Crystals of Diphenyl-Benzothiadiazole and Its Derivative with Terminal Trimethylsilyl Substituents: Growth from Solutions, Structure, and Fluorescence Properties.

Linear conjugated molecules consisting of benzothiadiazole (BTD) and phenyl rings are highly efficient organic luminophores. Crystals based on these compounds have great potential for use as light-emitting elements, in particular, scintillation detectors. This paper compares the peculiarities of growth, structure, and fluorescent properties of crystals based on 4,7-diphenyl-2,1,3-benzothiadiazole () and its organosilicon derivative 4,7-bis(4-(trimethylsilyl)phenyl) BTD ().

Tetrachromophoric Derivatives of Dibenzoylmethanatoboron Difluoride Based on Stereoregular Cyclotetrasiloxanes: Synthesis and Properties.

A series of new tetrachromophoric systems based on stereoregular tetracyclosiloxanes and dibenzoylmethanatoboron difluoride derivatives have been synthesized and characterized by a complex of physicochemical methods. The photophysical properties of the synthesized compounds are studied by electronic absorption, steady-state, and time-resolved fluorescence spectroscopy. In the synthesized compounds, four dibenzoylmethanatoboron difluoride (DBMBF)-based fluorophores are in an all-cis arrangement with respect to a cyclotetrasiloxane scaffold.

Synthesis and Photophysical Properties of Novel Meta-Conjugated Organic Molecules with 1,3,5-Benzene Branching Units.

The synthesis and photophysical investigation of three novel meta-conjugated molecules based on 3,1,2-benzothiadiazole and thiophene-2,5-diyl derivatives linked through 1,3,5-benzene branching units are described. Each of them is a symmetrical molecule with two branching units, four identical lateral thiophene-containing fragments, and one central benzothiadiazole-containing fragment. To study the effect of the chemical structure on their photophysical properties, the molecules with different linearly conjugated lateral and central fragments due to incorporation of additional thiophene rings were synthesized and compared.

A new linear phenyloxazole-benzothiadiazole luminophore: crystal growth, structure and fluorescence properties.

A new linear luminophore consisting of five conjugated units of oxazole, phenylene and a central benzothiadiazole fragment, 4,7-bis[4-(1,3-oxazol-5-yl)phenyl]-2,1,3-benzothiadiazole, has been synthesized and characterized. Needle-like single-crystal samples up to 10 mm in length were obtained by physical vapor transport. The crystal structure was determined at 95 K and 293 K using single-crystal X-ray diffraction.

Luminescent Coatings Based on (3-Aminopropyl)triethoxysilane and Europium Complex β-Diketophosphazene.

The reaction of β-diketophosphazene with the europium (III) salt synthesized the corresponding metal complex which was structured with (3-aminopropyl)triethoxysilane and treated with dibenzoylmethane for additional coordination of europium atoms. The polymer thus obtained exhibits luminescence with a maximum of 615 nm, which is characteristic of europium. The polymer is thermally stable up to 300 °C, the coating based on it has a contact angle of 101°, and the adhesive strength of the coating to non-finished glass (according to ISO 2409: 2013) is 1 point.

Excited state dynamics and exciton diffusion in triphenylamine/dicyanovinyl push-pull small molecule for organic optoelectronics.

Triphenylamine-based small push-pull molecules have recently attracted substantial research attention due to their unique optoelectronic properties. Here, we investigate the excited state de-excitation dynamics and exciton diffusion in TPA-T-DCV-Ph-F small molecule, having simple chemical structure with asymmetrical architecture and end-capped with electron-withdrawing p-fluorodicyanovinyl group. The excited state lifetime in diluted solutions (0.

Highly luminescent crystals of a novel linear π-conjugated thiophene-phenylene co-oligomer with a benzothiadiazole fragment.

The synthesis, growth from solutions and structure of crystals of a new linear thiophene-phenylene co-oligomer with a central benzothiadiazole fragment with a conjugated core, (TMS-2T-Ph)-BTD, are presented. Single-crystal samples in the form of needles with a length of up to 7 mm were grown and their crystal structure was determined at 85 K and 293 K using single-crystal X-ray diffraction. The conformational differences between the crystal structures are insignificant.

Impact of N-substitution on structural, electronic, optical, and vibrational properties of a thiophene-phenylene co-oligomer.

Properties of the organic semiconductors can be finely tuned changes in their molecular structure. However, the relationship between the molecular structure, molecular packing, and (opto)electronic properties of the organic semiconductors to guide their smart design remains elusive. In this study, we address computationally and experimentally the impact of subtle modification of a thiophene-phenylene co-oligomer CF-PTTP-CF on the molecular properties, crystal structure, charge transport, and optoelectronic properties.

