Formation of azaborines by photoelimination of B,N-heterocyclic compounds.

Highly fluorescent π-conjugated polycyclic azaborines can be prepared from B,N-heterocyclic compounds with a BR2 -CH2 unit through the elimination of an R-H molecule (see scheme). These clean photoelimination reactions occur both in solution and in polymers doped with the precursors.

Decorating BODIPY with three- and four-coordinate boron groups.

Two new BODIPY derivative molecules decorated by a Lewis acidic BMes(2)(vinyl) group and a photochromic four-coordinate boryl chromophore, respectively, have been synthesized. Significant mutual influence on photophysical and photochemical properties by the different boron-containing units has been observed.