RT Book,_Section
T1 Total Hydrolysis of a New Imidazolidine Induced by ZnII
A1 Fondo Busto, María Matilde
A1 Doejo Paz, Jesús
A1 García Deibe, Ana María
A1 Sanmartín Matalobos, Jesús
A1 González Bello, Concepción
K1 Imidazolidine
K1 Hydrolysis
K1 Zinc
K1 1D ladder
AB 2,2´-(2-(2-hydroxyphenyl)imidazolidin-1,3-diyl)diethanol(H3L) was obtained by condensation between 2-hydroxybenzaldehyde and N,N'-bis(2-hydroxyethyl)ethylenediamine. Its potential ability as NNOOO donor towards ZnII was tested. This study shows that zinc(II) mediates the fast hydrolysis of H3L, yielding the free aldehyde and amine. This latter was crystallographically characterised, showing a supramolecular 1D architecture based on hydrogen bond interactions
PB MDPI
SN 978-3-906980-55-3
YR 2015
FD 2015
LK http://hdl.handle.net/10347/25956
UL http://hdl.handle.net/10347/25956
LA eng
NO Fondo, M., Doejo, J., García-Deibe, A.M., Sanmartín-Matalobos, J. & González-Bello, C. (2015). Total Hydrolysis of a New Imidazolidine Induced by ZnII. In J.A. Seijas, M.P. Vázquez Tato & S.K. Lin, Proceedings ECSOC-18: The 18Th International Electronic Conference On Synthetic Organic Chemistry: November 1-30, 2014. MDPI. doi: 10.3390/ecsoc-18-a026
NO The 18th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis
DS Minerva
RD 24 abr 2026