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Synthesis of annulated dioxins as electron-rich donors for cation radical salts
KTH, Superseded Departments, Chemistry.
KTH, Superseded Departments, Chemistry.
KTH, Superseded Departments, Chemistry.
2004 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 60, no 40, 8899-8912 p.Article in journal (Refereed) Published
Abstract [en]

The synthesis of a series of new alkoxylated linearly annulated dioxins is described together with their cyclic voltammetric behavior and some preliminary result on their ability to form cation radical salts. Of these dioxins, seven (8, 12, 19, 21, 27, 33, 34) are the first representatives of entirely new heterocyclic systems. Dioxins 8, 21, 22 and 27 gave good quality cation radical salts upon electrocrystallization.

Place, publisher, year, edition, pages
2004. Vol. 60, no 40, 8899-8912 p.
Keyword [en]
dioxines, dibenzodioxines, cyclovoltammetry
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-40559DOI: 10.1016/j.tet.2004.07.017ISI: 000223935100015Scopus ID: 2-s2.0-4444350440OAI: oai:DiVA.org:kth-40559DiVA: diva2:441569
Note
QC 20110916Available from: 2011-09-16 Created: 2011-09-16 Last updated: 2017-12-08Bibliographically approved

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