TY  - JOUR
A1  - Zhang, Fangyuan
A1  - Radacki, Krzysztof
A1  - Braunschweig, Holger
A1  - Lambert, Christoph
A1  - Ravat, Prince
T1  - Zinc-[7]helicenocyanine and its discrete π-stacked homochiral Dimer
JF  - Angewandte Chemie International Edition
N2  - In this communication, we demonstrate a novel approach to prepare a discrete dimer of chiral phthalocyanine (Pc) by exploiting the flexible molecular geometry of helicenes, which enables structural interlocking and strong aggregation tendency of Pcs. Synthesized [7]helicene-Pc hybrid molecular structure, zinc-[7]helicenocyanine (Zn-7HPc), exclusively forms a stable dimeric pair consisting of two homochiral molecules. The dimerization constants were estimated to be as high as 8.96×10\(^6\) M\(^{−1}\) and 3.42×107 M\(^{−1}\) in THF and DMSO, respectively, indicating remarkable stability of dimer. In addition, Zn\(^{-7}\)HPc exhibited chiral self-sorting behavior, which resulted in preferential formation of a homochiral dimer also in the racemic sample. Two phthalocyanine subunits in the dimeric form strongly communicate with each other as revealed by a large comproportionation constant and observation of an IV-CT band for the thermodynamically stable mixed-valence state.
KW  - organic chemistry
KW  - supramolecular assembly
KW  - chirality
KW  - helicenes
KW  - homochiral dimer
KW  - phthalocyanines
Y1  - 2021
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-256534
VL  - 60
ER  - 
TY  - JOUR
A1  - Bold, Kevin
A1  - Stolte, Matthias
A1  - Shoyama, Kazutaka
A1  - Holzapfel, Marco
A1  - Schmiedel, Alexander
A1  - Lambert, Christoph
A1  - Würthner, Frank
T1  - Macrocyclic donor-acceptor dyads composed of a perylene bisimide dye surrounded by oligothiophene bridges
JF  - Angewandte Chemie Internationale Edition
N2  - Two macrocyclic architectures comprising oligothiophene strands that connect the imide positions of a perylene bisimide (PBI) dye have been synthesized via a platinum-mediated cross-coupling strategy. The crystal structure of the double bridged PBI reveals all syn-arranged thiophene units that completely enclose the planar PBI chromophore via a 12-membered macrocycle. The target structures were characterized by steady-state UV/Vis absorption, fluorescence and transient absorption spectroscopy, as well as cyclic and differential pulse voltammetry. Both donor–acceptor dyads show ultrafast Förster Resonance Energy Transfer and photoinduced electron transfer, thereby leading to extremely low fluorescence quantum yields even in the lowest polarity cyclohexane solvent.
KW  - organic chemistry
KW  - photoinduced electron transfer
KW  - donor–acceptor dyads
KW  - macrocycles
KW  - oligothiophenes
KW  - perylenebisimide
Y1  - 2022
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-256569
VL  - 61
IS  - 1
ER  -