Synthesis and characterization of a thermally stable triarylphosphine radical cation, [P(8-Br-CH)][BArF] ([][BArF], BArF = tetrakis(3,5-bis(trifluoromethyl)phenyl)borate), enabled by stabilization through -bromo-substituted naphthalenes, are described. Unlike previously reported phosphine radical cations that rely on sterically bulky substituents for stabilization, our approach leverages electronic stabilization via "through-space" radical delocalization. Single-crystal X-ray diffraction of [][BArF] reveals a tricapped tetrahedral geometry, resulting from the spatial proximity of the three bromine atoms to the phosphorus center, differentiated from the trigonal planar geometry observed in the previously reported triarylphosphine radical cations with sterically bulky substituents.
View Article and Find Full Text PDFNatural photosynthetic systems require spatiotemporal organization to optimize photosensitized reactions and maintain overall efficiency, involving the hierarchical self-assembly of photosynthetic components and their stabilization through synergistic interactions. However, replicating this level of organization is challenging due to the difficulty in efficiently communicating supramolecular nano-assemblies with nanoparticles or biological architectures, owing to their dynamic instability. Herein, we demonstrate that the supramolecular reconstruction of self-assembled amphiphilic rhodamine B nanospheres (RN) through treatment with metal-phenolic coordination complexes results in the formation of a stable hybrid structure.
View Article and Find Full Text PDFThe social transmission of food preference, a rudimentary form of social learning, has primarily been studied in pairs of adult rodents. Here, we present a protocol to explore the parent-offspring context in social learning using an adaptation of this classic paradigm for rodent dam-pup dyads. We describe steps for studying weanling mice from the same mother and present a worked example using weight-based (food consumption) and time-based (exploration) indices of social learning.
View Article and Find Full Text PDFA universal approach for enhancing water affinity in polymer photocatalysts by covalently attaching hydrophilic photocrosslinkers to polymer chains is presented. A series of bisdiazirine photocrosslinkers, each comprising bisdiazirine photophores linked by various aliphatic (CL-R) or ethylene glycol-based bridge chains (CL-TEG), is designed to prevent crosslinked polymer photocatalysts from degradation through a safe and efficient photocrosslinking reaction at a wavelength of 365 nm. When employing the hydrophilic CL-TEG as a photocrosslinker with polymer photocatalysts (F8BT), the hydrogen evolution reaction (HER) rate is considerably enhanced by 2.
View Article and Find Full Text PDFTin-lead (Sn-Pb) perovskite solar cells (PSCs) have gained interest as candidates for the bottom cell of all-perovskite tandem solar cells due to their broad absorption of the solar spectrum. A notable challenge arises from the prevalent use of the hole transport layer, PEDOT:PSS, known for its inherently high doping level. This high doping level can lead to interfacial recombination, imposing a significant limitation on efficiency.
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