[2.2]Paracyclophane derivatives containing tetrathiafulvalene moieties [PDF]
Beilstein Journal of Organic Chemistry, 2015 The synthesis of [2.2]paracyclophane derivatives containing tetrathiafulvalene units has been accomplished by the coupling reaction of 4-([2.2]paracyclophan-4-yl)-1,3-dithiol-2-thione in the presence of trimethylphosphite.
Laura G. Sarbu +4 more
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Synthesis of Thieno[2,3-d]-1,3-dithiol-2-thiones from Thieno[2,3-d]-1,2,3-thiadiazoles: Matryoshka-type autoclave for high-temperature, high-pressure thermolysis microscale reactions [PDF]
Molecules, 2002 Thieno[2,3-d]-1,2,3-thiadiazoles (1) react with carbon disulfide in a "Matryoshkatype" double compartment autoclave [1] to yield thieno[2,3-d]-1,3-dithiol-2-thiones (2).
Ving J. Lee +3 more
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An Improved Synthetic Method for Sensitive Iodine Containing Tricyclic Flavonoids [PDF]
Molecules, 2022 The synthesis of new iodine containing synthetic tricyclic flavonoids is reported. Due to the sensitivity of the precursors to the heat and acidic conditions required for the ring closure of the 1,3-dithiolium core, a new cyclization method has been ...
Mihail Lucian Birsa, Laura G. Sarbu
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An Approach to Paracyclophane-Based Tetrathiafulvalenes: Synthesis and Characterization of a Pseudo-Geminal [2.2]Paracyclophane 1,3-Dithia-2-Thione [PDF]
Molecules, 2020 The synthesis of paracyclophane-based tetrathiafulvalene precursors is described in the context of the importance of these compounds in the field of material chemistry.
Lucian G. Bahrin +4 more
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One-Dimensional Polycyclic Aromatic Hydrocarbons Incorporating Multiple Dithiafulvene Units-Novel Multi-Redox and Electrochromic Systems. [PDF]
Angew Chem Int Ed EnglPlanar polycyclic aromatic hydrocarbons (PAHs) incorporating three or four dithiafulvene (DTF) units were synthesized via Horner–Wadsworth–Emmons reactions to create large π‐conjugated redox‐active frameworks. These molecules display strong intermolecular associations and distinct odd–even redox behavior, enabling formation of mixed‐valence and radical‐
Rindom C +3 more
europepmc +3 more sources
Planar, Twisted, or Curved Extended Tetrathiafulvalenes with Polycyclic Aromatic Hydrocarbon Cores Featuring Five-Membered Rings. [PDF]
Chem Asian JTetrathiafulvalenes (TTFs) extended by polycyclic aromatic hydrocarbons (PAHs) constitute a class of redox‐active chromophores. This review summarizes PAH‐extended TTFs for which the PAH core features five‐membered rings together with six‐, seven‐, and/or eight‐membered rings.
Pedersen VBR, Nielsen MB.
europepmc +2 more sources
Bis-1,3-dithiolium Salts as Initiators for the Cationic Polylnerization of Vinyl Monomers [PDF]
Polymer Journal, 1996 Top of pageAbstract Keywords: Bis-1,3-dithiolium Salts; Radical Cation; Cationic Polymerization; Initiator; Vinyl ...
Eri Yoshida, Yoshida Eri
exaly +2 more sources
Tricyclic flavonoids with 1,3-dithiolium substructure [PDF]
Beilstein Journal of Organic Chemistry, 2012 Lucian G Bahrin, Henning Hopf
exaly +2 more sources
Reaction of 1,4,2-Dithiazolium and 1,3-Dithiolium Salts with Malononitrile [PDF]
Bulletin of the Chemical Society of Japan, 1989 Abstract The reaction of 5-substituted 3-phenyl-1,4,2-dithiazolium salts with malononitrile gave not only 5-dicyanomethylene-3-phenyl-1,4,2-dithiazole and an isothiazole derivative, but 4-amino-5-cyano-2-(1-cyano-2-dialkylamino-2-mercaptovinyl)-6-phenylpyrimidines (6) and a butadiene derivative, depending on substituents at C-5 and bases
Katsumi Yonemoto +2 more
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Tri(hetero)substituted Carbonium Ions. XI. A Novel Synthetic Route to 2-Dialkylamino-4-alkyl-1,3-dithiolium Salts [PDF]
Bulletin of the Chemical Society of Japan, 1976 Abstract Pyrolysis of 2-dialkylamino-4-(α-bromoalkyl)-1,3-dithiolanylium bromides (2) readily prepared by bromination of the β,γ-unsaturated dithiocarbamates (1) affords 2-dialkylamino-4-alkyl-1,3-dithiolium salts (3) in good yields, providing a useful way to prepare dithiolium salts.
Takeshi Nakai +2 more
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