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Pregled bibliografske jedinice broj: 162717

Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers


Čaplar, Vesna; Žinić, Mladen; Pozzo, Jean-Luc; Fages, Frederic; Mieden-Gundert, Gudrun; Voegtle, Fritz
Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers // European journal of organic chemistry, 2004 (2004), 19; 4048-4059 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 162717 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers

Autori
Čaplar, Vesna ; Žinić, Mladen ; Pozzo, Jean-Luc ; Fages, Frederic ; Mieden-Gundert, Gudrun ; Voegtle, Fritz

Izvornik
European journal of organic chemistry (1434-193X) 2004 (2004), 19; 4048-4059

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

Ključne riječi
Amino acids; Enantiomers; Fatty acids; Gelation; Racemates; Self-assembly

Sažetak
A new class of efficient low molecular weight gelator molecules has been designed by combining 11-aminoundecanoic acid (AUDA), lauric acid and aromatic and aliphatic amino acid units in the same molecule. This yields a special class of fatty acid amphiphiles with core chiral centres and hydrogen bonding sites. Some of the compounds with terminal carboxylic acid and sodium carboxylate functions exhibited ambidextrous gelation properties, being able to form gels both with highly polar solvents (water, DMSO) and also with highly lipophilic solvents, including two hydrocarbon fuels. At variance with several recent observations that the enantiomers are generally more efficient gelators than the corresponding racemates, some of the racemic gelators prepared in this work were found to be capable of gelling up to 16 times larger volumes of certain solvents than the pure enantiomers. Temperature-dependent FTIR and 1H NMR studies of the gels formed by derivatives with terminal carboxylic acid groups and lipophilic solvents revealed that intermolecular hydrogen bonding between amidic and carboxylic acid units was involved in the self-assembly of gel aggregates. Additional strong stabilization of the aggregates was observed in the gelators possessing terminal sodium carboxylate groups, and this was attributed to the electrostatic and ion-dipole interactions between the sodium carboxylate groups. This additional stabilization appears to be responsible for considerably higher thermal stability of the latter gels in relation to those formed by gelators with terminal carboxylic acid groups.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
0098053

Ustanove:
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Mladen Žinić (autor)

Avatar Url Vesna Čaplar (autor)


Citiraj ovu publikaciju:

Čaplar, Vesna; Žinić, Mladen; Pozzo, Jean-Luc; Fages, Frederic; Mieden-Gundert, Gudrun; Voegtle, Fritz
Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers // European journal of organic chemistry, 2004 (2004), 19; 4048-4059 (međunarodna recenzija, članak, znanstveni)
Čaplar, V., Žinić, M., Pozzo, J., Fages, F., Mieden-Gundert, G. & Voegtle, F. (2004) Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers. European journal of organic chemistry, 2004 (19), 4048-4059.
@article{article, author = {\v{C}aplar, Vesna and \v{Z}ini\'{c}, Mladen and Pozzo, Jean-Luc and Fages, Frederic and Mieden-Gundert, Gudrun and Voegtle, Fritz}, year = {2004}, pages = {4048-4059}, keywords = {Amino acids, Enantiomers, Fatty acids, Gelation, Racemates, Self-assembly}, journal = {European journal of organic chemistry}, volume = {2004}, number = {19}, issn = {1434-193X}, title = {Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers}, keyword = {Amino acids, Enantiomers, Fatty acids, Gelation, Racemates, Self-assembly} }
@article{article, author = {\v{C}aplar, Vesna and \v{Z}ini\'{c}, Mladen and Pozzo, Jean-Luc and Fages, Frederic and Mieden-Gundert, Gudrun and Voegtle, Fritz}, year = {2004}, pages = {4048-4059}, keywords = {Amino acids, Enantiomers, Fatty acids, Gelation, Racemates, Self-assembly}, journal = {European journal of organic chemistry}, volume = {2004}, number = {19}, issn = {1434-193X}, title = {Chiral Gelators Constructed from 11-Aminoundecanoic (AUDA), Lauric and Amino Acid Units. Synthesis, Gelling Properties and Preferred Gelation of Racemates vs. the Pure Enantiomers}, keyword = {Amino acids, Enantiomers, Fatty acids, Gelation, Racemates, Self-assembly} }

Časopis indeksira:


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





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