1937
DOI: 10.1002/prac.19371490801
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Innere Komplexsalze der Aldimin‐ und Azoreihe

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Cited by 190 publications
(62 citation statements)
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“…Pfeiffer et al (6) have reported that the Schiff bases (2) derived from salicylaldehyde or substituted salicylaldehyde and m-aminophenol do not form metal complexes, and we have also verified this for copper(ll) and oxovanadium(IV) in our laboratory. It would be interesting to see whether the Schiff bases of type (3) derived from salicylaldehyde or substituted salicylaldehyde and 3-aminothiophenol will form metal complexes.…”
Section: Introductionsupporting
confidence: 79%
“…Pfeiffer et al (6) have reported that the Schiff bases (2) derived from salicylaldehyde or substituted salicylaldehyde and m-aminophenol do not form metal complexes, and we have also verified this for copper(ll) and oxovanadium(IV) in our laboratory. It would be interesting to see whether the Schiff bases of type (3) derived from salicylaldehyde or substituted salicylaldehyde and 3-aminothiophenol will form metal complexes.…”
Section: Introductionsupporting
confidence: 79%
“…The reagent H 2 SA 2 en and its copper(II), nickel(II), iron(III), and dioxouranium(VI) complexes were prepared as reported [35]. The reagent H 2 SA 2 en was prepared by simple condensation of salisylaldehyde with ethylenediamine in 2:1 molar ratio in ethanol.…”
Section: Chemicals and Equipmentsmentioning
confidence: 99%
“…1) has been exclusively studied as the complexing reagent for copper(II), nickel(II), palladium(II), platinum(II), iron(II), iron(III), cobalt(II), cobalt(III), manganese(II), oxovanadium(IV), oxochromium(V), dioxomolybdenum(VI), and dioxouranium(VI) [20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37]. The uranyl complex of H 2 SA 2 en was reported as early as 1937 [35]. Pasini et al [24] and El-Sonbati [37] have reported the nature of uranyl complex with tetradentate shiff bases including H 2 SA 2 en.…”
Section: Introductionmentioning
confidence: 99%
“…The ir spectra are consistent with the formation of H 4 L 1 and H 2 L 2 ligands. The vibrational assignments were aided by comparison with the vibrational frequencies of the related compounds, such as, the Schiff bases of salicylaldehyde [16,17]. The fundamental stretching mode of the azomethine moiety, m(-C=N-), is readily assigned by comparison with the infrared spectra of 4,6-diacetylresorcinol (DAR), o-aminophenol and ophenylenediamine.…”
Section: Schiff Base Ligandsmentioning
confidence: 99%