Behavioural studies of stimulated luminescence from feldspars

Since the work of Mejdahl in the mid-1980s feldspars have been used widely for palaeodosimetry. They have proved particularly popular because of the technical ease with which an optically stimulated luminescence signal can be obtained, and the potential for their use in dating over a wider time range than quartz. However, while the use of infrared stimulated lminescence has been a great success, the realisation of the potential for dating over a wide time range has been hampered by a series of behavioural problems, in particular concerned with the stability of the luminescence signal. This paper surveys the current state of knowledge of a range of aspects of the stimulated luminescence behaviour of feldspar. Particular attention is paid to the thermal and optical properties of the thermoluminescence (TL) and optically stimulated luminescence (OSL) signals from feldspars since these are of greatest relevance to their use as palaeodosimeters. Results obtained from well-characterised museum specimens demonstrate the variety of responses that are seen from different types of feldspar, particularly in their TL behaviour. Less variation is seen in their OSL response. In contrast, the response of potassium-rich feldspars separated from Quaternary sediments tends to be very consistent when many grains are analysed simultaneously, suggesting that averaging of the signal simplifies the behaviour of the system.     

Spectral information from minerals relevant for luminescence dating

The paper reviews basic spectral features of luminescence from minerals used in dating and allied research. Luminescence production is a result of multiple interactions within the imperfect crystal lattice and spectral information is not limited to the emission of light. Results of spectral investigations of luminescence emission during thermal stimulation (TL) or optical stimulation (OSL) form the main part of the paper. However, information on luminescence excitation and light absorption spectroscopy is also presented and possible links between luminescence production in minerals and particular lattice defects are considered. Quartz and feldspars, the most commonly used minerals, receive special attention, but the review includes other materials such as polymineral fine-grained fractions from sediments, zircon, calcite and other salts (halite, sulfate), meteorites, flint, volcanic materials (obsidian, tephra), ceramics and metallurgical slags. Although a wide range of different luminescence emission wavebands occur, it can be shown that certain emissions dominate in particular materials. Basic dosimetric properties are often known just for single emission wavebands of a particular mineral, and are listed in this case. The paper also aims to provide a starting point and inspiration for the study of other TL and OSL emissions, with particular regard to their potential and suitability for dating and related dosimetry tasks. These investigations, involving palaeodose determination based on an emission waveband with known characteristics, need careful separation of the particular emission peak, which may be influenced by its behaviour during the dating procedure (sample preparation, irradiation, preheat treatments, luminescence measurements, etc.). Spectral information available in this context and some technical remarks on the experimental conditions will be given to pave the way for conventional TL or OSL measurements in luminescence dating and dosimetry using natural or semi-natural materials.     

Nafion-Induced Metal-Metal Interactions in a Platinum(II) Terpyridyl Acetylide Complex:a Luminescent Sensor for Detection of Volatile Organic Compounds

Introduction The design of new solid-state sensor materials that can selectively adsorb volatile organic compounds (VOC) and produce measurable color and/or lumines-cence changes is of potential significance in the sense of environmental and public safety control.1-5 The use of metal complexes as optical sensors for VOC detection has been reported, and most of them are based on the susceptibility of metal-to-ligand charge transfer (MLCT) and/or metal-metal-to-ligand charge transfer (MMLC…     

Synthesis,characterization, and electroluminescence of PPV copolymers containing electron and hole‐transporting units

Three series of poly(phenylene vinylene) (PPV) derivatives containing hole‐transporting triphenylamine derivatives [N‐(4‐octoxylphenyl)diphenylamine, N,N′‐di(4‐octyloxylphenyl)‐N,N′‐diphenyl‐1,4‐phenylenediamine, and N,N′‐di(4‐octoxylphenyl)‐N,N′‐diphenylbenzidine] (donor) and electron‐transporting oxadiazole unit (2,5‐diphenyl‐1,3,4‐oxadiazole) (acceptor) in the main chain were synthesized by improved Wittig copolymerization. The resulting donor–acceptor (D‐A) polymers are readily soluble in common organic solvents, such as chloroform, dichloroethane, THF, and toluene. The polymers containing oxadiazole group exhibit good thermal stability with 5% weight loss above 400 °C. The intramolecular charge‐transfer was observed in these D‐A polymers. In comparison with corresponding polymers without oxadiazole unit, the single‐layer devices based on the D‐A polymers showed much improved electroluminescent properties, because of the balanced charge injection and transport. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1566–1576, 2008     

Synthesis and ion‐sensing phenomena of two new helical conjugated oligomers containing 1,10‐phenanthroline and oligo‐alkylthiophene

