Polycyclic aromatic compound

US9741950B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9741950-B2
Application numberUS-201514832414-A
CountryUS
Kind codeB2
Filing dateAug 21, 2015
Priority dateMar 10, 2011
Publication dateAug 22, 2017
Grant dateAug 22, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention provides a polycyclic aromatic compound or a salt thereof having a partial structure represented by the following general formula (I): wherein X, ring A, ring B, ring C, and ring D are as defined in the specification.

First claim

Opening claim text (preview).

The invention claimed is: 1. A polycyclic aromatic compound or a salt thereof represented by the following formula (I): wherein X represents B, P, P═O, P═S, P═Se, As, As═O, As═S, As═Se, Sb, Sb═O, Sb═S, Sb═Se, an optionally substituted metal in groups 3 to 11 in the periodic table, or an optionally substituted metal or metalloid in group 13 or 14 of the periodic table; and ring A, ring B, ring C, and ring D are the same or different, and each represents an optionally substituted phenyl ring, an optionally substituted phenyl ring fused to an aryl or heteroaryl ring, an optionally substituted heteroaromatic ring, or an optionally substituted heteroaromatic ring fused to an aryl or heteroaryl ring, wherein at least one of ring A, ring B, ring C, and ring D is an optionally substituted heteroaromatic ring, or an optionally substituted heteroaromatic ring fused to an aryl or heteroaryl ring, wherein the heteroaromatic ring of ring A, ring B, ring C, and ring D is selected from the group consisting of thiophene, pyrrole and pyridine, and wherein the compound represented by formula (I) is not a heterofullerene. 2. The polycyclic aromatic compound or salt thereof according to claim 1 , represented by the following formula (II): wherein Y a s are the same or different, and each represents C— or N; or two adjacent Y a s on the same ring, together with a bond therebetween, form N—, or S; provided that all Y a s do not represent C— at the same time; and X represents B, P, P═O, P═S, P═Se, As, As═O, As═S, As═Se, Sb, Sb═O, Sb═S, Sb═Se, an optionally substituted metal in groups 3 to 11 in the periodic table, or an optionally substituted metal or metalloid in group 13 or 14 of the periodic table. 3. The polycyclic aromatic compound or salt thereof according to claim 1 , represented by any one of the following formulae (II-2) to (II-54): wherein X represents B, P, P═O, P═S, P═Se, As, As═O, As═S, As═Se, Sb, Sb═O, Sb═S, Sb═Se, an optionally substituted metal in groups 3 to 11 in the periodic table, or an optionally substituted metal or metalloid in group 13 or 14 of the periodic table; and Z represents S, or N—. 4. The polycyclic aromatic compound or salt thereof according to claim 1 represented by the following formula (II′): wherein Ys are the same or different, and each represents CR or N; or two adjacent Ys on the same ring, together with a bond therebetween, form NR, or S; provided that all Ys do not represent C— at the same time; X represents B, P, P═O, P═S, P═Se, As, As═O, As═S, As═Se, Sb, Sb═O, Sb═S, Sb═Se, an optionally substituted metal in groups 3 to 11 in the periodic table, or an optionally substituted metal or metalloid in group 13 or 14 of the periodic table; R represents a hydrogen atom, halogen atom, C 1-20 alkyl group, hydroxy C 1-20 alkyl group, trifluoromethyl group, C 2-12 perfluoroalkyl group, C 3-8 cycloalkyl group, C 2-20 alkenyl group, C 2-20 alkynyl group, mono- or di-aryl-substituted alkenyl group, mono- or di-heteroaryl-substituted alkenyl group, arylethynyl group, heteroarylethynyl group, hydroxy group, C 1-20 alkoxy group, aryloxy group, trifluoromethoxy group, trifluoroethoxy group, C 2-12 perfluoroalkoxy group, C 1-20 alkylcarbonyl group, C 1-20 alkylsulfonyl group, cyano group, nitro group, amino group, monoalkylamino group, monoarylamino group, monoheteroarylamino group, carbazole group, C 1-20 alkoxycarbonylamino group, carbamoyl group, mono- or di-alkylcarbamoyl group, sulfamoyl group, mono- or