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首页> 外文期刊>Beilstein journal of organic chemistry. >Oxalyl retro-peptide gelators. Synthesis, gelation properties and stereochemical effects
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Oxalyl retro-peptide gelators. Synthesis, gelation properties and stereochemical effects

机译:草酰逆肽胶凝剂。合成,凝胶性质和立体化学作用

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In this work we report on gelation properties, self-assembly motifs, chirality effects and morphological characteristics of gels formed by chiral retro-dipeptidic gelators in the form of terminal diacids (1a–5a) and their dimethyl ester (1b–5b) and dicarboxamide (1c–5c) derivatives. Terminal free acid retro-dipeptides (S,S)-bis(LeuLeu) 1a, (S,S)-bis(PhgPhg) 3a and (S,S)-bis(PhePhe) 5a showed moderate to excellent gelation of highly polar water/DMSO and water/DMF solvent mixtures. Retro-peptides incorporating different amino acids (S,S)-(LeuPhg) 2a and (S,S)-(PhgLeu) 4a showed no or very weak gelation. Different gelation effectiveness was found for racemic and single enantiomer gelators. The heterochiral (S,R)-1c diastereoisomer is capable of immobilizing up to 10 and 4 times larger volumes of dichloromethane/DMSO and toluene/DMSO solvent mixtures compared to homochiral (S,S)-1c. Based on the results of 1H NMR, FTIR, CD investigations, molecular modeling and XRPD studies of diasteroisomeric diesters (S,S)-1b/(S,R)-1b and diacids (S,S)-1b/(S,R)-1a, a basic packing model in their gel aggregates is proposed. The intermolecular hydrogen bonding between extended gelator molecules utilizing both, the oxalamide and peptidic units and layered organization were identified as the most likely motifs appearing in the gel aggregates. Molecular modeling studies of (S,S)-1a/(S,R)-1a and (S,S)-1b/(S,R)-1b diasteroisomeric pairs revealed a decisive stereochemical influence yielding distinctly different low energy conformations: those of (S,R)-diastereoisomers with lipophilic i-Bu groups and polar carboxylic acid or ester groups located on the opposite sides of the oxalamide plane resembling bola amphiphilic structures and those of (S,S)-diasteroisomers possessing the same groups located at both sides of the oxalamide plane. Such conformational characteristics were found to strongly influence both, gelator effectiveness and morphological characteristics of gel aggregates.
机译:在这项工作中,我们报告了由末端二酸(1a-5a)及其二甲酯(1b-5b)和二甲酰胺形成的手性逆二肽胶凝剂形成的凝胶的凝胶特性,自组装基序,手性效应和凝胶的形态学特征(1c-5c)导数。末端游离酸逆向二肽(S,S)-双(LeuLe​​u)1a,(S,S)-双(PhgPhg)3a和(S,S)-双(PhePhe)5a显示出中等至极好的高极性水凝胶化/ DMSO和水/ DMF溶剂混合物。掺入不同氨基酸(S,S)-(LeuPhg)2a和(S,S)-(PhgLeu)4a的逆肽显示没有或非常弱的凝胶化。对于外消旋和单一对映异构体胶凝剂发现了不同的胶凝效力。与同手性(S,S)-1c相比,杂手性(S,R)-1c非对映异构体能够固定多达10到4倍体积的二氯甲烷/ DMSO和甲苯/ DMSO溶剂混合物。基于1H NMR,FTIR,CD研究,非对映异构二酯(S,S)-1b /(S,R)-1b和二酸(S,S)-1b /(S,R)的分子建模和XRPD研究)-1a,提出了其凝胶聚集体的基本填充模型。利用草酰胺和肽单元以及分层组织,扩展的凝胶剂分子之间的分子间氢键被确定为最可能出现在凝胶聚集体中的基序。 (S,S)-1a /(S,R)-1a和(S,S)-1b /(S,R)-1b非对映异构体对的分子建模研究显示了决定性的立体化学影响,产生了截然不同的低能构象:那些(S,R)-非对映异构体的亲脂性i-Bu基团和极性羧酸或酯基位于草酰胺平面的相对侧,类似bola两亲性结构;(S,S)-非对映异构体的那些具有相同的基团草酰胺平面的两面。发现这种构象特征强烈影响胶凝剂效力和凝胶聚集体的形态特征。

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