Please use this identifier to cite or link to this item:
https://biore.bio.bg.ac.rs/handle/123456789/841
DC Field | Value | Language |
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dc.contributor.author | Alimmari, Adel | en_US |
dc.contributor.author | Mijin, Dušan | en_US |
dc.contributor.author | Vukićević, Radovan | en_US |
dc.contributor.author | Božić, Bojan | en_US |
dc.contributor.author | Valentić, Nataša | en_US |
dc.contributor.author | Vitnik, Vesna | en_US |
dc.contributor.author | Vitnik, Željko | en_US |
dc.contributor.author | Ušćumlić, Gordana | en_US |
dc.date.accessioned | 2019-07-13T22:16:45Z | - |
dc.date.available | 2019-07-13T22:16:45Z | - |
dc.date.issued | 2012-07-23 | - |
dc.identifier.uri | https://biore.bio.bg.ac.rs/handle/123456789/841 | - |
dc.description.abstract | Background: A series of some novel arylazo pyridone dyes was synthesized from the corresponding diazonium salt and 6-hydroxy-4-phenyl-3-cyano-2-pyridone using a classical reaction for the synthesis of the azo compounds.Results: The structure of the dyes was confirmed by UV-vis, FT-IR, 1 H NMR and 13 C NMR spectroscopic techniques and elemental analysis. The solvatochromic behavior of the dyes was evaluated with respect to their visible absorption properties in various solvents.Conclusions: The azo-hydrazone tautomeric equilibration was found to depend on the substituents as well as on the solvent. The geometry data of the investigated dyes were obtained using DFT quantum-chemical calculations. The obtained calculational results are in very good agreement with the experimental data. © 2012 Alimmari et al.; licensee Chemistry Central Ltd. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Chemistry Central Journal | en_US |
dc.subject | Arylazo pyridone dyes | en_US |
dc.subject | DFT caculation | en_US |
dc.subject | Solvent effect | en_US |
dc.subject | Substituent effect | en_US |
dc.subject | Tautomerism | en_US |
dc.title | Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl-3-cyano-2-pyridone dyes | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1186/1752-153X-6-71 | - |
dc.identifier.pmid | 22824496 | - |
dc.identifier.scopus | 2-s2.0-84873927057 | - |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/84873927057 | - |
dc.description.rank | M21 | en_US |
dc.description.startpage | 71 | en_US |
dc.description.volume | 6 | en_US |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.fulltext | With Fulltext | - |
item.grantfulltext | restricted | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | Chair of General Physiology and Biophysics | - |
crisitem.author.orcid | 0000-0001-9910-2741 | - |
Appears in Collections: | Journal Article |
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33 Synthesis, structure and solvatochromic properties of some novel 5-arylazo-6-hydroxy-4-phenyl.pdf | 746.99 kB | Adobe PDF | Request a copy |
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