A Pseudopeptide Polymer Micelle Used for Asymmetric Catalysis of the Aldol Reaction in Water.

Micelles assembled from amphiphilic molecules have proved to be ideal scaffolds to construct artificial catalysts mimicking enzymatic catalytic behavior. In this paper, we describe the synthesis of amphiphilic poly(2-oxazoline) derivatives with l-prolinamide units in the side chain and their application in asymmetric aldol reactions. Upon dissolution in water, the pseudopeptide polymers self-assembled into particles with different sizes, relying on the copolymer composition and distribution of hydrophilic/hydrophobic segments in the polymer chain. A preliminary study has demonstrated that the catalytic activity of these polymeric organocatalysts are strongly dependent on the aggregated architecture. The micelle-type assemblies can act as nanoreactors to efficiently promote the direct aldolisation of cyclohexanone with aromatic aldehydes in aqueous media, affording anti-aldol products in excellent yields (88⁻99%) and higher stereoselectivities (90/10 dr, 86% ee) compared to their nonmicellar systems under identical conditions.

Synthesis and evaluation of pseudopeptide chiral stationary phases for enantioselective resolution.

Poly(2-oxazoline)s are regarded as bioinspired polymers due to their structural relation to polypeptides. In this work, a new kind of poly(2-oxazoline)s containing dipeptide segments in the side chains was synthesized through a bottom-up protocol, which involves ring-opening copolymerization of 2-(N-Boc-l-2-pyrrolidinyl)-2-oxazoline (PyOXBoc) with 2-(3-butenyl)-2-oxazoline (BuOX) followed by deprotection and amide coupling with N-protected L-proline. The resulting vinyl-functionalized polymers were subsequently immobilized onto mercaptopropylated silica bead matrices by means of thio-click chemistry and their potential as the chiral stationary phase (CSP) for high-performance liquid chromatography was preliminarily evaluated with a series of structurally different racemates. The results showed that this class of pseudopeptide CSPs is particularly adapted to the enantiomeric separation of 1,1'-bi-2-naphthol and acyloin compounds (such as benzoin) under normal-phase conditions. Moreover, an increase in the length of polymer main chains is beneficial to the enhancement of both enantioselectivity and resolution ability. The chiral discrimination of analytes by the polymeric selectors stems primarily from hydrogen bonding and π-π interactions as well as steric hindrance.

A polymer-based probe for specific discrimination of cysteine.

A novel optically active methacrylic polymer with an amide-linked acrylate appendage as a chemosensor was synthesized by atom transfer radical polymerization (ATRP) followed by post-modification through a bottom-up design. The sensing behavior of the polymeric probe to various α-amino acids has been investigated through fluorescence, absorption, circular dichroism (CD), and visual color changes at physiological pH. It was found that the sensor exhibits specificity for the fluorescent recognition of cysteine against other amino acids and thiols in a turn-on mode, being significantly more effective than the corresponding small molecule counterpart. The detection limit was estimated to be in the micromolar range. In addition, the use of this chiral polymer allows the selective discrimination of cysteine enantiomers based on either fluorescence or CD spectral responses. Interestingly, the cysteine assay could also be visualized by the naked eye in the presence of small amounts of ferric ions.

Chiroptical inversion induced by rotation of a carbon-carbon single bond: an experimental and theoretical study.

We propose a new strategy to construct chiral molecular switches with highly reversible and sensitive chiroptical responses to variations in the external environment. Its fundamental concept involves a stimuli-triggered exchange of two conformations presenting significantly different chiroptical properties through the rotation of a carbon-carbon single bond, as demonstrated by chiral Schiff bases s-1, s-2, and a salicylamide analogue s-3. Upon addition of base in solution, the circular dichroism (CD) spectra of these molecular switches displayed unique changes featuring an inversion of the Cotton effect's signs, and the original CD profiles can be recoverd by acidification. Various spectroscopic studies as well as the conformational analysis combining with TDDFT computations allowed clear elucidation of the chiroptical inversion mechanism. It is expected that this kind of chiroptical switches is of great interest for molecular recognition, chemosensing, and the construction of molecular-scale devices. Furthermore, the present study indicates that the use of the conformational transition about a single bond may serve as the basis for designing chiroptical inversion systems.