Rapid synthesis of redox-active dodecaborane B₁₂(OR)₁₂clusters under ambient conditions

Abstract

We have developed a fast and efficient route to obtain perfunctionalized ether-linked alkyl and benzyl derivatives of the <i>closo</i>-[B₁₂(OH)₁₂]^2- icosahedral dodecaborate cluster via microwave-assisted synthesis. These icosahedral boron clusters exhibit three-dimensional delocalization of the cage-bonding electrons, tunable photophysical properties, and a high degree of stability in air in both solid and solution states. A series of <i>closo</i>-[B₁₂(OR)₁₂]^2-, <i>hypocloso</i>-[B₁₂(OR)₁₂]^1- and <i>hypercloso</i>-[B₁₂(OR)₁₂]⁰ clusters have been prepared with reaction times ranging from hours to several minutes. This method is superior to previously reported protocols since it dramatically decreases the reaction times required and eliminates the need for inert atmosphere conditions. The generality of the new microwave-based method has been further demonstrated through the synthesis of several new derivatives, which feature redox potentials up to 0.6 V more positive than previously known B₁₂(OR)₁₂ cluster compounds. We further show how this method can be applied to a one-pot synthesis of hybrid, vertex-differentiated species B₁₂(OR)₁₁(OR) that was formerly accessible only via multi-step reaction sequence.