Abstract
The functionalisation of macrocyclic p-tertbutylcalix[4]arenes at the lower rim with
hydroxamic acid and proline hydroxamic acid groups gives the calixarenes chelating
properties similar to siderophores. The
The functionalisation of macrocyclic p-tertbutylcalix[4]arenes at the lower rim with
hydroxamic acid and proline hydroxamic acid groups gives the calixarenes chelating
properties similar to siderophores. The