Two‐Dimensional Acetylenic Scaffolding: Extended Donor‐Substituted Perethynylated Dehydroannulenes |
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Authors: | Milan Kivala Frieder Mitzel Corinne Boudon Jean‐Paul Gisselbrecht Paul Seiler Maurice Gross Franois Diederich |
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Institution: | Milan Kivala,Frieder Mitzel,Corinne Boudon,Jean‐Paul Gisselbrecht,Paul Seiler,Maurice Gross,François Diederich |
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Abstract: | Starting from (Z)‐bis(N,N‐diisopropylanilino)‐substituted tetraethynylethene (TEE), perethynylated octadehydro12]‐ and dodecadehydro18]annulenes were prepared by oxidative Hay coupling. The dodecadehydro18]annulene with six peripheral N,N‐diisopropylanilino substituents was characterized by X‐ray crystallography. Elongation of the Z‐bisdeprotected TEE by Cadiot–Chodkiewicz coupling with 1‐bromo‐2‐(triisopropylsilyl)ethyne provided a Z‐configured bis(butadiyne), which after alkyne deprotection afforded under Hay coupling conditions N,N‐diisopropylanilino‐substituted perethynylated hexadecadehydro20]‐ and tetracosadehydro30]an‐nulenes. The diisopropylanilino substituents enhance the properties of these unprecedented all‐carbon perimeters in several distinct ways. They ensure their solubility, increase their stability, and importantly, engage in strong intramolecular charge‐transfer interactions with the electron‐accepting all‐carbon cores, resulting in intense, bathochromically shifted charge‐transfer bands in the UV/Vis spectra. The charge‐transfer character of these bands was confirmed by protonation‐neutralization experiments. The redox properties of the new carbon‐rich chromophores were investigated by cyclic voltammetry and rotating disk voltammetry, which indicated different redox behavior for aromatic (4n+2 π electrons) and antiaromatic (4n π electrons) dehydroannulenes. |
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Keywords: | alkynes charge transfer conjugation dehydroannulenes electrochemistry |
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