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Astron., 195, 10.18052\u002Fwww.scipress.com\u002FILCPA.39.195\nQikProp, Technical Information (2.1).\nRahaek, 1998, Circumdatins D, E, and F: further fungal benzodiazepine analogues from Aspergillus ochraceus, J. Nat. Prod., 62, 904, 10.1021\u002Fnp980495u\nRahaek, 1999, Circumdatin A, B, and C: three new benzodiazepine alkaloids isolated from a culture of the fungus aspergillus ochraceus, J. Org. Chem., 64, 1689, 10.1021\u002Fjo981536u\nSah, P.P., Peoples, S.A., 1954, Isonicotinyl hydrazones as antitubercular agents and derivatives for identification of aldehydes and ketones, J. Am. Pharm. Assoc. Am. Pharm. Assoc., 43, 513, 10.1002\u002Fjps.3030430902\nSelvam, 2011, Quinazoline marketed drugs – a review, Res. Pharm., 1, 1\nShah, 2016, Design, synthesis and characterization of quinoline–pyrimidine linked calix[4]arene scaffolds as anti-malarial agents, J. Incl. Phenom. Macrocycl. 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Chem. Int. Ed. Engl., 27, 1456, 10.1002\u002Fanie.198814561\nAlajarin, 2012, Recent Highlights in Ketenimine Chemistry, Eur. J. Org. Chem., 29, 5637, 10.1002\u002Fejoc.201200383\nAlajarin, 1996, Intramolecular [2 + 2] cycloaddition of ketenimines with imines, Tetrahedron Lett., 37, 8945, 10.1016\u002FS0040-4039(96)02054-0\nAumann, 1988, Keteniminkomplexe aus Carbenkomplexen und Isocyaniden – vielseitige Bausteine für Carbocyclen und N-Heterocyclen, Angew Chem., 100, 1512, 10.1002\u002Fange.19881001106\nAlajarin, 2000, Periselective intramolecular [4+2] cycloadditions of ketenimines: synthesis of pyrido[1,2-a] benzimidazoles, Tetrahedron Lett., 41, 7029, 10.1016\u002FS0040-4039(00)01197-7\nAriyaratne, 1963, Some ketenimine complexes of iron, J. Chem. Soc., 2976, 10.1039\u002Fjr9630002976\nAlajarin, 2012, Tandem [1,5]-H shift\u002F6p-electrocyclizations of ketenimines bearing 1,3-oxathiane units. Computational assessment of the experimental diastereoselection, Tetrahedron Lett., 68, 4672, 10.1016\u002Fj.tet.2012.04.021\nAnaraki-Ardakani, 2011, Three-component synthesis of dialkyl 2-(cyclohexyliminomethylene)-3-arylsulfonylamino succinate, J. Chem. Res., 35, 98, 10.3184\u002F174751911X12964930076881\nAsghari, 2013, One-pot synthesis of N-substituted 2,4-thiazolidinediones and computational investigation of the products, Monatsh. Chem., 144, 337, 10.1007\u002Fs00706-012-0815-4\nAlexander, 2017, Formation of Ketenimines via the Palladium-Catalyzed Decarboxylative π–Allylic Rearrangement of N-Alloc Ynamides, Org. Lett., 19, 5822, 10.1021\u002Facs.orglett.7b02780\nAlajarin, 2004, Imino-Ketenimines on an Ortho-Benzylic Scaffold. Nitrogen to Carbon [1,3] Shift of an Ortho-Functionalized Benzyl Group, Lett. Org. Chem., 1, 340, 10.2174\u002F1570178043400398\nBorrmann, 1968\nBeck, 1966, Über Metall-Stickoxid-Komplexe. XXI. Tricyanomethanido–Nitrosyl-Komplexe von Kobalt und Nickel, Z. Anorg. Allg. Chem., 344, 285, 10.1002\u002Fzaac.19663440508\nBeck, 1967, Pseudohalogeno—Metallverbindungen XVIII. Anionische (Tricyanomethanido)pentacarbonyl-Komplexe von Chrom, Molybdän und Wolfram, J. Organometal. Chem., 8, 547, 10.1016\u002FS0022-328X(00)83678-5\nBarker, 1972, Heterocycles from ketenimines. V. 2-Iminoazetidines through thermolysis, J. Heterocyclic Chem., 9, 1147, 10.1002\u002Fjhet.5570090535\nBayat, 2008, Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry, Synth. Commun., 38, 2567, 10.1080\u002F00397910802219213\nBissember, 2018, α-Cyanocarbanion complexes and their application in synthesis, J. Organomet. Chem., 869, 213, 10.1016\u002Fj.jorganchem.2018.04.010\nBendikov, 2005, An Unexpected Two-Group Migration Involving a Sulfonynamide to Nitrile Rearrangement. Mechanistic Studies of a Thermal N → C Tosyl Rearrangement, Org. Lett, 7, 783, 10.1021\u002Fol0477327\nCorey, 1995\nCheng, 2009, An Unprecedented Chemospecific and Stereoselective Tandem Nucleophilic Addition\u002FCycloaddition Reaction of Nucleophilic Carbenes with Ketenimines, J. Org. Chem., 74, 850, 10.1021\u002Fjo802289s\nCoffinier, 2011, A new multicomponent reaction for the synthesis of pyridines via cycloaddition of azadienes and ketenimines, Tetrahedron Lett., 52, 3023, 10.1016\u002Fj.tetlet.2011.04.007\nClarke, 1992, Relatively Stable N-Benzhydryl- and N-Benzyldiarylketene Imines and Their Conversion to Cyanodiarylmet hanes via an Isolable Radical, Org. Chem., 57, 362, 10.1021\u002Fjo00027a062\nDodd, 2018, Ketenimines Generated from Ynamides: Versatile Building Blocks for Nitrogen-Containing Scaffolds, Chem. Eur. J., 24, 2297, 10.1002\u002Fchem.201704689\nDijkstra, 1954, Imenes derived from methylsulphonyl-acetonitrile: (Properties of the sulphonyl group XLIII), Recl. Trav. Chim. Pays-Bas., 73, 575, 10.1002\u002Frecl.19540730710\nDenmark, 2012, Silyl Ketene Imines: Highly Versatile Nucleophiles for Catalytic, Asymmetric Synthesis, Angew. Chem. Int. Ed., 51, 9980, 10.1002\u002Fanie.201202139\nDomling, 2006, Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry, Chem. Rev., 106, 17, 10.1021\u002Fcr0505728\nDos Santos, 2017, Nef–Perkow–Mumm Cascade towards Imido Phosphate Derivatives, Synlett, 28, 2637, 10.1055\u002Fs-0036-1590856\nDwyer, 1999, An asymmetric oxazoline ketenimine rearrangement. Construction of chiral o -quaternary carbon ketones, Tetrahedron Lett., 40, 4765, 10.1016\u002FS0040-4039(99)00729-7\nDe Korver, 2010, A Divergent Mechanistic Course of Pd(0)-Catalyzed Aza-Claisen Rearrangement and Aza-Rautenstrauch-Type Cyclization of N-Allyl Ynamides, Org. Lett., 12, 1840, 10.1021\u002Fol100446p\nDe Korver, 2011, N-Allyl-N-sulfonyl Ynamides as Synthetic Precursors to Amidines and Vinylogous Amidines. An Unexpected N-to-C 1,3-Sulfonyl Shift in Nitrile Synthesis, J. Org. Chem, 76, 5092, 10.1021\u002Fjo200780x\nDoney, 1983, New Donors with Two-Electron Oxidation. Synthesis and Electrochemical Properties of Highly Conjugated Bis(4H-pyrans), Bis(4H-thiopyrans), and Bis(flavenes), J. Org. Chem., 4, 2757\nDekorver, 2010, A Divergent Mechanistic Course of Pd (0)-Catalyzed Aza-Claisen Rearrangement and Aza-Rautenstrauch-Type Cyclization of N-Allyl Ynamides, Org. Lett., 12, 1840, 10.1021\u002Fol100446p\nDekorver, 2012, Carbocyclization Cascades of Allyl Ketenimines via Aza-Claisen Rearrangements of N-Phosphoryl-N-allyl-ynamide, Org. Lett., 14, 1768, 10.1021\u002Fol300366e\nFalmagne, 1981, Cyclobutanone and Cyclobutenone Derivatives by Reaction of Tertiary Amides with Alkenes or Alkynes, Angew. Chem. Int., 20, 879, 10.1002\u002Fanie.198108791\nFedushkin, 2009, Magnesium (II) Complexes of the dpp-BIAN Radical-Anion: Synthesis, Molecular Structure, and Catalytic Activity in Lactide Polymerization, Eur. J. Inorg. Chem., 2009, 4995, 10.1002\u002Fejic.200900710\nGroult, 2017\nGambaryan, 1976, Fluorinated Ketenimines, Russ. Chem. Rev., 45, 630, 10.1070\u002FRC1976v045n07ABEH002698\nGuan, 2019, One-Pot Three-Component Synthesis of Pyrrolidin-2-ones via a Sequential Wittig\u002FNucleophilic Addition\u002FCyclization Reaction, Synth., 51, 2402, 10.1055\u002Fs-0037-1612279\nGrass, 2019, Ketenimine Formation Catalyzed by a High-Valent Cobalt Carbene in Bulky Alkoxide Ligand Environment, J. Organomet. Chem., 38, 962, 10.1021\u002Facs.organomet.8b00911\nGuérin, 2020, Synthesis and use of trifluoromethylthiolated ketenimines, Chem. Eur. J., 26, 14852, 10.1002\u002Fchem.202002723\nHaufe, 2019\nHiroi, 1985, Asymmetric Induction Reactions. I. Asymmetric [2, 3] Sigmatropic Rearrangements of Sulfur Ylides Derived from Chiral Ketenimines and Trimethylsulfonium YlideChem, Pharm. Bull., 33, 2331, 10.1248\u002Fcpb.33.2331\nHanessian, 2005, Synthetic Studies in the Intramolecular Carbocyclization of N-Acyloxyiminium Ions. Stereoelectronic and Steric Implications of Nucleophilic Alkene, Alkyne, and Allene Tethers, Org. Chem., 70, 5070, 10.1021\u002Fjo050326w\nInui, 2001, Control of C-C and C–N Bond Cleavage of 2H-Azirine by Means of the Excitation Wavelength: Studies in Matrices and in Solutions, Chem. Commun., 2001, 1036, 10.1039\u002Fb102384p\nIravani, 2003, Trimerization of Phenylacetonitrile. InMe3 as a Base for C-H Acidic Nitriles, Organometallics, 22, 4129, 10.1021\u002Fom0303956\nJochims, 1970, Ketenimines. Geometry and barriers to racemization, J. Am. Chem. Soc, 92, 5524, 10.1021\u002Fja00721a044\nJalli, 2015, One-pot four component synthesis of novel 3-furyl coumarin derivatives, J. Chem. Sci., 128, 217, 10.1007\u002Fs12039-015-1014-8\nJin, 2015, Hydroalumination of Ketenimines and Subsequent Reactions with Heterocumulenes: Synthesis of Unsaturated Amide Derivatives and 1,3-Diimines, J. Org. Chem., 80, 6062, 10.1021\u002Facs.joc.5b00466\nKirsch, 2004\nKrow, 1971, Synthesis and Reactions of Ketenimines, Angew. Chem. Ed, 10, 435, 10.1002\u002Fanie.197104351\nKim, 2011, Sulfonyl and Phosphoryl Azides: Going Further Beyond the Click Realm of Alkyl and Aryl Azides, Chem. Asian. J., 