Raymond Akong Akong , Helmar Görls , Joseph Anthony Orighomisan Woods , Blessing Ifeoma Nwadike , Abimbola Olumide Adekanmbi , Winfried Plass , Abiodun Omokehinde Eseola
{"title":"2-(1h -咪唑-2-基)苯胺配体及其钴配合物:邻氨基酚的合成、表征、抗菌活性和氧化偶联","authors":"Raymond Akong Akong , Helmar Görls , Joseph Anthony Orighomisan Woods , Blessing Ifeoma Nwadike , Abimbola Olumide Adekanmbi , Winfried Plass , Abiodun Omokehinde Eseola","doi":"10.1016/j.ica.2025.122716","DOIUrl":null,"url":null,"abstract":"<div><div>We report a family of imidazole based Schiff bases obtained by condensation of 2-(1<em>H</em>-imidazol-2-yl)aniline scaffolds with salicylaldehyde (<strong>HL</strong><sub><strong>1</strong></sub>, <strong>HL</strong><sub><strong>3</strong></sub> – <strong>HL</strong><sub><strong>5</strong></sub>) {<strong>HL</strong><sub><strong>1</strong></sub> = (<em>E</em>)-2-(((2-(4,5-diphenyl-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol; <strong>HL</strong><sub><strong>3</strong></sub> = (<em>E</em>)-2-(((2-(4,5-bis(4-methoxyphenyl)-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol; <strong>HL</strong><sub><strong>4</strong></sub> = (<em>E</em>)-2-(((2-(4,5-bis(4-methoxyphenyl)-1-methyl-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol; <strong>HL</strong><sub><strong>5</strong></sub> = (<em>E</em>)-2-(((2-(1,4,5-triphenyl-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol} and 2-pyridinecarboxaldehyde (<strong>L</strong><sub><strong>2</strong></sub> = (<em>E</em>)-2-(4,5-diphenyl-1<em>H</em>-imidazol-2-yl)-N-(pyridin-2-ylmethylene)aniline), as well as their homoleptic Co<sup>II</sup> (<strong>1</strong>, <strong>2</strong>–<strong>7</strong>) {<strong>1</strong> = [CoL<sub>1</sub>Cl]0.75H<sub>2</sub>O.0.5MeOH; <strong>2</strong> = [CoL<sub>1</sub>(OAc)]0.75H<sub>2</sub>O; <strong>3</strong> = [CoL<sub>2</sub>Cl<sub>2</sub>]; <strong>4</strong> = [CoL<sub>3</sub>Cl]1.5MeOH; <strong>5</strong> = [CoL<sub>3</sub>(OAc)]; <strong>6</strong> = [CoL<sub>4</sub>Cl]; <strong>7</strong> = [CoL<sub>5</sub>Cl]} and Co<sup>III</sup> (<strong>1v</strong> = [Co(L<sub>1</sub>)<sub>2</sub>]Cl.MeOH) complexes. The formulation of prepared compounds was determined by elemental analysis, NMR, MS, FT-IR, electronic absorption, magnetic susceptibility and single crystal X-ray analysis (<strong>1v</strong>, <strong>3</strong>, <strong>7</strong> and <strong>Co(I</strong><sub><strong>A4</strong></sub><strong>)Cl</strong><sub><strong>2</strong></sub>). In the imine complexes, the Co<img>N bond lengths are longer in the neutral ligand (<strong>3</strong>) than in the anionic ligands (<strong>1v</strong> and <strong>7</strong>) and suggests high spin (HS) state in <strong>3</strong> and <strong>7</strong> (Co-<em>N</em> > 2.0 Å) and low spin (LS) state in <strong>1v</strong> (Co-<em>N</em> < 2.0 Å). The compounds were tested against Gram (+) and Gram (−) bacteria and exhibited better activity than one of the control used (especially in the case of <em>K. pne</em> and <em>C. freundii</em>). The catalytic efficiency of the complexes depends on the nature of the counter ion deployed, subtle changes in the molecular scaffolds and geometry.</div></div>","PeriodicalId":13599,"journal":{"name":"Inorganica Chimica Acta","volume":"584 ","pages":"Article 122716"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"2-(1H-imidazol-2-yl)aniline bearing ligands and their cobalt complexes: Synthesis, characterisation, antimicrobial activity and oxidative coupling of o-aminophenol\",\"authors\":\"Raymond Akong Akong , Helmar Görls , Joseph Anthony Orighomisan Woods , Blessing Ifeoma Nwadike , Abimbola Olumide Adekanmbi , Winfried Plass , Abiodun Omokehinde Eseola\",\"doi\":\"10.1016/j.ica.2025.122716\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We report a family of imidazole based Schiff bases obtained by condensation of 2-(1<em>H</em>-imidazol-2-yl)aniline scaffolds with salicylaldehyde (<strong>HL</strong><sub><strong>1</strong></sub>, <strong>HL</strong><sub><strong>3</strong></sub> – <strong>HL</strong><sub><strong>5</strong></sub>) {<strong>HL</strong><sub><strong>1</strong></sub> = (<em>E</em>)-2-(((2-(4,5-diphenyl-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol; <strong>HL</strong><sub><strong>3</strong></sub> = (<em>E</em>)-2-(((2-(4,5-bis(4-methoxyphenyl)-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol; <strong>HL</strong><sub><strong>4</strong></sub> = (<em>E</em>)-2-(((2-(4,5-bis(4-methoxyphenyl)-1-methyl-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol; <strong>HL</strong><sub><strong>5</strong></sub> = (<em>E</em>)-2-(((2-(1,4,5-triphenyl-1<em>H</em>-imidazol-2-yl)phenyl)imino)methyl)phenol} and 2-pyridinecarboxaldehyde (<strong>L</strong><sub><strong>2</strong></sub> = (<em>E</em>)-2-(4,5-diphenyl-1<em>H</em>-imidazol-2-yl)-N-(pyridin-2-ylmethylene)aniline), as well as their homoleptic