Matches in SemOpenAlex for { <https://semopenalex.org/work/W1973588093> ?p ?o ?g. }
Showing items 1 to 97 of
97
with 100 items per page.
- W1973588093 endingPage "89" @default.
- W1973588093 startingPage "71" @default.
- W1973588093 abstract "Abstract Some new substituted polyhydroxy azo–azomethine compounds were prepared by reaction of tris(hydroxymethyl)aminomethane with (E)-2-hydroxy-5-(phenyldiazenyl) benzaldehyde and its substituted derivatives. The structures of azo and azo–azomethine compounds were determined by IR, UV–vis, 1H NMR and 13C NMR spectroscopic techniques, and/or X-ray diffraction studies. According to IR spectra, all azo–azomethine compounds adopt keto form in solid state. UV–vis analysis has shown the presence of keto–enol tautomerism in solution for all azo–azomethine compounds, except that for nitro substituted derivative, enol form is dominantly favored in solution. At the same time, above mentioned derivative compounds were studied in vitro for their antimicrobial properties. Among the phenylazosalicylaldehyde series compound tested, 4-phenylazosalicylaldehyde, 4-(3-chlorophenylazo)salicylaldehyde, 4-(2-chlorophenylazo)salicylaldehyde, 4-(4-fluorophenylazo)salicylaldehyde, 4-(3-chlorophenylazo)salicylaldehyde and 4-(4-ethylphenylazo)salicylaldehyde showed a weak antimicrobial activity only against gram positive bacteria. On the contrary, phenylazosalicylaldehyde series compounds were reacted tris(hydroxmethyl)aminomethane, that exhibited a strong antimicrobial activity against gram positive bacteria, yeast and mould. Moreover, while the 2-{[1,3-dihydroxy-2-(hydroxymethyl)propan-2-ylimino]methyl}phenol did not show an inhibition on tested microorganism, the addition of phenyldiazine groups to 2-{[1,3-dihydroxy-2-(hydroxymethyl)propan-2-ylimino]methyl}phenol resulted in a strong increases in antimicrobial activity." @default.
- W1973588093 created "2016-06-24" @default.
- W1973588093 creator A5000937098 @default.
- W1973588093 creator A5012035433 @default.
- W1973588093 creator A5041642994 @default.
- W1973588093 creator A5043656228 @default.
- W1973588093 creator A5073984639 @default.
- W1973588093 date "2007-09-01" @default.
- W1973588093 modified "2023-10-13" @default.
- W1973588093 title "Some polyhydroxy azo–azomethine derivatives of salicylaldehyde: Synthesis, characterization, spectroscopic, molecular structure and antimicrobial activity studies" @default.
- W1973588093 cites W1972681950 @default.
- W1973588093 cites W1981774553 @default.
- W1973588093 cites W1981917374 @default.
- W1973588093 cites W1985175885 @default.
- W1973588093 cites W1987995101 @default.
- W1973588093 cites W1998920258 @default.
- W1973588093 cites W2021263908 @default.
- W1973588093 cites W2034831518 @default.
- W1973588093 cites W2035631358 @default.
- W1973588093 cites W2036584393 @default.
- W1973588093 cites W2037741149 @default.
- W1973588093 cites W2056570403 @default.
- W1973588093 cites W2056953217 @default.
- W1973588093 cites W2059020082 @default.
- W1973588093 cites W2065806773 @default.
- W1973588093 cites W2068046003 @default.
- W1973588093 cites W2071438556 @default.
- W1973588093 cites W2079952765 @default.
- W1973588093 cites W2082964719 @default.
- W1973588093 cites W2131426328 @default.
- W1973588093 cites W2154479689 @default.
- W1973588093 cites W2164618483 @default.
- W1973588093 cites W2327444149 @default.
- W1973588093 doi "https://doi.org/10.1016/j.molstruc.2006.11.025" @default.
- W1973588093 hasPublicationYear "2007" @default.
- W1973588093 type Work @default.
- W1973588093 sameAs 1973588093 @default.
- W1973588093 citedByCount "103" @default.
- W1973588093 countsByYear W19735880932012 @default.
- W1973588093 countsByYear W19735880932013 @default.
- W1973588093 countsByYear W19735880932014 @default.
- W1973588093 countsByYear W19735880932015 @default.
- W1973588093 countsByYear W19735880932016 @default.
- W1973588093 countsByYear W19735880932017 @default.
- W1973588093 countsByYear W19735880932018 @default.
- W1973588093 countsByYear W19735880932019 @default.
- W1973588093 countsByYear W19735880932020 @default.
- W1973588093 countsByYear W19735880932021 @default.
- W1973588093 countsByYear W19735880932022 @default.
- W1973588093 countsByYear W19735880932023 @default.
- W1973588093 crossrefType "journal-article" @default.
- W1973588093 hasAuthorship W1973588093A5000937098 @default.
- W1973588093 hasAuthorship W1973588093A5012035433 @default.
- W1973588093 hasAuthorship W1973588093A5041642994 @default.
- W1973588093 hasAuthorship W1973588093A5043656228 @default.
- W1973588093 hasAuthorship W1973588093A5073984639 @default.
- W1973588093 hasConcept C171250308 @default.
- W1973588093 hasConcept C178790620 @default.
- W1973588093 hasConcept C185592680 @default.
- W1973588093 hasConcept C188027245 @default.
- W1973588093 hasConcept C192562407 @default.
- W1973588093 hasConcept C21951064 @default.
- W1973588093 hasConcept C2776428424 @default.
- W1973588093 hasConcept C2779256853 @default.
- W1973588093 hasConcept C2780841128 @default.
- W1973588093 hasConcept C4937899 @default.
- W1973588093 hasConceptScore W1973588093C171250308 @default.
- W1973588093 hasConceptScore W1973588093C178790620 @default.
- W1973588093 hasConceptScore W1973588093C185592680 @default.
- W1973588093 hasConceptScore W1973588093C188027245 @default.
- W1973588093 hasConceptScore W1973588093C192562407 @default.
- W1973588093 hasConceptScore W1973588093C21951064 @default.
- W1973588093 hasConceptScore W1973588093C2776428424 @default.
- W1973588093 hasConceptScore W1973588093C2779256853 @default.
- W1973588093 hasConceptScore W1973588093C2780841128 @default.
- W1973588093 hasConceptScore W1973588093C4937899 @default.
- W1973588093 hasIssue "1-3" @default.
- W1973588093 hasLocation W19735880931 @default.
- W1973588093 hasOpenAccess W1973588093 @default.
- W1973588093 hasPrimaryLocation W19735880931 @default.
- W1973588093 hasRelatedWork W1986972138 @default.
- W1973588093 hasRelatedWork W2095212420 @default.
- W1973588093 hasRelatedWork W2327390624 @default.
- W1973588093 hasRelatedWork W2340043059 @default.
- W1973588093 hasRelatedWork W2367384385 @default.
- W1973588093 hasRelatedWork W2396822601 @default.
- W1973588093 hasRelatedWork W2407390358 @default.
- W1973588093 hasRelatedWork W2949587191 @default.
- W1973588093 hasRelatedWork W2952073341 @default.
- W1973588093 hasRelatedWork W2127552504 @default.
- W1973588093 hasVolume "840" @default.
- W1973588093 isParatext "false" @default.
- W1973588093 isRetracted "false" @default.
- W1973588093 magId "1973588093" @default.
- W1973588093 workType "article" @default.