6, 2618, 10.1002\u002Fasia.201100340\nKaneti, 1982, Theoretical study of ketenimine: Geometry, electronic properties, force constants and barriers to inversion and rotation, J. Mol. Struct., 87, 205, 10.1016\u002F0166-1280(82)80054-7\nKaufman, 1970, Reaction of ethyl azidoformate with dimethyl- and diethylketen-N-(p-tolyl) imine, J. Org. Chem., 35, 4244, 10.1021\u002Fjo00837a011\nKatagiri, 2009, Preparations and reactions of 2-trifluoromethylketenimines, J. Fluor. Chem, 130, 714, 10.1016\u002Fj.jfluchem.2009.05.020\nKhlebnikov, 2003, Cascade Transformations of (2,2-Diaryl-3,3-dichloroaziridin-1-yl) acetates, Russ. J. Org. Chem, 39, 559, 10.1023\u002FA:1026068020111\nLu, 2012, The thriving chemistry of ketenimines. Chem. Soc. Rev. 41,5687–5705, Chem. Soc. Rev., 41, 5687, 10.1039\u002Fc2cs35159e\nLaouiti, 2014, Exploring the Anionic Reactivity of Ynimines, Useful Precursors of Metalated Ketenimines, Org. Lett., 16, 2252, 10.1021\u002Fol500749h\nLong, 2013, Efficient Aldol-Type Reaction of O-Protected α-Hydroxy Aldehydes and N-Trimethylsilyl Ketene Imines: Synthesis of β, γ-Dihydroxy-Nitriles, Eur. J. Org. Chem, 2013, 5127, 10.1002\u002Fejoc.201300430\nMoss, 1995, Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995), Pure. Appl. Chem., 67, 1307, 10.1351\u002Fpac199567081307\nMolina, 1991, Domino reactions. One-pot preparation of fluoreno[2,3,4-ij] isoquinoline derivatives from conjugated ketene imines, J. Org. Chem., 56, 4008, 10.1021\u002Fjo00012a039\nMarchand-Brynaert, 1972, Cycloadditions of keteneimmonium cations to olefins and dienes. New synthesis of four-membered rings, J. Am. Chem. Soc., 94, 2870, 10.1021\u002Fja00763a062\nMaity, 2018, Carbene Formation and Transfer at a Dinickel Active Site, J. Organomet. Chem., 37, 2437, 10.1021\u002Facs.organomet.8b00261\nNicolaou, 1996\nNicolaou, 2003\nNicolaou, 2000, The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century, Angew. Chem. Int. Ed., 39, 44, 10.1002\u002F(SICI)1521-3773(20000103)39:1\u003C44::AID-ANIE44>3.0.CO;2-L\nOrru, 2003, Recent Advances in Solution-Phase Multicomponent Methodology for the Synthesis of Heterocyclic Compounds, Synth., 10, 1471, 10.1055\u002Fs-2003-40507\nOsisioma, 2018, Wavelength-dependent photochemistry of 2-azidovinylbenzene and 2-phenyl-2H-azirine, J. Mol. Struct., 1172, 94, 10.1016\u002Fj.molstruc.2018.04.042\nPeng, 2015, C-terminal peptide extension via gas-phase ion\u002Fion reactions, Int. J. Mass Spectrom., 391, 17, 10.1016\u002Fj.ijms.2015.07.027\nPujol, 2017, A Nucleophilic Gold (III) Carbene Complex, Angew. Chem. Int. Ed., 56, 12264, 10.1002\u002Fanie.201706197\nQian, 2016, Palladium-Catalyzed Migratory Insertion of Isocyanides for Synthesis of C-Phosphonoketenimines, ACS Catal, 6, 4715, 10.1021\u002Facscatal.6b01253\nQiu, 2016, Ketenimines from Isocyanides and Allyl Carbonates: PalladiumCatalyzed Synthesis of β, γ-Unsaturated Amides and Tetrazoles, Angew. Chem., 128, 15603, 10.1002\u002Fange.201609034\nRautenstrauch, 1984, 2-Cyclopentenones from 1-ethynyl-2-propenyl acetates Org, Chem., 49, 950\nSimon, 1968, Stereochemistry of carbodiimides and ketenimines, Rev. Roum. Chim., 13, 381\nStaudinger, 1919, Uber neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine, Helv. Chim. Acta., 2, 635, 10.1002\u002Fhlca.19190020164\nStevens, 1953, Nitrogen Analogs of Ketenes. A New Method of Preparation, J. Am. Chem. Soc., 75, 657, 10.1021\u002Fja01099a043\nStevens, 1958, Nitrogen Analogs of Ketenes. V. Formation of the Peptide Bond, J. Am. Chem. Soc., 80, 4065, 10.1021\u002Fja01548a059\nStevens, 1964, Nitrogen Analogs of Ketenes. VI.1 Dehydration of Amides, Org. Chem., 29, 34, 10.1021\u002Fjo01024a007\nShi, 2005, Synthesis of 2-Cyclopentenones by Gold(I)-Catalyzed Rautenstrauch Rearrangement, J. Am. Chem. Soc., 127, 5802, 10.1021\u002Fja051689g\nSosa, 2008, Synthesis of Alkynyl Ethers and Low-Temperature Sigmatropic Rearrangement of Allyl and Benzyl Alkynyl Ethers, Org. Lett., 10, 5091, 10.1021\u002Fol802147h\nTlili, 2013, Formation of C-SCF3 Bonds through Direct TrifluoromethylthiolationAngew, Chem. Int., 52, 6818, 10.1002\u002Fanie.201301438\nToulgoat, 2014, Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept, Eur. J. Org. Chem., 2014, 2415, 10.1002\u002Fejoc.201301857\nWeragoda, 2017, Singlet Photoreactivity of 3-Methyl-2-phenyl-2H-azirine, J. Chem., 70, 413\nWolf, 1996, Novel Heterocumulenes: Bisiminopropadienes and Linear Ketenimines, Chem. Eur. J., 2, 1318, 10.1002\u002Fchem.19960021020\nWoodward, 1961, A NEW SYNTHESIS OF PEPTIDES, Am. Chem. Soc., 4, 1007, 10.1021\u002Fja01465a069\nWu, 2017, Trifluoroacetic Anhydride-Promoted Copper(I)-Catalyzed Interrupted Click Reaction: From 1,2,3-Triazoles to 3- Trifluoromethyl-Substituted 1,2,4-Triazinones, Angew. Chem Int., 56, 10476, 10.1002\u002Fanie.201705620\nWang, 2013, J. Org. Chem., 78, 6233, 10.1021\u002Fjo400960e\nXiong, 2021, One-Pot Synthesis of Polysubstituted Pyrroles via Sequential Ketenimine Formation\u002FAg(I)-Catalyzed Alkyne Cycloisomerisation Starting from Ylide Adducts, Chin. Chem. Lett., 39, 1553, 10.1002\u002Fcjoc.202000639\nYoo, 2009, Copper-Catalyzed Multicomponent Reactions: Securing a Catalytic Route to Ketenimine Intermediates and their Reactivities, Curr. Org. Chem., 13, 1766, 10.2174\u002F138527209789630497\nYoo, 2007, Copper-Catalyzed Synthesis of N-Sulfonyl-1,2,3-triazoles: Controlling SelectivityAngew, Chem. Int., 46, 1730, 10.1002\u002Fanie.200604241\nYavari, 2012, One-pot synthesis of 2,6-diamino-4-sulfonamidopyrimidines from sulfonyl azides, terminal alkynes and cyanoguanidine, Tetrahedron Lett., 53, 942, 10.1016\u002Fj.tetlet.2011.12.041\nYavari, 2012, Copper-catalyzed one-pot synthesis of tetrasubstituted pyrazoles from sulfonyl azides, terminal alkynes, and hydrazonoyl chloride, Tetrahedron Lett., 53, 1889, 10.1016\u002Fj.tetlet.2012.01.083\nYu, 2014, Synthesis of α, β-unsaturated amides and iminocoumarins from N, N-disulfonyl ynamides with aldehydes via the ketenimine intermediate, Org Biomol. Chem., 12, 3986, 10.1039\u002Fc4ob00513a\nZhu, J., Bienaymé, H., 2005. Multicomponent Reactions. France: Eds. Wiley: Weinheim.\nZhang, 2019, The Generation of Difluoroketenimine and Its Application in the Synthesis of α, α-Difluoro-β-amino Amides, Angew. Chem., 131, 5800, 10.1002\u002Fange.201901591\nZhang, 2014, Comparison of the Photochemistry of 3–Methyl-2-phenyl–2H–azirine and 2–Methyl-3-phenyl–2H–azirine, J. Org. Chem., 79, 653, 10.1021\u002Fjo402443w\nZhang, 2009, Synthesis of Amidines Using N-Allyl Ynamides. A Palladium-Catalyzed Allyl Transfer through an Ynamido-π-Allyl Complex, Org. 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J. Res. Phys. Chem. Chem. Phys., 230, 67\nAbdallah, 2014, Corrosion inhibition of aluminum in NaOH solutions using some bidentate azo dyes compounds and synergistic action with some metal ions, Int. J. Electrochem. Sci., 9, 4747, 10.1016\u002FS1452-3981(23)08129-4\nAbdallah, 2014, Influence of N-thiazolyl-2-cyanoacetamide derivatives on the corrosion of aluminum in 0.01 M sodium hydroxide, Prot. Metals Phys. Chem. Surf., 50, 659, 10.1134\u002FS2070205114050025\nAbdallah, 2016, Animal glue as green inhibitor for corrosion of aluminum and aluminum-silicon alloys in sodium hydroxide solutions, J. Mol. Liq., 220, 755, 10.1016\u002Fj.molliq.2016.04.062\nAbdallah, 2016, Gelatin as corrosion inhibitor for aluminum and aluminum silicon alloys in sodium hydroxide solutions, Prot. Metals Phys. Chem. Surf., 52, 140, 10.1134\u002FS2070205116010020\nAbdallah, 2012, Antihypertensive drugs as an inhibitors for corrosion of aluminum and aluminum silicon alloys in aqueous solutions, Arab. J. Chem., 5, 225, 10.1016\u002Fj.arabjc.2010.08.017\nAbdel-Gaber, 2010, Novel package for inhibition of aluminium corrosion in alkaline solutions, Mater. Chem. Phys., 124, 773, 10.1016\u002Fj.matchemphys.2010.07.059\nAbiola, 2010, Cocos nucifera L. water as green corrosion inhibitor for acid corrosion of aluminium in HCl solution, Chin. Chem. Lett., 21, 1449, 10.1016\u002Fj.cclet.2010.07.008\nAhmad, 2006\nAl-Juaid, 2007, Mono azo dyes compounds as corrosion inhibitors for dissolution of aluminium in sodium hydroxide solutions, Portugaliae Electrochim. Acta, 25, 363, 10.4152\u002Fpea.200703363\nAl-Rawashdeh, 2005, Cationic surfactant as corrosion inhibitor for aluminum in acidic and basic solutions, Anti-Corros. Meth. Mater., 52, 160, 10.1108\u002F00035590510595157\nAmin, 2009, Polyacrylic acid as a corrosion inhibitor for aluminium in weakly alkaline solutions. Part I: weight loss, polarization, impedance EFM and EDX studies, Corros. Sci., 51, 658, 10.1016\u002Fj.corsci.2008.12.008\nBalaskas, 2015, Effectiveness of 2-mercaptobenzothiazole, 8-hydroxyquinoline and benzotriazole as corrosion inhibitors on AA 2024-T3 assessed by electrochemical methods, Surf. Interface Anal., 47, 10.1002\u002Fsia.5810\nBalbo, 2013, Corrosion inhibition by anionic surfactants of AA2198 Li-containing aluminium alloy in chloride solutions, Corros. Sci., 73, 80, 10.1016\u002Fj.corsci.2013.03.027\nBanerjee, 2011, An electrochemical and quantum chemical investigation of some corrosion inhibitors on aluminium alloy in 0.6 M aqueous sodium chloride solution, Indian J. Chem. Technol., 18, 309\nBardal, 2004\nBeulah, 2012, A study of the use of 1-(4-hydroxyphenyl)-3-(2-hydroxyphenyl)-propenone as an inhibitor for the corrosion of aluminium in NaOH solution, Arch. Appl. Sci. Res., 4, 2012\nBoisier, 2010, Corrosion inhibition of 2024 aluminium alloy by sodium decanoate, Electrochim. Acta, 55, 6182, 10.1016\u002Fj.electacta.2009.10.080\nCatubig, 2014, The use of cerium and praseodymium mercaptoacetate as thiol-containing inhibitors for AA2024-T3, Corros. Sci., 81, 45, 10.1016\u002Fj.corsci.2013.12.001\nChaubey, 2016, Corrosion inhibition performance of different bark extracts on aluminium in alkaline solution, J. Assoc. Arab Univ. Basic Appl. Sci.