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Fourfold Diels–Alder Reaction of Tetraethynylsilane
Authors:Florian L Geyer  Alexander Rode  Prof Uwe H F Bunz
Affiliation:Organisch‐Chemisches Institut, Ruprecht‐Karls‐Universit?t Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg (Germany), Fax: (+49)?6221‐54‐8401
Abstract:A series of ethynylated silanes, including tetraethynylsilane, was treated with tetraphenylcyclopentadienone at 300 °C under microwave irradiation to give the aromatized Diels–Alder adducts as sterically encumbered mini‐dendrimers with up to 20 benzene rings. The sterically most congested adducts display red‐shifted emission through intramolecular π–π interactions in the excited state.
Keywords:dendrimer  Diels–  Alder reaction  ethynyl  oligophenyl  silane
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