{"@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/1361699994700849408.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/adfm.200304363"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fadfm.200304363"}},{"identifier":{"@type":"URI","@value":"https://advanced.onlinelibrary.wiley.com/doi/pdf/10.1002/adfm.200304363"}}],"dc:title":[{"@value":"Star‐Shaped Oligothiophenes for Solution‐Processible Organic Field‐Effect Transistors"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>We have designed and successfully synthesized star‐shaped oligothiophenes, which could be used as semiconducting materials for solution‐processible organic field‐effect transistors (FETs). By systematically changing the chemical structure of the star‐shaped oligothiophenes we obtained the structural requirements needed for making working FETs from them. UV‐vis fluorescence measurements showed that a molecule of the star‐shaped compounds under consideration is not a fully conjugated molecule, but it has three independently conjugated oligothienyl‐phenylene blocks. A possible scheme of molecular packing of the star‐shaped oligothiophenes in a lamellar structure was proposed and confirmed by atomic force microscopy (AFM) and X‐ray diffraction (XRD) measurements. Although the star‐shaped semiconductors show a somewhat lower mobility than their linear analogs, they possess better solubility and film‐forming properties, leading to improved spin‐coating processing. The best FETs were made by spin‐coating 1,3,5‐tris(5″‐decyl‐2,2′:5′,2″‐terthien‐5‐yl)benzene from a chloroform solution, which resulted in a mobility of 2 × 10<jats:sup>–4</jats:sup> cm<jats:sup>2</jats:sup> V <jats:sup>–1</jats:sup>s<jats:sup>–1</jats:sup>, a 10<jats:sup>2</jats:sup> on/off ratio at gate voltages of 0 V and –20 V, and a threshold voltage close to 0 V.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381699994700849413","@type":"Researcher","foaf:name":[{"@value":"S.A. Ponomarenko"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994700849409","@type":"Researcher","foaf:name":[{"@value":"S. Kirchmeyer"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994700849410","@type":"Researcher","foaf:name":[{"@value":"A. Elschner"}]},{"@id":"https://cir.nii.ac.jp/crid/1380861402952045056","@type":"Researcher","foaf:name":[{"@value":"B.‐H. Huisman"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994700849408","@type":"Researcher","foaf:name":[{"@value":"A. Karbach"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994700849412","@type":"Researcher","foaf:name":[{"@value":"D. Drechsler"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"1616301X"},{"@type":"EISSN","@value":"16163028"}],"prism:publicationName":[{"@value":"Advanced Functional Materials"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2003-08-05","prism:volume":"13","prism:number":"8","prism:startingPage":"591","prism:endingPage":"596"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fadfm.200304363"},{"@id":"https://advanced.onlinelibrary.wiley.com/doi/pdf/10.1002/adfm.200304363"}],"createdAt":"2003-08-21","modifiedAt":"2025-10-02","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002214438438272","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis, Electronic, and Morphological Properties of Tetrahedral Oligothiophenes with <i>n</i>‐Hexyl Terminal Groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704966392960","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Structure‐Dependent Electronic Nature of Star‐Shaped Oligothiophenes, Probed by Ensemble and Single‐Molecule Spectroscopy"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644041081728","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Self-assembly and Nanostructure Formation of Multi-functional Organic π-Donors"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848655193809792","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis and characterization of polythiophene derivatives with nitrogen heterocycles on the side chain"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/adfm.200304363"},{"@type":"CROSSREF","@value":"10.1002/asia.201100639_references_DOI_HobKNyCUQdkUQkjfYq2OvfobdCg"},{"@type":"CROSSREF","@value":"10.1002/chem.201300313_references_DOI_HobKNyCUQdkUQkjfYq2OvfobdCg"},{"@type":"CROSSREF","@value":"10.1246/cl.2007.1402_references_DOI_HobKNyCUQdkUQkjfYq2OvfobdCg"},{"@type":"CROSSREF","@value":"10.1002/pola.27228_references_DOI_HobKNyCUQdkUQkjfYq2OvfobdCg"}]}