\nCrotty, D., Girard, J., et al., 2008. Inhibiting Aluminum Corrosion with Mercapto-substituted Silanes, Google Patents.\nDavis, 1999\nDavis, 2000\nDhayabaran, 2004, Inhibition of corrosion of aluminium in presence of fluorescein in basic medium, Ionics, 10, 288, 10.1007\u002FBF02382831\nDomingues, 2003, Anodising of Al 2024-T3 in a modified sulphuric acid\u002Fboric acid bath for aeronautical applications, Corros. Sci., 45, 149, 10.1016\u002FS0010-938X(02)00082-3\nEdrah, 2010, Studies on thiourea derivatives as corrosion inhibitor for aluminum in sodium hydroxide solution, J. Appl. Sci. Res., 6, 1045\nEduok, 2013, Chemical and spectrophotometric studies of naphthol dye as an inhibitor for aluminium alloy corrosion in binary alkaline medium, Geosyst. Eng., 16, 146, 10.1080\u002F12269328.2013.803708\nEgan, 2013, Developments in electrode materials and electrolytes for aluminium–air batteries, J. Power Sources, 236, 293, 10.1016\u002Fj.jpowsour.2013.01.141\nEid, 2015, Corrosion inhibition of aluminum and aluminum silicon alloys in sodium hydroxide solutions by methyl cellulose, J. Mater. Environ. Sci., 6, 892\nEl-Shafei, 2004, The role of indole and its derivatives in the pitting corrosion of Al in neutral chloride solution, Corros. Sci., 46, 579, 10.1016\u002FS0010-938X(03)00067-2\nElango, 2009, Study on polyaniline-ZnO used as corrosion inhibitors of 57S aluminium in 2 M NaOH solution, Anti-Corros. Meth. Mater., 56, 266, 10.1108\u002F00035590910989561\nElango, 2010, Novel polymeric inhibitor for corrosion of 57S aluminium in 2M NaOH solutions, Anti-Corros. Meth. Mater., 57, 3, 10.1108\u002F00035591011009664\nFoster, K.E., Ciemiega, M.S., 2008. Paint Stripper with Corrosion Inhibitor for Aluminium, Google Patents.\nGarcia, 2013, Unravelling the corrosion inhibition mechanisms of bi-functional inhibitors by EIS and SEM–EDS, Corros. Sci., 69, 346, 10.1016\u002Fj.corsci.2012.12.018\nGarcía, 2010, The influence of pH on corrosion inhibitor selection for 2024–T3 aluminium alloy assessed by high-throughput multielectrode and potentiodynamic testing, Electrochim. Acta, 55, 2457, 10.1016\u002Fj.electacta.2009.12.013\nGarner, A., 2014. Corrosion Inhibitor Comprising Azole and Cellulose Nanocrystals, Google Patents.\nGarrigues, 1996, An investigation of the corrosion inhibition of pure aluminum in neutral and acidic chloride solutions, Electrochim. Acta, 41, 1209, 10.1016\u002F0013-4686(95)00472-6\nGerengi, 2012, Anticorrosive properties of Date palm (Phoenix dactylifera L.) fruit juice on 7075 type aluminum alloy in 3.5% NaCl solution, Ind. Eng. Chem. Res., 51, 12835, 10.1021\u002Fie301771u\nGolru, 2015, Effects of different surface cleaning procedures on the superficial morphology and the adhesive strength of epoxy coating on aluminium alloy 1050, Prog. Org. Coat., 87, 52, 10.1016\u002Fj.porgcoat.2015.05.005\nGolru, 2015, Morphological analysis and corrosion performance of zirconium based conversion coating on the aluminum alloy 1050, J. Ind. Eng. Chem., 24, 233, 10.1016\u002Fj.jiec.2014.09.036\nHakeem, 2014, Calcium gluconate as a corrosion inhibitor for aluminium, J. Eng., Comput. Appl. Sci., 3, 1\nHarvey, 2013, Cerium-based conversion coatings on aluminium alloys: a process review, Corros. Eng., Sci. Technol., 48, 248, 10.1179\u002F1743278213Y.0000000089\nHarvey, 2011, The effect of inhibitor structure on the corrosion of AA2024 and AA7075, Corros. Sci., 53, 2184, 10.1016\u002Fj.corsci.2011.02.040\nHill, 2011, Corrosion inhibition of 7000 series aluminium alloys with cerium diphenyl phosphate, J. Alloy. Compd., 509, 1683, 10.1016\u002Fj.jallcom.2010.09.151\nHo, 2006, Cerium dibutylphosphate as a corrosion inhibitor for AA2024-T3 aluminum alloys, J. Electrochem. Soc., 153, B392, 10.1149\u002F1.2217260\nHu, 2015, Cerium tartrate as a corrosion inhibitor for AA 2024–T3, Corros. Sci., 95, 152, 10.1016\u002Fj.corsci.2015.03.010\nJames, 2008, Aloe vera: an inhibitor of aluminium corrosion in hydrochloric acid solution, Int. J. Pure Appl. Chem., 3, 159\nJayalakshmi, 1997, Inhibitors for aluminium corrosion in aqueous medium, Corros. Rev., 15, 315, 10.1515\u002FCORRREV.1997.15.3-4.315\nJevremović, 2012, The inhibitive effect of ethanolamine on corrosion behavior of aluminium in NaCl solution saturated with CO2, Metall. Mater. Eng., 18, 241\nJung, I.N., Hwang, S.Y., et al., 1989. Antifreeze Corrosion Inhibitor Composition for Aluminum Engines and Radiators, Google Patents.\nKalaivani, 2013, Inhibition performance on the surface of aluminium in alkaline medium, Int. J. Chem Tech Res., 5, 1714\nKalaivani, 2013, Inhibitive nature of carboxymethylcellulose with Zn2+ ion, Chem. Sci. Trans., 2, 1352\nKaufman, 2000\nKumari, 2011, 3-ethyl-4-amino-5-mercapto-1,2,4-triazole as corrosion inhibitor for 6061-alloy in sodium hydroxide solution, Portugaliae Electrochim. Acta, 29, 445, 10.4152\u002Fpea.201106445\nKumari, 2011, 3-Methyl-4-amino-5-mercapto-1,2,4-triazole as corrosion inhibitor for 6061 Al alloy in 0.5 M sodium hydroxide solution, J. Coat. Technol. Res., 8, 685, 10.1007\u002Fs11998-011-9341-2\nLakshmi, 2013, The corrosion inhibition of aluminium in 3.5% NaCl by diisopropyl thiourea, Int. J. Chem Tech Res., 5, 1959\nLamaka, 2007, High effective organic corrosion inhibitors for 2024 aluminium alloy, Electrochim. Acta, 52, 7231, 10.1016\u002Fj.electacta.2007.05.058\nLewis, K.J,. Aklian, J., 1999. Non-chromate Corrosion Inhibitors for Aluminum Alloys, Google Patents.\nLi, 2007, Corrosion behavior of aluminum alloy 2024–T3 by 8-hydroxy-quinoline and its derivative in 3.5% chloride solution, Trans. Nonferr. Metals Soc. China, 17, 318, 10.1016\u002FS1003-6326(07)60092-2\nLi, 2011, Inhibition of tryptophan on AA 2024 in chloride-containing solutions, J. Mater. Eng. Perform., 20, 265, 10.1007\u002Fs11665-010-9680-7\nLiu, 2014, 8-Hydroxyquinoline as an effective corrosion inhibitor for 7075 aluminium alloy in 3.5% NaCl solution, Int. J. Electrochem. Sci., 9, 5574\nLiu, 2005, Corrosion resistance properties of organic–inorganic hybrid coatings on 2024 aluminum alloy, Appl. Surf. Sci., 246, 82, 10.1016\u002Fj.apsusc.2004.10.040\nLundvall, 2007, Copper modified chitosan for protection of AA-2024, Surf. Coat. Technol., 201, 5973, 10.1016\u002Fj.surfcoat.2006.11.005\nMa, 2013, Surface texture formed on AA2099 Al–Li–Cu alloy during alkaline etching, Corros. Sci., 66, 292, 10.1016\u002Fj.corsci.2012.09.032\nMaayta, 2006, Organic corrosion inhibitors for aluminium in sodium hydroxide, Asian J. Chem., 18, 566\nMarcelin, 2015, Synergistic effect between 8-hydroxyquinoline and benzotriazole for the corrosion protection of 2024 aluminium alloy: a local electrochemical impedance approach, Corros. Sci., 101, 66, 10.1016\u002Fj.corsci.2015.09.002\nMarkley, 2007, Corrosion protection of AA2024-T3 using rare earth diphenyl phosphates, Electrochim. Acta, 52, 4024, 10.1016\u002Fj.electacta.2006.11.028\nMcCafferty, 2010\nMontemor, 2016, Fostering green inhibitors for corrosion prevention, 107\nMoon, 1999, The formation and dissolution of anodic oxide films on pure aluminium in alkaline solution, Electrochim. Acta, 44, 2445, 10.1016\u002FS0013-4686(98)00368-5\nMukherjee, 1996, Complex behaviour of aluminium dissolution in alkaline aqueous 2-propanol solution, J. Power Sources, 58, 183, 10.1016\u002FS0378-7753(96)02388-9\nNa, 2006, Effect of sulphate and molybdate ions on pitting corrosion of aluminium by using electrochemical noise analysis, J. Electroanal. Chem., 596, 7, 10.1016\u002Fj.jelechem.2006.06.017\nNiknahad, 2010, The adhesion properties and corrosion performance of differently pretreated epoxy coatings on an aluminium alloy, Corros. Sci., 52, 1948, 10.1016\u002Fj.corsci.2010.02.014\nOguzie, 2009, Inhibiting effect of crystal violet dye on aluminum corrosion in acidic and alkaline media, Chem. Eng. Commun., 