Abstract
A series of newly designed and synthesized diacetylene-containing platinum(II) terpyridine complexes exhibited intriguing self-assembly properties. Facilitated by Pt⋅⋅⋅Pt, π-π stacking, hydrogen-bonding and hydrophobic-hydrophobic interactions, these complexes are preorganized to readily undergo topochemical polymerization reactions upon photoirradiation. The in situ polymerization of the diacetylene units to form polydiacetylene, indicated by the UV/Vis spectral changes, gel permeation chromatography and dynamic light scattering, was found to alter their assembly behaviours, as revealed by TEM images.
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