Enantiomers Of Chiral Molecules Research Articles

Chiral Control of Gas-Phase Molecules using Microwave Pulses.

Microwave three-wave mixing has emerged as a novel approach for studying chiral molecules in the gas phase. This technique employs resonant microwave pulses and is a non-linear and coherent approach. It serves as a robust method to differentiate between the enantiomers of chiral molecules and to determine the enantiomeric excess, even in complex chiral mixtures. Besides such analytical applications, the use of tailored microwave pulses allows us to control and manipulate chirality at the molecular level. Here, an overview of some recent developments in the area of microwave three-wave mixing and its extension to enantiomer-selective population transfer is provided. The latter is an important step towards enantiomer separation-in energy and finally in space. In the last section, we present new experimental results on how to improve enantiomer-selective population transfer to achieve an enantiomeric excess of about 40 % in the rotational level of interest using microwave pulses alone.

Chirale Kontrolle von Molekülen in der Gasphase mittels Mikrowellenpulsen

AbstractMikrowellen Drei‐Wellen Mischen ist ein bemerkenswerter, neuartiger Ansatz für tief gehende Untersuchungen an chiralen Molekülen. Diese nicht‐lineare und kohärente Technik, die auf resonanten Mikrowellenpulsen basiert, dient als robuste Methode zur Unterscheidung von Enantiomeren chiraler Moleküle und zur Bestimmung des Enantiomerenüberschusses, sogar für komplexe Mischungen chiraler Moleküle. Neben solchen analytischen Anwendungen erlaubt uns die Verwendung maßgeschneiderter Mikrowellenpulse die Kontrolle und Manipulation von Chiralität auf der Molekülebene. Der vorliegende Artikel liefert einen Überblick zu jüngsten Entwicklungen im Bereich des Mikrowellen Drei‐Wellen Mischens und seine Erweiterung zu enantiomerenspezifischem Populationstransfer. Letzteres ist ein entscheidender Schritt in Richtung Enantiomerentrennung – energetisch und schließlich auch räumlich. Im letzten Abschnitt präsentieren wir neue experimentelle Ergebnisse zur Verbesserung des enantiomerenspezifischen Populationstransfers, bei denen wir einen Enantiomerenüberschuss von 40 % in dem Rotationsenergieniveau von Interesse allein mit Hilfe von Mikrowellenpulsen erreichen konnten.

Screening Approach for Identifying Cocrystal Types and Resolution Opportunities in Complex Chiral Multicomponent Systems

Cocrystallization of racemic-compound-forming chiral molecules can result in conglomerate cocrystals or diastereomerically related cocrystals, which enable the application of chiral separation techniques such as preferential crystallization and classic resolution. Here, a systematic method to identify the types and phase diagrams of cocrystals formed by chiral target compounds and candidate coformers in a particular solvent system is presented, which allows the design of suitable chiral resolution processes. The method is based on saturation temperature measurements of specific solution compositions containing both enantiomers of chiral molecules and a coformer. This method is applied to analyze three different systems. For racemic phenylalanine (Phe) in water/ethanol mixtures one of the enantiomers selectively cocrystallizes with the opposite enantiomer of valine (Val), forming the more stable diastereomerically related cocrystal. The racemic compound ibuprofen crystallizes with the nonchiral coformer 1,2-bis(4-pyridyl)ethane (BPN) as racemic compound cocrystals. More interestingly, when it is combined with trans-1-(2-pyridyl)-2-(4-pyridyl)ethylene (BPE), the racemic compound ibuprofen cocrystallizes as a conglomerate, which in principle enables the application of preferential crystallization of this racemic compound. The systematic method shows the benefit of using pseudo-binary phase diagrams. Such pseudo-binary phase diagrams depict the saturation temperature on a very specific route through the quaternary phase diagram, allowing the identification of various cocrystal types as well as the corresponding cocrystallization conditions. The systematic method can be used to identify a suitable solid phase for chiral separation, and the obtained phase diagram information enables the performance of a crystallization-mediated chiral resolution process design. Such a guideline for a chiral resolution process design has never been reported for conglomerate cocrystal systems such as IBU:BPE, presented in this study.