Tetrahedral Silicon-Centered Dibenzoylmethanatoboron Difluorides: Synthesis, Crystal Structure, and Photophysical Behavior in Solution and the Solid State.

Four tetrahedral silicon-centered derivatives of dibenzoylmethanatoboron difluoride (DBMBF ) were synthesized and characterized. Their structural and optical features both in solution and the solid state were investigated by using X-ray crystallography, steady-state and time-dependent spectroscopy, and DFT-based calculations. In dilute solutions, the molar absorption coefficient increases from 40500 to 175200 M  cm as the number of DBMBF fragments in a molecule increases from one to four, while, in contrast, the nonradiative rate constant of fluorescence decay decreases from 0.

Fluorinated Thiophene-Phenylene Co-Oligomers for Optoelectronic Devices.

Organic optoelectronics requires materials combining bright luminescence and efficient ambipolar charge transport. Thiophene-phenylene co-oligomers (TPCOs) are promising highly emissive materials with decent charge-carrier mobility; however, they typically show poor electron injection in devices, which is usually assigned to high energies of their lowest unoccupied molecular orbitals (LUMOs). A widely used approach to lower the frontier orbitals energy levels of a conjugated molecule is its fluorination.

Influence of photoluminophore-modified agro textile spunbond on growth and photosynthesis of cabbage and lettuce plants.

Light-converting polypropylene spunbond was first used in the study of the key physiological parameters of plants. A comparative study of the functioning of the photosynthetic apparatus and the dynamics of growth in late cabbage plants (Olga variety) and leaf lettuce (Emerald variety) was conducted using the ordinary nonwoven polypropylene fabric (spunbond) (density 30 g·m) and the spunbond containing a photoluminophore (PL) (1.6% yttrium oxysulfide doped with europium).

Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers.

Owing to the combination of efficient charge transport and bright luminescence, thiophene-phenylene co-oligomers (TPCOs) are promising materials for organic light-emitting devices such as diodes, transistors and lasers. The synthetic flexibility of TPCOs enables facile tuning of their properties. In this study, we address the effect of various electron-donating and electron-withdrawing symmetric terminal substituents (fluorine, methyl, trifluoromethyl, methoxy, tert-butyl, and trimethylsilyl) on frontier orbitals, charge distribution, static polarizabilities, molecular vibrations, bandgaps and photoluminescence quantum yields of 5,5'-diphenyl-2,2'-bithiophene (PTTP).

Synthesis and photophysical properties of halogenated derivatives of (dibenzoylmethanato)boron difluoride.

A series of (dibenzoylmethanato)boron difluoride (BFDBM) derivatives with a halogen atom in one of the phenyl rings at the para-position were synthesized and used to elucidate the effects of changing the attached halogen atom on the photophysical properties of BFDBM. The room-temperature absorption and fluorescence maxima of fluoro-, chloro-, bromo- and iodo-substituted derivatives of BFDBM in THF are red-shifted by about 2-10nm relative to the corresponding peaks of the parent BFDBM. The fluorescence quantum yields of the halogenated BFDBMs (except the iodinated derivative) are larger than that of the unsubstituted BFDBM.

Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals.

Thiophene-phenylene co-oligomers (TPCOs) are among the most promising materials for organic light emitting devices. Here we report on record high among TPCO single crystals photoluminescence quantum yield reaching 60%. The solution-grown crystals are stronger luminescent than the vapor-grown ones, in contrast to a common believe that the vapor-processed organic electronic materials show the highest performance.

Nanostructured organosilicon luminophores and their application in highly efficient plastic scintillators.

Organic luminophores are widely used in various optoelectronic devices, which serve for photonics, nuclear and particle physics, quantum electronics, medical diagnostics and many other fields of science and technology. Improving their spectral-luminescent characteristics for particular technical requirements of the devices is a challenging task. Here we show a new concept to universal solution of this problem by creation of nanostructured organosilicon luminophores (NOLs), which are a particular type of dendritic molecular antennas.

Facile synthesis and optical properties of bithiophenesilane monodendrons and dendrimers.

Three generations of bithiophenesilane monodendrons and dendrimers consisting of 3-45 2,2'-bithiene-5,5'-diyl units were synthesized by means of effective coupling reactions between the corresponding bithienyllithium derivatives and chlorosilanes. These compounds show efficient photoluminescence in the violet-blue region, the quantum yield of which is 5-15 times higher than that for the parent bithiophene or bithiophenesilanes.