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filingDate 1988-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b09105ad22ce9709aa0ba2d172dac61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8bc0aef94f4ad83cfd4b1f36f7eabc5b
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publicationDate 1988-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0293749-A1
titleOfInvention N,N'-Biscyano-p-benzoquinonebisimines, charge-transfer complexes containing them and radical-ion salts of the biscyano-benzoquinonebisimines
abstract Biscyanimine of the general formula in the R¹ for 1- or 2-propyl, for C₅- to C₂₀-alkyl, C₃- to C₂₀-alkenyl or iodine and R², R³ and R⁴ independently represent hydrogen, chlorine, bromine, iodine, fluorine, phenyl, C₁- to C₂₀-alkyl, C₃- to C₂₀-alkenyl or C₁- to C₈-alkoxy.n n n The biscyanimines (I) give fulvalene compounds of the formula the ratio of (I): (II) = 1: 1, 2: 1, 3: 2, 1: 2 or 2: 3 mol is charge transfer complexes which are electrically conductive.n n n The biscyanimines (I) also give electrically conductive radical ion salts of the formula in the R¹, R² and R⁴ have the meaning given above and M m⊕ for an m-valent alkali metal, alkaline earth metal, transition metal, ammonium or phosphonium ion, k for 1 to 3, l for 1 to 3, m for 1 or 2, n for 1 to 3 and z stands for 0 to 2, where k, l, n and z can also be fractional numbers and the sum (l + z) = n · m.n n n The charge transfer complexes which can be prepared from (I) and the radical ion salts (III) are suitable, for example for electrical semiconductors and photoconductors, as electrode and storage material in electrical batteries, for fuel cells and for the antistatic finishing of plastics.
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priorityDate 1987-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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