Current advances in fused tetrathiafulvalene donor–acceptor systems

JJ Bergkamp, S Decurtins, SX Liu - Chemical Society Reviews, 2015 - pubs.rsc.org
Electron donor (D) and acceptor (A) systems have been studied extensively. Among them,
fused D–A systems have attracted much attention during the past decades. Herein, we will …

Heterocyclic nanographenes and other polycyclic heteroaromatic compounds: synthetic routes, properties, and applications

M Stepien, E Gonka, M Żyła, N Sprutta - Chemical reviews, 2017 - ACS Publications
Two-dimensionally extended, polycyclic heteroaromatic molecules (heterocyclic
nanographenes) are a highly versatile class of organic materials, applicable as functional …

A tetrathiafulvalene‐based electroactive covalent organic framework

H Ding, Y Li, H Hu, Y Sun, J Wang… - … A European Journal, 2014 - Wiley Online Library
Two‐dimensional covalent organic frameworks (2D COFs) provide a unique platform for the
molecular design of electronic and optoelectronic materials. Here, the synthesis and …

Synthesis, self-assembly, and charge transporting property of contorted tetrabenzocoronenes

X Zhang, X Jiang, K Zhang, L Mao, J Luo… - The Journal of …, 2010 - ACS Publications
A facile route has been developed for the preparation of a new family of contorted 1.2, 3.4,
7.8, 9.10-tetrabenzocoronenes (TBC s). A two-step cyclization reaction, ie, oxidative …

1, 5, 9‐Triazacoronenes: A Family of Polycyclic Heteroarenes Synthesized by a Threefold Pictet–Spengler Reaction

J Wei, B Han, Q Guo, X Shi, W Wang, N Wei - Angewandte Chemie, 2010 - infona.pl
Cyclisierung im Dreierpack: Mit einer dreifachen Pictet‐Spengler‐Reaktion als
Schlüsselschritt wurden Triazacoronen‐Derivate in vier Stufen ausgehend von Veratrol …

Photoinduced asymmetric charge trapping in a symmetric tetraazapyrene-fused bis (tetrathiafulvalene) conjugate

P Zhou, MNH Pashaki, HM Frey, A Hauser… - Chemical …, 2023 - pubs.rsc.org
In fused donor–acceptor (D–A) ensembles, rapid charge recombination often occurs
because the D and A units are spatially close and strongly coupled. To the best of our …

Giant Star‐Shaped Nitrogen‐Doped Nanographenes

JP Mora‐Fuentes, A Riaño… - Angewandte Chemie …, 2019 - Wiley Online Library
Star‐shaped nanographenes (SNGs) are large monodisperse polycyclic aromatic
hydrocarbons that are larger than a nanometer and have shown a lot of promise in a wide …

Rapid synthesis of crowded aromatic architectures from silyl acetylenes

SJ Hein, H Arslan, I Keresztes, WR Dichtel - Organic letters, 2014 - ACS Publications
Congested aromatic systems were prepared by benzannulating silyl-protected
arylacetylenes. The silyl groups may be retained in the naphthalene products and …

Effect of tert-butyl groups on electronic communication between redox units in tetrathiafulvalene-tetraazapyrene triads

P Zhou, U Aschauer, S Decurtins, T Feurer… - Chemical …, 2021 - pubs.rsc.org
The electronic effect of tert-butyl groups on intramolecular through-bond interactions
between redox units in tetrathiafulvalene-tetraazapyrene (TAP) triads is investigated. The …

Functionalized coronenes: synthesis, solid structure, and properties

D Wu, H Zhang, J Liang, H Ge, C Chi… - The Journal of …, 2012 - ACS Publications
The construction of coronenes using simple building blocks is a challenging task. In this
work, triphenylene was used as a building block to construct functionalized coronenes, and …