@prefix rdf: . @prefix dbr: . @prefix yago: . dbr:Diindenoperylene rdf:type yago:Material114580897 , yago:Substance100019613 , yago:WikicatMolecularFormulas , yago:Conductor114821043 , yago:OrganicCompound114727670 , yago:WikicatOrganicSemiconductors , yago:Message106598915 . @prefix wikidata: . dbr:Diindenoperylene rdf:type wikidata:Q11173 , yago:Abstraction100002137 , yago:Chemical114806838 , yago:Matter100020827 , yago:Part113809207 . @prefix owl: . dbr:Diindenoperylene rdf:type owl:Thing , yago:AromaticHydrocarbon114767996 , yago:Semiconductor114821248 , yago:Relation100031921 . @prefix dbo: . dbr:Diindenoperylene rdf:type dbo:ChemicalSubstance , yago:MolecularFormula106817173 . @prefix umbel-rc: . dbr:Diindenoperylene rdf:type umbel-rc:ChemicalSubstanceType , yago:Compound114818238 , yago:Hydrocarbon114911057 . @prefix ns7: . dbr:Diindenoperylene rdf:type ns7:ChemicalObject , yago:Formula106816935 , yago:Statement106722453 , dbo:ChemicalCompound , yago:PhysicalEntity100001930 , yago:WikicatPolycyclicAromaticHydrocarbons , yago:Communication100033020 . @prefix rdfs: . dbr:Diindenoperylene rdfs:label "\u30B8\u30A4\u30F3\u30C7\u30CE\u30DA\u30EA\u30EC\u30F3"@ja , "\u062F\u064A\u064A\u0646\u062F\u064A\u0646\u0648\u0628\u064A\u0631\u064A\u0644\u064A\u0646"@ar , "Diind\u00E9nop\u00E9ryl\u00E8ne"@fr , "Diindenoperylene"@en , "\u4E8C\u831A\u5E76\u82DD"@zh ; rdfs:comment "\u062F\u064A\u064A\u0646\u062F\u064A\u0646\u0648\u0628\u064A\u0631\u064A\u0644\u064A\u0646 (DIP) \u0647\u0648 \u0647\u064A\u062F\u0631\u0648\u0643\u0631\u0628\u0648\u0646 \u0639\u0637\u0631\u064A \u0645\u062A\u0639\u062F\u062F \u0627\u0644\u062D\u0644\u0642\u0627\u062A \u0644\u0647 \u0627\u0644\u0635\u064A\u063A\u0629 \u0627\u0644\u0643\u064A\u0645\u064A\u0627\u0626\u064A\u0629 C32H16\u061B \u0648\u064A\u0643\u0648\u0646 \u0639\u0644\u0649 \u0634\u0643\u0644 \u0635\u0644\u0628 \u0628\u0631\u062A\u0642\u0627\u0644\u064A \u0627\u0644\u0644\u0648\u0646. \u064A\u0635\u0646\u0641 \u0627\u0644\u0645\u0631\u0643\u0628 \u0628\u0646\u064A\u0648\u064A\u0627\u064B \u0639\u0644\u0649 \u0623\u0646\u0647 \u0645\u0634\u062A\u0642 \u0645\u0646 \u0627\u0644\u0628\u064A\u0631\u064A\u0644\u064A\u0646\u060C \u062D\u064A\u062B \u062A\u0646\u062F\u0645\u062C \u0648\u062D\u062F\u062A\u0627\u0646 \u0645\u0646 \u0627\u0644\u0625\u0646\u062F\u0627\u0646 \u0639\u0644\u0649 \u062C\u0627\u0646\u0628\u064A \u0648\u062D\u062F\u0629 \u0627\u0644\u0628\u064A\u0631\u064A\u0644\u064A\u0646."@ar , "Diindenoperylene (DIP) is an organic semiconductor which receives attention because of its potential application in optoelectronics (solar cells, OLEDs) and electronics (RFID tags). DIP is a planar perylene derivative with two indeno-groups attached to opposite sides of the perylene core. Its chemical formula is C32H16, the full chemical name is diindeno[1,2,3-cd:1',2',3'-lm]perylene. Its chemical synthesis has been described."