57526182-022F961A-A04D-42F2-A21D-34D1C05FC772Q57526184-D61233DD-50B5-4898-89ED-6B61FEA38A70Q57526186-DEA7661E-A5C2-4866-95F7-0DB9AA94DE34Q57526187-16BD7AC1-FA5B-452C-86B9-6052D58950C4Q57526189-346E7532-875F-4526-87A9-C8DDE95F968C
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-3700-7903
@en
name
Mauro Stener
@ast
Mauro Stener
@en
Mauro Stener
@es
Mauro Stener
@nl
type
label
Mauro Stener
@ast
Mauro Stener
@en
Mauro Stener
@es
Mauro Stener
@nl
prefLabel
Mauro Stener
@ast
Mauro Stener
@en
Mauro Stener
@es
Mauro Stener
@nl
P1053
B-7987-2014
P106
P21
P31
P3829
P496
0000-0003-3700-7903