A simple water-soluble naphthalenedithiol building block is converted quantitatively into a series of octameric [2]-catenanes, composed of two interlocked molecular squares. When this mixture is re-equilibrated in the presence of an adamantyl ammonium guest, the catenanes disassemble into their macrocyclic components that bind the guest with nanomolar affinity in water
Interlocked DNA rings (catenanes) are interesting reconfigurable nanostructures. The synthesis of ca...
Direct guest exchange reactions in one-dimensional (1D) poly-[n]-catenanes self-assembled by elusive...
Template-directed protocols provide, a routine approach to the synthesis of mechanically interlocked...
A simple water-soluble naphthalenedithiol building block is converted quantitatively into a series o...
We report the first dynamic combinatorial synthesis in water of an all-acceptor [2]catenane and of ...
We report the efficient condensation of imine-based macrocycles from dialdehyde A and aliphatic diam...
This thesis describes work on aqueous dynamic combinatorial libraries (DCLs) with inbuilt donor-acce...
The hydrophobic/hydrophilic ratio in a molecule largely affects its assembled properties in aqueous ...
A new azobenzene-based dithiol building block was developed which, upon oxidation, forms predominant...
The lure of self-assembly lies in its capability to construct complex covalent molecular architectur...
The mutual molecular recognition expressed between two classes of compounds has led to the self-asse...
Two chiral pi-electron-rich crown ethers incorporating either a binaphthol or two D-mannitol units h...
Using dynamic combinatorial chemistry, mixtures of dipeptide monomers were combined to probe how the...
Directed chemical synthesis can produce a vast range of molecular structures, but the intended produ...
Interlocked DNA rings (catenanes) are interesting reconfigurable nanostructures. The synthesis of ca...
Direct guest exchange reactions in one-dimensional (1D) poly-[n]-catenanes self-assembled by elusive...
Template-directed protocols provide, a routine approach to the synthesis of mechanically interlocked...
A simple water-soluble naphthalenedithiol building block is converted quantitatively into a series o...
We report the first dynamic combinatorial synthesis in water of an all-acceptor [2]catenane and of ...
We report the efficient condensation of imine-based macrocycles from dialdehyde A and aliphatic diam...
This thesis describes work on aqueous dynamic combinatorial libraries (DCLs) with inbuilt donor-acce...
The hydrophobic/hydrophilic ratio in a molecule largely affects its assembled properties in aqueous ...
A new azobenzene-based dithiol building block was developed which, upon oxidation, forms predominant...
The lure of self-assembly lies in its capability to construct complex covalent molecular architectur...
The mutual molecular recognition expressed between two classes of compounds has led to the self-asse...
Two chiral pi-electron-rich crown ethers incorporating either a binaphthol or two D-mannitol units h...
Using dynamic combinatorial chemistry, mixtures of dipeptide monomers were combined to probe how the...
Directed chemical synthesis can produce a vast range of molecular structures, but the intended produ...
Interlocked DNA rings (catenanes) are interesting reconfigurable nanostructures. The synthesis of ca...
Direct guest exchange reactions in one-dimensional (1D) poly-[n]-catenanes self-assembled by elusive...
Template-directed protocols provide, a routine approach to the synthesis of mechanically interlocked...