2022
DOI: 10.1016/j.inoche.2022.109839
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8–Hydroxyquinoline is key to the development of corrosion inhibitors: An advanced review

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Cited by 36 publications
(8 citation statements)
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“…FMO analysis estimated the electron distribution in HOMO and LUMO areas. The resulting HOMOs of pistiphloroglucinyl, pistaciaphenyl ether, and naringenin organic compounds are represented in Figures c, c, and c, respectively. The results and discussion found are given below: The HOMO regions are mainly cited around C5–C11C12 for pistiphloroglucinyl ether, C2–C1, C7–C8–C10, and C6–C5 for pistaciaphenyl ether, and C13–C11C12 and C15–C10C14 for naringenin organic compounds. The electrons mainly occupied the HOMO regions, and as a result, the molecules are negatively charged. The energies of HOMO orbitals for the selected compounds are as follows: pistaciaphenyl ether > pistiphloroglucinyl ether > naringenin organic compound.…”
Section: Resultsmentioning
confidence: 99%
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“…FMO analysis estimated the electron distribution in HOMO and LUMO areas. The resulting HOMOs of pistiphloroglucinyl, pistaciaphenyl ether, and naringenin organic compounds are represented in Figures c, c, and c, respectively. The results and discussion found are given below: The HOMO regions are mainly cited around C5–C11C12 for pistiphloroglucinyl ether, C2–C1, C7–C8–C10, and C6–C5 for pistaciaphenyl ether, and C13–C11C12 and C15–C10C14 for naringenin organic compounds. The electrons mainly occupied the HOMO regions, and as a result, the molecules are negatively charged. The energies of HOMO orbitals for the selected compounds are as follows: pistaciaphenyl ether > pistiphloroglucinyl ether > naringenin organic compound.…”
Section: Resultsmentioning
confidence: 99%
“…FMO analysis estimated the electron distribution in HOMO and LUMO areas. 73 75 The resulting HOMOs of pistiphloroglucinyl, pistaciaphenyl ether, and naringenin organic compounds are represented in Figures 9 c, 10 c, and 11 c, respectively. The results and discussion found are given below: The HOMO regions are mainly cited around C5–C11=C12 for pistiphloroglucinyl ether, C2–C1, C7–C8–C10, and C6–C5 for pistaciaphenyl ether, and C13–C11=C12 and C15–C10=C14 for naringenin organic compounds.…”
Section: Resultsmentioning
confidence: 99%
“…Leveraging the nonbonding electrons of oxygen and nitrogen, 8-HQ coordinates strongly with metallic surfaces, which strongly inhibits corrosion. 25 Wei et al 2 investigated the fabrication of a ZIF-8 loaded with a corrosion inhibitor, 8-HQ, based on in situ host−guest nanoconfinement by a one-step process at ambient temperature. The results indicated that 8-HQ had an inhibition efficiency exceeding 91% to protect the aluminum alloy substrate against corrosion in the corrosive medium after 2 days.…”
Section: Introductionmentioning
confidence: 99%
“…8-Hydroxyquinoline (8HQ) and its derivatives are widely known for their various properties, such as anticancer, antimicrobial, antioxidant, and corrosion resistance. It has been implicated in many applications in medicinal, analytical separations, optoelectronics, and photoconduction in organic solar cells. In addition, it is frequently used as a precursor for synthesizing many essential compounds .…”
Section: Introductionmentioning
confidence: 99%