di-alkylsulfamoyl group, C 1-20 alkylsulfonylamino group, C 1-20 alkylcarbonylamino group, aryl group, heteroaryl group, C 1-20 alkoxycarbonyl group, carboxyl group, 5-tetrazolyl group, sulfo group (—SO 2 OH), fluorosulfonyl group, SR a , N(R a ) 2 , B(R a ) 2 , Si(R a ) 3 , or —C≡C—Si(R a ) 3 , (wherein R a represents an optionally substituted alkyl group, an optionally substituted aryl group, or an optionally substituted heteroaryl group; or two R a s, together with an atom bound thereto, may form a bicyclic group or a tricyclic group optionally having a heteroatom); provided that, the alkyl group, alkenyl group, alkynyl group, and alkoxy group are each optionally substituted with 1 to 3 atoms or groups, selected from the group consisting of halogen atom, hydroxy group, C 1-20 alkoxy group, aryloxy group, amino group, carbazole group, N(R a ) 2 (wherein R a is as defined above), trifluoromethyl group, C 2-12 perfluoroalkyl group, C 3-8 cycloalkyl group, aryl group, and heteroaryl group; and the aryl group, aryl moiety, heteroaryl group, heteroaryl moiety, and carbazole group are each optionally substituted with 1 to 5 atoms or groups, selected from the group consisting of halogen atom, C 1-20 alkyl group, hydroxy C 1-20 alkyl group, trifluoromethyl group, C 2-12 perfluoroalkyl group, C 3-8 cycloalkyl group, C 2-20 alkenyl group, C 2-20 alkynyl group, mono- or di-aryl-substituted alkenyl group, mono- or di-heteroaryl-substituted alkenyl group, arylethynyl group, heteroarylethynyl group, hydroxy group, C 1-20 alkoxy group, aryloxy group, trifluoromethoxy group, trifluoroethoxy group, C 2-12 perfluoroalkoxy group, cyano group, nitro group, amino group, carbazole group, monoalkylamino group, monoarylamino group, monoheteroarylamino group, N(R a ) 2 (wherein R a is as defined above), carbamoyl group, mono- or di-alkylcarbamoyl group, sulfamoyl group, mono- or di-alkylsulfamoyl group, C 1-20 alkylcarbonyl group, C 1-20 alkylsulfonyl group, C 1-20 alkylsulfonylamino group, C 1-20 alkylcarbonylamino group, methylenedioxy group, heteroaryl group, and aryl group, (wherein the aryl group is optionally substituted with 1 to 5 atoms or groups, selected from the group consisting of halogen atom, C 1-20 alkyl group, C 3-8 cycloalkyl group, C 2-20 alkenyl group, C 2-20 alkynyl group, hydroxy group, trifluoromethyl group, C 2-12 perfluoroalkyl group, C 1-20 alkoxy group, aryloxy group, trifluoromethoxy group, trifluoroethoxy group, C 2-12 perfluoroalkoxy group, C 1-20 alkylcarbonyl group, C 1-20 alkylsulfonyl group, methylenedioxy group, cyano group, nitro group, amino group, carbazole group, and N(R a ) 2 (wherein R a is as defined above)); or, two adjacent Rs on the same ring, together with a carbon atom bound thereto, form a five- or six-membered monocyclic aromatic group, bicyclic aromatic group, or tricyclic aromatic group optionally having a heteroatom; or three adjacent Rs on the same ring, together with a carbon atom bound thereto, form a bicyclic aromatic group or a tricyclic group optionally having a heteroatom. 5. The polycyclic aromatic compound or salt thereof according to claim 1 represented by the following

Assignees

Inventors

Classifications

  • containing nitrogen {having a Si-N linkage} · CPC title

  • Organic PV cells · CPC title

  • Germanium compounds · CPC title

  • Compounds with one or more Sn-N linkages · CPC title

  • C07F5/02Primary

    Boron compounds · CPC title

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Frequently asked questions

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What does patent US9741950B2 cover?
The invention provides a polycyclic aromatic compound or a salt thereof having a partial structure represented by the following general formula (I): wherein X, ring A, ring B, ring C, and ring D are as defined in the specification.
Who is the assignee on this patent?
Univ Kyoto, Jnc Corp
What technology area does this patent fall under?
Primary CPC classification C07F5/02. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).