posted on 2017-06-12, 13:52authored byGiacomo Cecot, Mathieu Marmier, Silvano Geremia, Rita De Zorzi, Anna V. Vologzhanina, Philip Pattison, Euro Solari, Farzaneh Fadaei Tirani, Rosario Scopelliti, Kay Severin
The reaction of cis-blocked, square-planar MII complexes with tetratopic
N-donor ligands is known to give
metallasupramolecular assemblies of the formula M2nLn. These assemblies typically
adopt barrel-like structures, with the ligands paneling the sides
of the barrels. However, alternative structures are possible, as demonstrated
by the recent discovery of a Pt8L4 cage with
unusual gyrobifastigium-like geometry. To date, the factors that govern
the assembly of MII2nLn complexes are not well understood. Herein,
we provide a geometric analysis of M2nLn complexes, and we discuss how size
and geometry of the ligand is expected to influence the self-assembly
process. The theoretical analysis is complemented by experimental
studies using different cis-blocked PtII complexes and metalloligands with four divergent pyridyl groups.
Mononuclear metalloligands gave mainly assemblies of type Pt8L4, which adopt barrel- or gyrobifastigium-like structures.
Larger assemblies can also form, as evidenced by the crystallographic
characterization of a Pt10L5 complex and a Pt16L8 complex. The former adopts a pentagonal barrel
structure, whereas the latter displays a barrel structure with a distorted
square orthobicupola geometry. The Pt16L8 complex
has a molecular weight of more than 23 kDa and a diameter of 4.5 nm,
making it the largest, structurally characterized M2nLn complex described to date. A
dinuclear metalloligand was employed for the targeted synthesis of
pentagonal Pt10L5 barrels, which are formed
in nearly quantitative yields.