An Extraordinary Catalyst Allowing Time-Dependent Enantiodivergent Synthesis

Highly efficient access to both enantiomers of chiral molecules is a long-standing challenge in synthetic chemistry. In a recent paper published in <i>Nature Chemistry</i>, Shu-Li You and coworkers reported a time-dependent enantiodivergent synthesis of chiral amines through an iridium-catalyzed allylic substitution reaction involving two kinetic resolutions.

Time-dependent enantiodivergent synthesis via sequential kinetic resolution.

The preparation of both enantiomers of chiral molecules is among the most fundamental tasks in organic synthesis, medicinal chemistry and materials science. Achieving this goal typically requires reversing the absolute configuration of the chiral component employed in the reaction system that is being used. The task becomes challenging when the natural source of the chiral component is not available in both configurations. Herein, we report a time-dependent enantiodivergent synthesis, in which an Ir-catalysed allylic substitution reaction uses one catalyst sequentially to promote two kinetic resolution reactions, enabling the synthesis of both enantiomers of the product using the same enantiomer of a chiral catalyst. The appropriate permutation of individual reaction rates is essential for the isolation of the chiral products in opposite configurations with high enantiopurity when quenched at different reaction times. This work provides an alternative solution for the preparation of both enantiomers of chiral molecules.

Enantioselective selectors for chiral electrochemistry and electroanalysis: Stereogenic elements and enantioselection performance

The ability to select among different electroactive molecules, or among different redox centers on a single molecule, in both analytical and synthetic applications, is a typical asset of electrochemistry, based on fine control of the electrode potential, possibly enhanced by the choice of appropriate electrode surfaces and media. An attractive step further, of great fundamental and applicative interest, is represented by enantioselective electrochemistry, implying the ability to discriminate the enantiomers of chiral molecules (in electroanalysis), or to selectively activate or achieve a given enantiomer of a chiral molecule controlling the electrode potential (in electrosynthesis). Since the enantiomers of a chiral molecule have identical scalar physico-chemical properties and therefore the same electrochemical behavior except when interacting with some other chiral entity, enantioselective electrochemistry necessarily implies the electron transfer process to take place in asymmetric conditions. This can be achieved by the use of a chiral electrode surface or a chiral medium. Artificial selectors are particularly interesting on account of the virtually unlimited range of tailored structures possible as well as the possibility to have both enantiomers of a given selector equally available. Among the many approaches so far proposed for this ambitious target along either of the two above ways, outstanding results have been recently obtained, based on the use of "inherently chiral molecular materials" (either as electrode surfaces or as media) in which the same structural element endows the molecule with both its key functional property and with chirality.

The influence of microbial communities for triadimefon enantiomerization in soils with different pH values.

Enantiomers of chiral molecules can undergo interconversion leading to markedly different toxicities, which can introduce significant uncertainty when evaluating biological and environmental fates. However, enantiomerization (the reversible conversion of one enantiomer into the other) related to soil microorganism is rarely understood. For better understanding, S-triadimefon and R-triadimefon enantiopure were incubated in different soils with different pH value. Both high-performance liquid chromatography and high-throughput sequencing technology were used to explore target analytes quantitatively and microbial taxa related to the conversion process. Results revealed a significant enantiomerization among the soils. The alkaline soil from Beijing had a faster conversion than neutral soil from Changchun, while acidic soil from Wuhan had no conversion. At the same results, analysis of bacteria community showed higher abundance of Arthrobacter and Halomonas genus in alkaline soil than neutral soil after treatments, but the acidic soil was lower. Moreover, Arthrobacter and Halomonas were responsible for converting S-triadimefon to R-triadimefon and R-triadimefon to S-triadimefon in alkaline and neutral soil, respectively. Thus, these genera may be one of the reasons to explain the enantiomerization in different soils observed in this study. Thus, research at microbial level is necessary for efficient ecological risk assessment of chiral fungicide.

High resolution GHz and THz (FTIR) spectroscopy and theory of parity violation and tunneling for 1,2-dithiine (C4H4S2) as a candidate for measuring the parity violating energy difference between enantiomers of chiral molecules.

