Extended analogues of tetrathiafulvalene (TTF): 1,2-bis, 1,4-bis and 1,2,4,5-tetrakis(1,4-dithiafulven-6-yl) benzenes; Synthesis and π-donor abilities

التفاصيل البيبلوغرافية
العنوان: Extended analogues of tetrathiafulvalene (TTF): 1,2-bis, 1,4-bis and 1,2,4,5-tetrakis(1,4-dithiafulven-6-yl) benzenes; Synthesis and π-donor abilities
المؤلفون: N. Soyer, Alain Gorgues, A. Belyasmine, M. Jubault, Marc Sallé
المصدر: Tetrahedron Letters. 32:2897-2900
بيانات النشر: Elsevier BV, 1991.
سنة النشر: 1991
مصطلحات موضوعية: chemistry.chemical_compound, chemistry, Stereochemistry, Organic Chemistry, Drug Discovery, Wittig reaction, Moiety, Cyclic voltammetry, Benzene, Biochemistry, Medicinal chemistry, Tetrathiafulvalene
الوصف: The title compounds are prepared by Wittig or Wittig-Horner reactions between the corresponding benzenes di- and tetracarbaldehydes and the P-reagents W or P bearing the 1,3-dithiol-2-ylidene moiety; among them, the tetrakis(dithiafulvenyl)benzene 3c is shown by cyclic voltammetry to possess the best π-donor character and, also, is chemically or electrochemically oxidized.
تدمد: 0040-4039
DOI: 10.1016/0040-4039(91)80642-j
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::76c8835ec7b5a7026414990535d7d7ed
https://doi.org/10.1016/0040-4039(91)80642-j
Rights: CLOSED
رقم الانضمام: edsair.doi...........76c8835ec7b5a7026414990535d7d7ed
قاعدة البيانات: OpenAIRE
الوصف
تدمد:00404039
DOI:10.1016/0040-4039(91)80642-j