Signatures of directed and spontaneous flocking.

Collective motion-or flocking-is an emergent phenomena that underlies many biological processes of relevance, from cellular migrations to animal group movements. In this work, we derive scaling relations for the fluctuations of the mean direction of motion and for the static density structure factor (which encodes static density fluctuations) in the presence of a homogeneous, small external field. This allows us to formulate two different and complementary criteria capable of detecting instances of directed motion exclusively from easily measurable dynamical and static signatures of the collective dynamics, without the need to detect correlations with environmental cues. The static one is informative in large enough systems, while the dynamical one requires large observation times to be effective. We believe these criteria may prove useful to detect or confirm the directed nature of collective motion in in vivo experimental observations, which are typically conducted in complex and not fully controlled environments.

Asymmetric Phenyl Substitution: An Effective Strategy to Enhance the Photosensitizing Potential of Curcuminoids.

Curcumin has been demonstrated to exhibit photosensitized bactericidal activity. However, the full exploitation of curcumin as a photo-pharmaceutical active principle is hindered by fast deactivation of the excited state through the transfer of the enol proton to the keto oxygen. Introducing an asymmetry in the molecular structure through acting on the phenyl substituents is expected to be a valuable strategy to impair this undesired de-excitation mechanism competing with the therapeutically relevant ones. In this study, two asymmetric curcumin analogs were synthesized and characterized as to their electronic-state transition spectroscopic properties. Fluorescence decay distributions were also reconstructed. Their analysis confirmed the substantial stabilization of the fluorescent state with respect to the parent compound. Nuclear magnetic resonance experiments were performed with the aim of determining the structural features of the keto-enol ring and the strength of the keto-enol hydrogen bond. Electronic structure calculations were also undertaken to elucidate the effects of substitution on the features of the keto-enol semi-aromatic system and the proneness to proton transfer. Finally, their singlet oxygen-generation efficiency was compared to that of curcumin through the 9,10-dimethylanthracene fluorescent assay.