Chiral Oligomers Research Articles

Enantioselective Discrimination via Wireless Chemiresistive Devices.

Developing chemiresistive devices for the wireless detection of complex analytes has gained considerable interest. In particular, the enantioselective recognition of chiral molecules is still a challenge. Here, we design a hybrid chemiresistive device for the wireless enantioselective discrimination of chiral analytes by combining the enantiorecognition capabilities of an inherently chiral oligomer, that is, oligo-(3,3'-dibenzothiophene) (BT2T4) and the insulating/conducting transition of polypyrrole (Ppy). The device is obtained by modifying each extremity of an interdigitated electrode (IDE) with Ppy on the interdigitated area and oligo-BT2T4 on the connection pads. Due to the asymmetric electroactivity triggered by bipolar electrochemistry, the wireless enantioselective discrimination of both enantiomers of tryptophan and DOPA was achieved. A difference in the onset resistance values was obtained for both enantiomers due to a favorable or unfavorable diastereomeric interaction between the inherently chiral oligomer and the antipode of the chiral molecule. Interestingly, such a device showed a wide quantification range, from μM to mM levels. This work opens up new alternatives to designing advanced wireless devices in enantiorecognition.

Inherently Chiral Oligomers Based on Indole-Benzothiophene Core.

In recent years, transductors of chiral information based on conducting polymers have gained considerable attention. In particular, inherently chiral materials, which allow differentiation between the antipodes of a chiral analyte in terms of energetic variations, are highly desired. In this work, we successfully synthesized a novel inherently chiral oligomer based on an indole-benzothiophene core, namely, 2-([2,2'-bithiophen]-5-yl)-3-(2-([2,2'-bithiophen]-5-yl)benzo[b]thiophen-3-yl)-N-methylindole (BTIndT4). The electrochemical characterization evidences a stabilization of electrogenerated radical cations due to the presence of the indole group, which guides the oligomerization, producing well-ordered polymeric matrices. Furthermore, the insitu electrochemical conductance analysis demonstrates a simultaneous intrachain and interchain transfer of charge carriers. Finally, the highly efficient enantiorecognition capabilities of the antipodes of the oligo-BTIndT4 films toward the enantiomers of tryptophan and 3,4-dihydroxyphenylalanine (DOPA), as model chiral analytes, were demonstrated.

Wireless Hollow Miniaturized Objects for Electroassisted Chiral Resolution.

Chiral resolution plays a crucial role in the field of drug development, especially for a better understanding of biochemical processes. In such a context, classic separation methods have been used for decades due to their versatility and easy scale-up. Among the many attempts proposed for enantioselective separation, electroassisted methods are presented as an interesting alternative. Herein, we present the use of wirelessly activated hollow tubular systems for the effective, simple, and tunable separation of racemic and enantioenriched mixtures. These double-layered tubular objects consist of an external polypyrrole chassis, a polymer with good electromechanical properties, functionalized in its inner part with an inherently chiral oligomer. The synergy between the electromechanical pumping process of the outer layer and the enantioselective affinity of the inner part induces the system to behave as a miniaturized chiral column. These hybrid objects are able to separate racemic and enantioenriched solutions of chiral model analytes into the corresponding enantiomers in high enantiomeric purity. Finally, these electromechanical systems can resolve mixtures formed by chiral probes with completely uncorrelated molecular structures injected simultaneously into the single antipodes.

Wireless asymmetric umpolung electrosynthesis.

Electroorganic synthesis has become an exciting tool for the asymmetric conversion of pro-chiral compounds. Herein, we introduced a wireless methodology based on bipolar electrochemistry in synergy with the enantioselective capabilities of inherently chiral oligomers to induce an umpolung chirality transfer. This was exemplified by the electro-conversion of a racemic mixture of lansoprazole to an enantio-enriched solution of a single antipode.

On-Surface Synthesis of Multiple Cu Atom-Bridged Organometallic Oligomers.

A metal-metal bond between coordination complexes has the nature of a covalent bond in hydrocarbons. While bimetallic and trimetallic compounds usually have three-dimensional structures in solution, the high directionality and robustness of the bond can be applied for on-surface syntheses. Here, we present a systematic formation of complex organometallic oligomers on Cu(111) through sequential ring opening of 11,11,12,12-tetraphenyl-1,4,5,8-tetraazaanthraquinodimethane and bonding of phenanthroline derivatives by multiple Cu atoms. A detailed characterization with a combination of scanning tunneling microscopy and density functional theory calculations revealed the role of the Cu adatoms in both enantiomers of the chiral oligomers. Furthermore, we found sufficient strength of the bonds against sliding friction by manipulating the oligomers up to a hexamer. This finding may help to increase the variety of organometallic nanostructures on surfaces.

