Selectivity control towards CO versus H₂ for photo-driven CO₂ reduction with a novel Co(II) catalyst

• Lisa-Lou Gracia,
• Philip Henkel,
• Olaf Fuhr and
• Claudia Bizzarri

Beilstein J. Org. Chem. 2023, 19, 1766–1775, doi:10.3762/bjoc.19.129

• ]. Among the most employed earth-abundant metal-based PS, Cu(I) complexes have the first place, not only in artificial photosynthesis, but also in a large variety of photo(redox)catalyses [12][13][14][15][16][17]. On the other hand, several complexes based on 3d transition metals, like manganese [18], iron

• [19][20][21], cobalt [22][23], and nickel [24][25], have been designed as CO2 reduction catalysts. This (supra)molecular approach is appealing for gaining a structure–property understanding with the goal of tunable and efficient activity. Among the 3d transition metals, cobalt is relatively abundant

Recent developments and trends in the iron- and cobalt-catalyzed Sonogashira reactions

• Surendran Amrutha,
• Sankaran Radhika and
• Gopinathan Anilkumar

Beilstein J. Org. Chem. 2022, 18, 262–285, doi:10.3762/bjoc.18.31

• nature. Furthermore, the 3d transition metals show contrast in the reactive nature with 4d and 5d group members [19]. Catalysts based on Earth abundant metals such as Fe and Co are promising members of the 3d series in catalysis [20]. Recently, catalysts based on iron and cobalt complexes have been

Earth-abundant 3d transition metals on the rise in catalysis

• Nikolaos Kaplaneris and
• Lutz Ackermann

Beilstein J. Org. Chem. 2022, 18, 86–88, doi:10.3762/bjoc.18.8

• , Germany 10.3762/bjoc.18.8 Keywords: C–H activation; 3d transition metals; green chemistry; late-stage functionalization; sustainability; Transition metal catalysis has emerged as a transformative platform for the assembly of increasingly complex compounds, with enabling applications to natural product

• these indisputable advances, this approach has, thus far, predominantly relied on precious, often toxic, 4d and 5d transition metals, most prominently palladium, rhodium and iridium. In sharp contrast, the use of less expensive and less toxic Earth-abundant 3d transition metals continues to be

• underdeveloped. This lack of viable catalysis strategies involving 3d transition metals is largely due to a limited knowledge on the working mode of these metal catalysts, which often involve single-electron-transfer-based redox events. As a consequence, there is a strong demand for efficient and reliable

Copper-catalyzed monoselective C–H amination of ferrocenes with alkylamines

• Zhen-Sheng Jia,
• Qiang Yue,
• Ya Li,
• Xue-Tao Xu,
• Kun Zhang and
• Bing-Feng Shi

Beilstein J. Org. Chem. 2021, 17, 2488–2495, doi:10.3762/bjoc.17.165

• derivatives [13][14][15][16]. Especially, the 3d transition metals, such as Cu, Co and Ni, have been exploited to convert C–H bonds to various functional groups, attributing to the cost-effective and less toxic properties, which render C–H transformations both economically desirable and environmentally benign

Sustainable manganese catalysis for late-stage C–H functionalization of bioactive structural motifs

• Jongwoo Son

Beilstein J. Org. Chem. 2021, 17, 1733–1751, doi:10.3762/bjoc.17.122

• powerful synthetic strategy for accessing advanced agrochemicals, bioimaging materials, and drug candidates, among other complex molecules. While traditional late-stage diversification relies on the use of precious transition metals, the utilization of 3d transition metals is an emerging approach in

• biologically active small molecules and complex peptides. Keywords: bioactive molecules; 3d transition metals; late-stage functionalization; manganese catalyst; sustainable catalysis; Introduction Manganese, a 3d transition metal, allows for a potentially ideal sustainable catalytic system because of the

A perfluorocyclopentene based diarylethene bearing two terpyridine moieties – synthesis, photochemical properties and influence of transition metal ions

• Falk Wehmeier and
• Jochen Mattay

Beilstein J. Org. Chem. 2010, 6, No. 53, doi:10.3762/bjoc.6.53

• of the bis(terpyridinyl)diarylethenes 10a and 10b. Photochromic reaction of the free ligand 10a. Synthesis of the binuclear Ru(II)-complex 12. Influence of different 3d-transition metals on the photochromic reaction of 10a in solution. Supporting Information Supporting information contains UV–vis