Optical properties of a fs laser-created sphere inside a CYTOP fiber by Mueller polarimetry.

Optical elements embedded in an optical fiber can be used to shape and modulate the light transmitted within. We consistently observe, via Mueller polarimetry, that the optical properties of a femtosecond (fs) laser-created spherical cavity within a perfluorinated fiber exhibit predictable patterns. Specifically, linear birefringence is always induced at the periphery of the cavity, with its value showing a bell-shape distribution.

Carbon Dot Synthesis in CYTOP Optical Fiber Using IR Femtosecond Laser Direct Writing and Its Luminescence Properties.

Luminescent carbon dots (CDs) were locally synthesized in the core of CYTOP fibers using IR femtosecond laser direct writing (FLDW), a one-step simple method serving as a post-treatment of the pristine fiber. This approach enables the creation of several types of modifications such as ellipsoid voids. The CDs and photoluminescence (PL) distribute at the periphery of the voids.

LASU: An efficient and stable phthalocyanine dye with tolerable safety profile for self-disinfecting anti-COVID textiles activated by ambient light.

Background: Recent COVID crisis has demonstrated that modern society urgently needs an accessible protection against mass infections, especially viruses, as the new strains are appearing at an ever-increasing pace and cause severe harm to the population and the world economy.

Methods: We have developed an efficient phthalocyanine photosensitizer LASU, that is suitable for dyeing textiles and allows to prepare reusable self-disinfecting fabrics with strong antiviral properties. The safety profile of LASU was evaluated in accredited laboratories by several in vitro assays according to the OECD-guidelines.

Coating gold nanorods with silica prevents the generation of reactive oxygen species under laser light irradiation for safe biomedical applications.

Gold nanoparticles can produce reactive oxygen species (ROS) under the action of ultrashort pulsed light. While beneficial for photodynamic therapy, this phenomenon is prohibitive for other biomedical applications such as imaging, photo-thermal drug release, or targeted gene delivery. Here, ROS are produced in water by irradiating gold nanorods and silica-coated gold nanorods with near-infrared femtosecond laser pulses and are detected using two fluorescent probes.

Unravelling the true MOF-5 luminescence.

Highly pure millimeter-sized MOF-5 single crystals were synthesized and characterized. Photoluminescence (PL) spectroscopy and time-correlated single photon counting (TCSPC) demonstrate a solvent-guest dependency of MOF-5 emission and its ligand-centred nature. These results allow measuring the true MOF-5 luminescence free of solvent at a wavelength of 355 nm, a significantly lower wavelength than previously published.

Large irradiation doses can improve the fast neutron/gamma discriminating capability of plastic scintillators.

When new materials appear as potential alternatives for radiation detection, several criteria have to be fulfilled. The one presented herein is the response variation to large irradiation doses of neutron/gamma discriminating plastic scintillators. Thus, several samples were exposed to high gamma doses reaching 10 kGy.

Role of the Bridging Group in Bis-Pyridyl Ligands: Enhancing Both the Photo- and Electroluminescent Features of Cationic (IPr)Cu Complexes.

We report on the benefits of changing the bridging group X of bis-pyridyl ligands, that is, Py-X-Py where X is NH, CH , C(CH ) , or PPh, on the photo- and electroluminescent properties of a new family of luminescent cationic H-heterocyclic carbene (NHC) copper(I) complexes. A joint experimental and theoretical study demonstrates that the bridging group affects the molecular conformation from a planar-like structure (X is NH and CH ) to a boat-like structure (X is C(CH ) and PPh), leading to i) four-fold enhancement of the photoluminescence quantum yield (ϕ ) without affecting the thermally activated delayed fluorescence mechanism, and ii) one order of magnitude reduction of the ionic conductivity (σ) of thin films. This leads to an overall enhancement of the device efficacy and luminance owing to the increased ϕ and the use of low applied driving currents.

N-(2-Ethylhexyl)carbazole: A New Fluorophore Highly Suitable as a Monomolecular Liquid Scintillator.

The synthesis, photophysical properties, and applications in scintillation counting of N-(2-ethylhexyl)carbazole (EHCz) are reported. This molecule displays all of the required characteristics for an efficient liquid scintillator (emission wavelength, scintillation yield), and can be used without any extra fluorophores. Thus, its scintillation properties are discussed, as well as its fast neutron/gamma discrimination.

