Transition metal-mediated hydrolysis of the imine bond in 2-azomethine benzothiazoles

Crosbi ID324062
Bib IRB ID1264951
Year2022
StatusObjavljeno
Typeprilog u časopisu
Subtypeizvorni znanstveni rad
AuthorsRep Kaulić, Valentina ; Pantalon Juraj, Natalija ; Perić, Berislav ; Štefanić, Zoran ; Kirin, Srećko I. ; Raić-Malić, Silvana
JournalCroatica chemica acta
Volume95
Issue4
Pagesstr. 123-130
DOI10.5562/cca3907
ISSN0011-1643
EISSN1334-417X
Titles

en original Transition metal-mediated hydrolysis of the imine bond in 2-azomethine benzothiazoles

Abstracts
en original

An ultrasound-assisted synthesis has been used for the preparation of novel benzothiazole Schiff bases (1–3) as ligands for Zn(II) and Cu(II) metal complexes. In this class of Schiff base ligands, the isolated complexes 1a and 2a appear to be the only ones that have structures which include both the Schiff base ligand and the hydrolysis product 2-aminobenzothiazole in the same complex molecule. The aldehydes formed by Schiff base hydrolysis formed a rare example of a trans isomer in pentacoordinated 2, 4-disubstituted benzaldehyde complexes.

Keywords

en original ultrasound-assisted synthesis ; Schiff base ; hydrolytic cleavage ; metal complexes

Authors
Institutions
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Citations
Rep Kaulić, Valentina ; Pantalon Juraj, Natalija ; Perić, Berislav ; Štefanić, Zoran ; Kirin, Srećko I. ; Raić-Malić, Silvana
Transition metal-mediated hydrolysis of the imine bond in 2-azomethine benzothiazoles // Croatica chemica acta, 95 (2022), 4; 123-130. doi: 10.5562/cca3907
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