196, 591, 10.1080\u002F00986440802483848\nOguzie, 2006, Corrosion inhibition and adsorption behaviour of bismark brown dye on aluminium in sodium hydroxide solution, Mater. Lett., 60, 3376, 10.1016\u002Fj.matlet.2006.03.018\nOguzie, 2005, The inhibition of aluminium corrosion in potassium hydroxide by “Congo Red” dye, and synergistic action with halide ionsnull, Anti-Corros. Meth. Mater., 52, 293, 10.1108\u002F00035590510615794\nÖnal, 2000, Corrosion inhibition of aluminium alloys by tolyltriazole in chloride solutions, Anti-Corros. Meth. Mater., 47, 339, 10.1108\u002F00035590010354177\nPatil, 2014, Inhibition of corrosion of aluminum in potassium hydroxide solution by pyridine derivatives, ISRN Mater. Sci., 2014, 10.1155\u002F2014\u002F154285\nPopoola, 2013, Inhibitive action of ferrous gluconate on aluminum alloy in saline environment, Adv. Mater. Sci. Eng., 2013, 10.1155\u002F2013\u002F639071\nPrincey, 2012, Corrosion inhibition of aluminium using 3-hydroxy flavone in the presence of quarternary ammonium salts in NaOH medium, J. Kor. Chem. Soc., 56, 201, 10.5012\u002Fjkcs.2012.56.2.201\nPyun, 2000, Corrosion mechanism of pure aluminium in aqueous alkaline solution, J. Solid State Electrochem., 4, 267, 10.1007\u002Fs100080050203\nQafsaoui, 2009, Analysis of the inhibitive effect of BTAH on localized corrosion of Al 2024 from electrochemical noise measurements, J. Electrochem. Soc., 156, C67, 10.1149\u002F1.3040281\nQafsaoui, 2015, Effect of 1-pyrrolidine dithiocarbamate on the galvanic coupling resistance of intermetallics – aluminum matrix during corrosion of AA 2024–T3 in a dilute NaCl, Corros. Sci., 92, 245, 10.1016\u002Fj.corsci.2014.12.011\nRajendran, 2013, Inhibition of corrosion of aluminum in alkaline medium by glutaric acid in conjunction with zinc sulphate and diethylene triamine penta (methylene phosphonic acid), Arch. Appl. Sci. Res., 5, 202\nRajendran, 2012, Inhibition of corrosion of aluminium in alkaline medium by succinic acid in conjunction with zinc sulphate and diethylene triamine penta (Methylene phosphonic acid), J. Chem. Pharm. Res., 4, 4836\nRajendran, 2012, Study of synergistic effect of diethylene triamine penta (methylene phosphonic acid) and adipic acid on the inhibition of corrosion of alkaline aluminum, Der Chemica Sinica, 3, 1475\nRen, 2015, Experimental and theoretical studies of triisopropanolamine as an inhibitor for aluminum alloy in 3% NaCl solution, RSC Adv., 5, 101693, 10.1039\u002FC5RA21050J\nRevie, 2008\nRodič, 2016, Corrosion inhibition of pure aluminium and alloys AA2024-T3 and AA7075-T6 by cerium(III) and cerium(IV) salts, J. Electrochem. Soc., 163, C85, 10.1149\u002F2.0431603jes\nRosliza, 2010, Study on the effect of vanillin on the corrosion inhibition of aluminum alloy, J. Appl. Electrochem., 40, 833, 10.1007\u002Fs10800-009-0066-1\nRosliza, 2008, Electrochemical properties and corrosion inhibition of AA6061 in tropical seawater, Colloids Surf., A, 312, 185, 10.1016\u002Fj.colsurfa.2007.06.061\nSanthini, 2012, The inhibition effect of [3-(4-hydroxy-3-methoxy-phenyl)-1-(2-hydroxy-phenyl-propenone)] on the corrosion of the aluminium in alkaline medium, Arch. Appl. Sci. Res., 4, 2213\nShahrabi, 2008, Inhibition behaviour of 2-butine 1,4diol and tartrate salt, and their synergistic effects on corrosion of AA3003 aluminium alloy in 0.5% NaCl solution, J. Mater. Sci. Technol., 24, 427\nShao, 2003, The cooperative effect of calcium ions and tartrate ions on the corrosion inhibition of pure aluminum in an alkaline solution, Mater. Chem. Phys., 77, 305, 10.1016\u002FS0254-0584(02)00006-8\nSherif, 2011, Corrosion and corrosion inhibition of aluminum in Arabian Gulf seawater and sodium chloride solutions by 3-amino-5-mercapto-1,2,4-triazole, Int. J. Electrochem. Sci., 6, 1479\nSherif, 2012, Effects of 3-amino-1,2,4-triazole-5-thiol on the inhibition of pure aluminum corrosion in aerated stagnant 3.5 wt.% NaCl solution as a corrosion inhibitor, Int. J. Electrochem. Sci., 7, 4847\nSherif, 2013, Electrochemical investigations on the corrosion inhibition of aluminum by 3-amino-1,2,4-triazole-5-thiol in naturally aerated stagnant seawater, J. Ind. Eng. Chem., 19, 1884, 10.1016\u002Fj.jiec.2013.02.026\nSherif, 2005, Effects of 1,5-naphthalenediol on aluminum corrosion as corrosion inhibitor in 0.50 M NaCl, J. Electrochem. Soc., 152, B205, 10.1149\u002F1.1914752\nSherif, 2006, Effects of 1,4-naphthoquinone on aluminum corrosion in 0.50 M sodium chloride solutions, Electrochim. Acta, 51, 1313, 10.1016\u002Fj.electacta.2005.06.018\nShi, 2011, Corrosion protection of aluminium alloy 2024–T3 in 0.05 M NaCl by cerium cinnamate, Corros. Sci., 53, 2374, 10.1016\u002Fj.corsci.2011.03.012\nSinko, J., 2002. Corrosion Inhibitor Composition Applicable for Aluminum and Steel Protection and Procedure, Google Patents.\nSnihirova, 2016, Smart composite coatings for corrosion protection of aluminium alloys in aerospace applications, 85\nSnihirova, 2015, Comparison of the synergistic effects of inhibitor mixtures tailored for enhanced corrosion protection of bare and coated AA2024-T3, Surf. Coat. Technol.\nSoliman, 2011, Influence of 8-hydroxyquinoline addition on the corrosion behavior of commercial Al and Al-HO411 alloys in NaOH aqueous media, Corros. Sci., 53, 2994, 10.1016\u002Fj.corsci.2011.05.045\nSolmaz, 2008, Citric acid as natural corrosion inhibitor for aluminium protection, Corros. Eng., Sci. Technol., 43, 186, 10.1179\u002F174327807X214770\nUmoren, 2009, Synergistic effect of halide ions and polyethylene glycol on the corrosion inhibition of aluminium in alkaline medium, J. Appl. Polym. Sci., 113, 3533, 10.1002\u002Fapp.30258\nUmoren, 2007, Effect of halide ions on the corrosion inhibition of aluminium in alkaline medium using polyvinyl alcohol, J. Appl. Polym. Sci., 103, 2810, 10.1002\u002Fapp.25446\nVerma, 2015, Electrochemical, thermodynamic, surface and theoretical investigation of 2-aminobenzene-1,3-dicarbonitriles as green corrosion inhibitor for aluminum in 0.5 M NaOH, J. Mol. Liq., 209, 767, 10.1016\u002Fj.molliq.2015.06.039\nVrsalović, 2009, Application of phenolic acids in the corrosion protection of Al-0.8Mg alloy in chloride solution, Int. J. Electrochem. Sci., 4, 1568\nVrsalovic, 2007, Sinapinic acid as Al-2.5Mg alloy corrosion inhibitor in sodium chloride solution, J. Appl. Electrochem., 37, 325, 10.1007\u002Fs10800-006-9260-6\nWan Nik, 2013, Assessment of performance of sodium benzoate corrosion inhibitor performance on AA6063 in sea water, Biosci., Biotechnol. Res. Asia, 10, 637, 10.13005\u002Fbbra\u002F1175\nWang, 2016, Experimental and theoretical investigation on corrosion inhibition of AA5052 aluminium alloy by l-cysteine in alkaline solution, Mater. Chem. Phys., 169, 142, 10.1016\u002Fj.matchemphys.2015.11.041\nWang, 2015, Electrochemical and DFT studies of quinoline derivatives on corrosion inhibition of AA5052 aluminium alloy in NaCl solution, Appl. Surf. Sci., 357, 2176, 10.1016\u002Fj.apsusc.2015.09.206\nWinkler, 2016, Using high throughput experimental data and in silico models to discover alternatives to toxic chromate corrosion inhibitors, Corros. Sci., 106, 229, 10.1016\u002Fj.corsci.2016.02.008\nWinston Revie, 2011\nXhanari, 2016, Organic corrosion inhibitors for aluminium and its alloys in acid solutions: a review, RSC Adv., 6, 62833, 10.1039\u002FC6RA11818F\nYazdzad, 2008, Inhibition of 3003 aluminum alloy corrosion by propargyl alcohol and tartrate ion and their synergistic effects in 0.5% NaCl solution, Mater. Chem. Phys., 109, 199, 10.1016\u002Fj.matchemphys.2007.11.012\nYurt, 2005, Quantum chemical studies on inhibition effect of amino acids and hydroxy carboxylic acids on pitting corrosion of aluminium alloy 7075 in NaCl solution, J. Mol. Struct. (Thoechem), 725, 215, 10.1016\u002Fj.theochem.2005.01.048\nZheludkevich, 2005, Triazole and thiazole derivatives as corrosion inhibitors for AA2024 aluminium alloy, Corros. Sci., 47, 3368, 10.1016\u002Fj.corsci.2005.05.040\nZhou, 2015, Evolution of the corrosion process of AA 2024-T3 in an alkaline NaCl solution with sodium dodecylbenzenesulfonate and lanthanum chloride inhibitors, Appl. Surf. Sci., 357, 735, 10.1016\u002Fj.apsusc.2015.09.093\nZor, 2010, The inhibition effect of amides on aluminium corrosion in chloride solutions, Prot. Metals Phys. Chem. Surf., 46, 727, 10.1134\u002FS2070205110060171\nZor, 2014, Experimental and theoretical study of sulfathiazole as environmentally friendly inhibitor on aluminum corrosion in NaCl, Prot. Metals Phys. 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Pharm. Biomed. Anal., 17, 169, 10.1016\u002FS0731-7085(97)00211-2\nAnthony, 2004\nArranz, 1997, Analyst, 122, 849, 10.1039\u002Fa701210a\nAttia, 2012, Int. J. Curr. Pharm. Res., 4, 101\nBebawy, 2002, J. Pharm. Biomed. Anal., 27, 779, 10.1016\u002FS0731-7085(01)00523-4\nBritish Pharmacopoeia, 2011. Her Majesty's stationary office, London.