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.</p
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...
The hydrophobic/hydrophilic ratio in a molecule largely affects its assembled properties in aqueous ...
This thesis describes work on aqueous dynamic combinatorial libraries (DCLs) with inbuilt donor-acce...
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...
Using dynamic combinatorial chemistry, mixtures of dipeptide monomers were combined to probe how the...
Two chiral pi-electron-rich crown ethers incorporating either a binaphthol or two D-mannitol units h...
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...
The hydrophobic/hydrophilic ratio in a molecule largely affects its assembled properties in aqueous ...
This thesis describes work on aqueous dynamic combinatorial libraries (DCLs) with inbuilt donor-acce...
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...
Using dynamic combinatorial chemistry, mixtures of dipeptide monomers were combined to probe how the...
Two chiral pi-electron-rich crown ethers incorporating either a binaphthol or two D-mannitol units h...
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...