Two new 1,10‐phenanthroline (Phen) containing conjugated oligomers, oligo‐3,8‐bis(4‐octylthiophene‐2‐yl)‐1,10‐phenanthroline) (PDTPh) and oligo‐3,8‐bis‐(4‐octyl‐5‐(4‐ctylthiophene‐2‐yl)thiophene‐2‐yl)‐1,10‐phenanthroline) (PTTPh), as well as their corresponding monomers (OTPhOT and OTOTPhOTOT) were prepared and their metal ion‐sensing properties were investigated. The oligomers showed high thermal stability, good proccessibility, and gave varied color when reacted with different metal ions. Oligomers also showed distinct responses toward metal ions when compared with their corresponding monomers, suggesting that the ionochromic responses were determined by not only the coordinating ability of Phen unit but also the conformation of oligomer chains. Moreover, the differences in the ion‐sensing behaviors between OTPhOT and OTOTPhOTOT also suggested that the coordination ability of Phen depends on its substituents. The oligo‐alkylthiophene moieties in PDTPh and PTTPh acted as spacers to reorganize the conformation of the oligomer chains, as well as the electron donating groups to adjust the coordination ability of the Phen. These findings provide a clue for designing Phen‐containing ion‐sensors for specified ion‐sensing applications. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 1586–1597, 2008     

Anion recognition and sensing in organic and aqueous media using luminescent and colorimetric sensors

This review article focuses primarily on the work carried in our laboratories over the last few years using luminescent and colorimetric sensors, where the anion recognition occurs through hydrogen bonding in organic or aqueous solvents. This review begins with the story of the discovery of fluorescent photoinduced electron transfer (PET) sensors for anions using charged neutral urea or thiourea receptors where both fluorescent and NMR spectroscopic methods monitored anion recognition. This work led to the development of dual luminescent and colorimetric anion sensors based on the use of the ICT based naphthalimide chromophore, where ions such as fluoride gave rise to changes in both the fluorescence and the absorption spectra of the sensors, but at different concentrations. Here, the former changes were due to hydrogen bonding interactions, whereas the latter was due to the deprotonation of acidic protons, giving rise to the formation of the bifluoride anion (HF₂⁻). Modification of the 4-amino-l,8-naphthalimide moiety has facilitated the formation of colorimetric anion sensors that work both in organic or aqueous solutions. Such charge neutral receptor motifs have also been incorporated into organic scaffolds with norbomyl and calixarene backbones, which have enabled us to produce anion directed self-assembled structures.     

Radiation induced luminescence processes in c-BN

Spectral properties of cubic boron nitride have been studied using methods of photoluminescence (PL), X-ray excited luminescence (XL), thermoluminescence (TL) and optically stimulated luminescence. It is found that emission of cubic boron nitride is presented by 4 subbands, their relative yield is determined by the excitation type: blue, green (dominant) and red bands are observed in PL, ultraviolet, blue (dominant), green and red bands—in XL. Three thermal peaks are found in TL curves in the 0–700°C temperature range, their presence and intensity depend on radiation type used. A tentative correspondence between thermal peaks and emission bands is found.     

Photoluminescence spectra of copper-based planar nanostructures

We have studied the luminescence of planar nanostructures based on amorphous copper, excited by a low-intensity source in the UV region of the spectrum. We have shown that it is dependent on the packing density of copper granules on the surface of the quartz substrate, the presence of chains of granules, the optical properties of the surrounding medium, and the oxidation time. The observed maxima at the wavelengths of 400 nm and 520 nm correspond to luminescence of the quartz and copper oxide Cu₂O. The maximum at 650 nm is located in the region of plasma resonances of the oxidized copper chains and aggregates, and is enhanced in the “hot spot” region near the surface of interacting copper particles. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 73, No. 4, pp. 510–515, July–August, 2006.     

Cluster model for complex compounds of hexavalent uranium

We have studied the regular patterns of the change in the electronic transition frequency in low-temperature luminescence spectra of uranyl trinitrate and tetranitrate crystals with alkali metal cations or an NH ₄ ⁺ group as the outer-sphere cations, as a function of the ionization potential of the latter. An analogous study was carried out as a function of the ratio of the concentrations of impurity and matrix for different cations in mixed crystals and solid solutions. Analysis of the results obtained, together with available crystallographic data, allowed us to propose a cluster model for the uranyl complex. The observed regular patterns are also explained from the standpoint of statistical thermodynamics. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 73, No. 5, pp. 588–591, September–October, 2006.