Co<sup>II</sup> (<strong>1</strong>, <strong>2</strong>–<strong>7</strong>) {<strong>1</strong> = [CoL<sub>1</sub>Cl]0.75H<sub>2</sub>O.0.5MeOH; <strong>2</strong> = [CoL<sub>1</sub>(OAc)]0.75H<sub>2</sub>O; <strong>3</strong> = [CoL<sub>2</sub>Cl<sub>2</sub>]; <strong>4</strong> = [CoL<sub>3</sub>Cl]1.5MeOH; <strong>5</strong> = [CoL<sub>3</sub>(OAc)]; <strong>6</strong> = [CoL<sub>4</sub>Cl]; <strong>7</strong> = [CoL<sub>5</sub>Cl]} and Co<sup>III</sup> (<strong>1v</strong> = [Co(L<sub>1</sub>)<sub>2</sub>]Cl.MeOH) complexes. The formulation of prepared compounds was determined by elemental analysis, NMR, MS, FT-IR, electronic absorption, magnetic susceptibility and single crystal X-ray analysis (<strong>1v</strong>, <strong>3</strong>, <strong>7</strong> and <strong>Co(I</strong><sub><strong>A4</strong></sub><strong>)Cl</strong><sub><strong>2</strong></sub>). In the imine complexes, the Co<img>N bond lengths are longer in the neutral ligand (<strong>3</strong>) than in the anionic ligands (<strong>1v</strong> and <strong>7</strong>) and suggests high spin (HS) state in <strong>3</strong> and <strong>7</strong> (Co-<em>N</em> > 2.0 Å) and low spin (LS) state in <strong>1v</strong> (Co-<em>N</em> < 2.0 Å). The compounds were tested against Gram (+) and Gram (−) bacteria and exhibited better activity than one of the control used (especially in the case of <em>K. pne</em> and <em>C. freundii</em>). The catalytic efficiency of the complexes depends on the nature of the counter ion deployed, subtle changes in the molecular scaffolds and geometry.</div></div>\",\"PeriodicalId\":13599,\"journal\":{\"name\":\"Inorganica Chimica Acta\",\"volume\":\"584 \",\"pages\":\"Article 122716\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganica Chimica Acta\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0020169325001823\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganica Chimica Acta","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0020169325001823","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
2-(1H-imidazol-2-yl)aniline bearing ligands and their cobalt complexes: Synthesis, characterisation, antimicrobial activity and oxidative coupling of o-aminophenol
We report a family of imidazole based Schiff bases obtained by condensation of 2-(1H-imidazol-2-yl)aniline scaffolds with salicylaldehyde (HL1, HL3 – HL5) {HL1 = (E)-2-(((2-(4,5-diphenyl-1H-imidazol-2-yl)phenyl)imino)methyl)phenol; HL3 = (E)-2-(((2-(4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl)phenyl)imino)methyl)phenol; HL4 = (E)-2-(((2-(4,5-bis(4-methoxyphenyl)-1-methyl-1H-imidazol-2-yl)phenyl)imino)methyl)phenol; HL5 = (E)-2-(((2-(1,4,5-triphenyl-1H-imidazol-2-yl)phenyl)imino)methyl)phenol} and 2-pyridinecarboxaldehyde (L2 = (E)-2-(4,5-diphenyl-1H-imidazol-2-yl)-N-(pyridin-2-ylmethylene)aniline), as well as their homoleptic CoII (1, 2–7) {1 = [CoL1Cl]0.75H2O.0.5MeOH; 2 = [CoL1(OAc)]0.75H2O; 3 = [CoL2Cl2]; 4 = [CoL3Cl]1.5MeOH; 5 = [CoL3(OAc)]; 6 = [CoL4Cl]; 7 = [CoL5Cl]} and CoIII (1v = [Co(L1)2]Cl.MeOH) complexes. The formulation of prepared compounds was determined by elemental analysis, NMR, MS, FT-IR, electronic absorption, magnetic susceptibility and single crystal X-ray analysis (1v, 3, 7 and Co(IA4)Cl2). In the imine complexes, the CoN bond lengths are longer in the neutral ligand (3) than in the anionic ligands (1v and 7) and suggests high spin (HS) state in 3 and 7 (Co-N > 2.0 Å) and low spin (LS) state in 1v (Co-N < 2.0 Å). The compounds were tested against Gram (+) and Gram (−) bacteria and exhibited better activity than one of the control used (especially in the case of K. pne and C. freundii). The catalytic efficiency of the complexes depends on the nature of the counter ion deployed, subtle changes in the molecular scaffolds and geometry.
期刊介绍:
Inorganica Chimica Acta is an established international forum for all aspects of advanced Inorganic Chemistry. Original papers of high scientific level and interest are published in the form of Articles and Reviews.
Topics covered include:
• chemistry of the main group elements and the d- and f-block metals, including the synthesis, characterization and reactivity of coordination, organometallic, biomimetic, supramolecular coordination compounds, including associated computational studies;
• synthesis, physico-chemical properties, applications of molecule-based nano-scaled clusters and nanomaterials designed using the principles of coordination chemistry, as well as coordination polymers (CPs), metal-organic frameworks (MOFs), metal-organic polyhedra (MPOs);
• reaction mechanisms and physico-chemical investigations computational studies of metalloenzymes and their models;
• applications of inorganic compounds, metallodrugs and molecule-based materials.
Papers composed primarily of structural reports will typically not be considered for publication.