@en , "\u30B8\u30A4\u30F3\u30C7\u30CE\u30DA\u30EA\u30EC\u30F3\uFF08\u82F1\u8A9E: Diindenoperylene, DIP\uFF09\u3068\u306F\u3001\u591A\u74B0\u82B3\u9999\u65CF\u70AD\u5316\u6C34\u7D20\u306E\u4E00\u7A2E\u3067\u3042\u308B\u3002\u6709\u6A5F\u534A\u5C0E\u4F53\u3068\u3057\u3066\u7528\u3044\u3089\u308C\u308B\u3002\u5316\u5B66\u5F0F\u306FC32H16\u3001IUPAC\u540D\u306Fdiindeno[1,2,3-cd:1',2',3'-lm]perylene\u3002."@ja , "Le diind\u00E9nop\u00E9ryl\u00E8ne, souvent abr\u00E9g\u00E9 en DIP, \u00E9galement appel\u00E9 p\u00E9riflanth\u00E8ne, est un hydrocarbure aromatique polycyclique de formule C32H16 qui fait l'objet de recherches comme semiconducteur organique ayant des applications potentielles en \u00E9lectronique (pastilles RFID) et en opto\u00E9lectronique (cellules photovolta\u00EFques et diodes \u00E9lectroluminescentes organiques). La mol\u00E9cule est plane et d\u00E9rive structurellement du p\u00E9ryl\u00E8ne avec deux groupes ind\u00E9no fusionn\u00E9s de part et d'autre, ses dimensions \u00E9tant d'environ 1,84 \u00D7 0,7 nm. Sa masse molaire vaut 400,47 g\u00B7mol-1, et sa temp\u00E9rature de sublimation d\u00E9passe 330 \u00B0C. Il est apolaire et par cons\u00E9quent seulement faiblement soluble, par exemple dans l'ac\u00E9tone. Sa synth\u00E8se a \u00E9t\u00E9 d\u00E9crite en Allemagne d\u00E8s 1934 et aux \u00C9tats-Unis en 1964."@fr , "\u4E8C\u831A\u5E76\u82DD\uFF08\u82F1\u8A9E\uFF1ADiindenoperylene\uFF0C\u7B80\u79F0\uFF1ADIP\uFF09\u662F\u4E00\u79CD\u591A\u73AF\u82B3\u9999\u70C3\u3002\u4F5C\u4E3A\u4E00\u79CD\u6709\u673A\u534A\u5BFC\u4F53\u88AB\u4F7F\u7528\u3002\u5316\u5B66\u5F0F\u4E3AC32H16\u3001IUPAC\u540D\u4E3Adiindeno[1,2,3-cd:1',2',3'-lm]perylene\u3002"@zh . @prefix foaf: . dbr:Diindenoperylene foaf:depiction , . @prefix dcterms: . @prefix dbc: . dbr:Diindenoperylene dcterms:subject dbc:Organic_semiconductors , dbc:Polycyclic_aromatic_hydrocarbons ; dbo:wikiPageID 13955542 ; dbo:wikiPageRevisionID 1031257514 ; dbo:wikiPageWikiLink dbr:Optoelectronics , dbc:Organic_semiconductors , dbr:Acetone , dbc:Polycyclic_aromatic_hydrocarbons , dbr:Solar_cell , dbr:RFID , dbr:Chemical_synthesis , dbr:Field_effect_transistor , dbr:Electronics , dbr:OLED , dbr:Silicon_dioxide , dbr:Gate_dielectric , dbr:Organic_light_emitting_diode , dbr:Molecular_weight , dbr:Chemical_formula , dbr:Soluble , dbr:Optical_recording , dbr:Transistor , dbr:Perylene , dbr:Organic_semiconductor , dbr:Dye , dbr:Charge_carrier_mobility , dbr:Crystal , , dbr:Indeno ; owl:sameAs , , , , , , . @prefix dbpedia-sh: . dbr:Diindenoperylene owl:sameAs dbpedia-sh:Diindenoperilen , . @prefix dbpedia-sr: . dbr:Diindenoperylene owl:sameAs dbpedia-sr:Diindenoperilen , wikidata:Q3027899 . @prefix yago-res: . dbr:Diindenoperylene owl:sameAs yago-res:Diindenoperylene . @prefix dbp: . @prefix dbt: . dbr:Diindenoperylene dbp:wikiPageUsesTemplate dbt:PAHs , dbt:Stdinchicite , dbt:Chembox_Hazards , dbt:Chembox_Identifiers , dbt:Chembox , dbt:Chembox_Properties , dbt:Chemspidercite , dbt:Cascite , dbt:Fdacite , dbt:Reflist ; dbo:thumbnail ; dbp:imagealt "Ball-and-stick model"@en , "Skeletal formula"@en ; dbp:imagefile "Diindenoperylene-3D-balls.png"@en , "Diindenoperylene.svg"@en ; dbp:imagesize 240 ; dbp:othernames "Periflanthen; Periflanthene"@en ; dbp:pin "Diindeno[1,2,3-cd:1\u2032,2\u2032,3\u2032-lm]perylene"@en ; dbp:verifiedfields "changed"@en ; dbp:verifiedrevid 424894498 ; dbp:watchedfields "changed"@en ; dbo:abstract "Diindenoperylene (DIP) is an organic semiconductor which receives attention because of its potential application in optoelectronics (solar cells, OLEDs) and electronics (RFID tags). DIP is a planar perylene derivative with two indeno-groups attached to opposite sides of the perylene core. Its chemical formula is C32H16, the full chemical name is diindeno[1,2,3-cd:1',2',3'-lm]perylene. Its chemical synthesis has been described."@en , "\u4E8C\u831A\u5E76\u82DD\uFF08\u82F1\u8A9E\uFF1ADiindenoperylene\uFF0C\u7B80\u79F0\uFF1ADIP\uFF09\u662F\u4E00\u79CD\u591A\u73AF\u82B3\u9999\u70C3\u3002\u4F5C\u4E3A\u4E00\u79CD\u6709\u673A\u534A\u5BFC\u4F53\u88AB\u4F7F\u7528\u3002\u5316\u5B66\u5F0F\u4E3AC32H16\u3001IUPAC\u540D\u4E3Adiindeno[1,2,3-cd:1',2',3'-lm]perylene\u3002"@zh , "\u30B8\u30A4\u30F3\u30C7\u30CE\u30DA\u30EA\u30EC\u30F3\uFF08\u82F1\u8A9E: Diindenoperylene, DIP\uFF09\u3068\u306F\u3001\u591A\u74B0\u82B3\u9999\u65CF\u70AD\u5316\u6C34\u7D20\u306E\u4E00\u7A2E\u3067\u3042\u308B\u3002\u6709\u6A5F\u534A\u5C0E\u4F53\u3068\u3057\u3066\u7528\u3044\u3089\u308C\u308B\u3002\u5316\u5B66\u5F0F\u306FC32H16\u3001IUPAC\u540D\u306Fdiindeno[1,2,3-cd:1',2',3'-lm]perylene\u3002."@ja , "Le diind\u00E9nop\u00E9ryl\u00E8ne, souvent abr\u00E9g\u00E9 en DIP, \u00E9galement appel\u00E9 p\u00E9riflanth\u00E8ne, est un hydrocarbure aromatique polycyclique de formule C32H16 qui fait l'objet de recherches comme semiconducteur organique ayant des applications potentielles en \u00E9lectronique (pastilles RFID) et en opto\u00E9lectronique (cellules photovolta\u00EFques et diodes \u00E9lectroluminescentes organiques). La mol\u00E9cule est plane et d\u00E9rive structurellement du p\u00E9ryl\u00E8ne avec deux groupes ind\u00E9no fusionn\u00E9s de part et d'autre, ses dimensions \u00E9tant d'environ 1,84 \u00D7 0,7 nm. Sa masse molaire vaut 400,47 g\u00B7mol-1, et sa temp\u00E9rature de sublimation d\u00E9passe 330 \u00B0C. Il est apolaire et par cons\u00E9quent seulement faiblement soluble, par exemple dans l'ac\u00E9tone. Sa synth\u00E8se a \u00E9t\u00E9 d\u00E9crite en Allemagne d\u00E8s 1934 et aux \u00C9tats-Unis en 1964. Le DIP est un pigment rouge et a \u00E9t\u00E9 utilis\u00E9 comme mat\u00E9riau actif pour l'enregistrement optique. En raison de ses caract\u00E9ristiques d'\u00E9mission lumineuse proches de