We report high resolution spectroscopic results of 1,2-dithiine-(1,2-dithia-3,5-cyclohexadiene, C4H4S2) in the gigahertz and terahertz spectroscopic ranges and exploratory theoretical calculations of parity violation and tunneling processes in view of a possible experimental determination of the parity violating energy difference ΔpvE in this chiral molecule. Theory predicts that the parity violating energy difference between the enantiomers in their ground state (ΔpvE ≃ 1.1 × 10(-11)(hc) cm(-1)) is in principle measurable as it is much larger than the calculated tunneling splitting for the symmetrical potential ΔE± < 10(-24) (hc) cm(-1). With a planar transition state for stereomutation at about 2500 cm(-1) tunneling splitting becomes appreciable above 2300 cm(-1). This makes levels of well-defined parity accessible to parity selection by the available powerful infrared lasers and thus useful for one of the existing experimental approaches towards molecular parity violation. The new GHz spectroscopy leads to greatly improved ground state rotational parameters for 1,2-dithiine. These are used as starting points for the first successful analyses of high resolution interferometric Fourier transform infrared (FTIR, THz) spectra of the fundamentals ν17 (1308.873 cm(-1) or 39.23903 THz), ν22 (623.094 cm(-1) or 18.67989 THz) and ν3 (1544.900 cm(-1) or 46.314937 THz) for which highly accurate spectroscopic parameters are reported. The results are discussed in relation to current efforts to measure ΔpvE.

Infrared laser induced population transfer and parity selection in (14)NH3: A proof of principle experiment towards detecting parity violation in chiral molecules.

We have set up an experiment for the efficient population transfer by a sequential two photon-absorption and stimulated emission-process in a molecular beam to prepare quantum states of well defined parity and their subsequent sensitive detection. This provides a proof of principle for an experiment which would allow for parity selection and measurement of the time evolution of parity in chiral molecules, resulting in a measurement of the parity violating energy difference ΔpvE between enantiomers of chiral molecules. Here, we present first results on a simple achiral molecule demonstrating efficient population transfer (about 80% on the average for each step) and unperturbed persistence of a selected excited parity level over flight times of about 1.3 ms in the beam. In agreement with model calculations with and without including nuclear hyperfine structure, efficient population transfer can be achieved by a rather simple implementation of the rapid adiabatic passage method of Reuss and coworkers and considering also the stimulated Raman adiabatic passage technique of Bergmann and coworkers as an alternative. The preparation step uses two powerful single mode continuous wave optical parametric oscillators of high frequency stability and accuracy. The detection uses a sensitive resonantly enhanced multiphoton ionization method after free flight lengths of up to 0.8 m in the molecular beam. Using this technique, we were able to also resolve the nuclear hyperfine structure in the rovibrational levels of the ν1 and ν3 fundamentals as well as the 2ν4 overtone of (14)NH3, for which no previous data with hyperfine resolution were available. We present our new results on the quadrupole coupling constants for the ν1, ν3, and 2ν4 levels in the context of previously known data for ν2 and its overtone, as well as ν4, and the ground state. Thus, now, (14)N quadrupole coupling constants for all fundamentals and some overtones of (14)NH3 are known and can be used for further theoretical analysis.

Wavepacket Dynamics of the Axially Chiral Molecule Cl-O-O-Cl under Coherent Radiative Excitation and Including Electroweak Parity Violation.

We report detailed calculations of the quantum wavepacket dynamics of Cl-O-O-Cl, which serves as a prototype molecule for the stereomutation dynamics of an axially chiral molecule. We include the effects both from electroweak parity violation and from the interaction with a coherent monochromatic laser field. We use the quasiadiabatic channel reaction path Hamiltonian approach to approximately solve the six-dimensional Schrödinger equation describing the vibrational motion, including rotation by an effective Hamiltonian. We calculate time-dependent wave functions based on the time-dependent Schrödinger equation. We study stereomutation dynamics due to tunneling motion and laser-induced population transfer and show results on efficient methods for selectively populating single molecular states in chiral molecules by frequency-modulated laser pulses. We also discuss laser-induced stereomutation (LISM) and a process that may be called resonance Raman induced stereomutation (RRISM). The results are discussed in relation to current experimental attempts to measure the parity violating energy difference ΔpvE between the enantiomers of chiral molecules. Furthermore, we show detailed quantitative simulations of a selection of well-defined parity levels in chiral molecules ("parity isomers") that form the basis of a possible measurement of ΔpvE by the time evolution of parity.

