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https://hdl.handle.net/10356/150312
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DC Field | Value | Language |
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dc.contributor.author | Barát, Viktor | en_US |
dc.contributor.author | Budanović, Maja | en_US |
dc.contributor.author | Halilovic, Dzeneta | en_US |
dc.contributor.author | Huh, June | en_US |
dc.contributor.author | Webster, Richard David | en_US |
dc.contributor.author | Mahadevegowda, Surendra Hittanahalli | en_US |
dc.contributor.author | Stuparu, Mihaiela Corina | en_US |
dc.date.accessioned | 2021-06-11T02:09:39Z | - |
dc.date.available | 2021-06-11T02:09:39Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Barát, V., Budanović, M., Halilovic, D., Huh, J., Webster, R. D., Mahadevegowda, S. H. & Stuparu, M. C. (2019). A general approach to non-fullerene electron acceptors based on the corannulene motif. Chemical Communications, 55(21), 3113-3116. https://dx.doi.org/10.1039/C9CC00327D | en_US |
dc.identifier.issn | 1359-7345 | en_US |
dc.identifier.uri | https://hdl.handle.net/10356/150312 | - |
dc.description.abstract | Here, we show that oxidation of exo-cyclic sulfur atoms enhances the molecular reduction potential of non-planar polycyclic aromatic hydrocarbons and allows for a systematic bridging of the electron affinity gap between corannulene, a fragment of fullerene C₆₀, and the prevalent fullerene-based electron acceptor phenyl-C₆₁-butyric acid methyl ester (PCBM). | en_US |
dc.description.sponsorship | Agency for Science, Technology and Research (A*STAR) | en_US |
dc.description.sponsorship | Ministry of Education (MOE) | en_US |
dc.description.sponsorship | Nanyang Technological University | en_US |
dc.language.iso | en | en_US |
dc.relation | M4011792 | en_US |
dc.relation | M4012047 | en_US |
dc.relation | A1883c0006 | en_US |
dc.relation | M4081566 | en_US |
dc.relation.ispartof | Chemical Communications | en_US |
dc.rights | © 2019 The Royal Society of Chemistry. All rights reserved. | en_US |
dc.subject | Science::Chemistry | en_US |
dc.title | A general approach to non-fullerene electron acceptors based on the corannulene motif | en_US |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en_US |
dc.contributor.school | School of Materials Science and Engineering | en_US |
dc.identifier.doi | 10.1039/C9CC00327D | - |
dc.identifier.issue | 21 | en_US |
dc.identifier.volume | 55 | en_US |
dc.identifier.spage | 3113 | en_US |
dc.identifier.epage | 3116 | en_US |
dc.subject.keywords | Corannulene | en_US |
dc.subject.keywords | Fullerene | en_US |
dc.description.acknowledgement | Support from the MoE under the AcRF Tier 1 (M4011792) (M4012047); A*STAR AME IRG A1883c0006; and NTU (M4081566) is gratefully acknowledged. J. H. thanks Creative Materials Discovery Program through the National Research Foundation of Korea (NRF) funded by Ministry of Science and ICT (2018M3D1A1058536). | en_US |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | SPMS Journal Articles |
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