ORGANIC MOLECULES FOR OPTOELECTRONIC DEVICES

The invention relates to an organic molecule for optoelectronic devices. According to the invention, the organic molecule has: -a chemical moiety with a structure of formula I: and-one or two second chemical moieties with a structure of formula II: wherein RI, RII, RIII, RIV, RV, RVI, RVII, RVIII, R...

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description The invention relates to an organic molecule for optoelectronic devices. According to the invention, the organic molecule has: -a chemical moiety with a structure of formula I: and-one or two second chemical moieties with a structure of formula II: wherein RI, RII, RIII, RIV, RV, RVI, RVII, RVIII, RIX, and RX are at each occurrence independently selected from the group consisting of the binding site of a single bond linking the first chemical moiety to the second moiety, hydrogen, deuterium, OPh, SPh, CF3, CN, F, Si(C1-C5-alkyl)3, Si(Ph)3, C1-C5-alkyl, C1-C5-alkoxy, C1-C5-thioalkoxy, C2-C5-alkenyl, C2-C5-alkynyl, C6-C18-aryl, C3-C17-heteroaryl, N(C6-C18-aryl)2, N(C3-C17-heteroaryl)2; N(C3-C17-heteroaryl)(C6-C18-aryl); the dashed lines "Formula III" in formula II represent the binding sites of the first chemical moiety to the second chemical moiety; Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C═CR3R4, C═O, C═NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; Ar1 is C6-C60-aryl, which is optionally substituted with one or more substituents R6; wherein either RV and RVI, or RVI and RVII represent the binding sites of a single bond linking the first chemical moiety to the second chemical moiety to form a ring.
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According to the invention, the organic molecule has: -a chemical moiety with a structure of formula I: and-one or two second chemical moieties with a structure of formula II: wherein RI, RII, RIII, RIV, RV, RVI, RVII, RVIII, RIX, and RX are at each occurrence independently selected from the group consisting of the binding site of a single bond linking the first chemical moiety to the second moiety, hydrogen, deuterium, OPh, SPh, CF3, CN, F, Si(C1-C5-alkyl)3, Si(Ph)3, C1-C5-alkyl, C1-C5-alkoxy, C1-C5-thioalkoxy, C2-C5-alkenyl, C2-C5-alkynyl, C6-C18-aryl, C3-C17-heteroaryl, N(C6-C18-aryl)2, N(C3-C17-heteroaryl)2; N(C3-C17-heteroaryl)(C6-C18-aryl); the dashed lines "Formula III" in formula II represent the binding sites of the first chemical moiety to the second chemical moiety; Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C═CR3R4, C═O, C═NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; Ar1 is C6-C60-aryl, which is optionally substituted with one or more substituents R6; wherein either RV and RVI, or RVI and RVII represent the binding sites of a single bond linking the first chemical moiety to the second chemical moiety to form a ring.</description><language>eng ; fre ; ger</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; ADHESIVES ; CHEMISTRY ; DYES ; MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; ORGANIC CHEMISTRY ; PAINTS ; POLISHES</subject><creationdate>2023</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20230628&amp;DB=EPODOC&amp;CC=EP&amp;NR=4200380A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20230628&amp;DB=EPODOC&amp;CC=EP&amp;NR=4200380A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>DANZ, Michael</creatorcontrib><title>ORGANIC MOLECULES FOR OPTOELECTRONIC DEVICES</title><description>The invention relates to an organic molecule for optoelectronic devices. According to the invention, the organic molecule has: -a chemical moiety with a structure of formula I: and-one or two second chemical moieties with a structure of formula II: wherein RI, RII, RIII, RIV, RV, RVI, RVII, RVIII, RIX, and RX are at each occurrence independently selected from the group consisting of the binding site of a single bond linking the first chemical