Multiple Bismuth(III)−Thioether Secondary Interactions Integrate Metalloporphyrin Ligands into Functional Networks

We introduce the 1,2,3-tris(organylthiophenyl) group as a symmetrical, multidentate chelation link for building
coordination networks. For this, zinc(II) 5,10,15,20-tetrakis[3‘,4‘,5‘-tris(methylthio)phenyl]porphyrin was synthesized
and integrated into a two-dimensional network via coordination with BiBr3. The coordination link exhibits an unusually
complex bonding pattern, involving six S atoms from two neighboring ligands that form multiple Bi−S interactions
(distances ranging from 3.08 to 3.63 Å) with a dimerlike unit of Bi2Br6. The electronic interaction between the
porphyrin center and the Bi2Br6 block was illustrated by the diffuse-reflectance spectrum of the network compound,
in which a modest red-shifted feature at 1.8 eV was seen (while the Q-band absorption of the metalloporphyrin
core continues to be dominant at 1.9 eV).