posted on 2021-07-22, 16:03authored byErica Giraldi, Rosario Scopelliti, Farzaneh Fadaei-Tirani, Kay Severin
Molecular cages with arylboronate
ester caps at the vertices are
described. The cages were obtained by metal-templated polycondensation
reactions of a tris(2-formylpyridine oxime) ligand with arylboronic
acids. Suited templates are triflate or triflimide salts of ZnII, FeII, CoII, or MnII. In
the products, the metal ions are coordinated internally to the pyridyl
and oximato N atoms adjacent to the boronate ester, resulting in an
improved hydrolytic stability of the latter. It is possible to decorate
the cages with cyano or aldehyde groups using functionalized arylboronic
acids. The aldehyde groups allow for a postsynthetic modification
of the cages via an imine bond formation.