Molecular Weight-Dependent Physical and Photovoltaic Properties of Poly(3-alkylthiophene)s with Butyl, Hexyl, and Octyl Side-Chains

A series of poly-3-alkylthiophenes (P3ATs) with butyl (P3BT), hexyl (P3HT), and octyl (P3OT) sidechains and well-defined molecular weights (MWs) were synthesized using Grignard metathesis polymerization. The MWs of P3HTs and P3OTs obtained via gel permeation chromatography agreed well with the calculated MWs ranging from approximately 10 to 70 kDa. Differential scanning calorimetry results showed that the crystalline melting temperature increased with increasing MWs and decreasing alkyl side-chain length, whereas the crystallinity of the P3ATs increased with the growth of MWs. An MW-dependent red shift was observed in the UV–Vis and photoluminiscence spectra of the P3ATs in solution, which might be a strong evidence for the extended effective conjugation occurring in polymers with longer chain lengths. The photoluminescence quantum yields of pristine films in all polymers were lower than those of the diluted solutions, whereas they were higher than those of the phenyl-C61-butyric acid methyl ester-blended films. The UV–Vis spectra of the films showed fine structures with pronounced red shifts, and the interchain interaction-induced features were weakly dependent on the MW but significantly dependent on the alkyl side-chain length. The photovoltaic device performances of the P3BT and P3HT samples significantly improved upon blending with a fullerene derivative and subsequent annealing, whereas those of P3OTs mostly degraded, particularly after annealing. The optimal power conversion efficiencies of P3BT, P3HT, and P3OT were 2.4%, 3.6%, and 1.5%, respectively, after annealing with MWs of ~11, ~39, and ~38 kDa, respectively.

Dispersion Performance of Polycarboxylate Terpolymers with Different Alkyl Side-Chain Lengths in Pesticide Suspension Concentrate

A versatile dispersant plays a critical role in the suspension stability of pesticide suspension concentrate (SC) systems. Herein, a series of novel acrylate ester-based polycarboxylate terpolymers (PTs) were designed as dispersant for pesticide suspension concentrate and successfully synthesized in aqueous solutions from the copolymerization of α-methacrylic acid, allyl polyoxyethylene ether, and acrylate (methyl acrylate, ethyl acrylate, and n-butyl acrylate). Terpolymers were characterized by FT-IR and 1H-NMR to confirm their structure. The surface activities of PTs were evaluated according to critical micelle concentration (CMC) and the surface tension at CMC (γCMC). PT-3 with the longest alkyl side-chain length displayed the most superior surface activity due to its lowest CMC value compared with that of the other PTs. Additionally, the dispersion properties of PTs as dispersants in a 600 g/L imidacloprid SC were evaluated. Results showed that compared to the other two PTs, PT-3 contributes to the excellent dispersion properties on imidacloprid SC. Meanwhile, the obtained SC system exhibited shear thinning behavior under high-speed shearing showing typical features of pseudo-plastic non-Newtonian fluids, which conforms to the Herschel–Buckley model. Our results revealed that the effect of the alkyl side-chain length of dispersants could be considered the primary modulator of dispersion performance of SCs.

Investigation of the Anti-Methicillin-Resistant Staphylococcus aureus Activity of (+)-Tanikolide- and (+)-Malyngolide-Based Analogues Prepared by Asymmetric Synthesis

Herein, we report antibacterial and antifungal evaluation of a series of previously prepared (+)-tanikolide analogues. One analogue, (4S,6S)-4-methyltanikolide, displayed promising anti-methicillin-resistant Staphylococcus aureus activity with a MIC of 12.5 µg/mL. Based on the antimicrobial properties of the structurally related (−)-malyngolide, two further analogues (4S,6S)-4-methylmalyngolide and (4R,6S)-4-methylmalyngolide bearing a shortened n-nonyl alkyl side chain were prepared in the present study using a ZrCl4-catalysed deprotection/cyclisation as the key step in their asymmetric synthesis. When these were tested for activity against anti-methicillin-resistant Staphylococcus aureus, the MIC increased to 50 µg/mL.