553-26-4Relevant articles and documents
Intramolecular Electron Transfer from Pentacyanoferrate(II) to Pentaaminecobalt(III) with 3,3'-Dimethyl-4,4'-bipyridine, 4,4'-Bipyridylacetylene, 1,4-Bis(4-pyridyl)butadiyne, 2,7-Diazapyrene, and 3,8-Phenanthroline as Bridging Ligands: Adiabaticity and th
Lee, Gyu-Hwan,Ciana, Leopoldo Della,Haim, Albert
, p. 2535 - 2541 (1989)
Rate constants for intramolecular electron transfer from iron to cobalt in (NH3)5CO(III)LFe(II)(CN)5 (L=3,3'-dimethyl-4,4'-bipyridine, 4,4'-bipyridylacetylene, 1,4-bis(4-pyridyl)butadiyne, 2,7-diazapyrene, and 3,8-phenanthroline) have been measured at 25
Synthetic transformations of sesquiterpene lactones 9.*Synthesis of 13-(pyridinyl)eudesmanolides
Patrushev, Sergey S.,Shakirov, Makhmut M.,Shults, Elvira E.
, p. 165 - 171 (2016)
[Figure not available: see fulltext.]The reaction of isoalantolactone, a sesquiterpene α-methylidene-γ-lactone, with bromo(iodo)pyridines under the Heck reaction conditions gave 3-(pyridylmethylidene)-8а-methyldecahydronaphtho[2,3-b]furan-2(3Н)-ones and 3-(pyridylmethyl)-8а-methyloctahydronaphtho[2,3-b]-furan-2(4Н)-ones, products of double bond migration. The yield and product ratio depended on the reaction conditions and the nature of halopyridine. The effectiveness of Pd(OAc)2–caffeine catalytic system was demonstrated in this reaction.
Highly efficient removal of paraquat pesticide from aqueous solutions using a novel nano Kaolin modified with sulfuric acid via host–guest interactions
Mohammadzadeh Kakhki, Roya,Karimian, Azam,Saadati Rad, Masoud
, p. 307 - 313 (2020)
Contamination of wastewaters with pesticides has significant risk for environmental water. In spite of the rule of Europ, paraquat is used extensively as an herbicide in the all around the world and it is likely to be released into drinking water. Therefore the elimination of it from water is very important. In this paper a new sulfuric acid modified nano kaolin sorbent was synthesized with a simple and low cost method. Thereafter it was applied for removing of paraquat and the experimental conditions such as concentration of herbicide, dose of sorbent and pH of solution were optimized. The results showed the unmodified Kaolin wasn’t able to remove the paraquat efficiently. But with the proposed modified nano Kaolin removal percent reach to 98% in a short time 60 min. Also the results showed this system obeys from Frendluich adsorption isotherm.
Suzuki–Miyaura arylation of 2,3-, 2,4-, 2,5-, and 3,4-dibromothiophenes
Babkova, Mariia,Baran, Andrei,Petkus, Jana,Shubin, Kirill
, (2022/03/15)
A convenient and general method for Suzuki–Miyaura double cross-coupling of various dibromothiophenes was developed. Using a simple and cheap catalytic system Pd(OAc)2/PPh3 in 95% EtOH, various (hetero)arylboronic acids react with dibromothiophenes providing diarylthiophenes, useful in the synthesis of metal–organic frameworks (MOFs), in moderate to excellent yields. The overall efficiency of the catalytic process and slight excess of boronic acids allowed to suppress formation of side products and significantly simplify the purification of products.
Green-Synthesized Nickel Nanoparticles on Reduced Graphene Oxide as an Active and Selective Catalyst for Suzuki and Glaser-Hay Coupling Reactions
Murugan, Karthik,Nainamalai, Devarajan,Kanagaraj, Pavithara,Nagappan, Saravana Ganesan,Palaniswamy, Suresh
, (2020/07/09)
A mild and benign methodology to syntheses biaryls and 1,3-diynes has been demonstrated using the nickel nanoparticles supported on reduced graphene oxide (RGO-Ni) as a heterogeneous catalyst which is prepared using green reagents. A series of substituted biaryls and 1,3-diynes has been synthesised in good to excellent yields through C-C homocoupling reaction of arylboronic acids and terminal alkynes respectively using 1,4-dioxane as a benign solvent. The present ligand-free catalytic system proceeds smoothly under mild conditions, avoids noble and stoichiometric metal reagents and tolerates sensitive functional groups. Also has a wide substrate scope and feasible with other nitrogen and sulphur containing heteroaryl boronic acids. Hot filtration test unambiguously proves the true heterogeneity of the catalyst and which support for the further reusability of the catalyst for several times without any change in the activity. The easy preparation and simple magnetic separation, stability and reusability reveal that as-prepared RGO-Ni as a versatile catalyst for the synthesis of polyaromatic compounds both in academia and industries. Highlights: Green-synthesized RGO-Ni nanocomposite used as a heterogeneous catalyst for Suzuki type (C-C) and Glaser–Hay (C ≡ C) homocoupling coupling reactions. Ligand-free catalytic system and avoids noble and stoichiometric metal reagents Short reaction time with a minimum catalyst (nickel) loading RGO-Ni nanocomposite is highly stable, reusable, and magnetically retrievable.