Helitwistacenes-Combining Lateral and Longitudinal Helicity Results in Solvent-Induced Inversion of Circularly Polarized Light.

Helicity is expressed differently in ortho- and para-fused acenes-helicenes and twistacenes, respectively. While the extent of helicity is constant in helicenes, it can be tuned in twistacenes, and the handedness of flexible twistacenes is often determined by more rigid helicenes. Here, we combine helicenes with rigid twistacenes consisting of a tunable degree of twisting, forming helitwistacenes. While the X-ray structures reveal that the connection does not affect the helicity of each moiety, their electronic circular dichroism (ECD) and circularly polarized luminescence (CPL) spectra are strongly affected by the helicity of the twistacene unit, resulting in solvent-induced sign inversion. ROESY NMR and TD-DFT calculations support this observation, which is explained by differences in the relative orientation of the helicene and twistacene moieties.

The effect of axial and helical chirality on circularly polarized luminescence: lessons learned from tethered twistacenes.

The effect of axial and helical twisting on the circularly polarized luminescence of acenes was studied both experimentally and computationally, using four series of tethered twisted acenes. We find that the combination of axial and helical chirality yields the highest anisotropy factors, and that the ratio between the absorption and emission anisotropy factors is an intrinsic property for twistacenes.

Circularly polarized and total luminescence as probes of nucleation and growth in chiral nanocrystals.

Nucleation of crystals as well as their growth is difficult to study experimentally. We have recently demonstrated that chiral Eu3+ -doped terbium phosphate nanocrystals are an interesting system for studying nanocrystal formation mechanisms and chiral symmetry breaking, occurring during their formation, directed by chiral ligands, such as tartaric acid. In this paper, we show how simultaneous, in situ monitoring of both total emission intensity and circularly polarized luminescence magnitude and sign versus time during nanocrystal formation provides considerable information on the mechanisms of nanocrystal nucleation and growth. Specifically, we show that the presence of tartaric acid leads to the formation of chiral prenucleation clusters, which deterministically transform into nanocrystals of a specific handedness. Additionally, we demonstrate that both unseeded and seeded nanocrystal syntheses behave differently mechanistically and that the addition of seed nanocrystals catalyses both enantio-specific (also called secondary nucleation) as well as nonspecific nucleation.

A Kinetic Isotope Effect in the Formation of Lanthanide Phosphate Nanocrystals.

Mechanisms of nucleation and growth of crystals are still attracting a great deal of interest, in particular with recent advances in experimental techniques aimed at studying such phenomena. Studies of kinetic isotope effects in various reactions have been useful for elucidating reaction mechanisms, and it is believed that the same may apply for crystal formation kinetics. In this work, we present a kinetic study of the formation of europium-doped terbium phosphate nanocrystals under acidic conditions, including a strong H/D isotope effect. The nanocrystal growth process could be quantitatively followed through monitoring of the europium luminescence intensity. Hence, such lanthanide-based nanocrystals may serve as unique model systems for studying crystal nucleation and growth mechanisms. By combining the luminescence and NMR kinetics data, we conclude that the observed delayed nucleation occurs due to initial formation of pre-nucleation clusters or polymers of the lanthanide and phosphate ions, which undergo a phase transformation to crystal nuclei and further grow by cluster attachment. A scaling behavior observed on comparison of the H2O and D2O-based pre-nucleation and nanocrystal growth kinetics led us to conclude that both pre-nucleation and nanocrystal growth processes are of similar chemical nature.

Moral Injury and Suicide Ideation Among Combat Veterans: The Role of Trauma-Related Shame and Collective Hatred.

Exposure to potentially morally injurious events (PMIEs) among combat veterans has been acknowledged as a significant stressful combat event that may lead to mental health problems, including suicide ideation (SI). Several studies have examined the risk and protective factors that can explain the conditions in which PMIEs may contribute to the development and maintenance of SI. However, the contribution of social-emotional factors has yet to be examined. In the current study, we examined the association between PMIE-Self and SI among combat veterans and explored the mediating role of trauma-related shame and the moderation role of collective hatred in this association. A volunteer sample of 336 Israeli combat veterans was recruited, completing self-report questionnaires in a cross-sectional study. Results indicated that PMIE-Self was positively associated with SI, and trauma-related shame mediated this association. Moreover, collective hatred moderated both their direct (PMIE-SI) and indirect (PMIE-Shame-SI) association. Notably, collective hatred had an inverse role for each of the associations. Thus, collective hatred was found to comprise both a risk and a protective factor for SI following PMIE-Self. The current findings highlight the crucial contribution of trauma-related shame and collective hatred to the association between moral injury and suicidality. Moreover, the findings demonstrate that even years after their military service release, combat veterans exposed to PMIEs may still feel consumed by painful memories and maintain premonitions of a foreshortened future. Furthermore, the findings help to better understand the dynamics of collective hatred and the challenge of modifying it.

Time-resolved circularly polarized luminescence of Eu3+ -based systems.

Chiral Eu3+ -based systems are frequently studied via circularly polarized luminescence spectroscopy. The emission lifetimes of each circular polarization, however, are virtually always ignored, because in a homogeneous sample of emitters, there should be no difference between the two. However, we show that in less robust Eu3+ complex structures, as in the chiral complex Eu (facam)3 , a difference in the lifetimes of the two circularly polarized emission components arises due to heterogeneity of the complexes. In this case, each species within the sample could have different degrees of circularly polarized luminescence and decay rates at certain emission lines. The superposition of the emission components of the various chiral species leads to an overall difference in decay rate between the two circular polarizations. Such a difference is also shown for Eu3+ -doped chiral TbPO4 ·D2 O nanocrystals. We believe that this kind of measurement could be a unique tool for determining the homogeneity of a lanthanide-based chiral system, where other methods might fail in this task.