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Synthesis, structural characterization and extraction studies of 17-, 18-, 19- and 20- membered N2O2-donor macrocyclic Schiff bases


Balić, Tomislav; Matasović, Brunislav; Marković, Berislav; Šter, Anamarija; Štivojević, Marija; Matković-Čalogović, Dubravka
Synthesis, structural characterization and extraction studies of 17-, 18-, 19- and 20- membered N2O2-donor macrocyclic Schiff bases // Journal of Inclusion Phenomena and Macrocyclic Chemistry, 3 (2016), 85; 217-226 doi:10.1007/s10847-016-0621-4 (međunarodna recenzija, članak, znanstveni)


Naslov
Synthesis, structural characterization and extraction studies of 17-, 18-, 19- and 20- membered N2O2-donor macrocyclic Schiff bases

Autori
Balić, Tomislav ; Matasović, Brunislav ; Marković, Berislav ; Šter, Anamarija ; Štivojević, Marija ; Matković-Čalogović, Dubravka

Izvornik
Journal of Inclusion Phenomena and Macrocyclic Chemistry (1338-3127) 3 (2016), 85; 217-226

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Schiff base macrocycles ; N2O2-donor ; Crystal and molecular structure ; Metal ion extraction

Sažetak
Two new macrocyclic Schiff bases m 3 and m 4 (m 3 = 1, 5-diaza-2, 4:7, 8:17, 18-tribenzo-9, 16- dioxa-cyclononadeca-1, 5-dien ; m 4 = 1, 5- diaza-2, 4:7, 8:18, 19- tribenzo-9, 17-dioxa- cycloeicosa-1, 5-dien) were synthesized by reactions of the appropriate dialdehyde and diamine. The compounds were characterized by means of FT-IR and NMR spectroscopy, TG/DSC and elemental analysis. The crystal and molecular structures were determined by the single crystal X-ray diffraction method. Both molecules are N2O2-donor macrocyclic Schiff bases with 19 and 20 atoms in their inner macrocyclic rings and of a similar molecular structure. A different crystal packing arrangement of the molecules is caused by the differences in macrocycle planarity. The extraction experiments of the aforementioned compounds were performed by using metallic picrate salts, and simultaneously for the previously synthesized 17- and 18- membered macrocyclic analogues (m 2 and m 1). The metal cation extractability was determined for m 1, m 2, m 3 and m 4 by UV–Vis spectrophotometry in order to find correlation of structural features and the extraction capabilities of the Schiff bases. The highest metal cation extraction percentage was determined for the Hg2+ ion in the case of the m 2 macrocycle.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove
Prirodoslovno-matematički fakultet, Zagreb,
Sveučilište u Osijeku - Odjel za kemiju

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • SCI-EXP, SSCI i/ili A&HCI


Uključenost u ostale bibliografske baze podataka:


  • CA Search (Chemical Abstracts)
  • GeoRef


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