Photonic Orbital Angular Momentum Dichroism on Three-Dimensional Chiral Oligomers

Chiral oligomers in optics are photonic metamaterials inspired by the concept of chiral centers in chemistry. In recent years, chiral oligomers have attracted increasing attention in recent years due to their simple construction and unique chiroptical response. To date, research has predominantly focused on the photonic spin angular momentum (SAM)-dependent chiroptical response: circular dichroism (CD). However, for another photonic dimension parallel to the SAM, orbital angular momentum (OAM)-dominated chiroptical response of chiral oligomers still remains elusive. Here, we theoretically and experimentally demonstrate the individual three-dimensional (3D) chiral tetramers can exhibit a gigantic response to the photonic OAM with a maximum helical dichroism (HD) of ∼23%. Meanwhile, we also reveal the origin of the HD via simulation analysis of electric current distribution, reflected electric field, and the discrete OAM spectroscopy. Furthermore, by femtosecond direct laser writing, 3D oligomers with tailoring geometric parameters can be flexibly fabricated in one step for varying HD responses. Our research fills the gap of OAM-related chiroptical response of chiral oligomers, which has great implications for chiroptical spectroscopy and photonic angular momentum engineering.

Photoluminescent ellipsometric circular dichroism

A novel spectroscopic technique, photoluminescent ellipsometric circular dichroism (PECD), which distinguishes all radiative electronic transitions related to molecular chiral centers. Additionally, it is proposed as complementary to the ellipsometric Raman spectroscopy (ERS) technique, thus establishing a relationship between vibrational modes and electronic transitions, associated with molecular chiral centers. In this way, PECD turns into a powerful technique for chiral material characterization. The PECD technique was performed on a chiral oligomer (1R,2R)-diiminocyclohexane, and its derivative polymer. A complete photophysical characterization in solution was performed to corroborate the new PECD technique.

Enantioselective resolution of two model amino acids using inherently chiral oligomer films with uncorrelated molecular structures.

Preferential crystallization induced by chiral surfaces is an interesting alternative to isolate enantiopure antipodes. Herein, we take advantage of the outstanding enantiorecognition capabilities of inherently chiral oligomers to induce an enantioselective crystallization process. We exemplify this strategy with two amino acid model molecules, asparagine and glutamic acid, having a completely uncorrelated structure with respect to the template. This illustrates the versatility of the approach with potential applications in the resolution of pharmaceutical compounds.

Wireless electrochemical actuation of soft materials towards chiral stimuli.

Different areas of modern chemistry, require wireless systems able to transfer chirality from the molecular to the macroscopic event. The ability to recognize the enantiomers of a chiral analyte is highly desired, since in the majority of cases such molecules present different physico-chemical properties that could lead, eventually, to dangerous or harmful interactions with the environment or the human body. From an electrochemical point of view, enantiomers have the same electrochemical behavior except when they interact in a chiral environment. In this Feature Article, different approaches for the electrochemical recognition of chiral information based on the actuation of conducting polymers are described. Such a dynamic behavior of π-conjugated materials is based on an electrochemically induced shrinking/swelling transition of the polymeric matrix. Since all the systems, described so far in the literature, are achiral and require a direct connection to a power supply, new strategies will be presented in the manuscript, concerning the implementation of chirality in electrochemical actuators and their use in a wireless manner through bipolar electrochemistry. Herein, the synergy between the wireless unconventional actuation and the outstanding enantiorecognition of inherent chiral oligomers is presented as an easy and straightforward read out of chiral information in solution. This approach presents different advantages in comparison to classic electrochemical systems such as its wireless nature and the possible real-time data acquisition.

Wireless electromechanical enantio-responsive valves.

Microfluidic valves based on chemically responsive materials have gained considerable attention in recent years. Herein, a wireless enantio-responsive valve triggered by bipolar electrochemistry combined with chiral recognition is reported. A conducting polymer actuator functionalized with the enantiomers of an inherently chiral oligomer was used as bipolar valve to cover a tube loaded with a dye and immersed in a solution containing chiral analytes. When an electric field is applied, the designed actuator shows a reversible cantilever-type deflection, allowing the release of the dye from the reservoir. The tube can be opened and closed by simply switching the polarity of the system. Qualitative results show the successful release of the colorant, driven by chirality and redox reactions occurring at the bipolar valve. The device works well even in the presence of chemically different chiral analytes in the same solution. These systems open up new possibilities in the field of microfluidics, including also controlled drug delivery applications.

