Laure Guy

Progress toward the first observation of parity violation in chiral molecules by high-resolution laser spectroscopy†

Parity violation (PV) effects in chiral molecules have so far never been experimentally observed. To take up this challenge, a consortium of physicists, chemists, theoreticians, and spectroscopists has been established and aims at measuring PV energy differences between two enantiomers by using high-resolution laser spectroscopy. In this article, we present our common strategy to reach this goal, the progress accomplished in the diverse areas, and point out directions for future PV observations. The work of André Collet on bromochlorofluoromethane (1) enantiomers, their synthesis, and their chiral recognition by cryptophanes made feasible the first generation of experiments presented in this article.

Reversible, solvent-induced chirality switch in atrane structure: control of the unidirectional motion of the molecular propeller.

Here we demonstrate that atrane-hemicryptophane molecular cages exhibit a reversible change in chirality uniquely controlled by the solvent, thus establishing the feasibility of a new mode of stimulation for atrane-based molecular switches. The oxidovanadium(V) complexes of hemicryptophane molecules exist as diastereomeric mixtures because of the P or M handedness of the cyclotriveratrylene unit and the chiral ether groups with the S configuration. The Δ/Λ propeller-like arrangement of the atrane moiety introduces a new local dissymmetry because of the conformationally restricted helical structure. (1)H NMR experiments provided significant data for the Δ ⇆ Λ interconversion process, where the solvent profoundly influences the chirality sense of the propeller motion, making control of the chirality by the choice of solvent possible. The reversible chirality inversion process is induced by alternating changes of solvent from CDCl(3) to C(6)D(6). The ratio of the rates of the clockwise and anticlockwise tilting motions of the atrane structure shows that the solvent directs the rotational motion of the vanatrane moiety, so the propeller sense of the motion can be considered as unidirectional.

Efficient Dibenzo[c]acridine Helicene-like Synthesis and Resolution: Scaleup, Structural Control, and High Chiroptical Properties

Herein, we describe our recent expeditious synthesis of dibenzo[c]acridine helicene-like compounds on a large scale in pure enantiomeric form. This flexible synthesis allows for variation at several positions on the skeleton. Geometrical parameters related to these compounds have been obtained from monocrystal X-ray structure resolution. Additionally, chiroptical parameters have been recorded, highlighting the versatility of this family showing for example optical rotation at 589 nm varying between 135 and 150 deg g(-1)cm(2).

Absolute Configuration and Enantiodifferentiation of a Hemicryptophane Incorporating an Azaphosphatrane Moiety

The hemicryptophane racemate (±)-1 was optically resolved by semipreparative HPLC on Chiralpak IC column. The absolute configuration of each isolated enantiomer was established from the analysis of their electronic circular dichroism spectra. Enantiodifferentiation of the chiral cationic cage (±)-1 was evidenced in solution using Δ-TRISPHAT as chiral solvating agent, and the diastereomeric associations were observed in (1)H and (31)P NMR spectra.

Anion Binding in Water Drives Structural Adaptation in an Azaphosphatrane-Functionalized FeII4L4 Tetrahedron

Anion-templated aqueous self-assembly resulted in the formation of an endohedrally functionalized FeII4L4 tetrahedron from azaphosphatrane-based subcomponents. This new water-soluble cage is flexible and able to encapsulate anions with volumes ranging from 35 to 219 Å3 via hydrogen bonding and electrostatic interactions. It structurally adapts in response to the size and shape of the template anions, dynamically adopting a conformation either where all four azaphosphatrane +P-H vectors point inward, or else where one points outward and the other three inward. The two cage isomers can coexist in solution and interconvert. A shape memory phenomenon was observed during guest displacement because guest exchange occurs more rapidly than structural reconfiguration.

