Synthesis, structural characterization, theoretical studies and corrosion inhibition of a new pyrrole derivative:1-(1-benzyl-4-(4-chlorophenyl)-2,5-dimethyl-1H-pyrrol-3-yl)ethanone

Natural Hydroxyapatite: Green Catalyst for the Synthesis of Pyrroles, Inhibitors of Corrosion

“…ese results prove that this Journal of Chemistry method is extendable to a variety of nitroalkane compounds. e structures of products 1e and 1h were successfully confirmed by single-crystal X-ray crystallographic analysis [25,31].…”

“…ey are adsorbed onto the metal surface and prevent metal dissolution in aggressive media [24]. Lately, we investigated the corrosion inhibition of S300 steel in 1 M HCl using a pyrrole derivative [25].…”

Synthesis, spectral characterization, crystal structure and computational investigation of 2-formyl-6-methoxy-3-carbethoxy quinoline as potential SARS-CoV inhibitor

“…Density functional theory (DFT) is one of the popular computational chemistry techniques to understand the molecular structure and its application, which is growing quickly. It is a successful and promising approach in theoretical estimations such as total energy of the system, atomic charge, electric and magnetic properties, vibrational frequencies, atomization energies, ionization energies, and reaction pathways [ [31] , [32] , [33] , [34] , [35] , [36] ].…”

Experimental Study of Poly(1‐Acetamide‐3‐vinylimidazolium Bromide) as a Corrosion Inhibitor for N80 Carbon Steel in HCl

“…[3] In general, compounds containing N, O, S and P heteroatoms and/or π-electron conjugated functions are considered to be a great candidate for the anti-corrosive inhibitors, since such these functions make for the adsorption of inhibitors themselves on the metal surface mainly recurring to physical and/or chemical interactions. [4,5] In this regard, azole-type derivatives, such as imidazole, [6,7] pyrrole, [8] triazole, [9] pyrazole, [10] pyridine, [11] pyrimidine, [12] pyrazine, [13] and some Schiff and Mannich bases, [14,15] may perfectly fulfil the requirement for the chemical structure of inhibitors. Unfortunately, since many organic inhibitors are unhealthy and environ-mentally unfriendly, their use would result in a serious threat to human health and life, and the living environment, which motivates us to search for more suitable alternatives to overcome this challenge facing chemists.…”