We compare the ability of a prototypical dicarboxylic acid and its fluorinated analogue to act as molecular building blocks for the formation of self-assembled monolayers. Whilst fluorination is found to prevent homomolecular self-assembly, it greatly increases the ability of the carboxylic acid to act as a hydrogen bond donor for the formation of bimolecular networks
The properties of fluorine make it an attractive tool within medicinal chemistry to modulate the lip...
Exploiting coordination bonding of aromatic carboxylic acids at metal surfaces, this thesis explores...
The structure and function of self-assembled monolayers (SAMs) at the nanoscale are determined by th...
We compare the ability of a prototypical dicarboxylic acid and its fluorinated analogue to act as mo...
We report on the comparative performance of a simple diphenol and its fluorinated analogue as hydrog...
The role of non-covalent interactions involving fluorine atoms is of significant interest in the fie...
Support by The Leverhulme Trust (RGP-2013-177) and EPSRC via a doctoral training grant (H.A.) is gra...
Although hydrogen bonds have long been established as a highly effective intermolecular interaction ...
The ability to fine-tune structural parameters for partially fluorinated alkanethiols opens avenues ...
Although hydrogen bonds have long been established as a highly effective intermolecular interaction ...
The self-assembled behaviors of two fluorenone derivatives, 2,7-bis((11-hydroxyundecyl)oxy)-9-fluo...
Interfacial chemical transformations are an important way to control the physical and chemical prope...
Abstract Two new long-chain carboxylic acids (1, 2) bearing strong fluorescent group ...
AbstractThe field of self-assembled monolayers (SAMs) of organic compounds on different substrates i...
We elucidate the structure of assemblies formed by three conjugated molecules with very similar chem...
The properties of fluorine make it an attractive tool within medicinal chemistry to modulate the lip...
Exploiting coordination bonding of aromatic carboxylic acids at metal surfaces, this thesis explores...
The structure and function of self-assembled monolayers (SAMs) at the nanoscale are determined by th...
We compare the ability of a prototypical dicarboxylic acid and its fluorinated analogue to act as mo...
We report on the comparative performance of a simple diphenol and its fluorinated analogue as hydrog...
The role of non-covalent interactions involving fluorine atoms is of significant interest in the fie...
Support by The Leverhulme Trust (RGP-2013-177) and EPSRC via a doctoral training grant (H.A.) is gra...
Although hydrogen bonds have long been established as a highly effective intermolecular interaction ...
The ability to fine-tune structural parameters for partially fluorinated alkanethiols opens avenues ...
Although hydrogen bonds have long been established as a highly effective intermolecular interaction ...
The self-assembled behaviors of two fluorenone derivatives, 2,7-bis((11-hydroxyundecyl)oxy)-9-fluo...
Interfacial chemical transformations are an important way to control the physical and chemical prope...
Abstract Two new long-chain carboxylic acids (1, 2) bearing strong fluorescent group ...
AbstractThe field of self-assembled monolayers (SAMs) of organic compounds on different substrates i...
We elucidate the structure of assemblies formed by three conjugated molecules with very similar chem...
The properties of fluorine make it an attractive tool within medicinal chemistry to modulate the lip...
Exploiting coordination bonding of aromatic carboxylic acids at metal surfaces, this thesis explores...
The structure and function of self-assembled monolayers (SAMs) at the nanoscale are determined by th...