Pure chiral organic thin films with high isotropic optical activity synthesized by UV pulsed laser deposition

We show that the pulsed laser deposition (PLD) technique allows us to elaborate pure molecular solid state thin films based on binaphthyl molecules featuring high isotropic optical rotation (HIOR). The transfer of chirality from the ablated target to the substrate was probed by polarimetry and circular dichroism (CD) measurements. A rotary power of 12° mm at 546 nm has been obtained. CD spectroscopy confirms both the chiral and the isotropical nature of the deposited thin films and put into evidence the disorder between the naphthyl chromophores inside the molecular material. Finally, we highlight three regimes for the deposition mechanism depending on the laser fluence: desorption without racemisation, desorption with racemisation, and ablation with degradation. These results demonstrate that, by properly adjusting the growth conditions, isotropic purely organic chiral films can be grown by PLD, thereby opening the prospect for the synthesis of high value organic materials for applications such as waveguiding.

Helical, Axial, and Central Chirality Combined in a Single Cage: Synthesis, Absolute Configuration, and Recognition Properties

The synthesis of eight enantiopure molecular cages (four diastereomeric pairs of enantiomers) comprising a helically chiral cyclotriveratrylene (CTV) unit, three axially chiral binaphthol linkages, and three centrally asymmetric carbon atoms of a trialkanolamine core, is described. These new cages constitute a novel family of hemicryptophanes, which combine three classes of chirality. Their absolute configuration was successfully assigned by a chemical correlation method to overcome the signals overlap in the ECD spectra of the binaphtol and CTV units. Stereoselective recognition of glucose and mannose derivatives was investigated with these new chiral cages. Excellent enantio- and diastereoselectivity were reached, since in some cases, both exclusive enantio- and diastereo-discrimination have been observed. In addition, compared with the most relevant hemicryptophanes, these new cages also exhibit improved binding affinities.

Diastereoselective supramolecular ion-pairing between the TRISPHAT anion and pro-chiral heptamethine cyanine dyes

The supramolecular interactions between enantiopure TRISPHAT anion (tris(tetrachlorobenzenediolato)phosphate) and various non-chiral or pro-chiral heptamethine cyanine cations have been studied in the solid state by X-ray diffraction and in solution by NMR spectroscopy. The presence of the conformationally restricted tert-butyl functionalized cyclohexenyl moieties is responsible for the asymmetric shape interaction between the two ions revealing the chirality of the molecule. On the other hand, the strength of this interaction is controlled by the nature of the distal substituents.

Breathing Motion of a Modulable Molecular Cavity

A class of hemicryptophane cages that adopt imploded conformations in solution and in the solid state has been described and studied by NMR spectroscopy and X-ray crystallography. It is reported that the degree of collapse of the molecular cavity can be controlled by changing the stereochemistry of the chiral elements of the hemicryptophanes, leading to a modulation of their physical and chemical properties. Upon the binding of an oxidovanadium unit, the collapsed molecular cavity can inflate to give an expanded conformation. Removal of the vanadium core by an ancillary complexing ligand restores the initial folded structure. Thus, coordination/de-coordination of the metal ion controls the dynamic motions of the cage, leading to a reversible nanomechanical process. This controlled motion between a collapsed and expanded cavity can be seen as that of a breathable molecular cage.

Large-Scale Synthesis of Helicene-Like Molecules for the Design of Enantiopure Thin Films with Strong Chiroptical Activity

Helicenes are fascinating molecules owing to their unusual properties and applications in many fields from catalysis to organic electronics. Herein, we report a straightforward pathway for the synthesis of helicene-like molecules on a gram scale in an enantiopure form. Thin-film materials with good propagating optical properties and very high chiroptical responses have been grown by using pulsed laser ablation without altering the structure or the enantiopurity of the molecules. Moreover, electronic and vibrational circular dichroism spectroscopies coupled with theoretical calculations enabled some dependences of the chiroptical properties with the structure to be highlighted, for example, effects of rigidification, aromatization, or the state of matter (liquid versus solid).