Tunneling and Parity Violation in Trisulfane (HSSSH): An Almost Ideal Molecule for Detecting Parity Violation in Chiral Molecules.

Measuring the parity-violating energy difference Δpv E between the enantiomers of chiral molecules is a major challenge of current physical-chemical stereochemistry. An important step towards this goal is to identify suitable molecules for such experiments by means of theory. This step has been made by calculations for the complex dynamics of tunneling and electroweak quantum chemistry of parity violation in the "classic" molecule trisulfane, HSSSH, which satisfies the relevant conditions for experiments almost ideally, as the molecule is comparatively simple and parity violation clearly dominates over tunneling in the ground state. At the same time, the barrier for stereomutation is easily overcome by the S-H infrared chromophore.

A chiral rhenium complex with predicted high parity violation effects: synthesis, stereochemical characterization by VCD spectroscopy and quantum chemical calculations

With their rich electronic, vibrational, rotational and hyperfine structure, molecular systems have the potential to play a decisive role in precision tests of fundamental physics. For example, electroweak nuclear interactions should cause small energy differences between the two enantiomers of chiral molecules, a signature of parity symmetry breaking. Enantioenriched oxorhenium(VII) complexes S-(-)- and R-(+)-3 bearing a chiral 2-methyl-1-thio-propanol ligand have been prepared as potential candidates for probing molecular parity violation effects via high resolution laser spectroscopy of the Re=O stretching. Although the rhenium atom is not a stereogenic centre in itself, experimental vibrational circular dichroism (VCD) spectra revealed a surrounding chiral environment, evidenced by the Re=O bond stretching mode signal. The calculated VCD spectrum of the R enantiomer confirmed the position of the sulfur atom cis to the methyl, as observed in the solid-state X-ray crystallographic structure, and showed the presence of two conformers of comparable stability. Relativistic quantum chemistry calculations indicate that the vibrational shift between enantiomers due to parity violation is above the target sensitivity of an ultra-high resolution infrared spectroscopy experiment under active preparation.

Mikheev–Smirnov–Wolfenstein effect in chiral molecules

AbstractIn a recent article (Phys Rev A 2009, 80, 012110), we have proposed an alternative method to measure the parity‐violating energy difference between enantiomers of chiral molecules by modifying the dynamics of the two‐state system using an external chiral field, in particular circularly polarized light. When this field is properly tuned, the two‐state system becomes resonant, thus being maximal the probability of interconversion between enantiomers. In this work, we show that the resonance found in our previous work is identical to that found in two‐flavor neutrino oscillations, known as Mikheev–Smirnov–Wolfenstein (MSW) resonance. We use some analogies between neutrinos and chiral molecules to derive some interesting properties of the oscillations between enantiomers. In particular, we obtain an expression for the transition probability between them when their energy difference is time‐dependent. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem, 2011

Detection of parity violation in chiral molecules by external tuning of electroweak optical activity

A proposal is made to measure the parity-violating energy difference between enantiomers of chiral molecules by modifying the dynamics of the two-state system using an external chiral field, in particular, circularly polarized light. The intrinsic molecular parity-violating energy could be compensated by this external chiral field, with the subsequent change in the optical activity. From the observation of changes in the time-averaged optical activity of a sample with initial chiral purity and minimized environment effects, the value of the intrinsic parity-violating energy could be extracted. A discussion is made on the feasibility of this measurement.

High-Resolution Spectroscopic Studies and Theory of Parity Violation in Chiral Molecules

We review the high-resolution spectroscopic approach toward the study of intramolecular dynamics, emphasizing molecular parity violation. Theoretical work in the past decade has shown that parity-violating potentials in chiral molecules are much larger (typically one to two orders of magnitude) than anticipated on the basis of older theories. This makes experimental approaches toward small molecular parity-violating effects promising. The concepts and results of intramolecular dynamics derived from spectroscopy are analyzed as a sequence of symmetry breakings. We summarize the concepts of symmetry breakings (de facto and de lege) in view of parity violation in chiral molecules. The experimental schemes and the current status of spectroscopic experiments on molecular parity violation are established. We discuss the promises of detecting and accurately measuring parity-violating energy differences Delta(pv) E on the order of 10(11) J mol(1) (approximately 100 aeV) in enantiomers of chiral molecules with regard to their contribution to fundamental physics in the framework of the standard model of particle physics and more speculative future fundamental symmetry tests such as for the combined charge conjugation, parity, and time-reversal (CPT) symmetry violation.