moiety to the second moiety, hydrogen, deuterium, OPh, SPh, CF3, CN, F, Si(C1-C5-alkyl)3, Si(Ph)3, C1-C5-alkyl, C1-C5-alkoxy, C1-C5-thioalkoxy, C2-C5-alkenyl, C2-C5-alkynyl, C6-C18-aryl, C3-C17-heteroaryl, N(C6-C18-aryl)2, N(C3-C17-heteroaryl)2; N(C3-C17-heteroaryl)(C6-C18-aryl); the dashed lines "Formula III" in formula II represent the binding sites of the first chemical moiety to the second chemical moiety; Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C═CR3R4, C═O, C═NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; Ar1 is C6-C60-aryl, which is optionally substituted with one or more substituents R6; wherein either RV and RVI, or RVI and RVII represent the binding sites of a single bond linking the first chemical moiety to the second chemical moiety to form a ring.</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>ADHESIVES</subject><subject>CHEMISTRY</subject><subject>DYES</subject><subject>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</subject><subject>NATURAL RESINS</subject><subject>ORGANIC CHEMISTRY</subject><subject>PAINTS</subject><subject>POLISHES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2023</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNDxD3J39PN0VvD193F1DvVxDVZw8w9S8A8I8XcFCoQE-YMkXVzDPJ1dg3kYWNMSc4pTeaE0N4OCm2uIs4duakF-fGpxQWJyal5qSbxrgImRgYGxhYGjoTERSgBgDiTd</recordid><startdate>20230628</startdate><enddate>20230628</enddate><creator>DANZ, Michael</creator><scope>EVB</scope></search><sort><creationdate>20230628</creationdate><title>ORGANIC MOLECULES FOR OPTOELECTRONIC DEVICES</title><author>DANZ, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP4200380A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>2023</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>ADHESIVES</topic><topic>CHEMISTRY</topic><topic>DYES</topic><topic>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</topic><topic>NATURAL RESINS</topic><topic>ORGANIC CHEMISTRY</topic><topic>PAINTS</topic><topic>POLISHES</topic><toplevel>online_resources</toplevel><creatorcontrib>DANZ, Michael</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>DANZ, Michael</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>ORGANIC MOLECULES FOR OPTOELECTRONIC DEVICES</title><date>2023-06-28</date><risdate>2023</risdate><abstract>The invention relates to an organic molecule for optoelectronic devices. According to the invention, the organic molecule has: -a chemical moiety with a structure of formula I: and-one or two second chemical moieties with a structure of formula II: wherein RI, RII, RIII, RIV, RV, RVI, RVII, RVIII, RIX, and RX are at each occurrence independently selected from the group consisting of the binding site of a single bond linking the first chemical moiety to the second moiety, hydrogen, deuterium, OPh, SPh, CF3, CN, F, Si(C1-C5-alkyl)3, Si(Ph)3, C1-C5-alkyl, C1-C5-alkoxy, C1-C5-thioalkoxy, C2-C5-alkenyl, C2-C5-alkynyl, C6-C18-aryl, C3-C17-heteroaryl, N(C6-C18-aryl)2, N(C3-C17-heteroaryl)2; N(C3-C17-heteroaryl)(C6-C18-aryl); the dashed lines "Formula III" in formula II represent the binding sites of the first chemical moiety to the second chemical moiety; Z is at each occurrence independently selected from the group consisting of a direct bond, CR3R4, C═CR3R4, C═O, C═NR3, NR3, O, SiR3R4, S, S(O) and S(O)2; Ar1 is C6-C60-aryl, which is optionally substituted with one or more substituents R6; wherein either RV and RVI, or RVI and RVII represent the binding sites of a single bond linking the first chemical moiety to the second chemical moiety to form a ring.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
ADHESIVES
CHEMISTRY
DYES
MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE
METALLURGY
MISCELLANEOUS APPLICATIONS OF MATERIALS
MISCELLANEOUS COMPOSITIONS
NATURAL RESINS
ORGANIC CHEMISTRY
PAINTS
POLISHES
title ORGANIC MOLECULES FOR OPTOELECTRONIC DEVICES
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