Nonlinear optical (NLO) donor-acceptor (D-A) chromophores containing a fuse
d terthiophene, namely dithienothiophene (DTT) as electron relay, and vario
us strength acceptors were synthesized to evaluate the relay's role in the
solvatochromism as well as in the molecular nonlinearity, mu beta(0). Their
solvatochromic behavior, which is dependent on acceptor strength, is corre
lated to their mu beta(0). The static quadratic hyperpolarizability, beta(0
), of DTT-containing chromophores was determined by EFISH measurements. Fro
m the comparison of mu beta(0) values of D-A chromophores based on oligothi
ophenes, it was assessed that DTT as relay is significantly more efficient
compared to bithiophene (the same number of conjugated double bonds) and te
rthiophene. An additional merit of DTT is that chromophores containing DTT
have a noticeably high thermal stability.