Aggregation-Induced Polarization (AIP): Optical Rotation Amplification and Adjustment of Chiral Aggregates of Folding Oligomers and Polymers.

The phenomenon of aggregation-induced polarization (AIP) was observed showing optical rotation amplification and adjustment. The relationship between optical rotations of chiral aggregates of multilayered chiral folding oligomers and polymers with water% in THF (f w) has been established accordingly. New multilayered chiral oligomers were synthesized under the asymmetric catalytic systems established by our laboratory recently. These products were well-characterized by UV-vis, NMR, and MALDI-TOF spectra. Absolute stereochemistry (enantio- and diastereochemistry) was assigned by comparison with similar asymmetric induction by the same catalyst in our previous reactions. The present AIP work can serve as a new tool to determine chiral aggregates, especially for those that cannot display emission. AIP would also complement AIE-based CPL since AIP serves as a new tool providing enhanced right- or left-hand polarized lights with individual wavelengths. It will find many applications in chemical and materials science in the future.

Wireless light-emitting device for the determination of chirality in real samples

Bipolar electrochemistry can be employed in the context of chiral recognition in order to obtain useful analytical readouts of enantiomeric analytes. Herein, we employ this concept for the simultaneous determination of two enantiomers present in solution, and its possible use as transduction mechanism for complex real matrices analysis. This approach is based on the combination of the enantioselective electrooxidation of only one of the two antipodes of a chiral analyte with the emission of light from light-emitting diodes (LEDs). A double hybrid device was designed, using the enantiomers of an inherently chiral oligomer and a bare gold wire as the anode and cathode of a green and red LED. By applying an appropriate voltage, the wirelessly induced redox reactions trigger light emission only when the probe with the right configuration is present in solution. This device was used to simultaneously measure the ratio between L- and D-Tryptophan, both present in solution and to quantify L-ascorbic acid in a commercial juice sample. The measurement correlates with the value reported on the sample specifications. These results illustrate the possible use of such light-emitting bipolar devices as analytical tools for qualitative and quantitative measurements of enantiomeric excess, even in real samples.

Chiral discrimination of enantiomers based on different interactions with alterable chiral oligomer

Chiral discrimination of enantiomers based on different interactions with alterable chiral oligomer

Hybrid light-emitting devices for the straightforward readout of chiral information.

Bipolar electrochemistry has gained increasing attention in recent years as an attractive transduction concept in analytical chemistry in general and, more specifically, in the frame of chiral recognition. Herein, we use this concept of wireless electrochemistry, based on the combination of the enantioselective oxidation of a chiral probe with the emission of light from a light-emitting diode (LED), as an alternative for an easy and straightforward readout of the presence of chiral molecules in solution. A hybrid polymer-microelectronic device was designed, using an inherently chiral oligomer, that is, oligo-(3,3'-dibenzothiophene) and a polypyrrole strip as the anode and cathode of a miniaturized LED. The wireless induced redox reactions trigger light emission when the probe with the right chirality is present in solution, whereas no light emission is observed for the opposite enantiomer. The average light intensity shows a linear correlation with the analyte concentration, and the concept opens the possibility to quantify the enantiomeric excess in mixtures of the molecular antipodes.

A Pyrene-Modified Serinol Nucleic Acid Nanostructure Converts the Chirality of Threoninol Nucleic Acids into Circularly Polarized Luminescence Signals.

Herein is reported a circularly polarized luminescent (CPL) probe that can respond to the chirality of nucleic acids. An achiral nanostructure was prepared by the hybridization of symmetric serinol nucleic acid (SNA) containing pyrene-modified residues. When chiral oligomers that were complementary to the SNA were added, they induced helicity into the SNA nanowire. Efficient circular dichroism (CD) signal amplification was observed when pyrene was attached to uracil bases through a rigid alkynyl linker. Both CPL and CD signals were observed; they depended on the chirality of the added acyclic threoninol nucleic acid (aTNA) oligomer. This system can be used to convert the chirality of chiral biomolecules into chiroptical signals.

