1215112-72-3Relevant academic research and scientific papers
Cu(II) Coordination Polymers as Vehicles in the A3 Coupling
Loukopoulos, Edward,Kallitsakis, Michael,Tsoureas, Nikolaos,Abdul-Sada, Alaa,Chilton, Nicholas F.,Lykakis, Ioannis N.,Kostakis, George E.
, p. 4898 - 4910 (2017)
A family of benzotriazole based coordination compounds, obtained in two steps and good yields from commercially available materials, formulated as [CuII(L1)2(MeCN)2]·2ClO4·MeCN (1), [CuII(L
Silver(I) complexes as efficient source for silver oxide nanoparticles with catalytic activity in A3 coupling reactions
Trivedi, Manoj,Singh, Gurmeet,Kumar, Abhinav,Rath, Nigam P.
, p. 255 - 263 (2015)
New silver(I) complexes [Ag7(μ4-Cl)(μ3-Cl)2(μ2-Cl)3(MPI)6] (1), and [Ag(μ3-I)(BI)]n (2) [MPI = 1-(4-methoxyphenyl)-1H-imidazole; BI = 1-Benzylimidazole] hav
Ionic liquid assisted silver-catalyzed one-pot A3-coupling reactions for the synthesis of propargylamines
Zhu, Anlian,Du, Chunyan,Zhang, Yue,Li, Lingjun
, p. 289 - 293 (2019/02/06)
A series of ionic liquids with different cations and anions were synthesized and their performances for the silver catalyzed one-pot A3-coupling reactions were investigated. The selection showed that the combination of AgNO3 and ioni
Structural Diversity and Catalytic Properties in a Family of Ag(I)-Benzotriazole Based Coordination Compounds
Loukopoulos, Edward,Abdul-Sada, Alaa,Viseux, Eddy M. E.,Lykakis, Ioannis N.,Kostakis, George E.
, p. 5638 - 5651 (2018/08/03)
In this work we study the coordination chemistry of a series of semirigid benzotriazole based ligands (L1-L3) along with the low coordination number but versatile AgI ions. This has led to nine new coordination compounds formulated [Ag(L1)(CF3CO2)] (1), [Ag2(L1T)2(CF3SO3)2]·2Me2CO (2), [Ag(L2T)(ClO4)(Me2CO)] (3), [Ag(L2T)(BF4)(Et2O)] (4), [Ag2(L3T)2(ClO4)2]2 (5), [Ag(L3)(NO3)] (6), [Ag2(L3T)2(CF3CO2)2] (7), [Ag2(L3T)(CF3SO3)2] (8), and [Ag2(L3T)2(CF3CF2CO2)2]·2Me2CO (9). These compounds show structural diversity including dimers (5, 7, 9) and one-dimensional (1D) (3, 4, 6) and two-dimensional (2D) (1, 2, 8) coordination polymers. The presence of the two -CH2- units between the three rigid backbones, benzotriazole/-C6H4-/benzotriazole, provides a limited, but significant, flexibility in L1-L3, influencing their variety coordination abilities. Interestingly, certain structures exhibit an isomerism effect (L1T-L3T) in the benzotriazole unit when in solid state; a series of studies are indicative of the 1,1-form which is generally dominant in solution even in cases where the crystal structure does not contain this tautomer. The homogeneous catalytic efficacy of all compounds against the well-known multicomponent A3 coupling reaction and the hydration of alkynes were investigated. Compound 4 was identified as the optimal catalyst for both reactions, promoting the multicomponent coupling as well as the alkyne hydration reaction under low loadings (0.5 and 3 mol %, respectively) and in high yields (up to 99 and 93% in each case).
Ultrasonic and bio-assisted synthesis of Ag@HNTs-T as a novel heterogeneous catalyst for the green synthesis of propargylamines: A combination of experimental and computational study
Malmir, Masoumeh,Heravi, Majid M.,Sadjadi, Samahe,Hosseinnejad, Tayebeh
, (2018/04/05)
A novel heterogeneous catalyst is prepared through functionalization of halloysite nanotube with 1H-1,2,3-triazole-5-methanol and subsequent immobilization of silver nanoparticles through bio-assisted approach using Arctiumplatylepis extract. The resulting catalyst, Ag@HNTs-T, was characterized by using SEM/EDX, BET, XRD, FTIR, ICP-AES, TGA, DTGA and elemental mapping analysis. Moreover, we computationally assessed metal-ligand interactions in Ag@HNTs-T complex model to interpret the immobilization behavior of silver nanoparticles on HNTs surface via quantum chemistry computations. The catalytic activity of the catalyst was studied for the synthesis of propargylamines via A3 and KA2 coupling reactions under ultrasonic irradiation. The results demonstrated that Ag@HNTs-T could efficiently promote these reactions to furnish the corresponding products in high yields and short reaction times. The study of the recyclability of the catalyst and Ag(0) leaching confirmed that the catalyst was recyclability up to four reaction runs with slight Ag(0) leaching.