\nCaira, 2004, J. Therm. Anal. Calorim., 77, 653, 10.1023\u002FB:JTAN.0000039001.05945.42\nCides, 2006, J. Therm. Anal. Calorim., 84, 441, 10.1007\u002Fs10973-005-7131-8\nCraig, 2007\nDe Betono, 1996, Anal. Chim. Acta, 329, 25, 10.1016\u002F0003-2670(96)00096-7\nEl-Ries, 2011, Insight Pharm. Sci., 1, 18, 10.5567\u002FIPHARMA-IK.2011.18.23\nEl-Ries, 2010, J. Drug Res., 31, 89\nFreitas, 2007, J. Therm. Anal. Calorim., 87, 905, 10.1007\u002Fs10973-006-7710-3\nGabbott, 2008\nHatakeyama, 1998\nJckman, 1991, J. Chromatogr. Biomed. Appl., 104, 234, 10.1016\u002F0378-4347(91)80129-Z\nLiu, 2010, J. Chromatogr., B, 878, 2415, 10.1016\u002Fj.jchromb.2010.07.027\nMacedo, 2002, J. Therm. Anal. Calorim., 67, 483, 10.1023\u002FA:1013901332759\nMathkar, 2009, J. Pharm. Biomed. Anal., 49, 627, 10.1016\u002Fj.jpba.2008.12.030\nOjha, 2003, J. Pharm. Biomed. Anal., 31, 775, 10.1016\u002FS0731-7085(02)00689-1\nOliveira, 2005, J. Therm. Anal. Calorim., 79, 267, 10.1007\u002Fs10973-005-0047-5\nOwens, 1997, J. Chromatogr., 9, 184\nOzgur, 1997, Pharmazie, 52, 561\nRadha, 2010, J. Pharm. Res., 3, 590\nStulzer, 2008, J. Therm. Anal. Calorim., 91, 323, 10.1007\u002Fs10973-006-7935-1\nSweetman, 2009\nWassel, 2011, J. Pharm. 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Phys. D Appl. Phys., 40, 7024, 10.1088\u002F0022-3727\u002F40\u002F22\u002F024\nAgrawal, 2008, New J. Phys., 10, 043023, 10.1088\u002F1367-2630\u002F10\u002F4\u002F043023\nAlbinson, 1993, Solid State Ionics, 60, 63, 10.1016\u002F0167-2738(93)90275-8\nAppetecchi, 2000, Electrochim. Acta, 45, 1481, 10.1016\u002FS0013-4686(99)00363-1\nAppetecchi, 2001, J. Power Sources, 1, 4335\nAppetecchi, 2003, J. Power Sources, 114, 105, 10.1016\u002FS0378-7753(02)00543-8\nBaril, 1997, Solid State Ionics, 97, 35, 10.1016\u002FS0167-2738(96)00614-5\nBhide, 2006, J. Power Source, 159, 1450, 10.1016\u002Fj.jpowsour.2005.11.096\nChandra, 2009, J. Phys. D Appl. Phys., 42, 135107, 10.1088\u002F0022-3727\u002F42\u002F13\u002F135107\nChandra, 2010\nChandra, 2010, Eur. Phys. J. Appl. Phys., 50, 21103, 10.1051\u002Fepjap\u002F2010035\nChandra, 2011, Indian J. Pure Appl. Phys., 49, 698\nChandra, 2012, Int. J. Chem., 1, 209\nChandra, 2013, Indian J. Pure Appl. Phys., 51, 44\nChandra, 1981\nChandra, 1988, Solid State Ionics, 28–30, 651, 10.1016\u002FS0167-2738(88)80119-X\nChoudhary, 2011, Indian J. Eng. Mater. Sci., 18, 147\nChoudhary, 2011, Indian J. Pure Appl. Phys., 49, 204\nChu, 2003, Solid State Ionics, 156, 141, 10.1016\u002FS0167-2738(02)00582-9\nCroce, 1998, Nature, 394, 456, 10.1038\u002F28818\nDey, 2008, Solid State Ionics, 178, 1963, 10.1016\u002Fj.ssi.2007.12.063\nDey, 2009, Solid State Commun., 149, 1282, 10.1016\u002Fj.ssc.2009.05.021\nDissanayak, 2004, Ionics, 10, 221, 10.1007\u002FBF02382820\nGray, 1991\nHashmi, 1995, Mater. Sci. Eng. B, 34, 18, 10.1016\u002F0921-5107(95)01219-2\nHu, 2007, J. Power Sources, 166, 226, 10.1016\u002Fj.jpowsour.2007.01.028\nKumar, 2007, J. Mater. Sci., 42, 5752, 10.1007\u002Fs10853-006-0743-y\nLaskar, 1989\nLakshmi, 2001, Phys. Stat. Sol. (a), 186, 395\nLakshmi, 2002, J. Mater. Sci., 37, 249, 10.1023\u002FA:1013683724965\nMahan, 1976\nMaier, 2000\nMaier, 2006, vol. 177\nMohan, 2006, Ionics, 12, 219, 10.1007\u002Fs11581-006-0035-1\nMohapatra, 2008, Ionics, 14, 255, 10.1007\u002Fs11581-007-0171-2\nQian, 2001, Electrochim. Acta, 46, 1829, 10.1016\u002FS0013-4686(00)00723-4\nShukla, 2009, Ionics, 15, 357, 10.1007\u002Fs11581-008-0275-3\nStephan, 2009, J. Phys. Chem. B, 113, 1963, 10.1021\u002Fjp808640j\nThakur, 2011, Ionics, 17, 109, 10.1007\u002Fs11581-010-0498-y\nVan Gool, 1973\nWieczorek, 1998, Phys. Chem. B, 102, 6968, 10.1021\u002Fjp981397k\nWen, 1996, J. Electroanal. 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Surf. Sci., 459, 788, 10.1016\u002Fj.apsusc.2018.08.063\nAsadi, 2021, Multifunctional hydrogels for wound healing: Special focus on biomacromolecular based hydrogels, Int. J. Biol. Macromol., 170, 728, 10.1016\u002Fj.ijbiomac.2020.12.202\nAshraf, 2021, Nanofibers of polycaprolactone containing hydroxyapatite doped with aluminum\u002Fvanadate ions for wound healing applications, New J. Chem., 45, 22610, 10.1039\u002FD1NJ03455C\nBao, 2020, Bioactive Self-Pumping Composite Wound Dressings with Micropore Array Modified Janus Membrane for Enhanced Diabetic Wound Healing, Adv. Funct. Mater., 30, 2005422, 10.1002\u002Fadfm.202005422\nBeladi, 2017, Cellular compatibility of nanocomposite scaffolds based on hydroxyapatite entrapped in cellulose network for bone repair, Mater. Sci. Eng., C, 75, 385, 10.1016\u002Fj.msec.2017.02.040\nBishop, 2003, Importance of moisture balance at the wound-dressing interface, Journal of wound care, 12, 125, 10.12968\u002Fjowc.2003.12.4.26484\nBraiman-Wiksman, 2007, Novel insights into wound healing sequence of events, Toxicologic pathology, 35, 767, 10.1080\u002F01926230701584189\nDlugosz, 1994, Protein kinase C regulates keratinocyte transglutaminase (TGK) gene expression in cultured primary mouse epidermal keratinocytes induced to terminally differentiate by calcium, J, Invest. Dermatol., 102, 409, 10.1111\u002F1523-1747.ep12372171\nDoozandeh, 2020, Preparation of novel Arabic gum-C6H9NO biopolymer as a bedsore for wound care application, Acta Medica Iranica, 520\nFarazin, 2021, A Review on Polymeric Wound Dress for the Treatment of Burns and Diabetic Wounds, International Journal of Basic Science in Medicine, 6, 44, 10.34172\u002Fijbsm.2021.08\nHan, 2009, A simple route to prepare stable hydroxyapatite nanoparticles suspension, J. Nanopart. Res., 11, 1235, 10.1007\u002Fs11051-008-9507-8\nHan, 2016, Interactive wound dressings, 39\nHosgood, 2006, Stages of wound healing and their clinical relevance, Veterinary Clinics: Small Animal Practice, 36, 667\nJunker, 2013, Clinical impact upon wound healing and inflammation in moist, wet, and dry environments, Advances in wound care, 2, 348, 10.1089\u002Fwound.2012.0412\nKawai, 2011, Calcium-based nanoparticles accelerate skin wound healing, PloS one, 6, e27106, 10.1371\u002Fjournal.pone.0027106\nKlein, 2018, Enhanced in vitro biocompatibility and water dispersibility of magnetite and cobalt ferrite nanoparticles employed as ROS formation enhancer in radiation cancer therapy, Small, 14, 1704111, 10.1002\u002Fsmll.201704111\nKulanthaivel, 2016, Cobalt doped proangiogenic hydroxyapatite for bone tissue engineering application, Mater. Sci. Eng., C, 58, 648, 10.1016\u002Fj.msec.2015.08.052\nLansdown, 2002, Calcium: a potential central regulator in wound healing in the skin, Wound repair and regeneration, 10, 271, 10.1046\u002Fj.1524-475X.2002.10502.x\nLee, 1998, Iontophoresis itself on hairless mouse skin induces the loss of the epidermal calcium gradient without skin barrier impairment, J, Invest. Dermatol., 111, 39, 10.1046\u002Fj.1523-1747.1998.00226.x\nLickmichand, 2019, In vitro biocompatibility and hyperthermia studies on synthesized cobalt ferrite nanoparticles encapsulated with polyethylene glycol for biomedical applications, Mater. Today:. Proc., 15, 252\nLowe, 2016, Preparation and characterization of chitosan-natural nano hydroxyapatite-fucoidan nanocomposites for bone tissue engineering, Int. J. Biol. Macromol., 93, 1479, 10.1016\u002Fj.ijbiomac.2016.02.054\nMaalej, 2014, Rhelogical, dermal wound healing and in vitro antioxidant properties of exopolysaccharide hydrogel from Pseudomonas stutzeri AS22, Colloids Surf. BBiointerfaces, 123, 814, 10.1016\u002Fj.colsurfb.2014.10.017\nMagee, 1987, Calcium-induced changes in cytoskeleton and motility of cultured human keratinocytes, Exp. Cell Res., 172, 43, 10.1016\u002F0014-4827(87)90091-7\nMaver, 2015, Functional wound dressing materials with highly tunable drug release properties, RSC Adv., 5, 77873, 10.1039\u002FC5RA11972C\nMohammadi, 2019, The effect of chrysin–curcumin-loaded nanofibres on the wound-healing process in male rats, Artif. Cells Nanomed. Biotechnol., 47, 1642, 10.1080\u002F21691401.2019.1594855\nRaisi, 2020, A soft tissue fabricated using a freeze-drying technique with carboxymethyl chitosan and nanoparticles for promoting effects on wound healing, Journal of Nanoanalysis, 7, 262\nRajalekshmy, 2021, Strontium ion cross-linked alginate-g-poly (PEGMA) xerogels for wound healing applications: in vitro studies, Carbohydr. Polym., 251\nRawat, 2016, Review on transdermal drug delivery system, Indo Am J Pharm Sci, 3, 423\nSaber-Samandari, 2018, The role of titanium dioxide on the morphology, microstructure, and bioactivity of grafted cellulose\u002Fhydroxyapatite nanocomposites for a potential application in bone repair, Int. J. Biol. Macromol., 106, 481, 10.1016\u002Fj.ijbiomac.2017.08.031\nStojanović, 2009, Hydrothermal synthesis of nanosized pure and cobalt-exchanged hydroxyapatite, Mater. Manuf. Processes, 24, 