Designing NHC-Copper(I) Dipyridylamine Complexes for Blue Light-Emitting Electrochemical Cells.

This study presents the influence of various substituents on the photophysical features of heteroleptic copper(I) complexes bearing both N-heterocyclic carbene (NHC) and dipyridylamine (dpa = dipyridylamine skeleton corresponding to ligand L1) ligands. The luminescent properties have been compared to our recently reported archetypal blue emitting [Cu(IPr)(dpa)][PF6] complex. The choice of the substituents on both ligands has been guided to explore the effect of the electron donor/acceptor and "push-pull" on the emission wavelengths and photoluminescence quantum yields.

Giant Amplification of Photoswitching by a Few Photons in Fluorescent Photochromic Organic Nanoparticles.

Controlling or switching the optical signal from a large collection of molecules with the minimum of photons represents an extremely attractive concept. Promising fundamental and practical applications may be derived from such a photon-saving principle. With this aim in mind, we have prepared fluorescent photochromic organic nanoparticles (NPs), showing bright red emission, complete ON-OFF contrast with full reversibility, and excellent fatigue resistance.

Efficient sensing of explosives by using fluorescent nonporous films of oligophenyleneethynylene derivatives thanks to optimal structure orientation and exciton migration.

The fluorescence of thin films of a diimine-substituted phenyleneethynylene compound can be efficiently quenched by nitroaromatic vapors, which is not the case for the unsubstituted parent compound. Thin-film porosity is usually considered to be an essential factor for efficient quenching, but in the present case the origin of the quenching is completely different, as both films are nonporous and hermetic to 2,4-dinitrotoluene (DNT) molecules. The molecular organization in the two crystallized thin films offers a low level of π stacking for both compounds, but the orientation of the phenylenethynylene fluorophore differs markedly with respect to the surface of the films.

A spiral designed surface based on amino-perylene grafted polyacrylic acid.

This communication shows the possibility of inducing spontaneous special surface organisation by means of grafting a fluorescent aminobenzo[g,h,i]perylene derivative onto surface grown polyacrylic chains.

Nanoparticle organization through photoinduced bulk mass transfer.

A series of dipolar triphenylaminoazo derivatives, with largely distinct charge transfer and glass transition temperatures, has been synthesized. Their photomigration capability in the solid state to form surface relief gratings (SRGs) under interferential illumination has been investigated with respect to their photochromic properties and showed a prevailing influence of the bulkiness of the azo substituent. The azo mass transfer was utilized to efficiently photoalign 200 nm polystyrene nanoparticles along the SRG crests, which were initially deposited on nonirradiated azo surfaces.

Spectroscopy of BODIPY in solid phase: crystal and nanoparticles.

We compare the absorption and fluorescence spectra of single crystals and suspensions of nanoparticles with the prediction of the Frenkel theory. The single crystals of a novel synthesized fluorescent BODIPY derivative dye, adamantyl mesityl BODIPY (4,4-difluoro-3,5-di-(adamantyl)-8-mesityl-4-bora-3a,4a-diaza-s-indacene), have been prepared. Their birefringence and dichroism have been studied.

Fluorescent labeling of a bisurea-based supramolecular polymer.

Bisurea-based supramolecular polymer 2-ethylhexyl-3-[3-(3-(2-ethylhexyl)ureido)-4-methyl-phenyl]urea (EHUT) has been shown previously to self-assemble through hydrogen bonding into high-molecular-weight structures. The present publication reports the study of the thermodynamics of these tubular structures by time-resolved fluorescence spectroscopy, with the help of a tetrazine labeled monomer. Results of calorimetry and time-resolved fluorescence spectroscopy show that the as-modified monomer EHUTz does not interfere with the formation of the supramolecular assembly.

Quenching dynamics in CdSe nanoparticles: surface-induced defects upon dilution.

We have analyzed the decays of the fluorescence of colloidal CdSe quantum dots (QDs) suspensions during dilution and titration by the ligands. A ligand shell made of a combination of trioctylphosphine (TOP), oleylamine (OA), and stearic acid (SA) stabilizes the as-synthesized QDs. The composition of the shell was analyzed and quantified using high resolution liquid state 1H nuclear magnetic resonance (NMR) spectroscopy.

