Fluorine-Substituted Molecular Motors with a Quaternary Stereogenic Center

A series of unprecedented second generation molecular motors featuring a quaternary stereogenic center substituted with a fluorine atom has been synthesized. It is demonstrated that a seemingly benign replacement of the stereogenic hydrogen for a fluorine atom, regarded as a common substituent in pharmacology, resulted in a dramatic change in the energetic profile of thermal helix inversion. The barrier for the thermal helix inversion was found to increase considerably (by 20-30kJmol(-1)), presumably due to destabilization of the transition state by increased steric hindrance when the fluorine atom is forced to pass over the lower half of the motor. This results in the activation barrier for the thermal helix inversion to be higher than the barrier for backward thermal E-Z isomerization, impairing the motor function. A fluorine-substituted motor capable of performing unidirectional rotation is successfully prepared when these limitations are considered in the design phase

Pedagogía social : revista interuniversitaria

Monográfico con el título: "Redes territoriales de acción socioeducativa: una apuesta por la innovación social colaborativa"Título, resumen y palabras clave también en portuguésResumen basado en el de la publicaciónEstudio cualitativo, localizado en Estados Unidos, presenta un análisis en profundidad sobre el liderazgo en escuelas y organizaciones comunitarias que ayudan a conectar a los alumnos y a las familias con recursos educativos fundamentales. Los datos han sido recopilados a partir de 132 entrevistas con personas que han experimentado las complejidades sociales de la indigencia. Los resultados sugieren que el liderazgo participativo fomenta el aprendizaje, el simbolismo, el desarrollo de la identidad y la responsabilidad. El tipo de liderazgo promete brindar oportunidades para los desfavorecidos, que no tienen acceso a recursos o relaciones de importancia.ES

Structural Dynamics of Overcrowded Alkene-Based Molecular Motors during Thermal Isomerization

Synthetic light-driven rotary molecular motors show complicated structural dynamics during the rotation process. A combination of DFT calculations and various spectroscopic techniques is employed to study the effect of the bridging group in the lower half of the molecule on the conformational dynamics. It was found that the extent to which the bridging group can accommodate the increased folding in the transition state is the main factor in rationalizing the differences in barrier height and, as a consequence, the rotary speed. These findings will be essential in designing future rotary molecular motors

Molecular Stirrers in Action

A series of first-generation light-driven molecular motors with rigid substituents of varying length was synthesized to act as "molecular stirrers". Their rotary motion was studied by H-1 NMR and UV-vis absorption spectroscopy in a variety of solvents with different polarity and viscosity. Quantitative analyses of kinetic and thermodynamic parameters show that the rotary speed is affected by the rigidity of the substituents and the length of the rigid substituents and that the differences in speed are governed by entropy effects. Most pronounced is the effect of solvent viscosity on the rotary motion when long, rigid substituents are present. The alpha values obtained by the free volume model, supported by DFT calculations, demonstrate that during the rotary process of the motor, as the rigid substituent becomes longer, an increased rearranging volume is needed, which leads to enhanced solvent displacement and retardation of the motor

Multi-State Regulation of the Dihydrogen Phosphate Binding Affinity to a Light- and Heat-Responsive Bis-Urea Receptor

A responsive bis-urea receptor can be switched between three isomers using light and heat as evidenced by H-1 NMR and UV-vis spectroscopy. Anion binding experiments H-1 NMR titrations, ESI-MS) reveal a high selectivity for dihydrogen phosphate. Importantly, a large difference in binding affinity to the interchangeable isomers is observed, which is further rationalized by DFT calculations. As a consequence, the amount of bound substrate can be controlled via photo- and thermal isomerization in a three-step process

Solvent effects on the thermal isomerization of a rotary molecular motor

As molecular machines move to exciting applications in various environments, the study of medium effects becomes increasingly relevant. It is difficult to predict how, for example, the large apolar structure of a light-driven rotary molecular motor is affected by a biological setting or surface proximity, while for future nanotechnology precise fine tuning and full understanding of the isomerization process are of the utmost importance. Previous investigations into solvent effects have mainly focused on the relatively large solvent-solute interaction of hydrogen bonding or polarization induced by the isomerization process. We present a detailed study of a key step in the rotary process i.e. the thermal helix inversion of a completely apolar rotary molecular motor in 50 different solvents and solvent mixtures. Due to the relative inertness of this probe, we are able to study the influence of subtle solvent-solvent interactions upon the rate of rotation. Statistical analysis reveals which solvent parameters govern the isomerization process

Dicyanovinyl-based fluorescent sensors for dual mechanism amine sensing

Food wastage due to spoiling is a global economic issue and contributes to over-farming and overfishing with real environmental consequences. Smart food packaging is a promising solution to this problem, the concept of which is to incorporate responsive sensors that allow direct monitoring of the gasses released from the decay of food into a label that provides a visual indicator to the consumer as to whether the food is fresh or has spoiled. Here we report two dicyanovinyl-fluorene-benzothiadiazole-based fluorescent compounds,\ua0K12\ua0and\ua0K12b, both of which showed rapid response to biogenic amines\ua0via\ua0two independent mechanisms. When primary alkyl amines were present in solution, they underwent an aza-Michael addition with the dicyanovinyl group of the sensing material, resulting in a rapid colour change. The reaction products of\ua0K12\ua0and\ua0K12b\ua0with primary amines showed a decrease and increase in the fluorescence quantum yield, respectively, enabling a unique dual-sensor array with turn-off/turn-on response. In addition, fluorescence quenching\ua0via\ua0photoinduced hole transfer was observed in the solid-state sensor films with a wide range of primary, secondary and tertiary amines, enabling rapid and sensitive detection of amine vapours. Finally, we show as proof-of-concept that the fluorescence quenching response of sensing films was observable at cadaverine concentrations relevant to the food industry

Spectroscopic and Theoretical Identification of Two Thermal Isomerization Pathways for Bistable Chiral Overcrowded Alkenes

Chiroptical molecular switches play an important role in responsive materials and dynamic molecular systems. Here we present the synthesis of four chiral overcrowded alkenes and the experimental and computational study of their photochemical and thermal behavior. By irradiation with UV light, metastable diastereoisomers with opposite helicity were generated through high yielding E-Z isomerizations. Kinetic studies on metastable 1-4 using CD spectroscopy and HPLC analysis revealed two pathways at higher temperatures for the thermal isomerization, namely a thermal E-Z isomerization (TEZI) and a thermal helix inversion (THI). These processes were also studied computationally whereby a new strategy was developed for calculating the TEZI barrier for second-generation overcrowded alkenes. To demonstrate that these overcrowded alkenes can be employed as bistable switches, photochromic cycling was performed, which showed that the alkenes display good selectivity and fatigue resistance over multiple irradiation cycles. In particular, switch 3 displayed the best performance in forward and backward photoswitching, while 1 excelled in thermal stability of the photogenerated metastable form. Overall, the alkenes studied showed a remarkable and unprecedented combination of switching properties including dynamic helicity, reversibility, selectivity, fatigue resistance, and thermal stability