1096, 10.1080\u002F10426910903032113\nTrump, 1984, Cell calcium, cell injury and cell death, Environ. Health Perspect., 57, 281, 10.1289\u002Fehp.8457281\nUnnithan, 2012, Wound-dressing materials with antibacterial activity from electrospun polyurethane–dextran nanofiber mats containing ciprofloxacin HCl, Carbohydr. Polym., 90, 1786, 10.1016\u002Fj.carbpol.2012.07.071\nVenus, 2010, Basic physiology of the skin, Surgery (Oxford), 28, 469, 10.1016\u002Fj.mpsur.2010.07.011\nWeller, 2006, Wound dressings update, J. Pharm. Pract. Res., 36, 318, 10.1002\u002Fj.2055-2335.2006.tb00640.x\nWinter, 1963, Effect of air exposure and occlusion on experimental human skin wounds, Nature, 200, 378, 10.1038\u002F200378a0\nWuriantika, 2021, Nanostructure, porosity and tensile strength of PVA\u002FHydroxyapatite composite nanofiber for bone tissue engineering, Mater. Today:. Proc., 44, 3203\nYang, 2009, Synthesis and characterization of Eu-doped hydroxyapatite through a microwave assisted microemulsion process, Solid State Sci., 11, 1923, 10.1016\u002Fj.solidstatesciences.2009.07.013\nYusof, 2003, Flexible chitin films as potential wound-dressing materials: Wound model studies, Journal of Biomedical Materials Research Part A: An Official Journal of The Society for Biomaterials, The Japanese Society for Biomaterials, and The Australian Society for Biomaterials and the Korean Society for Biomaterials, 66, 224, 10.1002\u002Fjbm.a.10545\nZhou, 2017, Multifunctional and biomimetic fish collagen\u002Fbioactive glass nanofibers: Fabrication, antibacterial activity and inducing skin regeneration in vitro and in vivo, Int. J. 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Mater., 12, 1689, 10.1002\u002F1521-4095(200011)12:22\u003C1689::AID-ADMA1689>3.0.CO;2-9\nBao, 2007, Bifunctional Au-Fe3O4 nanoparticles for protein separation, ACS Nano., 1, 293, 10.1021\u002Fnn700189h\nChandran, 2006, Synthesis of gold nanotriangles and silver nanoparticles using Aloevera plant extract, Biotechnol. Prog., 22, 577, 10.1021\u002Fbp0501423\nDubey, 2010, Bioprospective of Sorbus aucuparia leaf extract in development of silver and gold nanocolloids, Colloids Surf., B, 80, 26, 10.1016\u002Fj.colsurfb.2010.05.024\nDwivedi, 2010, Biosynthesis of silver and gold nanoparticles using Chenopodium album leaf extract, Colloids Surf., A, 369, 27, 10.1016\u002Fj.colsurfa.2010.07.020\nElechiguerra, 2005, Interaction of silver nanoparticles with HIV-1, J. Nanobiotech., 3, 6, 10.1186\u002F1477-3155-3-6\nGardea-Torresdey, 2003, Alfalfa Sprouts: a natural source for the synthesis of silver nanoparticles, Langmuir, 13, 1357, 10.1021\u002Fla020835i\nGardea-Torresdey, 2002, Formation and growth of Au nanoparticles inside live Alfalfa plants, Nano Lett., 2, 397, 10.1021\u002Fnl015673+\nGils, 2010, Designing of silver nanoparticles in gum arabic based semi-IPN hydrogel, Int. J. Biol. Macromol., 46, 237, 10.1016\u002Fj.ijbiomac.2009.12.014\nHuang, 2008, Continuous-flow biosynthesis of silver nanoparticles by lixivium of sundried Cinnamomum camphora leaf in tubular microreactors, Ind. Eng. Chem. Res., 47, 6081, 10.1021\u002Fie701698e\nJaidev, 2010, Fungal mediated biosynthesis of silver nanoparticles, characterization and antimicrobial activity, Colloids Surf., B, 81, 430, 10.1016\u002Fj.colsurfb.2010.07.033\nJun, 2005, Nanoscale size effect of magnetic nanocrystals and their utilization for cancer diagnosis via magnetic resonance imaging, J. Am. Chem. Soc., 127, 5732, 10.1021\u002Fja0422155\nKaviya, 2011, Biosynthesis of silver nanoparticles using citrus sinensis peel extract and its antibacterial activity, Spectrochim. Acta A, 79, 594, 10.1016\u002Fj.saa.2011.03.040\nKhalil, M.M.H., Ismail, E.H., Magdoub, F.E., in press. Biosynthesis of Au nanoparticles using olive leaf extract. Arab. J. Chem.\nKonwarh, 2011, Biomimetic preparation of polymer-supported free radical scavenging, cytocompatible and antimicrobial green silver nanoparticles using aqueous extract of Citrus sinensis peel, Colloids Surf., B, 84, 338, 10.1016\u002Fj.colsurfb.2011.01.024\nMorones, 2005, The bactericidal effect of silver nanoparticles, Nanotechnology, 16, 2346, 10.1088\u002F0957-4484\u002F16\u002F10\u002F059\nPal, 2007, Does the antibacterial activity of silver nanoparticles depend on the shape of the nanoparticle? A study of the Gram-Negative bacterium Escherichia coli, Appl. Environ. Microbiol., 73, 1712, 10.1128\u002FAEM.02218-06\nPhilip, 2011, Extracellular biosynthesis of gold and silver nanoparticles using Krishna tulsi (Ocimum sanctum) leaf, Physica E, 43, 1318, 10.1016\u002Fj.physe.2010.10.006\nRajakumar, 2011, Larvicidal activity of synthesized silver nanoparticles using Eclipta prostrata leaf extract against filariasis and malaria vectors, Acta Trop., 118, 196, 10.1016\u002Fj.actatropica.2011.03.003\nRajesh, 2009, Phytosynthesis of silver nanoparticle using Gliricidia sepium (Jacq.), Curr. Nanosci., 5, 117, 10.2174\u002F157341309787314674\nRavel, 2002, Oxidation of iron in iron\u002Fgold core\u002Fshell nanoparticles, J. Appl. Phys., 91, 8195, 10.1063\u002F1.1453941\nRavindran, 2001, Black pepper, Piper nigrum medicinal and aromatic plants – industrial profiles, Phytochemistry, 58, 827, 10.1016\u002FS0031-9422(01)00241-2\nSatyavathi, 2010, Biosynthesis of silver nanoparticles using Coriandrum sativum leaf extract and their application in nonlinear optics, Adv. Sci. Lett., 3, 1\nShankar, 2003, Geranium leaf assisted biosynthesis of silver nanoparticles, Biotechnol. Prog., 19, 1627, 10.1021\u002Fbp034070w\nShankar, 2004, Rapid synthesis of Au, Ag, and bimetallic Au core–Ag shell nanoparticles using neem (Azadirachta indica) leaf broth, J. Colloid Interface Sci., 275, 496, 10.1016\u002Fj.jcis.2004.03.003\nShankar, 2004, Biological synthesis of triangular gold nanoprisms, Nature Mater., 3, 482, 10.1038\u002Fnmat1152\nSinha, 2009, Nanoparticles fabrication using ambient biological resources, J. Appl. Biosci., 19, 1113\nSong, 2009, Biological synthesis of gold nanoparticles using Magnolia kobus and Diopyros kaki leaf extracts, Process Biochem., 44, 1133, 10.1016\u002Fj.procbio.2009.06.005\nTsujino, 2007, Morphology of nanoholes formed in silicon by wet etching in solutions containing HF and H2O2 at different concentrations using silver nanoparticles as catalysts, Electrochim. Acta, 53, 28, 10.1016\u002Fj.electacta.2007.01.035\nZhang, 2006, Synthesis of Ag–Fe3O4 heterodimeric nanoparticles, J. 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Eng. Process. Process Intensif., 139, 1, 10.1016\u002Fj.cep.2019.03.012\nBarrett, 1989, Glancing angle EXAFS investigation of the habit modification of ADP by the incorporation of iron, J. Cryst. Growth., 94, 689, 10.1016\u002F0022-0248(89)90093-6\nBuffo, 2002, Modeling the rheology of concentrated beverage emulsions, J. Food Eng., 51, 267, 10.1016\u002FS0260-8774(01)00067-X\nCarpenter, 2016, Hydrodynamic cavitation: An emerging technology for the intensification of various chemical and physical processes in a chemical process industry, Rev. Chem. Eng., 33, 1\nCarpenter, 2017, Low pressure hydrodynamic cavitating device for producing highly stable oil in water emulsion: Effect of geometry and cavitation number, Chem. Eng. Process. Process Intensif., 116, 97, 10.1016\u002Fj.cep.2017.02.013\nDai, 2017, Liquid−liquid microextraction of Cu2+ from water using a new circle microchannel device, Ind. Eng. Chem. Res., 56, 12717, 10.1021\u002Facs.iecr.7b01888\nDavey, 1974, Growth of the 101 faces of ammonium dihydrogen phosphate crystals in the presence of ionic specie, J. Cryst. Growth., 23, 89, 10.1016\u002F0022-0248(74)90106-7\nDhanalakshmi, M., Parthiban, S., Swaminathan, M., 2020. Crystal growth and optical properties of ammonium dihydrogen phosphate (ADP) crystals doped with Fe(II) and Fe(III): Oxidation number effects. Mater. Today. P. 29 (4), 1119-1124. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.matpr.2020.05.200.\nEl-Bayaa, 2011, Purification of wet process phosphoric acid by decreasing iron and uranium using white silica sand, J. Hazard. Mater., 190, 324, 10.1016\u002Fj.jhazmat.2011.03.037\nFan, 2020, Gas-liquid-liquid flow patterns and extraction in a rotating microchannel extractor, Can. J. Chem. Eng., 99, S668\nFeng, 2016, Growth and highly efficient third harmonic generation of ammonium dihydrogen phosphate crystals, Rsc Adv., 6, 33983, 10.1039\u002FC6RA02283A\nGupta, 2014, Role of phosphate fertilizers in heavy metal uptake and detoxification of toxic metals, Chemosphere., 108, 134, 10.1016\u002Fj.chemosphere.2014.01.030\nJoshi, 2018, Effect of Sr2+ on growth and properties of ammonium dihydrogen phosphate single crystal, J. Mater. Sci-mater. El., 29, 5837, 10.1007\u002Fs10854-018-8556-8\nJoshi, 2020, Crystal growth, spectroscopic, second and third order nonlinear optical spectroscopic studies of L-phenylalanine doped ammonium dihydrogen phosphate single crystals, Arab. J. Chem., 13, 5018, 10.1016\u002Fj.arabjc.2020.01.024\nJoshi, 2019, Influence of l-serine on microstructural, spectroscopic, electrical and nonlinear optical performance of ammonium dihydrogen phosphate single crystal, J. Mater. Sci-mater. El., 30, 14243, 10.1007\u002Fs10854-019-01793-0\nJoshi, 2019, Crystal growth, A.C. electrical and nonlinear optical studies of pure and dl-methionine doped ammonium dihydrogen phosphate single crystals, J. Mater. Sci.