journal article·2003-01

Oligothiophene as photonic/electronic property modulator

O.-K Kim, K.-S Lee, Z Huang, W.B Heuer, C.S Paik-Sung

Optical Materials· Volume 21· Issue 1-3
Publisher page

Abstract

Several different series of conjugated oligomers bearing various π-centers such as dithienothiophene (DTT), fluorene and terthiophene moieties, attaching electron donor and/or electron acceptor units through conjugation were synthesized and assessed for their nonlinear optical, two-photon absorption and redox properties. Discussion is made on the property modulation role of the π-centers, particularly by DTT oligothiophene, which displays a unique and efficient electronic mediation.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nonlinear Optical Materials Studies · Photochromic and Fluorescence Chemistry · Nonlinear Optical Materials Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (29)

Show source-provided references
1. Polythiophene and its derivatives
2. Oligothiophenes in electronic materials
3. Garnier · Synth. Met. · 1996 · 81 · 16310.1016/S0379-6779(96)03761-7 ↗
4. Li · J. Am. Chem. Soc. · 1998 · 120 · 220610.1021/ja9735968 ↗
5. Geiger · Adv. Mater. · 1993 · 5 · 92210.1002/adma.19930051210 ↗
6. Gill · Adv. Mater. · 1994 · 6 · 13210.1002/adma.19940060206 ↗
7. Moreira · J. Chem. Soc. Chem. Commun. · 1992 · 45010.1039/C39920000450 ↗
8. Takahashi · J. Chem. Soc. Chem. Commun. · 1992 · 62010.1039/c39920000620 ↗
9. Hock · J. Chem. Soc. Dalton · 1996 · 425710.1039/dt9960004257 ↗
10. Gruener · J. Chem. Soc. Chem. Commun. · 1999 · 109710.1039/a902249j ↗
11. Kim · J. Mater. Chem. · 1999 · 9 · 222710.1039/a902297j ↗
12. Jen · Adv. Mater. · 1997 · 9 · 13210.1002/adma.19970090207 ↗
13. Raimundo · J. Chem. Soc. Chem. Commun. · 2000 · 159710.1039/b001700k ↗
14. Kim · Chem. Mater. · 2000 · 12 · 28410.1021/cm990662r ↗
15. Ventelon · Angew. Chem. Int. Ed. · 2001 · 40 · 209810.1002/1521-3773(20010601)40:11<2098::AID-ANIE2098>3.0.CO;2-0 ↗
16. Kim · Chem. Phys. Lett. · 1996 · 255 · 14710.1016/0009-2614(96)00358-2 ↗
17. Bourhill · J. Am. Chem. Soc. · 1994 · 116 · 261910.1021/ja00085a052 ↗
18. Blanchard-Desce · Chem. Eur. J. · 1997 · 3 · 109110.1002/chem.19970030717 ↗
19. Jen · J. Chem. Soc. Chem. Commun. · 1993 · 9010.1039/c39930000090 ↗
20. Albota · Science · 1998 · 281 · 165310.1126/science.281.5383.1653 ↗
21. Reinhardt · Chem. Mater. · 1998 · 10 · 186310.1021/cm980036e ↗
22. Rumi · J. Am. Chem. Soc. · 2000 · 122 · 950010.1021/ja994497s ↗
23. He · Opt. Soc. Am. B · 1997 · 14 · 107910.1364/JOSAB.14.001079 ↗
24. Ehrlich · J. Opt. Lett. · 1997 · 22 · 184310.1364/OL.22.001843 ↗
25. Swiatkiewicz · Opt. Commun. · 1998 · 157 · 13510.1016/S0030-4018(98)00474-X ↗
26. K.-S. Lee, O.-K. Kim, et al. unpublished results
27. Kim · Synth. Metals · 2001 · 121 · 160710.1016/S0379-6779(00)00662-7 ↗
28. O.-K. Kim, H.Y. Woo, W.B. Heuer, K.-S. Lee, unpublished results
29. O.-K. Kim, Z. Huang, et al. unpublished results