In this work, we present the innovative synthesis of salophen (acetaminosalol) derivatives in a solvent-free environment by high-speed ball milling, using a non-conventional activation method, which allowed obtaining compounds in a shorter time and with a better yield. Furthermore, for the first time, the salophen derivatives were deposited as composite films, using a matrix of poly 3,4-ethylene dioxythiophene:polystyrene sulfonate (PEDOT:PSS) polymer. Significant findings include the transformation from the benzoid to the quinoid form of PEDOT post-IPA treatment, as evidenced by Raman spectroscopy. SEM analysis revealed the formation of homogeneous films, and AFM provided insights into the changes in surface roughness and morphology post-IPA treatment, which may be crucial for understanding potential applications in electronics. The optical bandgap ranges between 2.86 and 3.2 eV for PEDOT:PSS-salophen films, placing them as organic semiconductors. The electrical behavior of the PEDOT:PSS-salophen films undergoes a transformation with the increase in voltage, from ohmic to space charge-limited conduction, and subsequently to constant current, with a maximum of 20 mA. These results suggest the possible use of composite films in organic electronics.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11435523PMC
http://dx.doi.org/10.3390/polym16182622DOI Listing

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ACS Omega

April 2024

Laboratorio de Química Inorgánica, Catálisis y Bioinorgánica. Departamento de Química, Facultad de Ciencias, Universidad de los Andes, Bogotá 111711, Colombia.

8-Formyl-7-hydroxycoumarin () and their derived salophen-type organocatalysts , , and were used for the synthesis of cyclic carbonates from carbon dioxide (CO) and epoxides under solvent-, halide-, and metal-free conditions. According to previous optimization tests, and had the best catalytic activity presenting 89 and 92% conversion toward the synthesis of 3-chloropropylene carbonate () using 8 bar CO, 100 °C at 9 h. Therefore, they were used as organocatalysts to complete the catalytic screening with 11 terminal epoxides () exhibiting the highest TOF values of 20 and 22 h using and , respectively.

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