-Mater. El., 30, 2985, 10.1007\u002Fs10854-018-00577-2\nJoshi, 2020, Effect of L-threonine on growth and properties of ammonium dihydrogen phosphate crystal, Arab. J. Chem., 13, 1532, 10.1016\u002Fj.arabjc.2017.12.005\nKong, 2018, In situ polymerization of furfuryl alcohol with ammonium dihydrogen phosphate in poplar wood for improved dimensional stability and flame retardancy, ACS Sustain. Chem. Eng., 6, 3349, 10.1021\u002Facssuschemeng.7b03518\nLampila, 2013, Applications and functions of food-grade phosphates, Ann. N.Y. Acad. Sci., 1301, 37, 10.1111\u002Fnyas.12230\nLee, 2015, Simultaneous treatment (cell disruption and lipid extraction) of wet microalgae using hydrodynamic cavitation for enhancing the lipid yield, Bioresour. Technol., 186, 246, 10.1016\u002Fj.biortech.2015.03.045\nLee, 2019, Design optimization of hydrodynamic cavitation for effectual lipid extraction from wet microalgae, J. Environ. Chem. Eng., 7, 10.1016\u002Fj.jece.2019.102942\nLi, 2020, Mass transfer process study of Fe(III) extraction from ammonium dihydrogen phosphate solution, J. Ser. Chem. Soc., 85, 1055, 10.2298\u002FJSC191017032L\nLo, 1983\nLuo, 2013, Extraction of Fe3+ from sodium dihydrogen phosphate with colloidal liquid aphrons, Ind. Eng. Chem. Res., 52, 4306, 10.1021\u002Fie3031899\nLuo, 2009, Study on Mg2+ removal from ammonium dihydrogen phosphate solution by predispersed solvent extraction, Ind. Eng. Chem. Res., 48, 2056, 10.1021\u002Fie801277t\nLuo, 2014, Study on Mg2+ removal from ammonium dihydrogen phosphate solution by an emulsion liquid membrane, Hem. Ind., 68, 341, 10.2298\u002FHEMIND130511058L\nLuo, 2011, Study on Mg2+ removal from ammonium dihydrogen phosphate solution by solvent extraction with di-2-ethylhexyl phosphoric acid, Korean J. Chem. Eng., 28, 1105, 10.1007\u002Fs11814-010-0468-0\nMaddikeri, 2014, Intensified synthesis of biodiesel using hydrodynamic cavitation reactors based on the interesterification of waste cooking oil, Fuel., 137, 285, 10.1016\u002Fj.fuel.2014.08.013\nMevada, 2019, Large scale microbial cell disruption using hydrodynamic cavitation: Energy saving options, Biochem. Eng. J., 143, 151, 10.1016\u002Fj.bej.2018.12.010\nMohammad, 1997, Extraction of Al(III) from phosphoric acid by HDDNSA, Sep. Sci. Technol., 12, 13\nOtu, 2001, Thermodynamics of the extraction of metal ions by dialkyl-substituted diphosphonic acids. II. The U(VI) and Sr(II) case, Solvent Extr. Ion Exc., 19, 1017, 10.1081\u002FSEI-100107617\nPanda, 2018, Sonochemical degradation of endocrine-disrupting organochlorine pesticide Dicofol: Investigations on the transformation pathways of dechlorination and the influencing operating parameters, Chemosphere., 204, 101, 10.1016\u002Fj.chemosphere.2018.04.014\nPanda, 2019, Hydrodynamic cavitation assisted degradation of persistent endocrine-disrupting organochlorine pesticide Dicofol: Optimization of operating parameters and investigations on the mechanism of intensification, Ultrason. Sonochem., 51, 526, 10.1016\u002Fj.ultsonch.2018.04.003\nPanda, 2020, Controlled hydrodynamic cavitation: A review of recent advances and perspectives for greener processing, Processes., 8, 220, 10.3390\u002Fpr8020220\nPetkovšek, 2013, Rotation generator of hydrodynamic cavitation for water treatment, Sep. Purifi. Technol., 118, 415, 10.1016\u002Fj.seppur.2013.07.029\nPreece, 2017, Intensification of protein extraction from soybean processing materials using hydrodynamic cavitation, Innov. Food Sci. Emerg. Technol., 41, 47, 10.1016\u002Fj.ifset.2017.01.002\nRajoriya, 2017, Degradation of reactive blue 13 using hydrodynamic cavitation: Effect of geometrical parameters and different oxidizing additives, Ultrason. Sonochem., 37, 192, 10.1016\u002Fj.ultsonch.2017.01.005\nRamisetty, 2014, Novel approach of producing oil in water emulsion using hydrodynamic cavitation reactor, Ind. Eng. Chem. Res., 53, 16508, 10.1021\u002Fie502753d\nSaxena, 2018, Enhanced synergistic degradation efficiency using hybrid hydrodynamic cavitation for treatment of tannery waste effluent, J. Clean. Prod., 198, 1406, 10.1016\u002Fj.jclepro.2018.07.135\nShah, 1999\nVanchinathan, 2012, Growth of cerium(III)-doped ADP crystals and characterization studies, J. Cryst. Growth., 354, 57, 10.1016\u002Fj.jcrysgro.2012.05.012\nVan de Voorde, 2005, Influence of acetate ions and the role of the diluents on the extraction of copper (II), nickel (II), cobalt (II), magnesium (II) and iron (II, III) with different types of extractants, Hydrometallurgy., 78, 92, 10.1016\u002Fj.hydromet.2005.02.008\nXue, D.F., Ratajczak, H., 2005. Effect of hydrogen bonds on physical properties of ammonium dihydrogenphosphate crystals. J. Mol. Struc.-theochem. 716 (1-3), 207-210. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.theochem.2004.11.026.\nYan, 2020, Study on mechanism of chitosan degradation with hydrodynamic cavitation, Ultrason. Sonochem., 64, 10.1016\u002Fj.ultsonch.2020.105046\nZhu, 2017, Preparation of porous hybrid adsorbents based on fluor(calcium silicate)\u002Factivated carbon and its application in the removal of iron (III) from ammonium phosphate solutions, Arab. J. 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2012, A three phase dispersive liquid-liquid microextraction tech nique for the extraction of antibiotics in milk, Microchim. Acta, 179, 179, 10.1007\u002Fs00604-012-0843-0\nArroyo-Manzanares, N., Lara, F. J., Airado-Rodríguez, D., Gámiz-Gracia, L. & A, A. G. 2015. Determination of sulfonamides in serum by on-line solid-phase extraction coupled to liquid chromatography with photoinduced fluorescence detection. Talanta 138, 258-262. doi:10.1016\u002Fj.talanta.2015.03.012.\nBenito-Peña, 2005, Development of a Novel and Automated Fluorescent Immunoassay for the Analysis of β-Lactam Antibiotics, J. Agric. Food. Chem., 53, 6635, 10.1021\u002Fjf0511502\nBenito-Peña, 2009, Quantitative determination of penicillin V and amoxicillin in feed samples by pressurised liquid extraction and liquid chromatography with ultraviolet detection, J. Pharm. Biomed. Anal., 49, 289, 10.1016\u002Fj.jpba.2008.11.016\nCasu, 2013, Can changes in renal function predict variations in β-lactam concentrations in septic patients?, Int. J. Antimicrob. Agents, 42, 422, 10.1016\u002Fj.ijantimicag.2013.06.021\nChatterjee, 2016, Multiresidue analysis of multiclass pesticides and polyaromatic hydrocarbons in fatty fish by gas chromatography tandem mass spectrometry and evaluation of matrix effect, Food Chem., 196, 1, 10.1016\u002Fj.foodchem.2015.09.014\nChen, 2017, Quantification of 16 β-lactams in chicken muscle by QuEChERS extraction and UPLC-Q-Orbitrap-MS with parallel reaction monitoring, Journal of Pharmaceutical and Biomedical Analysis, 145, 525, 10.1016\u002Fj.jpba.2017.07.019\nChina Food and Drug Administration. 2019. National Food Safety Standard–Maximum Residue Limits for Pesticides in Food,\nChun, 2005, Simultaneous Determination of the Novel Antithrombotic Agent, Acetylsalicylic Acid Maltol Ester (Aspalatone) and its Metabolites in Rat Plasma and Urine by HPLC, J. Liq. Chromatogr. Relat. Technol., 28, 2403, 10.1080\u002F10826070500187608\nCommission, E. 2010. COMMISSION DECISION (EU) No 37\u002F2010 of December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin.\nDasenaki, 2015, Multi-residue determination of 115 veterinary drugs and pharmaceutical residues in milk powder, butter, fish tissue and eggs using liquid chromatography–tandem mass spectrometry, Anal. Chim. Acta, 880, 103, 10.1016\u002Fj.aca.2015.04.013\nde Sousa, 2012, Evaluation of matrix effect on the GC response of eleven pesticides by PCA, Food Chem., 135, 179, 10.1016\u002Fj.foodchem.2012.04.063\nDorival-García, 2016, Simultaneous determination of quinolone and β-lactam residues in raw cow milk samples using ultrasound-assisted extraction and dispersive-SPE prior to UHPLC MS\u002FMS analysis, Food Control, 382–393\nFeledziak, 2013, An unprecedented reversible mode of action of β-lactams for the inhibition of human fatty acid amide hydrolase (hFAAH), Eur. J. Med. Chem., 60, 101, 10.1016\u002Fj.ejmech.2012.11.035\nGuedes, 2016, Matrix effect in guava multiresidue analysis by QuEChERS method and gas chromatography coupled to quadrupole mass spectrometry, Food Chem., 199, 380, 10.1016\u002Fj.foodchem.2015.12.007\nJank, 2012, β-lactam antibiotics residues analysis in bovine milk by LC-ESI-MS\u002FMS: a simple and fast liquid–liquid extraction method, Food Additives & Contaminants, 29, 497, 10.1080\u002F19440049.2011.604044\nKantiani, 2009, Analytical methodologies for the detection of β-lactam antibiotics in milk and feed samples, TrAC, Trends Anal. Chem., 28, 729, 10.1016\u002Fj.trac.2009.04.005\nKarageorgou, 2012, Ultrasound-assisted matrix solid phase dispersive extraction for the simultaneous analysis of β-lactams (four penicillins and eight cephalosporins) in milk by high performance liquid chromatography with photodiode array detection, J. Sep. Sci., 35, 2599, 10.1002\u002Fjssc.201200514\nKruve, 2008, Matrix effects in pesticide multi-residue analysis by liquid chromatography–mass spectrometry, J. Chromatogr. A, 1187, 58, 10.1016\u002Fj.chroma.2008.01.077\nLara, F. J., Olmo-Iruela, M. D., Cruces-Blanco, C., Quesada-Molina, C. & A, A. G. 2012. Advances in the determination of β-lactam antibiotics by liquid chromatography. Trac Trends in Analytical Chemistry 38. doi:10.1016\u002Fj.trac.2012.03.020.