Recent advances in heterocyclic nanographenes and other polycyclic heteroaromatic compounds
A Borissov, YK Maurya, L Moshniaha… - Chemical …, 2021 - ACS Publications
This review surveys recent progress in the chemistry of polycyclic heteroaromatic molecules
with a focus on structural diversity and synthetic methodology. The article covers literature …
with a focus on structural diversity and synthetic methodology. The article covers literature …
The Scholl reaction as a powerful tool for synthesis of curved polycyclic aromatics
The past decade has witnessed remarkable success in the synthesis of curved polycyclic
aromatics through Scholl reactions which enable oxidative aryl–aryl coupling even in …
aromatics through Scholl reactions which enable oxidative aryl–aryl coupling even in …
Efficient iodine uptake of ultra thermally stable conjugated copolymers bearing biaceanthrylenyl moieties and contorted aromatic units using a [3+ 2] palladium …
A novel series of copolymers made from alternating aromatic surrogates with contorted and
spiro compounds, denoted as BCP1–3, was successfully synthesized employing a …
spiro compounds, denoted as BCP1–3, was successfully synthesized employing a …
The design, synthesis and application of rubicene based polycyclic aromatic hydrocarbons (PAHs)
Rubicene, a key nanofragment of C70, is attracting great attention owing to its unique
molecular structure and physicochemical properties. As an indeno-annelated polycyclic …
molecular structure and physicochemical properties. As an indeno-annelated polycyclic …
Synthesis and Photophysical Properties of Soluble N‐Doped Rubicenes via Ruthenium‐Catalyzed Transfer Hydrogenative Benzannulation
WG Shuler, SP Parvathaneni… - … A European Journal, 2021 - Wiley Online Library
Ruthenium‐catalyzed butadiene‐mediated benzannulation enabled the first synthesis of 3,
10‐(di‐tert‐butyl) rubicene and its N‐doped derivatives as well as preliminary studies on …
10‐(di‐tert‐butyl) rubicene and its N‐doped derivatives as well as preliminary studies on …
Electron Acceptors Based on Cyclopentannulated Anthanthrenes
We demonstrate the preparation of anthanthrene derivatives with fused five-membered
rings. These new derivatives are prepared by a palladium catalyzed cyclopentannulation …
rings. These new derivatives are prepared by a palladium catalyzed cyclopentannulation …
Post-Functionalization of End-Capping Twistacenes with Pyrene Units
J Xiao, S Wang, T Ye - Organic Chemistry Frontiers, 2024 - pubs.rsc.org
The size, shape, edge structure of nanographenes can significantly affect their physical
properties. Meanwhile, the introduction of pentagon, heptagon, octagon into the parent …
properties. Meanwhile, the introduction of pentagon, heptagon, octagon into the parent …
Quadrupolar Cyclopenta[hi]aceanthrylene‐Based Electron Donor‐Acceptor‐Donor Conjugates: Charge Transfer versus Charge Separation
C Schierl, W Alex, LM Mateo, B Ballesteros… - Angewandte …, 2019 - Wiley Online Library
Abstract Cyclopenta [hi] aceanthrylenes (CPAs) have been functionalized at two of the
peripheral positions with electronically inert trimethylsilylethynyl (1), as well as with electron …
peripheral positions with electronically inert trimethylsilylethynyl (1), as well as with electron …
Donor‐acceptor copolymers from cyclopentannulation polymerizations with dicyclopenta [cd, jk] pyrene and dicyclopenta [cd, lm] perylene acceptors
A Uddin, KN Plunkett - Journal of Polymer Science, 2020 - Wiley Online Library
A series of donor‐acceptor copolymers with dicyclopenta [cd, jk] pyrene and dicyclopenta
[cd, lm] perylene acceptor units was prepared via palladium catalyzed cyclopenta …
[cd, lm] perylene acceptor units was prepared via palladium catalyzed cyclopenta …
Synthesis of anthradithiophene containing conjugated polymers via a cross-coupling strategy
WA Hussain, KN Plunkett - RSC advances, 2021 - pubs.rsc.org
New conjugated polymers that incorporate dihexylanthradithiophene (DHADT) in the main
chain were prepared by Stille, Sonogashira, and Yamamoto cross-coupling polymerization …
chain were prepared by Stille, Sonogashira, and Yamamoto cross-coupling polymerization …