RESUMEN
Three metal-free organic D-π-A dyes with benzothieno[3,2-b]indole as electron donor, cyanoacrylic acid as both electron acceptor and anchoring group with benzene (BID-1), thiophene (BID-2) and furan (BID-3) as π-spacers were designed and synthesized for application in dye-sensitized solar cells (DSSCs). A planar and electron-rich heterocycle such as benzothieno[3,2-b]indole offers better backbone rigidity and improves charge transport properties in comparison to indolo[3,2-b]indole donor, previously reported from our group. Additionally, we synthesized a benzothieno[3,2-b]indole donor grafted with longer alkyl chains which efficiently prevented the approach of oxidized species in the electrolyte coming closer to semiconductor thereby arresting recombination. A power conversion efficiency of 4.11 % was achieved for dye-sensitized solar cells based on the furan π-spacer benzothieno[3,2-b]indole dye BID-3 in comparison to the corresponding indolo[3,2-b]indole dye (IID-3) having an efficiency of 1.71 %. Detailed interfacial electrical measurements along with theoretical calculations disclosed the mechanism of back electron transfer and improvement in photovoltaic performance with respect to variation in both donor and π-spacer.
RESUMEN
A palladium-catalyzed aminocarbonylation strategy exploiting chloroform as a CO source has been developed for the synthesis of biologically potent 2-amidoimidazopyridine scaffolds. The aminocarbonylation reaction was found to be general with a range of amines and substituted imidazopyridines. Preliminary biological evaluation of cytotoxicity on selected examples provides scope for future investigations.
RESUMEN
Novel glycoconjugated squaraine dyes were synthesized, which exhibited excellent internalization in tumor cells and are potent fluorogenic imaging probes for tumor selective optical imaging.
