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The effect of ultrasound on electrochenical processes : dye effluent remediation and the anodic behaviour of copperPlattes, M. January 2003 (has links)
No description available.
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Fast photochromic systemsBradshaw, C. January 1988 (has links)
No description available.
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Kinetic factors in textile printing with fibre-reactive dyesArifoglu, M. January 1987 (has links)
No description available.
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An investigation into the measurement of particle size in concentrated dispersions by means of angular dependent light scatteringHiggs, D. M. J. January 1989 (has links)
No description available.
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Novel dyestuffs and alkenylidenecyclopropanes in synthesisJones, Nigel R. January 1995 (has links)
No description available.
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Synthesis and luminescence studies of some organometallic complexesStunt, R. A. January 1987 (has links)
No description available.
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Properties of organosiloxane liquid crystals for dye guest host ferroelectric display devicesShoosmith, Dean Edward January 2001 (has links)
No description available.
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A continuous-wave dye laser for Raman spectroscopy /Chiu, James Kwan-Hung. January 1976 (has links)
Thesis (M.S.)--Oregon Graduate Center, 1976.
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Continuous-wave dye laser for Raman spectroscopyChiu, James Kwan-Hung 07 1900 (has links) (PDF)
M.S. / Applied Physics / This monograph summarizes the theory and construction of a tunable continuous wave (CW) Rhodamine 6G dye laser longitudinally pumped by an argon laser. (from Introduction; no abstract available)
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Synthesis of nucleoside analogues and fluorescent labels for DNA sequencing and other applications in biotechnologyPredescu, Mihaela Narcisa 01 November 2005 (has links)
Two pyrrolo[2,3-d]pyrimidines and a nucleoside analogue have been prepared. The nucleobases were obtained by spontaneous cyclisation of 4-aminopyrimidyl-acetaldehydes as an acetal. The adenosine analogue has been made by glycosylation of a suitable sugar derivative with the corresponding heterocyclic base. This nucleoside can be converted into fluorescently-labeled chain-terminating substrates for DNA polymerase after subsequent triphosphorylation and coupling to through-bond energy transfer systems. Fluorescein-based donor components to be incorporated into through-bond energy transfer systems have been prepared. The synthesis of 5-ethynylfluorescein-(5-tert-butoxycarbonyl)-pentyl ester has been executed in five steps from 1,3-dihydroxybenzene and phthalic anhydride. The donor fluorescein carboxylate has been alkylated with the tert-butyl ester of 6-bromohexanoic acid to provide a handle for attachment to biomolecules. In the context of regioisomerically pure halofluoresceins, besides the synthesis of pure regioisomers of bromofluorescein derivatives, 5-iodosulfofluorescein and pure regioisomers of 5-nitrofluorescein diacetate, as an intermediate in the synthesis of 5-iodofluoresceins, have been synthesized. New rhodamine-based acceptor components with extended aromatic systems have been prepared from an affordable starting material, tetralin. The attempts to isolate them via repeated recrystallizations and flash chromatography have been unsuccessful. However, these pyrylium cations are expected to fluoresce at longer wavelengths.
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