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Four donor-acceptor-donor compounds consisting of 9,9-dimethyl-9,10-dihydroacridine donors differently linked to a benzothiadiazole acceptor were designed using DFT calculations and synthesized, namely 4,7-bis(4-(9,9-dimethyl-9,10-dihydroacridine)phenyl)benzo[c][1,2,5]thiadiazole (1), 4,7-bis(2,5-dimethyl-4-(9,9-dimethyl-9,10-dihydroacridine)phenyl)benzo[c][1,2,5]thiadiazole (2), 4,7-bis(3,5-di(9,9-dimethyl-9,10-dihydroacridine)phenyl)benzo[c][1,2,5]thiadiazole (3), and 4-(3,5-di(9,9-dimethyl-9,10-dihydroacridine)phenyl)-7-(thiophen-2-yl)benzo[c][1,2,5]thiadiazole (4). As predicted theoretically, all studied compounds were electrochemically active both in the reduction as well as in the oxidation modes. They underwent one electron quasi-reversible reduction. Oxidation of 1 and 2 involved a two electron process transforming them into dications and carrying out, in parallel, their dimerization. Oxidation of 3 and 4 resulted in their oligomerization (polymerization). The electrochemically determined ionisation potentials (IP) of 1-4 were similar, covering a narrow range of 5.28-5.33 eV and were consistent with DFT calculations. Larger differences were found for experimentally determined electron affinity (EA) values, being significantly lower for 2 (|EA| = 2.59 eV) as compared to 1, 3 and 4 whose |EA| values were higher by 0.15-0.25 eV, again consistent with DFT calculations. DFT calculations predict positive values of ΔE(S1-T1) for all compounds i.e. in the range of 0.18 eV to 0.43 eV for 1, 3 and 4 and a significantly lower value for 2 (0.06 eV), indicating a possible RISC process in this case. DFT calculations of ΔE(S1-T2) lead to negative and very small values for 2-4 implying a possible involvement of higher lying triplets in the generation of singlet excitons. The investigated derivatives exhibited fluorescence in the orange-red spectral range (550-770 nm) and were strongly dependent on the solvent polarity. The highest PLQY value of 37% was measured for 1 in toluene. The PLQY values significantly improved upon deoxygenation of the studied solutions. Solid state samples also exhibited higher PLQY values as compared to those determined for DCM solutions. These findings were rationalized by partial suppression of the vibrationally induced emission quenching in the solid state due to the intermolecular interaction confinement. [ABSTRACT FROM AUTHOR]