{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T10:07:28Z","timestamp":1791972448549,"version":"4.3.4"},"reference-count":21,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Science Progress"],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:p>The synthesis and application of metal complexes of 2-(4-nitrophenyl)-1H-benzimidazole, a significant heterocyclic compound, are rooted in the formation of its mono Schiff base precursor, N-(4-nitrobenzyl) benzene-1,2-diamine. This precursor is synthesized via the condensation of o-phenylenediamine (OPD) with 4-nitrobenzaldehyde (NBA). The formation of the Schiff base involves the nucleophilic attack of OPD's amino groups on the carbonyl carbon of 4-nitrobenzaldehyde, resulting in an imine linkage essential for subsequent cyclization reactions. Cyclization of the mono Schiff base N-(4-nitrobenzyl) benzene-1,2-diamine (NBD) is a crucial step in forming the benzimidazole ring. This compound's significance lies in its structural and electronic properties, influenced by the electron-withdrawing nitro group, making it valuable in coordination chemistry, medicinal chemistry, and materials science. In coordination chemistry, metal complexes of 2-(4-nitrophenyl)-1H-benzimidazole (NBI) acts as a ligand, forming stable complexes with transition metals that exhibit enhanced catalytic activity. These metal complexes are essential for various catalytic processes, including organic transformations and polymerization reactions. In medicinal chemistry, the benzimidazole core is a common motif in biologically active compounds. The presence of the nitro group can modulate the biological activity, making derivatives of 2-(4-nitrophenyl)-1H-benzimidazole (NBI) promising candidates for antimicrobial, anticancer, and antiviral agents. Research has also highlighted the applications of Schiff bases and their metal complexes in various fields. Schiff bases serve as versatile intermediates in the synthesis of heterocyclic compounds, while their metal complexes are explored for their catalytic, antimicrobial, and anticancer properties. The synthesis of 2-(4-nitrophenyl)-1H-benzimidazole and its derivatives remains a topic of significant interest due to their potential in developing new materials and pharmaceuticals. The synthesis of metal complexes of 2-(4-nitrophenyl)-1H-benzimidazole from its Schiff base precursor is a critical process with wide-ranging applications in coordination chemistry, medicinal chemistry, and materials science. The optimization of reaction conditions and the exploration of the compound's properties continue to drive research in this area, highlighting its importance in both fundamental and applied sciences.<\/jats:p>","DOI":"10.1177\/00368504251323767","type":"journal-article","created":{"date-parts":[[2025,3,17]],"date-time":"2025-03-17T02:48:26Z","timestamp":1742179706000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":3,"title":["The synthesis and characterization of Various metal complexes of 2-(4-nitrophenyl)-1H-benzimidazole and its mono schiff base precursor"],"prefix":"10.1177","volume":"108","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9097-6741","authenticated-orcid":false,"given":"Zolt\u00e1n","family":"K\u00f6nt\u00f6s","sequence":"first","affiliation":[{"name":"IOI Investment Zrt., Budapest, Hungary"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M\u00e1t\u00e9","family":"Bartek","sequence":"additional","affiliation":[{"name":"Budapest University of Technology and Economics"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2025,3,16]]},"reference":[{"key":"e_1_3_3_2_2","first-page":"62","article-title":"Synthesis and biological activities of Schiff bases and their derivatives: a review of recent work","volume":"6","author":"Sarkar A","year":"2019","unstructured":"Sarkar A, et al. 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