\nLi, 2018, Multiclass analysis of 25 veterinary drugs in milk by ultra-high performance liquid chromatography-tandem mass spectrometry, Food Chem., 257, 259, 10.1016\u002Fj.foodchem.2018.02.144\nLiu, 2014, Solid phase extraction using magnetic core mesoporous shell microspheres with C18-modified interior pore-walls for residue analysis of cephalosporins in milk by LC-MS\u002FMS, Food Chem., 150, 206, 10.1016\u002Fj.foodchem.2013.10.145\nLopes, 2012, Multiresidue determination of veterinary drugs in aquaculture fish samples by ultra high performance liquid chromatography coupled to tandem mass spectrometry, J. Chromatogr. B, 895–896, 39, 10.1016\u002Fj.jchromb.2012.03.011\nMacarov, 2012, Multi residue determination of the penicillins regulated by the European Union, in bovine, porcine and chicken muscle, by LC-MS\u002FMS, Food Chem., 135, 2612, 10.1016\u002Fj.foodchem.2012.06.126\nMoreno-González, 2017, Salting-out assisted liquid–liquid extraction coupled to ultra-high performance liquid chromatography–tandem mass spectrometry for the determination of tetracycline residues in infant foods, Food Chem., 221, 1763, 10.1016\u002Fj.foodchem.2016.10.107\nPrez-Burgos, 2012, Quechers methodologies as an alternative to solid phase extraction (SPE) for the determination and characterization of residues of cephalosporins in beef muscle using LC-MS\u002FMS, J. Chromatogr. B, 899, 57, 10.1016\u002Fj.jchromb.2012.05.002\nRezende, 2012, Optimisation and validation of a quantitative and confirmatory LC-MS method for multi-residue analyses of β-lactam and tetracycline antibiotics in bovine muscle, Food Additives & Contaminants: Part A, 29, 541, 10.1080\u002F19440049.2011.627883\nRuiz-Medina, 2012, Automated optosensor for the determination of carbaryl residues in vegetable edible oils and table olive extracts, J. Food Compos. Anal., 26, 66, 10.1016\u002Fj.jfca.2012.02.003\nSANTE. 2019. Guidance document on analytical quality control and method validation procedures for pesticides residues and analysis in food and feed (2019), from https:\u002F\u002Fwww.eurl-pesticides.eu\u002Fuserfiles\u002Ffile\u002FEurlALL\u002F AqcGuidance_SANTE_2019_12682.pdf.\nShendy, 2016, Development and validation of a modified QuEChERS protocol coupled to LC–MS\u002FMS for simultaneous determination of multi-class antibiotic residues in honey, Food Chem., 190, 982, 10.1016\u002Fj.foodchem.2015.06.048\nShin, 2018, Multi-residue Determination of Veterinary Drugs in Fishery Products Using Liquid Chromatography-Tandem Mass Spectrometry, Food Anal. Methods, 11, 1815, 10.1007\u002Fs12161-018-1179-0\nSouza, 2021, Development of a Methodology for the Simultaneous Analysis of Multiclass Contaminants in Milk, Food Anal. Methods, 14, 1075, 10.1007\u002Fs12161-020-01953-7\nTong, 2015, Comparison of resistance to third-generation cephalosporins in Shigella between Europe-America and Asia-Africa from 1998 to 2012, Epidemiol. Infect., 143, 2687, 10.1017\u002FS0950268814003446\nWang, 2021, Multi-class analysis of veterinary drugs in eggs using dispersive-solid phase extraction and ultra-high performance liquid chromatography-tandem mass spectrometry, Food Chem., 334, 10.1016\u002Fj.foodchem.2020.127598\nWang, 2015, Development of a Method for the Analysis of Multiclass Antibiotic Residues in Milk Using QuEChERS and Liquid Chromatography-Tandem Mass Spectrometry, Foodborne Pathogens and Disease, 12, 693, 10.1089\u002Ffpd.2014.1916\nYahaya, 2015, Dispersive Micro-Solid Phase Extraction Combined with High-Performance Liquid Chromatography for the Determination of Three Penicillins in Milk Samples, Food Anal. 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Acta A, 60, 271, 10.1016\u002FS1386-1425(03)00216-6\nAbdellattif, 2018, Int. J. Pharm. Sci. Res., 9, 1000\nAeschlach, 1994, Food Chem. Toxicol., 32, 31, 10.1016\u002F0278-6915(84)90033-4\nAlthagafi, 2019, Molecules, 24, 1741, 10.3390\u002Fmolecules24091741\nAvaji, 2009, Eur. J. Med. Chem., 44, 3552, 10.1016\u002Fj.ejmech.2009.03.032\nChristensen, 1971, Science, 174, 459, 10.1126\u002Fscience.174.4008.459\nCoats, 1964, Nature, 201, 68, 10.1038\u002F201068a0\nCovington, 1973\nda Gonçalves, 2014, J. Biomol. Struct. Dyn., 32, 301, 10.1080\u002F07391102.2013.765361\nDe Lima, 2017, J. Biomol. Struct. Dyn., 35, 1272, 10.1080\u002F07391102.2016.1178173\nDenizot, 1986, J. Immunol. Methods, 22, 271, 10.1016\u002F0022-1759(86)90368-6\nEl-Dossoki, 2008, J. Mol. Liquids, 142, 53, 10.1016\u002Fj.molliq.2008.04.013\nEl-Metwaly, 2019, J. Inorg. Organometal. Polym. Mater., 30, 907, 10.1007\u002Fs10904-019-01233-w\nEl-Metwaly, 2019, Appl. Organometal Chem., e5095, 10.1002\u002Faoc.5095\nEl-Shishtawi, 2010, J. Chem. Eng. Data, 55, 5422, 10.1021\u002Fje100534s\nFekri, 2014, Spectrochimi. Acta Part A, 132, 846, 10.1016\u002Fj.saa.2014.05.062\nFilippovic, 2009, Inorg. Chim. Acta, 362, 1996, 10.1016\u002Fj.ica.2008.09.019\nFrisch, M.J., Trucks, G.W., Pople, J.A., 2009. Gaussian 09, Revision B.2, Gaussian, Inc., Pittsburgh, PA.\nFrost, 1961\nGoodin, 1993, Biochemistry, 32, 3313, 10.1021\u002Fbi00064a014\nGrzybkowski, 1980, Electrochimica. Acta, 25, 279, 10.1016\u002F0013-4686(80)90006-7\nHamada, 2009, South Braz. J. Chem., 17, 33\nHawkey, 1994, 181\nHehre, 1986\nHorowitz, 1963, Anal. Chem., 25, 1464, 10.1021\u002Fac60203a013\nJohari, 1988, J. Indian Chem. Soc., 65, 793\nKhalifa, 1995, Anal. Fr., 23, 453\nKhan, 2013, Inorg. Chem. Commun., 35, 104, 10.1016\u002Fj.inoche.2013.06.014\nKostova, 2013, Curr. Med. Chem., 20, 4609, 10.2174\u002F09298673113209990149\nKuca, 2018, BMC Pharmacol. Toxicol., 19, 8, 10.1186\u002Fs40360-018-0196-3\nLever, 1968\nLima, 2008, Eur. J. Med. Chem., 43, 348, 10.1016\u002Fj.ejmech.2007.03.032\nMadhankumar, 2019, J. Mol. Struc., 1181, 118, 10.1016\u002Fj.molstruc.2018.12.048\nMadrakian, 2007, Talanta, 71, 610, 10.1016\u002Fj.talanta.2006.05.002\nMauceri, 1998, Nature, 394, 287, 10.1038\u002F28412\nMomma, 2011, J. Appl. Crystallogr., 44, 1272, 10.1107\u002FS0021889811038970\nMosmann, 1983, J. Immunol. Methods, 65, 55, 10.1016\u002F0022-1759(83)90303-4\nNagar, 1990, J. Inorg. Biochem., 40, 349, 10.1016\u002F0162-0134(90)80069-A\nNarang, 1996, Trans. Met. Chem., 21, 507, 10.1007\u002FBF00229701\nÖzmen, 2009, Spectrochim. Acta Part A, 70, 641, 10.1016\u002Fj.saa.2007.08.012\nPanchal, 2005, Toxicol. Environ. Chem., 87, 313, 10.1080\u002F02772240500126911\nRahmi-Nasrabadi, 2009, J. Mol. Liquids, 144, 97, 10.1016\u002Fj.molliq.2008.10.012\nRakha, 1996, Synth. React. Inorg. Met.-Org. Chem., 26, 1705, 10.1080\u002F00945719608004402\nSeleem, 2009, Spectrochim. Acta Part A, 74, 869, 10.1016\u002Fj.saa.2009.08.024\nSeth, 2011, Cryst. Eng. Comm., 13, 4528, 10.1039\u002Fc1ce05037k\nShaaban, 2018, Bioorg. Chem., 80, 43, 10.1016\u002Fj.bioorg.2018.05.019\nShoukry, 2008, Spectrochim. Acta Part A, 70, 686, 10.1016\u002Fj.saa.2007.08.022\nSingh, 2008, Spectrochim. Acta Part A, 71, 17, 10.1016\u002Fj.saa.2007.11.004\nSkovsen, 2010, Inorg. Chem., 49, 9343, 10.1021\u002Fic100990a\nTanak, 2011, Bull. Korean Chem. Soc., 32, 673, 10.5012\u002Fbkcs.2011.32.2.673\nTekeda, 1983, Bull. Chem. Soc. Jpn, 56, 3600, 10.1246\u002Fbcsj.56.3600\nThimmaiah, 1984, Polyhedron, 3, 1237, 10.1016\u002FS0277-5387(00)84669-0\nTurner, 2011, Cryst. Eng. Comm., 13, 1804, 10.1039\u002FC0CE00683A\nVogel, 1989\nde Willian, E.A., Ander, F.P., Alexandre, A. de C., Elaine, F.F. da C., Teodorico, C.R., 2016. Lett. Drug Des. Discov. 13(5), 360.\nYousef, 2011, J. Med. Med. Sci., 3, 37\nYusuff, 1990, Thermochim. Acta, 159, 357, 10.1016\u002F0040-6031(90)80121-E\nZaky, 2015, J. Mol. Struct., 1079, 203, 10.1016\u002Fj.molstruc.2014.09.033\nZaky, R.R., 2011. Phosphorus Sulfer Silicon and Related Elements, 186, 365.\nZang, 2010, Inorg. Chim. 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