Phenoxy-benzothiadiazole dyes: Synthesis,photophysical properties and preliminary application in OLEDs

The synthesis of a phenoxy-benzothiadiazole (BTD) derivative is reported for the first time. This derivative was employed as an intermediate in the obtention of two novel highly fluorescent aryl-phenoxy-BTD dyes. Their photophysical properties were evaluated in solution and the results indicate a strong intramolecular charge transfer (ICT) character in the excited state. The luminophore 3a, possessing a donor-BTD-phenoxide architecture, exhibits superior fluorescence quantum yield (0.67) than the designed acceptor-BTD-phenoxide dye (0.06). After electrochemical and photoluminescence characterization of thin films of 3a, an OLED with the configuration ITO/PEDOT:PSS/3a/TPBi/LiF/Al was constructed. This device displayed a green emission centered at 547?nm, with CIE coordinates of (0.40, 0.55). For comparison, an OLED using a previously reported luminescent BTD-pyridyl derivative was also constructed. The OLED made with the phenoxy-BTD derivative operated using less current density and led to higher irradiance and electrical stability, indicating the high potential of ArO-BTD dyes for future application in electroluminescent devices.     

Closed-loop recirculating manifold for matrix isolation in flow injection flame atomic absorption spectrometry. Analysis of silver electrolysis solutions

Two flow injection procedures have been investigated for the determination of some elements in silver electrolysis solutions, for which the problem of the formation of silver acetylide needs to be addressed. A single line manifold was found to give acceptable results for limited time periods, but for prolonged operation it was necessary to remove the silver. This was achieved with a recirculating reactor in which the silver was precipitated as the chloride and retained on a filter of nylon fibers. Good recoveries of copper, iron, nickel and zinc from solutions containing up to 100 g/l. silver were obtained with over 95% of the silver retained on the filter. The filter was regenerated rapidly by flushing with ammonia solution.     

Fluorescence of ammonia-d3 from its first excited singlet state

Structured emission spectra have been observed from ND₃ excited at 2139 Å and 2144 Å. The emission is short-lived (τ_{$\text{1}\text{2}$} < 10^?10 s) and has been assigned to the ND₃($\text{A}$) → ND₃($\text{X}$) fluorescence transition.     

Atomic spectrometric detectors for flow-injection analysis

The distinction between liquid chromatography and flow injection analysis is discussed in terms of the underlying concepts, the performance characteristics and the hardware involved. For the last aspect, attention is focused on the role of the detector and the development of spectroscopic detectors for these techniques is discussed. The limitations of atomic spectrometric detectors are discussed for the three most widely used techniques, flame atomic absorption spectrometry, plasma spectrometry and electrothermal atomisation atomic absorption spectrometry, and the recent literature concerned with the use of these techniques for chromatographic detectors is summarized. The use of flow-injection methods to extend the capabilities of the techniques, particularly as far as detection limits and matrix interferences are concerned, is discussed. These topics are illustrated by a detailed review of relevant papers from 1988 and 1989. It is concluded that there is a considerable sustained research effort in this field.     

Synthesis of the quinolizidine alkaloids (-)-lasubine II and (+/-)-myrtine by conjugate addition and intramolecular acylation of amino esters with acetylenic sulfones

The conjugate additions of (2-piperidyl)acetate esters to acetylenic sulfones, followed by LDA-promoted intramolecular acylations, afforded cyclic enaminones that were readily converted into the corresponding 4-substituted 2-keto- or 2-hydroxyquinolizidines by stereoselective reduction and desulfonylation. This procedure was applied to the total synthesis of (-)-lasubine II from methyl (S)-(2-piperidyl)acetate and 2-(3,4-dimethoxyphenyl)-1-(p-toluenesulfonyl)ethyne. Similarly, methyl (+/-)-(2-piperidyl)acetate and 1-(p-toluenesulfonyl)propyne provided (+/-)-myrtine.     

Atomic spectrometry and flow injection analysis: a synergic combination

The combination of flow-injection techniques with atomic spectrometry (flame atomic absorption and emission spectrometry and inductively-coupled plasma/atomic emission spectrometry) is reviewed, with particular reference to the more recent contributions. The considerable growth in the number of directly couple pre-concentration and matrix isolation is noted, together with the increasing number of reports of indirect methods for metals, inorganic anions and even drug molecules. Many developments are motivated by a desire to increase the performance of the spectrometry over that obtained with conventional methods of sample introduction. Conflicting statements concerning the possible benefits of reduced uptake rate, of air compensation and of peak-area measurement are examined critically. The conflicting requirements of obtaining freedom from stable-compound interferences coupled with god detection limits are discussed, as are means of obtaining the best detection limits. Modifications to nebuliser and spray-chamber design are suggested for maximising peak height (to obtain detection limits) and for working with reduced uptake rates (to reduce stable-compound interferences in flame-based spectrometries). The single well-stirred tank model is used to model nebuliser response and results are presented for the flow-injection behaviour of a Philips Scientific SP9 instrument under conditions of low flow rate which show reasonable agreement with the model. With the instrument, the best detection limits are obtained on the basis of peak-height measurements at the flow rate producing maximum signal-to-noise ratio.