Researchers developed new cisplatin-like platinum metalloenediynes using thermally resistant phosphine enediyne ligands, demonstrating how different ligand substituents affect cyclization kinetics.
The first crystallographic studies of these complexes revealed they have short inter alkyne distances, indicating a potential for spontaneous cyclization at room temperature, influenced by their electronic properties.
Kinetic studies showed that complexes with electron-donating groups cyclized much faster than those with electron-withdrawing groups due to their unique electronic effects on bond formation and cyclization barriers.