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Transition Metal-Mediated Hydrolysis of the Imine Bond in 2-Azomethine Benzothiazoles (CROSBI ID 324062)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

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

Podaci o odgovornosti

Rep Kaulić, Valentina ; Pantalon Juraj, Natalija ; Perić, Berislav ; Štefanić, Zoran ; Kirin, Srećko I. ; Raić-Malić, Silvana

engleski

Transition Metal-Mediated Hydrolysis of the Imine Bond in 2-Azomethine Benzothiazoles

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.

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

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Podaci o izdanju

95 (4)

2022.

123-130

objavljeno

0011-1643

1334-417X

10.5562/cca3907

Povezanost rada

Kemija

Poveznice
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