@techreport{oai:soar-ir.repo.nii.ac.jp:00014565,
 author = {鈴木,  正浩 and 白井,  汪芳 and 英,  謙二},
 month = {Mar},
 note = {We have focused on the self-assembling properties of organogelators in organic solvents and challenged the development of them as hydrogelators. Organogelators generally have not only amphiphilic groups such as amides, ureas, carboxylic acids, and hydroxyls, but also hydrophilic segments such as long alkyl chains and aromatic rings; therefore, most organogelators are water-insoluble. One of the simplest strategies in order to form hydrogelators is the introduction of charge into organogelators. The successful conversion of L-lysine-based organogelators into hydrogelators is achieved by linking the positively charged groups. Another approach is the introduction of a negative charge that is simply achieved by conversion of the ester to a carboxylate (alkali metal salt). We now describe new gelators based on an L-lysine., Article, 先進ファイバー工学研究教育拠点研究成果報告書 10: 27-28(2004)},
 title = {15-1-3 : L-リシンを基盤としたゲル化剤による溶媒のゲル化},
 year = {2004}
}