Direct functionalization at the boron center of antiaromatic chloroborole
Literature Information
Holger Braunschweig, Thomas Kupfer
The presence of a reactive B–Cl bond allowed for the direct functionalization of the boron center in antiaromatic chloroborole ClBC4Ph4, thus allowing for a selective fine tuning of the optical properties of borole derivatives and facilitating a potential new approach toward the introduction of borole moieties into the backbone of organic π-conjugated frameworks.
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