Abstract
Multifunctional chromophores are synthesized based on dithienothiophene, DDT (π-center) linked through conjugation by donor/donor (D/D) or D/acceptor (D/A) pair segments at the molecular end. Novel electronic/photonic properties are assessed by cyclic voltammetry (CV) and two-photon absorption (TPA). CV shows that the D/D system displays two oxidation/one reduction waves, while the D/A system shows two oxidation/two reduction waves. Such unusual redox is reflected in the amphotericity particularly with D/D system and can be accounted for solely by the involvement of DTT. Exceptionally large TPA cross-section values of these chromophores relative to those based on benzenoid π-center seem to be the result of unique electronic modulation effect of DTT.
| Original language | English |
|---|---|
| Pages (from-to) | 795-796 |
| Number of pages | 2 |
| Journal | American Chemical Society, Polymer Preprints, Division of Polymer Chemistry |
| Volume | 41 |
| Issue number | 1 |
| Publication status | Published - 2000 Mar 1 |
| Externally published | Yes |
| Event | The San Francisco Meeting - San Francisco, CA, USA Duration: 2000 Mar 26 → 2000 Mar 31 |
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ASJC Scopus subject areas
- Polymers and Plastics
Cite this
Electronic/photonic property modulations of D-π-D(A) chromophores by DTT as π-center. / Kim, O. K.; Woo, Han Young; Heuer, W. B.; Kim, K. S.; Lee, K. S.
In: American Chemical Society, Polymer Preprints, Division of Polymer Chemistry, Vol. 41, No. 1, 01.03.2000, p. 795-796.Research output: Contribution to journal › Conference article
}
TY - JOUR
T1 - Electronic/photonic property modulations of D-π-D(A) chromophores by DTT as π-center
AU - Kim, O. K.
AU - Woo, Han Young
AU - Heuer, W. B.
AU - Kim, K. S.
AU - Lee, K. S.
PY - 2000/3/1
Y1 - 2000/3/1
N2 - Multifunctional chromophores are synthesized based on dithienothiophene, DDT (π-center) linked through conjugation by donor/donor (D/D) or D/acceptor (D/A) pair segments at the molecular end. Novel electronic/photonic properties are assessed by cyclic voltammetry (CV) and two-photon absorption (TPA). CV shows that the D/D system displays two oxidation/one reduction waves, while the D/A system shows two oxidation/two reduction waves. Such unusual redox is reflected in the amphotericity particularly with D/D system and can be accounted for solely by the involvement of DTT. Exceptionally large TPA cross-section values of these chromophores relative to those based on benzenoid π-center seem to be the result of unique electronic modulation effect of DTT.
AB - Multifunctional chromophores are synthesized based on dithienothiophene, DDT (π-center) linked through conjugation by donor/donor (D/D) or D/acceptor (D/A) pair segments at the molecular end. Novel electronic/photonic properties are assessed by cyclic voltammetry (CV) and two-photon absorption (TPA). CV shows that the D/D system displays two oxidation/one reduction waves, while the D/A system shows two oxidation/two reduction waves. Such unusual redox is reflected in the amphotericity particularly with D/D system and can be accounted for solely by the involvement of DTT. Exceptionally large TPA cross-section values of these chromophores relative to those based on benzenoid π-center seem to be the result of unique electronic modulation effect of DTT.
UR - http://www.scopus.com/inward/record.url?scp=0033751833&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033751833&partnerID=8YFLogxK
M3 - Conference article
AN - SCOPUS:0033751833
VL - 41
SP - 795
EP - 796
JO - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry
JF - American Chemical Society, Polymer Preprints, Division of Polymer Chemistry
SN - 0032-3934
IS - 1
ER -