A Highly Sensitive Deep-Sea Hydrodynamic Pressure Sensor Inspired by Fish Lateral Line.

Hydrodynamic pressure sensors offer an auxiliary approach for ocean exploration by unmanned underwater vehicles (UUVs). However, existing hydrodynamic pressure sensors often lack the ability to monitor subtle hydrodynamic stimuli in deep-sea environments. In this study, we present the development of a deep-sea hydrodynamic pressure sensor (DSHPS) capable of operating over a wide range of water depths while maintaining exceptional hydrodynamic sensing performance. The DSHPS device was systematically optimized by considering factors such as piezoelectric polyvinylidene fluoride-trifluoroethylene/barium titanate [P(VDF-TrFE)/BTO] nanofibers, electrode configurations, sensing element dimensions, integrated circuits, and packaging strategies. The optimized DSHPS exhibited a remarkable pressure gradient response, achieving a minimum pressure difference detection capability of approximately 0.11 Pa. Additionally, the DSHPS demonstrated outstanding performance in the spatial positioning of dipole sources, which was elucidated through theoretical charge modeling and fluid-structure interaction (FSI) simulations. Furthermore, the integration of a high Young's modulus packaging strategy inspired by fish skull morphology ensured reliable sensing capabilities of the DSHPS even at depths of 1000 m in the deep sea. The DSHPS also exhibited consistent and reproducible positioning performance for subtle hydrodynamic stimulus sources across this wide range of water depths. We envision that the development of the DSHPS not only enhances our understanding of the evolutionary aspects of deep-sea canal lateral lines but also paves the way for the advancement of artificial hydrodynamic pressure sensors.

Prototropic equilibria, tautomerization and electronic absorption properties of dibenzofluorescein in aqueous solution related to its capability as a fluorescence probe.

The protolytic equilibria of 1,2,7,8-dibenzofluorescein in aqueous solution have been characterized by visible absorption and fluorescence spectra. The species involved are identified as dianion, monoanion, neutral form and cation. The neutral form includes both the quinoid and lactone structures. The pKas were calculated by an improved procedure to be 3.14, 4.04 and 6.28, respectively. The absorption spectra for each protolytic form were resolved. The absorption maxima (molar absorption coefficient, x10(5), M(-1) cm(-1)) are 532 nm (0.87) for the dianion, 510 nm (0.39) for the monoanion, 500 nm (0.16) for the neutral form, and 494 nm (0.19) for the cation, respectively. Contrary to the assumption in the literature, we found that the monoanion is highly fluorescent (Phif=0.66, compared to Phif=0.25 for dianion) and its molar ratio can reach 50% at neutral pH. It is therefore concluded that under physiological pH conditions the monoanion plays a major role when it is used as a fluorescence probe.

Photophysical properties of dibenzofluorescein and the presence of its tautomers or prototropic forms in organic solvents.

The UV/Vis absorption and fluorescence properties of dibenzofluorescein (DBFL) in organic solvents were measured and used to shed light on the possible presence of its tautomers or various prototropic forms. DBFL in aprotic solvents mainly exists in two tautomeric forms, viz. quinoid and lactone, but neither are efficiently fluorescent. In protic solvents, such as methanol and ethanol, both the monoanion and neutral quinoid are present and showed the highest fluorescence quantum yield. In contrast, DBFL is fully dissociated to the monoanion and dianion in deionized water.

Fluorescence properties of dibenzofluorescein in aqueous solution.

The deprotonation of dibenzofluorescein (DBFL), a long wavelength fluorescence probe, results in the simultaneous occurrence of neutral form, monoanion and dianion under physiological conditions. The fluorescence properties of the former two cannot be measured directly because they are always coexistent with some other species. By measuring the fluorescence under various pHs we computed the fluorescence parameters for each species involved in the prototropic equilibria of DBFL, including each species' emission spectrum, excitation spectrum, emission and excitation maximum, fluorescence quantum yield and lifetime. It was found that the monoanion is the most fluorescent chromospheres (Phif=0.66, compared to Phif=0.25 for dianion, 0.18 for cation and 0.0 for the neutral form). Together with the computed pKas, we are able to suggest that the monoanion plays a major role under physiological conditions when DBFL is used as a fluorescence probe, contrary to the assumption in literature.

Self-assembled nanowire networks of aryloxy zinc phthalocyanines based on Zn-O coordination.

Tetrakis(aryloxy)phthalocyanine (4c) and its Zn congeners (4a and 4b) and Ni congener (4d) were synthesized, and their self-assembling properties in coordinating and non-coordinating solvents were investigated by absorption and fluorescence spectroscopy, matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS), and transmission electron microscopy (TEM). Compounds 4a and 4b in non-coordinating solvents exhibit red-shifted and split Q-bands in absorption spectra even at very low concentrations, suggesting J-aggregate formation. The MALDI-TOF MS for the samples of 4a and 4b prepared from chloroform solutions gives the monomer and aggregate signals. The TEM images of such samples display an indefinite two-dimensional network structure. The aggregates break up into monomers when a coordinating solvent is added to the solution. The driving force for the aggregate formation is proposed to be the complementary coordination of the ether oxygen in the aryloxy groups of one molecule to the core Zn of another molecule of phthalocyanine.

3,4-Dicyano-phenyl 2,3,4,6-tetra-O-acetyl-α-d-glucopyran-oside.

The title compound, C(22)H(22)N(2)O(10), was prepared by the glycosidation method through nitrite displacement on substituted nitro-phthalonitrile. The mol-ecule contains a benzene ring, two nitrile groups and an acetyl-protected d-glucose fragment which adopts a chair conformation. The absolute configuration was determined by the use of d-glucose as starting material. All substituents of the protected sugar are in equatorial positions, with the exclusive presence of the α-anomer. The crystal packing is stabilized by C-H⋯O and C-H⋯N hydrogen-bonding inter-actions.