133113-92-5Relevant academic research and scientific papers
Highly Conjugated ?-Electron Donors for Organic Metals: Synthesis and Redox Chemistry of New 1,3-Dithiole and 1,3-Selenathiole Derivatives
Moore, Adrian J.,Bryce, Martin R.
, p. 157 - 168 (2007/10/02)
The bis(1,3-dithiolium) dication salts 8a-c have been synthesised in three steps (31-51percent overall yields) starting from 1,4-bis(bromomethyl)naphthalene, 9,10-bis(chloromethyl)anthracene and 4,4'-bis(chloromethyl)biphenyl, respectively.The bis(halogenomethyl) compounds 5 were converted into the dipiperidiniumbis(dithiocarboxylate) salts 6, which on alkylation with 3-chlorobutan-2-one yielded bis(dithioesters) 7; cyclisation of 7 occurred on treatment with concentrated sulphuric acid to give dication salts 8.Dimethyl 1,3-dithiol-2-ylphosphonate 20, dimethyl 4,5-dimethyl-1,3-dithiol-2-ylphosphonate 21 and dimethyl 1,3-selenathiol-2-ylphosphonate 22 were treated with butyllithium in the presence of a range of carbonyl compounds and quinones, e.g., cyclopentanone, cyclohexanone, benzophenone, acetophenone, benzaldehyde, thioxanthen-9-one, anthraquinone, bianthrone and naphthacene-5,12-quinone to yield Wittig-Horner products, e.g., alkenes 26-34 and the anthracenediylidene derivatives 35, 36, 40-43 and 53.Unsymmetrical derivatives 37-39 were prepared in two steps as follows: anthrone reacted with 2-methylthio-1,3-dithiolium iodides 45 and 46 in pyridine-acetic acid to yield ketones 48 and 49 which were then treated with the Wittig-Horner reagents 23-25.Cyclic voltammetric data for the new tetrathiafulvalene, selenatrithiafulvalene and diselenadithiafulvalene derivatives 35-43 and 53, show that these systems undergo two-electron redox behaviour which is observed as a single wave.Complexes of these donors with electron acceptors, e.g. 7,7,8,8-tetracyano-p-quinodimethane (TCNQ), have been obtained, some of which are organic semiconductors.
