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Improving the performance of p-type photoelectrodes represents a key challenge toward significant advancement in the field of tandem dye-sensitized solar cells. Herein, we demonstrate the application of boron-doped nanocrystalline diamond (B:NCD) thin films, covalently functionalized with a dithienopyrrole-benzothiadiazole push-pull chromophore, as alternative photocathodes. First, a primary functional handle is introduced on H-terminated diamond electrochemical diazonium grafting. Afterwards, Sonogashira cross-coupling and Cu(i) catalyzed azide-alkyne cycloaddition (CuAAC) reactions are employed to attach the chromophore, enabling the comparison of the degree of surface functionalization and the importance of the employed linker at the diamond-dye interface. X-ray photoelectron spectroscopy shows that surface functionalization CuAAC results in a slightly higher chromophore coverage compared to the Sonogashira cross-coupling. However, photocurrents and photovoltages, obtained by photoelectrochemical and Kelvin probe measurements, are approximately three times larger on photocathodes functionalized Sonogashira cross-coupling. Surface functionalization Sonogashira cross-coupling is thus considered the preferential method for the development of diamond-based hybrid photovoltaics.
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http://dx.doi.org/10.1039/c8ra07545j | DOI Listing |
J Org Chem
September 2025
Department of Pharmaceutical Engineering & Technology, IIT-Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India.
A visible light-driven, KSO-mediated one-step synthesis of 2-halo glycals has been reported, employing potassium salts as halogen source (KI, KBr, and KCl). Versatility of the proposed methodology to generate chloro-, bromo-, and iodo-substituted d-glycals containing both aliphatic and aromatic substitutions emphasizes the reproducibility of the methodology. The synthesized halogenated derivatives were subjected to Suzuki, Heck, and Sonogashira cross-coupling reactions, showcasing the utility of the halogenated derivatives for subsequent C-2 functionalization reactions of d-glycals.
View Article and Find Full Text PDFOrg Lett
September 2025
Shanghai Institute for Advanced Immunochemical Studies & School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
To address the current limitations of DNA-compatible Sonogashira cross-coupling reactions capable of accommodating a broad range of commercially available phenolic building blocks (BBs), an SuFEx-Sonogashira cross-coupling protocol has been developed. This protocol involves the conversion of readily accessible phenolic compounds into the corresponding aryl fluorosulfates within 96-well microplates via a highly efficient liquid-phase SuFEx reaction, followed by Sonogashira cross-coupling with DNA-conjugated terminal alkynes.
View Article and Find Full Text PDFJ Org Chem
August 2025
CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Chemistry, University of Science and Technology of China, Hefei 230026, China.
Substituted furans serve as pivotal building blocks for pharmaceutical agents and functional materials. In this study, we developed a Cu/Pd-catalyzed decarbonylative/acylative Sonogashira cross-coupling protocol, employing biomass-derived 2,5-furandicarboxylic dichloride and terminal alkynes as reactants, establishing a novel synthetic route for the production of unsymmetrically disubstituted furans. Both alkyl- and aryl-terminal alkynes are amenable to this tunable decarbonylative alkynylation transformation, yielding furan-based alkyne products bearing diverse electron-withdrawing and electron-donating substituents.
View Article and Find Full Text PDFOrg Biomol Chem
August 2025
Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Chemical Engineering, Hubei Normal University, Huangshi 435002, P. R. China.
A gold-catalyzed C(sp)-C(sp) cross-coupling reaction between hypervalent iodine(III) reagents and boronic acids has been developed, enabling the efficient synthesis of alkyne derivatives. This methodology features a broad substrate scope and high functional-group tolerance, and proceeds under mild reaction conditions without requiring external bases. Notably, the reaction is scalable to the gram level, and the resulting alkyne products can be readily transformed into structurally diverse derivatives.
View Article and Find Full Text PDFOrg Lett
August 2025
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
A palladium-catalyzed ligand-controlled acyl and decarbonylative Sonogashira reaction of alkenyl thioesters with terminal alkynes was developed. 1,3-Enynes and enynone products were obtained by using 1,3-bis(diphenylphosphino)propane and P(3,5-(CF)CH) as the ligands, respectively. To demonstrate the synthetic utilities, late-stage constructions of 1,3-enyne and enynone skeletons in natural products and drugs were showcased.
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