SUBSTITUTED BISACYLOXYNAPHTHACENE AND PRODUCTION OF TETRATHIOTETRACENE USING THE SAME

Compounds of the formula I (I) in which R1 to R8 independently of one another are H and at least one of R1 and R8 is a substituent belonging to the group -F, -Si(C1-C4alkyl)3 or -COOR10; or each pair of adjacent radicals of R1 to R8 is -CO-O-CO-; or at least one of R1 to R8 is C1-C20alkyl-(X)p-, C2-...

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Bibliographische Detailangaben
Hauptverfasser:	BUORUFUGANGU BUERUNETSUTO, BUARUTAA FUISHIYAA, KAARU DABURIYU MAIERU, MARUKUSU BAUMAN
Format:	Patent
Sprache:	eng
Schlagworte:	ACYCLIC OR CARBOCYCLIC COMPOUNDS ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ADHESIVES APPLYING LIQUIDS OR OTHER FLUENT MATERIALS TO SURFACES, IN GENERAL BASIC ELECTRIC ELEMENTS CABLES CHEMISTRY COMPOSITIONS BASED THEREON CONDUCTORS DYES ELECTRICITY HETEROCYCLIC COMPOUNDS INSULATORS MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS MANUFACTURE OR TREATMENT OF NANOSTRUCTURES MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS NANOTECHNOLOGY NATURAL RESINS ORGANIC CHEMISTRY ORGANIC MACROMOLECULAR COMPOUNDS PAINTS PERFORMING OPERATIONS POLISHES PROCESSES FOR APPLYING LIQUIDS OR OTHER FLUENT MATERIALS TOSURFACES, IN GENERAL SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING ORDIELECTRIC PROPERTIES SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES SPRAYING OR ATOMISING IN GENERAL THEIR PREPARATION OR CHEMICAL WORKING-UP TRANSPORTING
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Beschreibung
Zusammenfassung:	Compounds of the formula I (I) in which R1 to R8 independently of one another are H and at least one of R1 and R8 is a substituent belonging to the group -F, -Si(C1-C4alkyl)3 or -COOR10; or each pair of adjacent radicals of R1 to R8 is -CO-O-CO-; or at least one of R1 to R8 is C1-C20alkyl-(X)p-, C2-C20alkenyl-(X)p-, C2-C20-alkynyl-(X)p-, C3-C8cycloalkyl-(X)p-, (C1-C12alkyl-C3-C8cycloalkyl-(X)p-, C3-C8-cycloalkyl-CH2-(X)p-, C1-C12alkyl-C3-C8cycloalkyl-CH2-(X)p-, C6-C10aryl-X-, C7-C20alkaryl-X-, C7-C12aralkyl-(X)p- or C8-C20-alkaralkyl-(X)p- or -Y- (CmH2m-O)-nR10 each of which is unsubstituted or substituted by -F, -OH, -CN, C1-C12alkoxy, C1-C12acyloxy or -COOR10; R10 is H or C1-C18alkyl, X is -O-, -S-, -SO- or -SO2- and Y is -O- or -S-, and p is 0 or 1, m is a number from 2 to 6 and n is a number from 2 to 20; and R9 is C1-C4acyl which is unsubstituted or substituted by -F. The compounds of the formula I can be reacted directly with sulfur in the presence of catalytic amounts of a sulfonic acid to give 5,6,11,12-tetrathiotetracenes which form electrically conducting charge-transfer complexes with electron donors.