%0 Journal Article %1 Mahl_2020 %A Mahl, Magnus %A Shoyama, Kazutaka %A Krause, Ana-Maria %A Schmidt, David %A Würthner, Frank %D 2020 %I Wiley %J Angew. Chem. Int. Ed. %K myown %N 32 %P 13401--13405 %R 10.1002/anie.202004965 %T Base-Assisted Imidization: A Synthetic Method for the Introduction of Bulky Imide Substituents to Control Packing and Optical Properties of Naphthalene and Perylene Imides %U https://doi.org/10.1002%2Fanie.202004965 %V 59 %X We report the direct imidization of naphthalene and perylene dicarboxylic anhydrides/esters with bulky ortho ,ortho‐diaryl‐ and ortho ,ortho‐dialkynylaniline derivatives. This imidization method uses n‐butyllithium as a strong base to increase the reactivity of bulky amine derivatives, proceeds under mild reaction conditions, requires only stoichiometric amounts of reactants and gives straightforward access to new sterically crowded rylene dicarboximides. Mechanistic investigations suggest an isoimide as intermediary product, which was converted to the corresponding imide upon addition of an aqueous base. Single‐crystal X‐ray diffraction analyses reveal dimeric packing motifs for monoimides, while two‐side shielded bisimides crystallize in isolated molecules without close π–π‐interactions. Spectroscopic investigations disclose the influence of the bulky substituents on the optical properties in the solid state.

@article{Mahl_2020, abstract = {We report the direct imidization of naphthalene and perylene dicarboxylic anhydrides/esters with bulky ortho ,ortho‐diaryl‐ and ortho ,ortho‐dialkynylaniline derivatives. This imidization method uses n‐butyllithium as a strong base to increase the reactivity of bulky amine derivatives, proceeds under mild reaction conditions, requires only stoichiometric amounts of reactants and gives straightforward access to new sterically crowded rylene dicarboximides. Mechanistic investigations suggest an isoimide as intermediary product, which was converted to the corresponding imide upon addition of an aqueous base. Single‐crystal X‐ray diffraction analyses reveal dimeric packing motifs for monoimides, while two‐side shielded bisimides crystallize in isolated molecules without close π–π‐interactions. Spectroscopic investigations disclose the influence of the bulky substituents on the optical properties in the solid state.}, added-at = {2020-08-11T09:39:30.000+0200}, author = {Mahl, Magnus and Shoyama, Kazutaka and Krause, Ana-Maria and Schmidt, David and Würthner, Frank}, biburl = {https://www.bibsonomy.org/bibtex/20b647628ca4b864e9dc1a4e3b4ddbfcf/wuerthner_group}, doi = {10.1002/anie.202004965}, interhash = {5731f7d6fa4fae3528abd9300e72fdd4}, intrahash = {0b647628ca4b864e9dc1a4e3b4ddbfcf}, journal = {Angew. Chem. Int. Ed.}, keywords = {myown}, month = may, number = 32, pages = {13401--13405}, publisher = {Wiley}, timestamp = {2020-08-11T09:39:30.000+0200}, title = {Base-Assisted Imidization: A Synthetic Method for the Introduction of Bulky Imide Substituents to Control Packing and Optical Properties of Naphthalene and Perylene Imides}, url = {https://doi.org/10.1002%2Fanie.202004965}, volume = 59, year = 2020 }