TY  - JOUR
A1  - Zhang, Fangyuan
A1  - Michail, Evripidis
A1  - Saal, Fridolin
A1  - Krause, Ana-Maria
A1  - Ravat, Prince
T1  - Stereospecific Synthesis and Photophysical Properties of Propeller-Shaped C\(_{90}\)H\(_{48}\) PAH
JF  - Chemistry - A European Journal
N2  - Herein, we have synthesized an enantiomerically pure propeller‐shaped PAH, C\(_{90}\)H\(_{48}\), possessing three [7]helicene and three [5]helicene subunits. This compound can be obtained in gram quantities in a straightforward manner. The photophysical and chiroptical properties were investigated using UV/Vis absorption and emission, optical rotation and circular dichroism spectroscopy, supported by DFT calculations. The nonlinear optical properties were investigated by two‐photon absorption measurements using linearly and circularly polarized light. The extremely twisted structure and packing of the homochiral compound were investigated by single‐crystal X‐ray diffraction analysis.
KW  - chirality
KW  - enantiomers
KW  - helicenes
KW  - polycyclic aromatic hydrocarbons
KW  - stereospecific sythesis
Y1  - 2019
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-208682
VL  - 25
IS  - 71
ER  - 
TY  - JOUR
A1  - Farrell, Jeffrey  M.
A1  - Grande, Vincenzo
A1  - Schmidt, David
A1  - Würthner, Frank
T1  - A Highly Warped Heptagon-Containing sp\(^2\) Carbon Scaffold via Vinylnaphthyl π-Extension
JF  - Angewandte Chemie International Edition
N2  - A new strategy is demonstrated for the synthesis of warped, negatively curved, all‐sp\(^2\)‐carbon π‐scaffolds. Multifold C−C coupling reactions are used to transform a polyaromatic borinic acid into a saddle‐shaped polyaromatic hydrocarbon (2 ) bearing two heptagonal rings. Notably, this Schwarzite substructure is synthesized in only two steps from an unfunctionalized alkene. A highly warped structure of 2 was revealed by X‐ray crystallographic studies and pronounced flexibility of this π‐scaffold was ascertained by experimental and computational studies. Compound 2 exhibits excellent solubility, visible range absorption and fluorescence, and readily undergoes two reversible one‐electron oxidations at mild potentials.
KW  - arenes
KW  - carbon
KW  - C-C coupling
KW  - curvature
KW  - polycyclic aromatic hydrocarbons
Y1  - 2019
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-206682
VL  - 58
IS  - 46
ER  -