Chemistry of selenium and tellurium with tetrachelate and macrocyclic ligands

Abstract

Treatment of meso(tetra- p-tolyl)porphryin, H 2(TTP), or Li 2(TTP) with O SeCl 2 or O Se(NMe 2) 2 in toluene or THF resulted in the formation of the diprotonated porphyrin, [H 4(TTP)]Cl 2 and indicated the reluctance of selenium to insert into the porphyrin core. The molecular structure of [H 4(TTP)]Cl 2 was determined by single-crystal X-ray diffraction and exhibited the typical saddle-shape distortion of diprotonated porphyrins. The molecular structure of ( p-MeO–Ph) 2Te(salen) was reexamined by X-ray diffraction. The geometry of the Te(IV) center is strongly influenced by a stereochemically active lone pair and is best described as having an AX 4E disphenoid structure in which the salen oxygen atoms occupy axial positions and the two anisyl ligands reside in equatorial sites. Distances between Te and the salen nitrogen atoms are 2.852(3) and 2.984(3) Å and are largely nonbonding.