Electronic influence of pyrazole-appended pyridine/pyrazine based N,N,N-tridentate ligands on Ru complexes: Impact on selectivity of catalytic alkene oxidation with mild oxidant NaIO4

Sustainable Synthesis Strategies: A Comparative Life Cycle Perspective on LaFeO3 Nanoparticles

“…FeB showcases more than 50% more impact in majority of midpoint categories compared to other Fe precursors due to the usage of anhydrous tetrahydrofuran (THF) and sodium tert-butoxide (NaOt-Bu). THF produces hazardous peroxides upon exposure to air and light, whereas, NaOt-Bu is a strong base due to the presence of the tert-butoxide ion (Ot-Bu-), which deprotonates acidic hydrogens in various organic compounds, leading to the formation of corresponding alkoxides . The input organic solvents and other chemicals needed for production are the main cause of the increased impacts of organic precursors.…”

Design of a Copper(II) Complex with Tetradentate Bis‐Benzotriazole‐Appended Bipyridine Ligand and its Catalytic Application in A3 Coupling Reaction

“…However, attempts with aliphatic aldehydes or acyclic secondary amines did not yield significant amounts of propargylamine, which might be due to the relatively less stability of the iminium ion generated in situ from the aliphatic aldehydes or acyclic secondary amines, under the applied reaction conditions of the present protocol. Finally, switching from phenylacetylene to the aliphatic alkyne 1-octyne (23)(24)(25)(26)(27)(28)(29)(30) showcased successful product production, with yields ranging from 93 % to 80 %.…”

“…[16] Recently, we became interested to design and study the electronic and chelating effect of several benzotriazole-based N-enriched ligands in their transition metal complexes. [19][20][26][27][28][29] Inspired by these studies, we rationally employed benzotriazole-appended N,N-bidentate and N,N,N-tridentate suitable chelating ligands for ready access and effective utilization of air-stable, structurally well-defined and discrete Cu(II) complexes as precatalysts for A 3 coupling reactions (Figure 1, B-C). [18][19][20] The results showed that the multidentate chelate binding of these ligands to the Cu centre facilitated the catalytic processes, most probably via efficient stereo-electronic effect exerted to the catalytically active low-valent Cu(I) centre.…”

“…Previously, Lykakis and Kostakis recently used coordination polymers of Cu(II) with substituted benzotriazole ligands in catalytic A 3 coupling reaction (Figure 1A). [16] Recently, we became interested to design and study the electronic and chelating effect of several benzotriazole‐based N‐enriched ligands in their transition metal complexes [19–20,26–29] . Inspired by these studies, we rationally employed benzotriazole‐appended N,N‐bidentate and N,N,N‐tridentate suitable chelating ligands for ready access and effective utilization of air‐stable, structurally well‐defined and discrete Cu(II) complexes as precatalysts for A 3 coupling reactions (Figure 1, B–C) [18–20] .…”