Donor- and/or Acceptor-Substituted Expanded Radialenes: Theory, Synthesis, and Properties

Abstract

The synthesis of donor- (D) and/or acceptor (A)-expanded [4]­radialenes has been developed on the basis of readily available dibromoolefin (<b>7</b>), tetraethynylethene (<b>10</b> and <b>20</b>), and vinyl triflate (<b>12</b>) building blocks. The successful formation of D/A radialenes relies especially on (1) effective use of a series alkynyl protecting groups, (2) Sonogashira cross-coupling reactions, and (3) the development of ring closing reactions to form the desired macrocyclic products. The expanded [4]­radialene products have been investigated by spectroscopic (UV–vis absorption and emission) and quantum chemical computational methods (density functional theory and time dependent DFT). The combined use of theory and experiment provides a basis to evaluate the extent of D/A interactions via the cross-conjugated radialene framework as well as an interpretation of the origin of D/A interactions at an orbital level