{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1361699994359965568.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/adma.201001402"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fadma.201001402"}},{"identifier":{"@type":"URI","@value":"https://advanced.onlinelibrary.wiley.com/doi/pdf/10.1002/adma.201001402"}}],"dc:title":[{"@value":"Rylene and Related Diimides for Organic Electronics"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>Organic electron‐transporting materials are essential for the fabrication of organic p‐n junctions, photovoltaic cells, n‐channel field‐effect transistors, and complementary logic circuits. Rylene diimides are a robust, versatile class of polycyclic aromatic electron‐transport materials with excellent thermal and oxidative stability, high electron affinities, and, in many cases, high electron mobilities; they are, therefore, promising candidates for a variety of organic electronics applications. In this review, recent developments in the area of high‐electron‐mobility diimides based on rylenes and related aromatic cores, particularly perylene‐ and naphthalene‐diimide‐based small molecules and polymers, for application in high‐performance organic field‐effect transistors and photovoltaic cells are summarized and analyzed.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381699994359965568","@type":"Researcher","foaf:name":[{"@value":"Xiaowei Zhan"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994359965569","@type":"Researcher","foaf:name":[{"@value":"Antonio Facchetti"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994359965574","@type":"Researcher","foaf:name":[{"@value":"Stephen Barlow"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994359965573","@type":"Researcher","foaf:name":[{"@value":"Tobin J. Marks"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994359965570","@type":"Researcher","foaf:name":[{"@value":"Mark A. Ratner"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994359965572","@type":"Researcher","foaf:name":[{"@value":"Michael R. Wasielewski"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994359965571","@type":"Researcher","foaf:name":[{"@value":"Seth R. Marder"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"09359648"},{"@type":"EISSN","@value":"15214095"}],"prism:publicationName":[{"@value":"Advanced Materials"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2010-12-10","prism:volume":"23","prism:number":"2","prism:startingPage":"268","prism:endingPage":"284"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fadma.201001402"},{"@id":"https://advanced.onlinelibrary.wiley.com/doi/pdf/10.1002/adma.201001402"}],"createdAt":"2010-12-10","modifiedAt":"2025-10-06","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050008613567333760","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Dinaphthothiepine Bisimide and Its Sulfoxide: Soluble Precursors for Perylene 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