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Two alternating copolymers of dithienosilole (DTS) were designed and synthesized with small optical band gaps, flanked by thienyl units as electron-donor moieties and benzothiadiazole dicarboxylic imide (BTDI) as electron-acceptor moieties. The BTDI moieties were anchored to two different solubilizing side chains, namely 3,7-dimethyloctyl and n-octyl chains. An analysis of the effect of the electrochemical, optical, thermal, and structural characteristics of the resulting polymers along with their solubility and molecular weight is the subject of this paper. The Stille polymerization was used to synthesize PDTSDTBTDI-DMO and PDTSDTBTDI-8. The average molecular weight of PDTSDTBTDI-DMO and PDTSDTBTDI-8 is 14,600 and 5700 g mol−1, respectively. Both polymers have shown equivalent optical band gaps around 1.4 eV. The highest occupied molecular orbital (HOMO) levels of the polymers were comparable, around −5.2 eV. The lowest unoccupied molecular orbital (LUMO) values were −3.56 and −3.45 eV for PDTSDTBTDI-DMO and PDTSDTBTDI-8, respectively. At decomposition temperatures above 350 °C, both copolymers showed strong thermal stability. The studies of powder X-ray diffraction (XRD) have shown that they are amorphous in a solid-state. [ABSTRACT FROM AUTHOR]

A series of alternating copolymers containing cyclopentadithiophene (CPDT) flanked by thienyl moieties as electron-donor units and benzothiadiazole dicarboxylic imide (BTDI) as electron-acceptor units were designed and synthesized for solar cell applications. Different solubilizing side chains, including 2-ethylhexyl chains and n-octyl chains were attached to CPDT units, whereas 3,7-dimethyloctyl chains and n-octyl chains were anchored to the BTDI moieties. The impact of these substituents on the solubilities, molecular weights, optical and electrochemical properties, and thermal and structural properties of the resulting polymers was investigated. PCPDTDTBTDI-EH, DMO was synthesized via Suzuki polymerization, whereas PCPDTDTBTDI-8, DMO, and PCPDTDTBTDI-EH, 8 were prepared through direct arylation polymerization. PCPDTDTBTDI-8, DMO has the highest number average molecular weight (Mn = 17,400 g mol−1) among all polymers prepared. The PCPDTDTBTDI-8, DMO and PCPDTDTBTDI-8, 8 which have n-octyl substituents on their CPDT units have comparable optical band gaps (Eg ~ 1.3 eV), which are around 0.1 eV lower than PCPDTDTBTDI-EH, DMO analogues that have 2-ethylhexyl substituents on their CPDT units. The polymers have their HOMO levels between −5.10 and −5.22 eV with PCPDTDTBTDI-EH, DMO having the deepest highest occupied molecular orbital (HOMO) energy level. The lowest unoccupied molecular orbital (LUMO) levels of the polymers are between −3.4 and −3.5 eV. All polymers exhibit good thermal stability with decomposition temperatures surpassing 350 °C. Powder X-ray diffraction (XRD) studies have shown that all polymers have the amorphous nature in solid state. [ABSTRACT FROM AUTHOR]

Two novel low band gap donor–acceptor (D–A) copolymers, poly[9,10-bis(4-(dodecyloxy)phenyl)-2,6-anthracene-alt-5,5-(4′,7′-bis(2-thienyl)-2′,1′,3′-benzothiadiazole-N-5,6-(3,7-dimethyloctyl)dicarboxylic imide)] (PPADTBTDI-DMO) and poly[9,10-bis(4-(dodecyloxy)phenyl)-2,6-anthracene-alt-5,5-(4′,7′-bis(2-thienyl)-2′,1′,3′-benzothiadiazole-5,6-N-octyl-dicarboxylic imide)] (PPADTBTDI-8) were synthesized in the present work by copolymerising the bis-boronate ester of 9,10-phenylsubstituted anthracene flanked by thienyl groups as electron–donor units with benzothiadiazole dicarboxylic imide (BTDI) as electron–acceptor units. Both polymers were synthesized in good yields via Suzuki polymerisation. Two different solubilizing alkyl chains were anchored to the BTDI units in order to investigate the impact upon their solubilities, molecular weights, optical and electrochemical properties, structural properties and thermal stability of the resulting polymers. Both polymers have comparable molecular weights and have a low optical band gap (Eg) of 1.66 eV. The polymers have low-lying highest occupied molecular orbital (HOMO) levels of about −5.5 eV as well as the similar lowest unoccupied molecular orbital (LUMO) energy levels of −3.56 eV. Thermogravimetric analyses (TGA) of PPADTBTDI-DMO and PPADTBTDI-8 did not prove instability with decomposition temperatures at 354 and 313 °C, respectively. Powder X-ray diffraction (XRD) studies have shown that both polymers have an amorphous nature in the solid state, which could be used as electrolytes in optoelectronic devices. [ABSTRACT FROM AUTHOR]