کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
610215 880643 2010 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Birefringent physical gels of N-(4-n-alkyloxybenzoyl)-l-alanine amphiphiles in organic solvents: The role of hydrogen-bonding
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
پیش نمایش صفحه اول مقاله
Birefringent physical gels of N-(4-n-alkyloxybenzoyl)-l-alanine amphiphiles in organic solvents: The role of hydrogen-bonding
چکیده انگلیسی

A new class of amphiphiles, N-(4-n-alkyloxybenzoyl)-l-alanine was designed and synthesized. These amphiphiles have been shown to form thermoreversible gels in organic solvents such as aromatic hydrocarbons, cyclohexane, and chlorinated hydrocarbons at room temperature. The effects of amide functionality, chain length of the hydrocarbon tail, and the chirality of the head group of the amphiphiles on the ability to promote gelation in organic solvents have been studied. The n-tetradecyl derivative showed the best gelation ability, whereas the amphiphile with dl-alanine as the head group formed weak organogels. The 4-dodecyloxybenzoic-1-carboxyethyl ester derivative in which the amide group is replaced by an ester group also formed weak organogels at a slightly lower temperature (293 K). The gelation number and the gel melting temperature of the gelators in different solvents were determined. The rheological measurements suggested that the organogels of n-tetradecyl derivatives are stronger than those of amphiphiles containing n-dodecyl chains. Also the organogels of the amphiphiles, except the one with an ester group, were found to have gel-to-sol transition temperatures, Tgs, higher than room temperature (∼303 K), which increased with the increase of chain length and total concentration of the gelator. SEM pictures of the gels show fibrous structures. Small-angle XRD and optical microscopy were also employed to characterize the gels. The organogels of alanine derivatives, except that of 4-dodecyloxybenzoic-1-carboxyethyl ester, showed optical birefringence. The mechanism of gelation was studied using 1H NMR and FTIR spectroscopy. Hydrogen-bonding between –CO2H groups as well as π–π interactions were found to be important for the gelation process.

This article explores the mechanisms of physical gelation and liquid crystal properties of N-(4-n-alkyloxybenzoyl)-l-alanine amphiphiles in organic solvents.Figure optionsDownload high-quality image (117 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Colloid and Interface Science - Volume 344, Issue 1, 1 April 2010, Pages 10–20
نویسندگان
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