Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3ob40982a
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dc.titleBisacenaphthopyrazinoquinoxaline derivatives: Synthesis, physical properties and applications as semiconductors for n-channel field effect transistors
dc.contributor.authorTong, C.
dc.contributor.authorChang, J.
dc.contributor.authorTan, J.M.
dc.contributor.authorDai, G.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorChan, H.S.O.
dc.contributor.authorChi, C.
dc.date.accessioned2014-10-16T08:21:34Z
dc.date.available2014-10-16T08:21:34Z
dc.date.issued2013-09-14
dc.identifier.citationTong, C., Chang, J., Tan, J.M., Dai, G., Huang, K.-W., Chan, H.S.O., Chi, C. (2013-09-14). Bisacenaphthopyrazinoquinoxaline derivatives: Synthesis, physical properties and applications as semiconductors for n-channel field effect transistors. Organic and Biomolecular Chemistry 11 (34) : 5683-5691. ScholarBank@NUS Repository. https://doi.org/10.1039/c3ob40982a
dc.identifier.issn14770520
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93203
dc.description.abstractSeveral bisacenaphthopyrazinoquinoxaline (BAPQ) based derivatives 1-3 were synthesized by condensation between the acenaphthenequinones and 1,2,4,5-tetraaminobenzene tetrahydrochloride. Their optical, electrochemical and self-assembling properties are tuned by different substituents. Among them, compound 3 possesses a homogeneously distributed low-lying LUMO due to the peripheral substitution with four cyano groups. The corresponding n-channel field effect transistors showed a field effect electron mobility of 5 × 10-3 cm2 V-1 s-1. © 2013 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3ob40982a
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c3ob40982a
dc.description.sourcetitleOrganic and Biomolecular Chemistry
dc.description.volume11
dc.description.issue34
dc.description.page5683-5691
dc.description.codenOBCRA
dc.identifier.isiut000323800900015
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