celles du p\u00E9ryl\u00E8ne, il a \u00E9t\u00E9 utilis\u00E9 pour r\u00E9aliser des diodes \u00E9lectroluminescentes organiques. Des transistors \u00E0 effet de champs organiques en DIP ont \u00E9galement \u00E9t\u00E9 \u00E9tudi\u00E9s ; la mobilit\u00E9 des porteurs de charge obtenue pour ces transistors en couches minces \u00E0 grille en dioxyde de silicium atteignait 0,1 cm2\u00B7V-1\u00B7s-1, faisant du DIP un bon candidat pour investiguer de futures optimisations. La structure de cristaux de DIP a \u00E9t\u00E9 r\u00E9cemment \u00E9tudi\u00E9e par Pflaum et al, qui ont mis en \u00E9vidence deux phases distinctes \u00E0 temp\u00E9rature ambiante et au-dessus de 160 \u00B0C. On a montr\u00E9 que le DIP adopte une structure tr\u00E8s bien ordonn\u00E9e dans les couches minces d\u00E9pos\u00E9es par jet mol\u00E9culaire organique en quasi \u00E9quilibre, c'est-\u00E0-dire ici pour des temp\u00E9ratures de substrat voisines de 130 \u00B0C. La structure des couches minces de DIP a \u00E9t\u00E9 caract\u00E9ris\u00E9e apr\u00E8s \u00E9pitaxie avec des structures diff\u00E9rant de celles observ\u00E9es \u00E0 temp\u00E9rature ambiante sur des \u00E9chantillons massifs. Ces structures en couches minces d\u00E9pendent du substrat sur lequel les couches ont \u00E9t\u00E9 d\u00E9pos\u00E9es ainsi que de la temp\u00E9rature d'\u00E9pitaxie."@fr , "\u062F\u064A\u064A\u0646\u062F\u064A\u0646\u0648\u0628\u064A\u0631\u064A\u0644\u064A\u0646 (DIP) \u0647\u0648 \u0647\u064A\u062F\u0631\u0648\u0643\u0631\u0628\u0648\u0646 \u0639\u0637\u0631\u064A \u0645\u062A\u0639\u062F\u062F \u0627\u0644\u062D\u0644\u0642\u0627\u062A \u0644\u0647 \u0627\u0644\u0635\u064A\u063A\u0629 \u0627\u0644\u0643\u064A\u0645\u064A\u0627\u0626\u064A\u0629 C32H16\u061B \u0648\u064A\u0643\u0648\u0646 \u0639\u0644\u0649 \u0634\u0643\u0644 \u0635\u0644\u0628 \u0628\u0631\u062A\u0642\u0627\u0644\u064A \u0627\u0644\u0644\u0648\u0646. \u064A\u0635\u0646\u0641 \u0627\u0644\u0645\u0631\u0643\u0628 \u0628\u0646\u064A\u0648\u064A\u0627\u064B \u0639\u0644\u0649 \u0623\u0646\u0647 \u0645\u0634\u062A\u0642 \u0645\u0646 \u0627\u0644\u0628\u064A\u0631\u064A\u0644\u064A\u0646\u060C \u062D\u064A\u062B \u062A\u0646\u062F\u0645\u062C \u0648\u062D\u062F\u062A\u0627\u0646 \u0645\u0646 \u0627\u0644\u0625\u0646\u062F\u0627\u0646 \u0639\u0644\u0649 \u062C\u0627\u0646\u0628\u064A \u0648\u062D\u062F\u0629 \u0627\u0644\u0628\u064A\u0631\u064A\u0644\u064A\u0646."@ar . @prefix gold: . dbr:Diindenoperylene gold:hypernym dbr:Semiconductor . @prefix prov: . dbr:Diindenoperylene prov:wasDerivedFrom . @prefix xsd: . dbr:Diindenoperylene dbo:wikiPageLength "6710"^^xsd:nonNegativeInteger ; dbo:alternativeName "Periflanthen; Periflanthene"@en ; dbo:iupacName "Diindeno[1,2,3-cd:1\u2032,2\u2032,3\u2032-lm]perylene"@en . @prefix wikipedia-en: . dbr:Diindenoperylene foaf:isPrimaryTopicOf wikipedia-en:Diindenoperylene .