Abstract

This paper reports an investigation into organocatalytic hydrogels as prebiotically relevant systems. Gels are interesting prebiotic reaction media, combining heterogeneous and homogeneous characteristics with a structurally organized active “solid-like” catalyst separated from the surrounding environment, yet in intimate contact with the solution phase and readily accessible via “liquid-like” diffusion. A simple self-assembling glutamine amide derivative 1 was initially found to catalyze a model aldol reaction between cyclohexanone and 4-nitrobenzaldehyde, but it did not maintain its gel structure during reaction. In this study, it was observed that compound 1 could react directly with the benzaldehyde to form a hydrogel in situ based on Schiff base 2 as a low-molecular-weight gelator (LMWG). This new dynamic gel is a rare example of a two-component self-assembled LMWG hydrogel and was fully characterized. It was demonstrated that glutamine amide 1 could select an optimal aldehyde component and preferentially assemble from mixtures. In the hunt for an organocatalyst, reductive conditions were applied to the Schiff base to yield secondary amine 3, which is also a highly effective hydrogelator at very low loadings with a high degree of nanoscale order. Most importantly, the hydrogel based on 3 catalyzed the prebiotically relevant aldol dimerization of glycolaldehyde to give threose and erythrose. In buffered conditions, this reaction gave excellent conversions, good diastereoselectivity, and some enantioselectivity. Catalysis using the hydrogel of 3 was much better than that using non-assembled 3—demonstrating a clear benefit of self-assembly. The results suggest that hydrogels offer a potential strategy by which prebiotic reactions can be promoted using simple, prebiotically plausible LMWGs that can selectively self-organize from complex mixtures. Such processes may have been of prebiotic importance.

Highlights

  • Gels are a colloidal state of matter in which a solid-like network is dispersed through a continuous liquid-like phase, leading to solvent immobilization.[1]

  • Compound 1 was synthesized by coupling dodecylamine and Boc-protected glutamine using 1-ethyl-3-(3dimethylaminopropyl)carbodiimide (EDC) and dimethylaminopyridine (DMAP), followed by acid-mediated removal of the Boc-protecting group (Scheme 2)

  • We reported a self-assembling glutamine amide derivative 1, capable of organocatalysis of the reaction between cyclohexanone and 4-nitrobenzaldehyde in “solution”, but which could not maintain its gel structure during reaction

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Summary

Introduction

Gels are a colloidal state of matter in which a solid-like network is dispersed through a continuous liquid-like phase, leading to solvent immobilization.[1]. On addition of 4-nitrobenzaldehyde, the emergence of a new peak in the DLS (SI, Figure S36) clearly indicated that the self-assembly mode changes as the two components react with one another, consistent with the formation of a more effective selfassembled gel in situ.

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Conclusion
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