Controlling state populations of enantiomers of real chiral molecules by using a circularly polarized pulsed laser

The interaction of a pulsed circularly polarized laser with the enantiomers of a chiral molecule is described within the rotating-wave approximation as a means for studying the possibility of separating chiral species from a racemic mixture. For freely tumbling molecules, it is found that the separation efficiency depends on the magnitude of electric and magnetic transition dipole moments, and on the angle between them. The method is applied to evaluating the separation efficiency of five small organic molecules, whose molecular properties are computed by time-dependent density functional theory. By choosing an appropriate transition, the efficiency of chiral separation can be increased significantly.

Harmonic and anharmonic contributions to parity-violating vibrational frequency difference between enantiomers of chiral molecules

A general perturbative procedure for the computation of harmonic and anharmonic contributions to parity-violating vibrational shifts is introduced and applied to PHBrF and AsHBrF. The results point out the importance of both diagonal and off-diagonal anharmonic contributions and indicate that some parity-violating shift of AsHBrF approaches the resolution forecasted for next generation experiments. The proposed approach is sufficiently general and computationally effective to allow studies of similar and larger molecular systems.

Theoretical determination of parity-violating vibrational frequency differences between the enantiomers of chiral molecules

A perturbation treatment has been used to compute the leading first- and second-order parity-violating corrections to the vibrational energy levels of a chiral molecule. Assuming the molecular equilibrium geometry as expansion point of both parity-violating and parity-conserving potential-energy surfaces, it is shown that these corrections, i.e., harmonic and anharmonic contributions, are of the same order of magnitude and that none of them can be neglected for a realistic determination of vibrational frequency differences. Numerical tests based on ab initio MP2 force fields and quantum-relativistic calculations of the parity-violating potential for each normal mode of PHBrF and AsHBrF molecules confirm this conclusion. In particular, it is shown that a normal mode of AsHBrF is characterized by one of the largest vibrational frequency difference ever found--the prediction is approximately 0.1 Hz--only one order of magnitude less than the presumed resolution limit of current experimental investigations.

Antivirals at the mirror: the lack of stereospecificity of some viral and human enzymes offers novel opportunities in antiviral drug development.

The enantioselectivity of enzymes, namely the property of enzymes to recognise and metabolise only one of the two enantiomers of chiral molecules, is related to the chiral structure of the enzymes, reflecting the three-dimensional folding of the polypeptide backbone and the orientation of the amino acid side chains in the folded molecule. Because of the chirality of the amino acids (L), the chemistry of life should be highly sensitive to different enantiomers of chiral substrates. However, in a world consisting only of D-nucleosides and L-amino acids, an enzyme which lacks enantio-selectivity does not reduce its fitness, since there is no chance of molecular misunderstanding when no other choice is available. Thus, although enantioselectivity is theoretically essential for life we do not expect to be always present among the biochemical properties of enzymes. If this is the case for key enzymes involved in virus infection or cancer, how to exploit such lack of enantioselectivity for a novel approach to antiviral or anticancer chemotherapy? The present review will discuss the possible lack of enantioselectivity of enzymes and its relevance for the developing of novel drugs with the inverted optical configuration.

Molecular parity violation in electronically excited states

One of the greatest challenges in the field of molecular physics is the still outstanding measurement of the parity violating energy difference (ΔEpv) which electroweak theory predicts to exist between the enantiomers of chiral molecules. Apparently, previous attempts to detect signals of parity violation in molecules almost exclusively focused on electronic ground state systems. But as this study reveals, there are good reasons to believe that compounds which are chiral in an electronically excited state are particularly suited for a possible proof of molecular parity violation. Here, first calculations of the parity violating energy difference in electronically excited states are presented and routes to its measurement are discussed.