Green bio-based synthesis of Fe2O3@SiO2-IL/Ag hollow spheres and their catalytic utility for ultrasonic-assisted synthesis of propargylamines and benzo[b]furans
Sadjadi, Samahe,Heravi, Majid M.,Malmir, Masoumeh
, (2017/10/09)
A novel magnetic hybrid system containing nano-magnetic Fe2O3 hollow spheres, silica shell, [pmim]Cl ionic liquid and silver nanoparticles was synthesized and characterized. The silver nanoparticles were prepared via biosynthesis usi
Preparation of Ag-doped g-C3N4 Nano Sheet Decorated Magnetic γ-Fe2O3@SiO2 Core–Shell Hollow Spheres through a Novel Hydrothermal Procedure: Investigation of the Catalytic activity for A3, KA2 Coupling Reactions and [3?+?2] Cycloaddition
Sadjadi, Samahe,Malmir, Masoumeh,Heravi, Majid M.
, (2018/07/31)
Taking advantageous of both g-C3N4 and magnetic core-shell hollow spheres, for the first time a heterogeneous and magnetically separable hybrid system was prepared through a novel and simple hydrothermal procedure and used for immobilization of bio-synthesized Ag(0) nanoparticles. The hybrid system was fully characterized by using SEM/EDS, FTIR, VSM, TEM, XRD, TGA, DTGA, ICP-AES, BET and elemental mapping analysis. The catalytic utility of the obtained system, h-Fe2O3@SiO2/g-C3N4/Ag, for promoting ultrasonic-assisted A3, KA2 coupling reactions and [3?+?2] cycloaddition has been confirmed. The results established that the catalyst could efficiently catalyze the reaction to afford the corresponding products in high yields in short reaction times. The reusability study confirmed that the catalyst could be recovered and reused for at least five reaction runs with only slight loss of the catalytic activity. The hot filtration test also proved low silver leaching, indicating the heterogeneous nature of the catalysis.
Merging Photoredox with Copper Catalysis: Decarboxylative Alkynylation of α-Amino Acid Derivatives
Zhang, Hao,Zhang, Pengxiang,Jiang, Min,Yang, Haijun,Fu, Hua
, p. 1016 - 1019 (2017/03/15)
A novel and efficient decarboxylative alkynylation of N-(acetoxy)phthalimides of α-amino acids with terminal alkynes has been developed by merging photoredox with copper catalysis at room temperature, and the reaction provided the valuable propargylamines in good to excellent yields with assistance of [Ru(bpy)3]Cl2/CuI and visible light. The simple protocol, mild reaction conditions, and high efficiency of this method make it an important strategy for synthesis of diverse molecules containing amino acid fragments.
Cu@furfural imine-decorated halloysite as an efficient heterogeneous catalyst for promoting ultrasonic-assisted A3 and KA2 coupling reactions: A combination of experimental and computational study
Sadjadi, Samahe,Hosseinnejad, Tayebeh,Malmir, Masoumeh,Heravi, Majid M.
, p. 13935 - 13951 (2017/11/27)
Halloysite nanoclays (HNTs) were functionalized with (3-chloropropyl) trimethoxysilan and subsequently reacted with thiosemicarbazide and furfural to furnish furfural imine functionalized HNTs, which could serve as an efficient support for immobilization
Well-defined dinuclear silver phosphine complexes based on nitrogen donor ligand and their high efficient catalysis for A3-coupling reaction
Chen, Jing-Jing,Gan, Zhi-Liang,Huang, Qi,Yi, Xiao-Yi
, p. 93 - 99 (2017/06/07)
Nitrogen donor ligands HL1, HL3, HL4 and their silver complexes 1·OTf–4·OTf are prepared and fully characterized. Treatment of HL1-HL4 with AgOTf (OTf??=?triflato) in presence of base Etsu
