Self‐assembled monolayers of N‐heterocyclic carbenes (NHCs) on copper are reported. The monolayer structure is highly dependent on the N,N‐substituents on the NHC. On both Cu(111) and Au(111), bulky isopropyl substituents force the NHC to bind perpendicular to the metal surface while methyl‐ or ethyl‐substituted NHCs lie flat. Temperature‐programmed desorption studies show that the NHC binds to Cu(111) with a desorption energy of Edes=152±10 kJ mol−1. NHCs that bind upright desorb cleanly, while flat‐lying NHCs decompose leaving adsorbed organic residues. Scanning tunneling microscopy of methylated NHCs reveals arrays of covalently linked dimers which transform into adsorbed (NHC)2Cu species by extraction of a copper atom from the surface a...
N-Heterocyclic carbenes (NHCs) are an emerging alternative to thiols for the formation of stable sel...
Exploiting coordination bonding of aromatic carboxylic acids at metal surfaces, this thesis explores...
Two different positional isomers of 1,2-dicarba-<i>closo</i>-dodecaboranedithiols, 1,2-(HS)<sub>2</s...
Funding: EPSRC PhD studentship (EP/M506631/1).Self‐assembled monolayers of N‐heterocyclic carbenes (...
International audienceBy means of scanning tunnelling microscopy (STM), complementary density functi...
EA and FG acknowledge funding from EPSRC grants (EA: EP/R512199/1; FG: EP/S027270/1). We thank the E...
11siN-heterocyclic carbenes (NHCs) bind very strongly to transition metals due to their unique elect...
8Fundamental understanding of the correlation between the structure and reactivity of chemically add...
N-Heterocyclic carbenes (NHCs) have superior properties as building blocks of self-assembled monolay...
Fundamental understanding of the correlation between the structure and reactivity of chemically addr...
13siThe creation of stable molecular monolayers on metallic surfaces is a fundamental challenge of s...
Tuning the binding mode of N-heterocyclic carbenes on metal surfaces is crucial for the development ...
The formation of flexible self-assembled monolayers (SAMs) in which an external trigger modifies the...
Tuning the properties of oxide surfaces through the adsorption of designed ligands is highly desirab...
N-heterocyclic carbenes (NHCs) have emerged as a unique molecular platform for the formation of self...
N-Heterocyclic carbenes (NHCs) are an emerging alternative to thiols for the formation of stable sel...
Exploiting coordination bonding of aromatic carboxylic acids at metal surfaces, this thesis explores...
Two different positional isomers of 1,2-dicarba-<i>closo</i>-dodecaboranedithiols, 1,2-(HS)<sub>2</s...
Funding: EPSRC PhD studentship (EP/M506631/1).Self‐assembled monolayers of N‐heterocyclic carbenes (...
International audienceBy means of scanning tunnelling microscopy (STM), complementary density functi...
EA and FG acknowledge funding from EPSRC grants (EA: EP/R512199/1; FG: EP/S027270/1). We thank the E...
11siN-heterocyclic carbenes (NHCs) bind very strongly to transition metals due to their unique elect...
8Fundamental understanding of the correlation between the structure and reactivity of chemically add...
N-Heterocyclic carbenes (NHCs) have superior properties as building blocks of self-assembled monolay...
Fundamental understanding of the correlation between the structure and reactivity of chemically addr...
13siThe creation of stable molecular monolayers on metallic surfaces is a fundamental challenge of s...
Tuning the binding mode of N-heterocyclic carbenes on metal surfaces is crucial for the development ...
The formation of flexible self-assembled monolayers (SAMs) in which an external trigger modifies the...
Tuning the properties of oxide surfaces through the adsorption of designed ligands is highly desirab...
N-heterocyclic carbenes (NHCs) have emerged as a unique molecular platform for the formation of self...
N-Heterocyclic carbenes (NHCs) are an emerging alternative to thiols for the formation of stable sel...
Exploiting coordination bonding of aromatic carboxylic acids at metal surfaces, this thesis explores...
Two different positional isomers of 1,2-dicarba-<i>closo</i>-dodecaboranedithiols, 1,2-(HS)<sub>2</s...