New N-acylamino acids and derivatives from renewable fatty acids: gelation of hydrocarbons and thermal properties


Autoria(s): Duarte, Rodrigo da Costa; Ongaratto, Renata; Piovesan, Luciana Almeida; Lima, Vânia Rodrigues de; Soldi, Valdir; Merlo, Aloir Antônio; D’Oca, Marcelo G. Montes
Data(s)

12/08/2016

12/08/2016

2012

Resumo

This work reports the synthesis of new fatty N-acylamino acids and N-acylamino esters from the C16:0, C18:0, C18:1, and C18:1(OH) fatty acid families and demonstrates the activity of these compounds as organogel agents. Compounds were heated and dissolved in various solvents (n-hexane, toluene, and gasoline). Only saturated C16:0 and C18:0 derived from alanine were able to form gels in toluene, and saturated C16:0 derived from phenylalanine showed gelation in n-hexane. This is the first evidence that fatty N-acylamino esters and N-acylamino acid derivatives of l-serine and fatty acids C16:0, C18:0, and C18:1 are able to form gels with hexane. This observation confirms the importance of the hydroxyl group in the segment derivative of l-serine in forming good gels.

Identificador

DUARTE, Rodrigo da Costa; ONGARATTO, Renata; PIOVESAN, Luciana Almeida. et al. New N-acylamino acids and derivatives from renewable fatty acids: gelation of hydrocarbons and thermal properties. Tetrahedron Letters, v. 53, maio, p. 2454-2460, 2012. Disponível em:<http://ac.els-cdn.com/S0040403912003930/1-s2.0-S0040403912003930-main.pdf?_tid=b1b94d3e-1833-11e4-acef-00000aab0f26&acdnat=1406757283_aa2879851a9e3a0623c503eeb5ca88ec>. Acesso em: 12 ago. 2016.

0040-4039

http://repositorio.furg.br/handle/1/6305

10.1016/j.tetlet.2012.03.015

Publicador

Elsevier

Direitos

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Palavras-Chave #Low-molecular-weight gelators #Fatty amino acids #Lo L-Serine #Ricinoleic acid
Tipo

article