@phdthesis{Fritze2021,
  author    = {Fritze, Lars},
  title     = {Ways to Novel Inorganic-Organic Hybrid Materials Applying New B-C Bond Formation Strategies},
  doi       = {10.25972/OPUS-24217},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-242173},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2021},
  abstract  = {π-Conjugated oligomers and polymers with tricoordinate boron centers incorporated into the main chain have attracted considerable attention as the interaction of the vacant p orbital on boron with an adjacent π system of the chain leads to conjugated materials with intriguing optical and electronic properties. This enables applicability in organic electronics and optoelectronics (OLEDs, OFETs, photovoltaics) or as sensory materials. The potential of our B-C coupling protocol using metal-free catalytic Si/B exchange condensation is demonstrated by the synthesis of a series of π-conjugated monodisperse (het)aryl oligoboranes. Variation of the (het)aryl moieties allowed for tunability of the optoelectronic properties of the materials. Additionally, catalytic C-C cross-coupling strategies were applied to synthesize oligofuryl-based mono- and bisboranes, as well as polymers. These studies led to very robust and highly emissive compounds (f up to 97 \%), which allow for tuning of their emission color from blue to orange. Furthermore, this work includes investigations of reaction routes to a kinetically stabilized tetraoxaporphyrinogen. Being a key aspect of this work, a full investigation of the mechanism of the catalytic Si/B exchange was carried out. Additionally, this work presents the use of borenium cations to perform B-C coupling via intermolecular electrophilic borylation. Similar to the Si/B exchange, this route is capable of giving access to diaryl(bromo)boranes.},
  subject      = {Konjugierte Polymere},
  language  = {en}
}