Breast Cancer Treatment: The Case of Gold(I)-Based Compounds as a Promising Class of Bioactive Molecules

Breast cancers (BCs) may present dramatic diagnoses, both for ineffective therapies and for the limited outcomes in terms of lifespan. For these types of tumors, the search for new drugs is a primary necessity. It is widely recognized that gold compounds are highly active and extremely potent as anticancer agents against many cancer cell lines. The presence of the metal plays an essential role in the activation of the cytotoxicity of these coordination compounds, whose activity, if restricted to the ligands alone, would be non-existent. On the other hand, gold exhibits a complex biochemistry, substantially variable depending on the chemical environments around the central metal. In this review, the scientific findings of the last 6–7 years on two classes of gold(I) compounds, containing phosphane or carbene ligands, are reviewed. In addition to this class of Au(I) compounds, the recent developments in the application of Auranofin in regards to BCs are reported. Auranofin is a triethylphosphine-thiosugar compound that, being a drug approved by the FDA—therefore extensively studied—is an interesting lead gold compound and a good comparison to understand the activities of structurally related Au(I) compounds.

Tailoring graphene-supported Ru nanoparticles by functionalization with pyrene-tagged N-heterocyclic carbenes

The catalytic properties of graphene-supported ruthenium nanoparticles (Ru@rGO) have been finely tuned by modifying their metal surface with pyrene-tagged N-heterocyclic-carbene ligands (pyr-IMes). The nature and interaction modes of the pyr-IMes...

Carbene Ligand-Doped Fe2O3 Composite for Rapid Removal of Multiple Dyes under Sunlight

Contaminated water due to industrial organic dyes presents a significant challenge to sustainability. As a material of green energy, photocatalysts offer an effective and environmentally friendly way to deal with organic dyes for water treatment. A series of simple and highly efficient iron photocatalysts with carbene ligands were developed, which, under the illumination of sunlight, can rapidly degrade multiple organic dyes in water at room temperature, including rhodamine B (RhB), indigo carmine (IC), methyl blue (MB), and congo red (CR). The field-only surface integral method was carried out to determine the absorption spectrum of photocatalyst particles. Under the optimized experimental conditions which were selected by the orthogonal experiments for four dyes, 0.5a@Fe2O3 and 2c@Fe2O3 demonstrated good stability and photocatalytic activity. These two composite materials not only have the ability to remove 98.0% of the degradation in 10 s, but also maintain high reactivity after a few cycles of repeated use.

Efficient electrocatalytic acetylene semihydrogenation by electron–rich metal sites in N–heterocyclic carbene metal complexes

Electrocatalytic acetylene semihydrogenation is a promising alternative to thermocatalytic acetylene hydrogenation due to its environmental benignity and economic efficiency, but its performance is far below that of the thermocatalytic reaction because of strong competition from side reactions, including hydrogen evolution, overhydrogenation and carbon–carbon coupling reactions. We develop N–heterocyclic carbene–metal complexes, with electron–rich metal centers owing to the strongly σ–donating N–heterocyclic carbene ligands, as electrocatalysts for selective acetylene semihydrogenation. Experimental and theoretical investigations reveal that the copper sites in N–heterocyclic carbene–copper facilitate the absorption of electrophilic acetylene and the desorption of nucleophilic ethylene, ultimately suppressing the side reactions during electrocatalytic acetylene semihydrogenation, and exhibit superior semihydrogenation performance, with faradaic efficiencies of ≥98 % under pure acetylene flow. Even in a crude ethylene feed containing 1 % acetylene (1 × 104 ppm), N–heterocyclic carbene–copper affords a specific selectivity of >99 % during a 100–h stability test, continuous ethylene production with only ~30 ppm acetylene, a large space velocity of up to 9.6 × 105 mL·gcat−1·h−1, and a turnover frequency of 2.1 × 10−2 s−1, dramatically outperforming currently reported thermocatalysts.