TY - JOUR
T1 - Benzo[4,5]cyclohepta[1,2-b]fluorene: an isomeric motif for pentacene containing linearly fused five-, six- and seven-membered rings
AU - Yang, Xuejin
AU - Shi, Xueliang
AU - Aratani, Naoki
AU - Goncalves, Theo
AU - Huang, Kuo-Wei
AU - Yamada, Hiroko
AU - Chi, Chunyan
AU - Miao, Qian
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We are grateful to Prof. Michael M. Haley (University of
Oregon) and Prof. Yoshito Tobe (Osaka University) for their
kind support and helpful discussion. X. Yang and Q. Miao thank
financial support from the Research Grants Council of Hong
Kong (project number: GRF402412, CRF C4030-14G). X. Shi and
C. Chi thank financial support from MOE Tier 1 grant (R-143-
000-623-112), Tier 2 grant (MOE2014-T2-1-080) and Tier 3
programme (MOE2014-T3-1-004). N. Aratani and H. Yamada
thank support from the Grants-in-Aid for Scientific Research from JSPS (Nos. 16H02286, 26105004 and 26288038) and
CREST, JST. T. P. Gonçalves and K.-W. Huang acknowledge the
financial support from KAUST.
PY - 2016
Y1 - 2016
N2 - Benzo[4,5]cyclohepta[1,2-b]fluorene (5a), a new π-conjugated polycyclic hydrocarbon containing linearly fused six-, five-, six-, seven- and six-membered rings (C6-C5-C6-C7-C6), was designed and its stable derivatives 5b and 5c were synthesized. With 22 π electrons, 5a is an isomer of pentacene with quinoidal, dipolar ionic and diradical resonance forms. Molecules 5b and 5c were experimentally investigated with cyclic voltammetry, electronic absorption spectroscopy and X-ray crystallographic analysis, and theoretically studied by calculating the NICS value, diradical character and dipole moment. A comparison of 5a–c with pentacene and other pentacene analogues containing linearly fused five- or seven- membered rings was also conducted and discussed. It was found that 5b behaved as a p-type organic semiconductor in solution-processed thin film transistors with field effect mobility of up to 0.025 cm2/Vs.
AB - Benzo[4,5]cyclohepta[1,2-b]fluorene (5a), a new π-conjugated polycyclic hydrocarbon containing linearly fused six-, five-, six-, seven- and six-membered rings (C6-C5-C6-C7-C6), was designed and its stable derivatives 5b and 5c were synthesized. With 22 π electrons, 5a is an isomer of pentacene with quinoidal, dipolar ionic and diradical resonance forms. Molecules 5b and 5c were experimentally investigated with cyclic voltammetry, electronic absorption spectroscopy and X-ray crystallographic analysis, and theoretically studied by calculating the NICS value, diradical character and dipole moment. A comparison of 5a–c with pentacene and other pentacene analogues containing linearly fused five- or seven- membered rings was also conducted and discussed. It was found that 5b behaved as a p-type organic semiconductor in solution-processed thin film transistors with field effect mobility of up to 0.025 cm2/Vs.
UR - http://hdl.handle.net/10754/612971
UR - http://pubs.rsc.org/en/Content/ArticleLanding/2016/SC/C6SC01795A
UR - http://www.scopus.com/inward/record.url?scp=84983319985&partnerID=8YFLogxK
U2 - 10.1039/C6SC01795A
DO - 10.1039/C6SC01795A
M3 - Article
C2 - 30034757
SN - 2041-6520
VL - 7
SP - 6176
EP - 6181
JO - Chem. Sci.
JF - Chem. Sci.
IS - 9
ER -