Mixed copper, silver, and gold cyanides, (M(x)M'(1-x))CN: tailoring chain structures to influence physical properties.

Binary mixed-metal variants of the one-dimensional MCN compounds (M = Cu, Ag, and Au) have been prepared and characterized using powder X-ray diffraction, vibrational spectroscopy, and total neutron diffraction. A solid solution with the AgCN structure exists in the (Cu(x)Ag(1-x))CN system over the range (0 ≤ x ≤ 1). Line phases with compositions (Cu(1/2)Au(1/2))CN, (Cu(7/12)Au(5/12))CN, (Cu(2/3)Au(1/3))CN, and (Ag(1/2)Au(1/2))CN, all of which have the AuCN structure, are found in the gold-containing systems.

Contraction behaviors of sp. stalk investigated using high-speed video camera. II: Viscosity effect of several types of polymer additives.

The contraction process of living sp. in polymer solutions with various viscosities has been investigated by image processing using a high-speed video camera. The viscosity of the external fluid ranges from 1 to 5mPa·s for different polymer additives such as hydroxypropyl cellulose, polyethylene oxide, and Ficoll.

Contraction behaviors of sp. stalk investigated using high-speed video camera. I: Nucleation and growth model.

The contraction process of living sp. has been investigated by image processing using a high-speed video camera. In order to express the temporal change in the stalk length resulting from the contraction, a damped spring model and a nucleation and growth model are applied.

Solvatochromic dissociation of non-covalent fluorescent organic nanoparticles upon cell internalization.

Amorphous red-emitting materials involving solvatochromic small molecules have been processed by the reprecipitation method as non-doped nanospheres characterized by a remarkably low polydispersity. Their mean diameter could simply be tuned by the concentration of the organic solution giving rise to time-stable dispersion of 85-200 nm-sized nanoparticles. Time-resolved measurements performed on solid nanoparticles showed significant size-dependence effects of the emission lifetime and maxima evidencing populations with distinct molecular conformations.

Light-driven directed motion of azobenzene-coated polymer nanoparticles in an aqueous medium.

Azobenzene-coated polymer nanoparticles in the 16-nm-diameter range act as phototriggered nanomotors combining photo to kinetic energy conversion with optical control through light intensity gradients. The grafted dyes act as molecular propellers: their photoisomerization supplies sufficient mechanical work to propel the particles in an aqueous medium toward the intensity minima with velocities of up to 15 μm/s. It is shown that nanoparticles can be driven over tens of micrometers by translating the intensity gradients in the plane.

Designing dye-nanochannel antenna hybrid materials for light harvesting, transport and trapping.

We discuss artificial photonic antenna systems that are built by incorporating chromophores into one-dimensional nanochannel materials and by organizing the latter in specific ways. Zeolite L (ZL) is an excellent host for the supramolecular organization of different kinds of molecules and complexes. The range of possibilities for filling its one-dimensional channels with suitable guests has been shown to be much larger than one might expect.

Tunable emissive thin films through ICT photodisruption of nitro-substituted triarylamines.

UV-assisted photocleavage in the solid state of orange emitting nitro-substituted triarylamines leads to the appearance of blue emission following photodisruption of the ICT state.

Synthesis and optical properties of 2-(benzo[b]thiophene-3-yl)pyrroles and a new BODIPY fluorophore (BODIPY = 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene).

2-(Benzo[b]thiophene-3-yl)-1-vinylpyrrole has been synthesized directly from 3-acetylbenzo[b]thiophene oxime and acetylene (flow system, KOH-DMSO, 120 degrees C, 5 h) in 68% yield. Devinylation of the synthesized pyrrole (Hg(OAc)(2), NaBH(4), 50 degrees C) led to the corresponding 2-(benzo[b]thiophene-3-yl)pyrrole in 63% yield. Trifluoroacetylation of both the pyrroles with trifluoroacetic anhydride (80 degrees C, 1 h) gave the corresponding 5-trifluoroacetyl pyrroles in 97% and 76% yields, respectively.