Tetrazoles: Synthesis, Structures, Physico-Chemical Properties and Application

The paper represents a brief review of works published by the authors over a period of 1980-2003 years in the field of synthesis and investigations of properties of tetrazole derivatives. The main attention is given to problems of regioselective functionalization of the tetrazole ring and the development of simple and convenient methods for the synthesis of N- and C-substituted tetrazoles, to peculiarities of structure of crystalline tetrazoles including quaternary salts and complexes with transition metal salts as well as to the data on electronic, spatial structure and energetic characteristics of tetrazoles obtained using both quantum-chemical methods and IR-, XH , 13C and 15N NMR spectroscopy. The features of thermal decomposition and combustion of various tetrazoles and polyvinyltetrazoles determining the prospects of their use as effective components of different kind combustible and thermally decomposing systems, including those capable of liquid-flame combustion, which has been revealed for the first time, are considere

Selectively Tunable Luminescence of Perovskite Nanocrystals Embedded in Polymer Matrix Allows Direct Laser Patterning

Cesium lead halide perovskite nanocrystals (NCs) have gained enormous attention as promising light-emitting and light-converting materials. Most of their applications require embedding NCs in various matrices, which is a challenging task due to their low stability, especially in the case of red-emitting CsPbI3 NCs. In this work, a new approach is proposed allowing the formation of red-emitting perovskite NCs by anion exchange induced directly inside a solid polymer matrix using green-emitting CsPbBr3 NCs as templates and iodododecane as an iodine source. Moreover, a simple and efficient route to photo-assisted termination of the anion exchange reaction in the polymer composite after reaching desired optical properties is demonstrated. The findings allow the authors to pattern a thin composite film with an ultrashort UV laser resulting in a selective generation of green- and red-emitting features with a 15 µm resolution

Dual-color emitting quantum-dot-quantum-well CdSe-ZnS heteronanocrystals hybridized on InGaN/GaN light emitting diodes for high-quality white light generation

Cataloged from PDF version of article.We report white light generation by hybridizing green-red emitting (CdSe)ZnS/CdSe (core)shell/shell quantum-dot-quantum-well heteronanocrystals on blue InGaN/GaN light emitting diodes with the photometric properties of tristimulus coordinates (x,y)=(0.36,0.30), luminous efficacy of optical radiation LE=278 lm/W, correlated color temperature CCT=3929 K, and color-rendering index CRI=75.1. We present the photometric analysis and the quantum mechanical design of these dual-color emitting heteronanocrystals synthesized to achieve high-quality white light when hybridized on light emitting diodes. Using such multicolor emitting heteronanocrystals facilitates simple device implementation while providing good photometric properties. (C) 2008 American Institute of Physics

Colloidal Nanocrystals Embedded in Macrocrystals: Robustness, Photostability, and Color Purity

Cataloged from PDF version of article.The incorporation of colloidal quantum dots (QDs) into ionic crystals of various salts (NaCl, KCl, KBr, etc.) is demonstrated. The resulting mixed crystals of various shapes and beautiful colors preserve the strong luminescence of the incorporated QDs. Moreover, the ionic salts appear to be very tight matrices, ensuring the protection of the QDs from the environment and as a result providing them with extraordinary high photo- and chemical stability. A prototype of a white light-emitting diode (WLED) with a color conversion layer consisting of this kind of mixed crystals is demonstrated. These materials may also find applications in nonlinear optics and as luminescence standards

trans-Dichloridotetrakis­[1-(2-hydroxy­ethyl)-1H-tetrazole-κN 4]cobalt(II)

The title cobalt(II) complex, [CoCl2(C3H6N4O)4], was obtained from metallic cobalt by direct synthesis. There are two Co atoms in the asymmetric unit, each lying on an inversion centre and adopting a distorted octa­hedral coordination. Classical and non-classical hydrogen bonds are responsible for formation of a three-dimensional polymeric network in the crystal

Influence of the stabilizing ligand on the quality, signal-relevant optical properties, and stability of near-infrared emitting Cd1₁₋ₓHgₓTe nanocrystals

Bright and stable near-infrared (NIR) and infrared (IR) emitting chromophores are in high demand for applications in telecommunication, solar cells, security barcodes, and as fluorescent reporters in bioimaging studies. The best choice for wavelengths >750 nm are semiconductor nanocrystals, especially ternary or alloy nanocrystals like CdHgTe, which enable size and composition control of their optical properties. Here, we report on the influence of growth time and surface chemistry on the composition and optical properties of colloidal CdHgTe. Up to now, these are the only NIR and IR emissive quantum dots, which can be synthesized in high quality in water, using a simple one-pot reaction. For this study we utilized and compared three different thiol ligands, thioglycolic acid (TGA), 3-mercaptopropionic acid (MPA), and glutathione (GSH). Aiming at the rational design of bright NIR- and IR-emissive alloy materials, special emphasis was dedicated to a better understanding of the role of the surface ligand and adsorption–desorption equilibria on the photoluminescence quantum yield and stability. In this respect, dilution and protonation studies were performed. Our results show that with this simple synthetic procedure, strongly fluorescent CdHgTe colloids can be obtained with MPA as stabilizing ligand revealing quantum yields as high as 45% independent of particle concentration

Structural tuning of color chromaticity through nonradiative energy transfer by interspacing CdTe nanocrystal monolayers

Cataloged from PDF version of article.We proposed and demonstrated architectural tuning of color chromaticity by controlling photoluminescence decay kinetics through nonradiative Forster resonance energy transfer in the heterostructure of layer-by-layer spaced CdTe nanocrystal (NC) solids. We achieved highly sensitive tuning by precisely adjusting the energy transfer efficiency from donor NCs to acceptor NCs via controlling interspacing between them at the nanoscale. By modifying decay lifetimes of donors from 12.05 to 2.96 ns and acceptors from 3.68 to 14.57 ns, we fine-tuned chromaticity coordinates from (x,y)=(0.575,0.424) to (0.632, 0.367). This structural adjustment enabled a postsynthesis color tuning capability, alternative or additive to using the size, shape, and composition of NCs

Macrocrystals of Colloidal Quantum Dots in Anthrancene: Exciton Trannsfer and Polarized Emission

Cataloged from PDF version of article.In this work, centimeter-scale macrocrystals of nonpolar colloidal quantum dots (QDs) incorporated into anthracene were grown for the first time. The exciton transfer from the anthracene host to acceptor QDs was systematically investigated, and anisotropic emission from the isotropic QDs in the anthracene macrocrystals was discovered. Results showed a decreasing photoluminescence lifetime of the donor anthracene, indicating a strengthening energy transfer with increasing QD concentration in the macrocrystals. With the anisotropy study, QDs inside the anthracene host acquired a polarization ratio of similar to 1.5 at 0 degrees collection angle, and this increases to similar to 2.5 at the collection angle of 60 degrees. A proof-of-concept application of these excitonic macrocrystals as tunable color converters on light-emitting diodes was also demonstrated