TCNQ-embedded heptacene and nonacene: Synthesis, characterization and physical properties
KAUST DepartmentChemical Science Program
Homogeneous Catalysis Laboratory (HCL)
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/562527
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AbstractIncorporation of 7,7,8,8-tetracyanoquinodimethane (TCNQ) moieties into the acene backbone has been successfully achieved and two heptacene-TCNQ derivatives and one nonacene-TCNQ derivative have been synthesized and well characterized. Two TCNQ moieties have been embedded into heptacene and nonacene backbones for the first time. All the three compounds have good stability and solubility due to the presence of TCNQ moieties. Single crystal analysis revealed a bent butterfly-like conformation of these molecules. Their charge transport properties have been characterized using organic field effect transistors (OFETs). © 2013 The Royal Society of Chemistry.
SponsorsThis work was financially supported by Singapore MOE AcRF grant R-143-000-510-112 (C. C.), NUS Start Up grant R-143-000-486-133 (C. C.) and KAUST (K.-W. H.). We thank Mdm. Tan Geok Kheng for the crystallographic analysis.
PublisherRoyal Society of Chemistry (RSC)
RelationsIs Supplemented By:
Ye, Q., Chang, J., Huang, K.-W., Dai, G., & Chi, C. (2013). CCDC 934854: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc10cslr. DOI: 10.5517/cc10cslr HANDLE: 10754/624214
Ye, Q., Chang, J., Huang, K.-W., Dai, G., & Chi, C. (2013). CCDC 934853: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc10cskq. DOI: 10.5517/cc10cskq HANDLE: 10754/624213