Evidence for new enantiospecific interaction force in chiral biomolecules

Evidence for new enantiospecific interaction force in chiral biomolecules

Influence of molecular weight on helical twisting power of oligomer chiral dopants

Chiral mesogenic monomers have been widely used in applications based on chiral liquid crystals, where polymerization is normally required to fulfill the device function. The change of molecular weight has a notable impact on the properties of the formed polymers. Herein, we systematically investigate the influence of molecular weight on the helical twisting power (HTP) of chiral oligomers when used as chiral dopants. Two series of side-chain and main-chain liquid crystal oligomers are synthesized and examined in terms of phase behavior, HTP value and dependence on temperature. The relationship between the HTP value and molecular weight of the oligomer is established, which is markedly dependent on the molecular structure. The insights obtained from the current study could help develop methods to in-situ analyze functional devices based on chiral liquid crystal polymers.

En Route to a Chiral Melanin: The Dynamic "From-Imprinted-to-Template" Supramolecular Role of Porphyrin Hetero-Aggregates During the Oxidative Polymerization of L-DOPA.

Chiral porphyrin hetero-aggregates, produced from meso-tetrakis(4-N-methylpyridyl) porphyrin H2T4 and copper(II) meso-tetrakis(4-sulfonatophenyl)porphyrin CuTPPS by an imprinting effect in the presence of L-3,4-dihydroxyphenylalanine (L-DOPA), are shown herein to serve as templates for the generation of chiral structures during the oxidative conversion of the amino acid to melanin. This remarkable phenomenon is suggested to involve the initial role of L-DOPA and related chiral intermediates like dopachrome as templates for the production of chiral porphyrin aggregates. When the entire chiral pool from DOPA is lost, chiral porphyrin hetero-aggregate would elicit axially chiral oligomer formation from 5,6-dihydroxyindole intermediates in the later stages of melanin synthesis. These results, if corroborated by further studies, may open unprecedented perspectives for efficient strategies of asymmetric melanin synthesis with potential biological and technological applications.

Characterization of Inherently Chiral Electrosynthesized Oligomeric Films by Voltammetry and Scanning Electrochemical Microscopy (SECM).

A voltammetric and scanning electrochemical microscopy (SECM) investigation was performed on an inherently chiral oligomer-coated gold electrode to establish its general properties (i.e., conductivity and topography), as well as its ability to discriminate chiral electroactive probe molecules. The electroactive monomer (S)-2,2′-bis(2,2′-bithiophene-5-yl)-3,3′-bibenzothiophene ((S)-BT2T4) was employed as reagent to electrodeposit, by cyclic voltammetry, the inherently chiral oligomer film of (S)-BT2T4 (oligo-(S)-BT2T4) onto the Au electrode surface (resulting in oligo-(S)-BT2T4-Au). SECM measurements, performed in either feedback or competition mode, using the redox mediators [Fe(CN)6]4− and [Fe(CN)6]3− in aqueous solutions, and ferrocene (Fc), (S)-FcEA, (R)-FcEA and rac-FcEA (FcEA is N,N-dimethyl-1-ferrocenylethylamine) in CH3CN solutions, indicated that the oligomer film, as produced, was uncharged. The use of [Fe(CN)6]3− allowed establishing that the oligomer film behaved as a porous insulating membrane, presenting a rather rough surface. This was inferred from both the approach curves and linear and bidimensional SECM scans, which displayed negative feedback effects. The oligomer film acquired semiconducting or fully conducting properties when the Au electrode was biased at potential more positive than 0.6 V vs. Ag|AgCl|KCl. Under the latter conditions, the approach curves displayed positive feedback effects. SECM measurements, performed in competition mode, allowed verifying the discriminating ability of the oligo-(S)-BT2T4 film towards the (S)-FcEA and (R)-FcEA redox mediators, which confirmed the results obtained by cyclic voltammetry. SECM linear scans indicated that the enantiomeric discriminating ability of the oligo-(S)-BT2T4 was even across its entire surface.

Widening the Scope of “Inherently Chiral” Electrodes: Enantiodiscrimination of Chiral Electroactive Probes with Planar Stereogenicity

AbstractA series of planar‐stereogenicity ferrocenes, important as chiral promoters in enantioselective catalysis, is characterized in terms of relationships between structure and electronic properties. The enantiomers of six selected model cases are then successfully discriminated in voltammetry experiments on electrodes modified with electrodeposited inherently chiral oligomer films, in terms of significant potential differences, specular inverting probe or selector configuration. Small substituent changes do not alter the enantiomer peak sequence, but result in significant modulation of peak potential differences, which appear consistent with the availability of chiral/selector matching elements. The present stereogenic plane case, combined with former ones involving stereogenic centers, axes, and/or helices, shows that the inherent chirality strategy in electroanalysis can be effective with all four rigid stereogenic elements.