about
Site-selective adsorption of phthalocyanine on h-BN/Rh(111) nanomesh.Alkali metal doped organic molecules on insulators: charge impact on the optical properties.Line-on-line organic-organic heteroepitaxy of quaterrylene on hexa-peri-hexabenzocoronene on Au(111).On-Surface Growth Dynamics of Graphene Nanoribbons: The Role of Halogen Functionalization.Heteroatom-Doped Perihexacene from a Double Helicene Precursor: On-Surface Synthesis and Properties.On-Surface Synthesis of Heptacene Organometallic Complexes.Controlled synthesis of single-chirality carbon nanotubes.Interplay between Energy-Level Position and Charging Effect of Manganese Phthalocyanines on an Atomically Thin Insulator.Designing Dye-Nanochannel Antenna Hybrid Materials for Light Harvesting, Transport and TrappingBuilding Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic HydrocarbonsOn-surface synthesis of graphene nanoribbons with zigzag edge topologyPurely Armchair or Partially Chiral: Noncontact Atomic Force Microscopy Characterization of Dibromo-Bianthryl-Based Graphene Nanoribbons Grown on Cu(111)Resolving Atomic Connectivity in Graphene Nanostructure JunctionsInitiating and Monitoring the Evolution of Single Electrons Within Atom-Defined StructuresOptical absorption spectra of ultrathin PTCDA films on gold single crystals: Charge transfer beyond the first monolayerFormation of solid-state excitons in ultrathin crystalline films of PTCDA: from single molecules to molecular stacksDehalogenation and coupling of a polycyclic hydrocarbon on an atomically thin insulatorCombinatorial design of molecular seeds for chirality-controlled synthesis of single-walled carbon nanotubesElectrostatic Landscape of a Hydrogen-Terminated Silicon Surface Probed by a Moveable Quantum DotOn-Surface Synthesis and Characterization of Acene-Based Nanoribbons Incorporating Four-Membered Rings
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Q34419966-9368A81F-8B54-45B9-9B21-A4B89F65260BQ42935469-4D28C722-2403-4AD4-B0A5-6A48878AED72Q43254932-5A542573-3FFB-43C6-902E-9E66651689CCQ47376159-70B58C55-DAF6-44F3-876D-65AD70854BEBQ48044021-59EF0B12-AA26-415D-8C6A-5C7D015B567EQ48056501-68A141C7-5D35-418B-8645-1AEFA23D5F68Q51064392-0AAFA841-0F03-4C14-ACF3-45710C165518Q51713247-6788F0D5-FEC8-4276-BC0F-1D721971356FQ56504030-586C02D2-0F47-4E05-953A-0363F558D79DQ58338177-3258B505-BA90-471C-BA52-A577684EACAEQ58338194-1029CE04-CB9C-4361-A451-C678048AB8F3Q58338196-91E8F2D3-2144-45DC-ACA4-DF25654DB419Q58338282-57612B97-64B2-4978-B232-E7B555929CB2Q58589983-F0228353-DA2A-4ADE-8B68-A28A89548DCFQ70996620-115A9716-6BFE-4546-ADAC-3EFAE8A7C01AQ80785302-AB643CBE-1C6E-4720-ADA5-FCE81EA59371Q88033430-0BF3EA9C-772C-465C-B31B-5FD3170EAA7BQ92092284-9DDC1776-287E-4910-8D7B-3FCE8B03018CQ92448189-D481E7DE-0586-4DA4-B70A-A9799C5733E0Q92693958-E7B9D616-5E00-4C82-B0A8-FD9D5642647E
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description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
Thomas Dienel
@ast
Thomas Dienel
@en
Thomas Dienel
@es
Thomas Dienel
@nl
Thomas Dienel
@sl
type
label
Thomas Dienel
@ast
Thomas Dienel
@en
Thomas Dienel
@es
Thomas Dienel
@nl
Thomas Dienel
@sl
prefLabel
Thomas Dienel
@ast
Thomas Dienel
@en
Thomas Dienel
@es
Thomas Dienel
@nl
Thomas Dienel
@sl
P108
P214
P106
P21
P214
P31
P496
0000-0001-8146-8841
P735
P7859
viaf-86163123