Synthesis of 1,3-substituted cyclobutyls enabled by zinc insertion into functionalized iodocyclobutyl derivatives followed by Negishi coupling with halo-heteroaromatics is reported. Two distinct sets of conditions were developed; the first involved a two-step batch protocol using activated Rieke zinc, and the second involved a multistep continuous flow process. Both methods showed complementarity and allowed for rapid access to these medicinally relevant motifs, the possibility of scaling up, and automation for library synthesis.

Since the Industrial Revolution, technological advances have generated enormous emissions of various pollutants affecting all ecosystems. The detection and degradation of pollutants has therefore become a critical issue. More than 59 different remediation technologies have already been developed, such as biological remediation, and physicochemical and electrochemical methods. Among these techniques, advanced oxidation processes (AOPs) have been popularized in the treatment of wastewater. The use of ZnO as a photocatalyst for water remediation has been developing fast in recent years. In this work, the goals are to produce ZnO photocatalysts with different morphologies, by using a green sol-gel process, and to study both the influence of the synthesis parameters on the resulting morphology, and the influence of these different morphologies on the photocatalytic activity, for the degradation of an organic pollutant in water. Multiple morphologies were produced (nanotubes, nanorods, nanospheres), with the same crystalline phase (wurtzite). The most important parameter controlling the shape and size was found to be pH. The photoactivity study on a model of pollutant degradation shows that the resulting activity is mainly governed by the specific surface area of the material. A comparison with a commercial TiO2 photocatalyst (Evonik P25) showed that the best ZnO produced with this green process can reach similar photoactivity without a calcination step.

No abstract

No abstract

Earth‐abundant photosensitizers are highly sought after for light‐mediated applications, such as photoredox catalysis, depollution and energy conversion schemes. Homoleptic and heteroleptic copper(I) complexes are promising candidates in this field, as copper is abundant and the corresponding complexes are easily obtained in smooth conditions. However, some heteroleptic copper(I) complexes suffer from low (photo)stability that leads to the gradual formation of the corresponding homoleptic complex. Such degradation pathways are detrimental, especially when recyclability is desired. In here, we report a novel approach for the heterogenization of homoleptic and heteroleptic Cu complexes on silica nanoparticles. In both cases, the photophysical properties upon surface immobilization were only slightly affected. Excited‐state quenching with aryl diazonium derivatives occurred efficiently (108‐1010 M–1 s–1) with heterogeneous and homogeneous photosensitizers. Moderate but almost identical yields were obtained for the a‐arylation of enol acetate using the homoleptic complex in homogeneous or heterogeneous conditions. Importantly, the silica‐supported photocatalysts were recycled with moderate loss in photoactivity over multiple experiments. Transient absorption spectroscopy confirmed that excited‐state electron transfer occurred from the homogeneous and heterogeneous homoleptic copper(I) complexes to aryl diazonium derivatives, generating the corresponding copper(II) center that persisted for several hundreds of microseconds, compatible with photoredox catalysis applications.

No abstract