✦ LIBER ✦

New vinylogous tetrathiafulvalene .pi.-electron donors with peripheral alkylseleno substitution

✍ Scribed by Bryce, Martin R.; Coffin, Malcolm A.; Clegg, William

Book ID: 127003273
Publisher: American Chemical Society
Year: 1992
Tongue: English
Weight: 535 KB
Volume: 57
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00032a018

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: New Vinylogous Tetr

ChemInform Abstract: New Vinylogous Tetrathiafulvalene π-Electron Donors with Lower Oxidation Potentials.

✍ L. YU; D. ZHU 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

New Vinylogous Tetrathiafulvalene π-Electron Donors with Lower Oxidation Potentials. -Mild and efficient syntheses of new vinylogous tetrafulvalenes (VI) and 1,3-dithiole-2-thiones (V) via base-catalyzed ring opening of (III) are described. Cyclic voltammetry establishes that the new donors (VI) ha

New extended .pi.-electron donors. Tetra

New extended .pi.-electron donors. Tetrathiafulvalene systems with heterocyclic spacer groups

✍ Hansen, Thomas K.; Lakshmikantham, M. V.; Cava, Michael P.; Niziurski-Mann, Rene 📂 Article 📅 1992 🏛 American Chemical Society 🌐 English ⚖ 624 KB

Synthesis of Several Isomeric Tetrathiaf

Synthesis of Several Isomeric Tetrathiafulvalene .pi.-Electron Donors with Peripheral Sulfur Atoms. A Study of Their Radical Cations

✍ Rovira, Concepcio; Veciana, Jaume; Santalo, Nuria; Tarres, Judit; Cirujeda, Joan 📂 Article 📅 1994 🏛 American Chemical Society 🌐 English ⚖ 844 KB

Tetrathiafulvalene- and dithiafulvene-su

Tetrathiafulvalene- and dithiafulvene-substituted mesitylenes, new .pi.-donor molecules with 3-fold symmetry and the formation of an unprecedented new class of electroactive polymers

✍ Fourmigue, Marc; Johannsen, Ib; Boubekeur, Kamal; Nelson, Catherine; Batail, Pat 📂 Article 📅 1993 🏛 American Chemical Society 🌐 English ⚖ 946 KB