Please use this identifier to cite or link to this item: https://doi.org/10.1021/acsmaterialslett.2c00223
DC FieldValue
dc.titleDibenzylidene-s-indacenetetraone Linked n-Type Semiconducting Covalent Organic Framework via Aldol Condensation
dc.contributor.authorX. Hou
dc.contributor.authorK. Geng
dc.contributor.authorJ. Li
dc.contributor.authorS. Wu
dc.contributor.authorJ. Wu
dc.date.accessioned2023-05-05T01:34:54Z
dc.date.available2023-05-05T01:34:54Z
dc.date.issued2022-05-17
dc.identifier.citationX. Hou, K. Geng, J. Li, S. Wu, J. Wu (2022-05-17). Dibenzylidene-s-indacenetetraone Linked n-Type Semiconducting Covalent Organic Framework via Aldol Condensation. ACS Mater. Lett. 4 : 1154-1159. ScholarBank@NUS Repository. https://doi.org/10.1021/acsmaterialslett.2c00223
dc.identifier.issn2639-4979
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/239202
dc.description.abstractAcid-mediated aldol condensation between s-indacene-1,3,5,7(2H,6H)-tetraone (INDO4) and aromatic aldehydes was used as a new method for the synthesis of olefin-linked, π-conjugated covalent organic framework. Specifically, a dibenzylidene-sindacenetetraone-based COF (NCOF-1) was obtained in crystalline form. It exhibits eclipsed (AA) stacking in the solid state, with a BET surface area of about 368 m2 /g. The electron-deficient nature of the INDO4 unit endows the COF with n-type semiconducting character, and chemical doping by electron-rich N-DMBI gave the radical anion-based material with a small energy gap of about 1.08 eV and an electrical conductivity of about 7.44 × 10−3 S/cm.
dc.publisherAmerican Chemical Society
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/acsmaterialslett.2c00223
dc.description.sourcetitleACS Mater. Lett.
dc.description.volume4
dc.description.page1154-1159
dc.published.statePublished
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