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 …

Heterocycle-appended porphyrins: synthesis and challenges

IA Abdulaeva, KP Birin… - Coordination Chemistry …, 2020 - Elsevier
Porphyrin and their versatile metal complexes represent a special class of coordination
compounds possessing unique physical-chemical properties. The achievements in the …

Tetrathiafulvalene-(TTF-) derived oligopyrrolic macrocycles

A Jana, M Ishida, JS Park, S Bahring… - Chemical …, 2017 - ACS Publications
After the epochal discovery of the “organic metal”, namely, tetrathiafulvalene (TTF)–7, 7, 8, 8-
tetracyano-p-quinodimethane (TCNQ) dyad in 1973, scientists have made efforts to …

Embedding heteroatoms: an effective approach to create porphyrin-based functional materials

N Fukui, K Fujimoto, H Yorimitsu, A Osuka - Dalton Transactions, 2017 - pubs.rsc.org
Incorporation of planarized heteroatom (s) onto the porphyrin periphery is an effective
approach to create porphyrin-based functional materials. In the last three decades, such an …

Porphyrins fused with strongly electron-donating 1, 3-dithiol-2-ylidene moieties: Redox control by metal cation complexation and anion binding

NL Bill, M Ishida, S Bahring, JM Lim, S Lee… - Journal of the …, 2013 - ACS Publications
A new class of redox-active free base and metalloporphyrins fused with the 1, 3-dithiol-2-
ylidene subunits present in tetrathiafulvalene, termed MTTFP (M= H2, Cu, Ni, Zn), have been …

Structurally-modified subphthalocyanines: Molecular design towards realization of expected properties from the electronic structure and structural features of …

S Shimizu, N Kobayashi - Chemical Communications, 2014 - pubs.rsc.org
This feature article summarizes recent contributions of the authors in the synthesis of
structurally-modified subphthalocyanines. The structural modification covers (1) modification …

Multi-(phenylthio) porphyrinato Ni (II) compounds: Synthesis, structures and properties

P Jiang, T Zhao, J Rong, B Yin, Y Rao, M Zhou… - Chinese Chemical …, 2021 - Elsevier
A series of multi-(phenylthio) porphyrinato Ni (II) compounds were synthesized without the
participation of transition metal catalysts. All of these products were well characterized by 1 …

Porphyrin/platinum (II) C^ N^ N acetylide complexes: synthesis, photophysical properties, and singlet oxygen generation

A Jana, L McKenzie, AB Wragg, M Ishida… - … A European Journal, 2016 - Wiley Online Library
A new class of substituted porphyrins has been developed in which a different number of
cyclometalated PtII C^ N^ N acetylides and polyethylene glycol (PEG) chains are attached to …

Synthesis of 2-Azulenyltetrathiafulvalenes by Palladium-Catalyzed Direct Arylation of 2-Chloroazulenes with Tetrathiafulvalene and Their Optical and Electrochemical …

T Shoji, T Araki, S Sugiyama, A Ohta… - The Journal of …, 2017 - ACS Publications
Tetrathiafulvalene (TTF) derivatives with 2-azulenyl substituents 5–11 were prepared by the
palladium-catalyzed direct arylation reaction of 2-chloroazulenes with TTF in good yield …

Photoinduced electron transfer from a tetrathiafulvalene-calix [4] pyrrole to a porphyrin carboxylate within a supramolecular ensemble

CM Davis, Y Kawashima, K Ohkubo… - The Journal of …, 2014 - ACS Publications
A supramolecular assembly is formed upon mixing millimolar concentrations of a tetrakis-
tetrathiafulvalene calix [4] pyrrole (TTF-C4P) and a porphyrin tetraethylammonium …