Atomically precise graphene nanoribbons: interplay of structural and electronic properties
RSK Houtsma, J de la Rie, M Stöhr - Chemical Society Reviews, 2021 - pubs.rsc.org
Graphene nanoribbons hold great promise for future applications in nanoelectronic devices,
as they may combine the excellent electronic properties of graphene with the opening of an …
as they may combine the excellent electronic properties of graphene with the opening of an …
On‐Surface Reactions
R Lindner, A Kühnle - ChemPhysChem, 2015 - Wiley Online Library
On‐surface synthesis constitutes a rapidly growing field of research due to its promising
application for creating stable molecular structures on surfaces. While self‐assembled …
application for creating stable molecular structures on surfaces. While self‐assembled …
From graphene nanoribbons on Cu (111) to nanographene on Cu (110): critical role of substrate structure in the bottom-up fabrication strategy
Bottom-up strategies can be effectively implemented for the fabrication of atomically precise
graphene nanoribbons. Recently, using 10, 10′-dibromo-9, 9′-bianthracene (DBBA) as a …
graphene nanoribbons. Recently, using 10, 10′-dibromo-9, 9′-bianthracene (DBBA) as a …
Gap opening in double-sided highly hydrogenated free-standing graphene
Conversion of free-standing graphene into pure graphane─ where each C atom is sp3
bound to a hydrogen atom─ has not been achieved so far, in spite of numerous …
bound to a hydrogen atom─ has not been achieved so far, in spite of numerous …
Controllable conversion of quasi-freestanding polymer chains to graphene nanoribbons
In the bottom-up synthesis of graphene nanoribbons (GNRs) from self-assembled linear
polymer intermediates, surface-assisted cyclodehydrogenations usually take place on …
polymer intermediates, surface-assisted cyclodehydrogenations usually take place on …
Synthesis of armchair graphene nanoribbons from the 10, 10′-dibromo-9, 9′-bianthracene molecules on Ag (111): the role of organometallic intermediates
KA Simonov, AV Generalov, AS Vinogradov… - Scientific Reports, 2018 - nature.com
We investigate the bottom-up growth of N= 7 armchair graphene nanoribbons (7-AGNRs)
from the 10, 10′-dibromo-9, 9′-bianthracene (DBBA) molecules on Ag (111) with the …
from the 10, 10′-dibromo-9, 9′-bianthracene (DBBA) molecules on Ag (111) with the …
Stabilizing edge fluorination in graphene nanoribbons
The on-surface synthesis of edge-functionalized graphene nanoribbons (GNRs) is
challenged by the stability of the functional groups throughout the thermal reaction steps of …
challenged by the stability of the functional groups throughout the thermal reaction steps of …
On-Surface Synthesis of Graphene Nanoribbons: Photoelectron Spectroscopy Reveals Impact of Substrate Reactivity
Graphene nanoribbons (GNRs) show favorable electronic and optical properties due to their
excellent stability at ambient conditions and are suitable materials for nanoscale electronic …
excellent stability at ambient conditions and are suitable materials for nanoscale electronic …
Critical role of phenyl substitution and catalytic substrate in the surface-assisted polymerization of dibromobianthracene derivatives
Understanding the nature and hierarchy of on-surface reactions is a major challenge for
designing coordination and covalent nanostructures by means of multistep synthetic routes …
designing coordination and covalent nanostructures by means of multistep synthetic routes …
Aryl radical geometry determines nanographene formation on Au (111)
PH Jacobse, A van den Hoogenband… - Angewandte Chemie …, 2016 - Wiley Online Library
The Ullmann coupling has been used extensively as a synthetic tool for the formation of C−
C bonds on surfaces. Thus far, most syntheses made use of aryl bromides or aryl iodides …
C bonds on surfaces. Thus far, most syntheses made use of aryl bromides or aryl iodides …