Chiral bis(tyrosinol) and bis(p-hydroxyphenylglycinol) oxalamide gelators. influence of aromatic groups and hydrogen bonding on gelation properties

Crosbi ID101350
Bib IRB ID122425
Year2004
StatusObjavljeno
Typeprilog u časopisu
Subtypeizvorni znanstveni rad
AuthorsMakarević, Janja ; Jokić, Milan ; Raza, Zlata ; Čaplar, Vesna ; Katalenić, Darinka ; Štefanić, Zoran ; Kojić-Prodić, Biserka ; Žinić, Mladen
JournalCroatica chemica acta
Volume77
Issue1-2
Pages403-414
ISSN0011-1643
EISSN1334-417X
Titles

en original Chiral bis(tyrosinol) and bis(p-hydroxyphenylglycinol) oxalamide gelators. influence of aromatic groups and hydrogen bonding on gelation properties

Abstracts
en original

Enantiomerically pure R, R-bis(4-hydroxyphenylglycinol) oxalamides 3 and S, S-bis(tyrosinol) oxalamides 4 were prepared and tested for their gelling properties toward organic solvents water and aqueous mixtures with polar organic solvents. It was found that oxalamide compounds with aryl substituted phenolic hydroxy groups are efficient organogelators of highly polar solvent systems while the derivatives with free phenolic hydroxy groups tend to crystallize. The revealed different behaviour is explained on the basis of specific hydrogen bonding motifs found in the crystal structures.

Keywords

en original hydrogels; low molecular weight organogelators; self-assembly; oxalamide; hydrogen bonding; supramolecular chemistry

Authors
Institutions
Disciplines
Citations
Makarević, Janja ; Jokić, Milan ; Raza, Zlata ; Čaplar, Vesna ; Katalenić, Darinka ; Štefanić, Zoran ; Kojić-Prodić, Biserka ; Žinić, Mladen
Chiral bis(tyrosinol) and bis(p-hydroxyphenylglycinol) oxalamide gelators. influence of aromatic groups and hydrogen bonding on gelation properties // Croatica chemica acta, 77 (2004), 1-2; 403-414-x
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