TY - JOUR
T1 - The effects of cross conjugation on the optical absorption and frontier orbital levels of donor-acceptor polymers
AU - Pruissen, van, G.W.P.
AU - Brebels, J.
AU - Hendriks, K.H.
AU - Wienk, M.M.
AU - Janssen, R.A.J.
PY - 2015
Y1 - 2015
N2 - The influence of cross-conjugation on the optical and electrochemical properties of donor–acceptor copolymers is investigated. Isoindigo, substituted at the 6,6' or the 5,5' positions, and thieno[3,2-b]thiophene and thieno[2,3-b]thiophene are taken as conjugated and cross-conjugated electron-deficient and electron-rich building blocks from which four isomeric donor–acceptor polymers were synthesized. Introducing cross-conjugation in isoindigo has only a small effect on the electrochemical band gap and on the onset of the absorption, which remains in the near-infrared. The optical absorption spectra, however, differ strongly because cross-conjugation strongly reduces the absorption coefficient. DFT calculations confirm that the transition to the lowest excited singlet state has a small oscillator strength in cross-conjugated isoindigo model compounds. Cross-conjugation in thienothiophene exerts a different effect. It causes a moderate but distinct blue-shift of the optical absorption and a deeper HOMO energy level.
AB - The influence of cross-conjugation on the optical and electrochemical properties of donor–acceptor copolymers is investigated. Isoindigo, substituted at the 6,6' or the 5,5' positions, and thieno[3,2-b]thiophene and thieno[2,3-b]thiophene are taken as conjugated and cross-conjugated electron-deficient and electron-rich building blocks from which four isomeric donor–acceptor polymers were synthesized. Introducing cross-conjugation in isoindigo has only a small effect on the electrochemical band gap and on the onset of the absorption, which remains in the near-infrared. The optical absorption spectra, however, differ strongly because cross-conjugation strongly reduces the absorption coefficient. DFT calculations confirm that the transition to the lowest excited singlet state has a small oscillator strength in cross-conjugated isoindigo model compounds. Cross-conjugation in thienothiophene exerts a different effect. It causes a moderate but distinct blue-shift of the optical absorption and a deeper HOMO energy level.
U2 - 10.1021/acs.macromol.5b00046
DO - 10.1021/acs.macromol.5b00046
M3 - Article
SN - 0024-9297
VL - 48
SP - 2435
EP - 2443
JO - Macromolecules
JF - Macromolecules
IS - 8
ER -