Dual Fluorescence (dual + fluorescence)

Distribution by Scientific Domains


Selected Abstracts


Abnormal Endothelial Tight Junctions in Active Lesions and Normal-appearing White Matter in Multiple Sclerosis

BRAIN PATHOLOGY, Issue 2 2002
Jonnie Plumb
Blood-brain barrier (BBB) breakdown, demonstrable in vivo by enhanced MRI is characteristic of new and expanding inflammatory lesions in relapsing-remitting and chronic progressive multiple sclerosis (MS). Subtle leakage may also occur in primary progressive MS. However, the anatomical route(s) of BBB leakage have not been demonstrated. We investigated the possible involvement of interendothelial tight junctions (TJ) by examining the expression of TJ proteins (occludin and ZO-1) in blood vessels in active MS lesions from 8 cases of MS and in normal-appearing white (NAWM) matter from 6 cases. Blood vessels (10,50 per frozen section) were scanned using confocal laser scanning microscopy to acquire datasets for analysis. TJ abnormalities manifested as beading, interruption, absence or diffuse cytoplasmic localization of fluorescence, or separation of junctions (putative opening) were frequent (affecting 40% of vessels) in oil-red-O-positive active plaques but less frequent in NAWM (15%), and in normal (<2%) and neurological controls (6%). Putatively "open" junctions were seen in vessels in active lesions and in microscopically inflamed vessels in NAWM. Dual fluorescence revealed abnormal TJs in vessels with pre-mortem serum protein leakage. Abnormal or open TJs, associated with inflammation may contribute to BBB leakage in enhancing MRI lesions and may also be involved in subtle leakage in non-enhancing focal and diffuse lesions in NAWM. BBB disruption due to tight junctional pathology should be regarded as a significant form of tissue injury in MS, alongside demyelination and axonopathy. [source]


Spectroscopic and Computational Study on New Blue Emitting ReL(CO)3Cl Complexes Containing Pyridylimidazo[1,5- a]pyridine Ligands

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 23 2008
Claudio Garino
Abstract The structural and photophysical properties of three new ReL(CO)3Cl complexes (ReL1,ReL3) and their 1-(2-pyridyl)imidazo[1,5- a]pyridine ligands, namely 3-methyl-1-(2-pyridyl)imidazo[1,5- a]pyridine (L1), 1-(2-pyridyl)-3-[4-(trifluoromethyl)phenyl]imidazo[1,5- a]pyridine (L2), and 3-(4-nitrophenyl)-1-(2-pyridyl)imidazo[1,5- a]pyridine (L3), were studied by spectroscopy, X-ray diffraction, and computational methods. ReL1,ReL3 have high-energy singlet emissions arising from a , , ,* ligand-centered state. In oxygen-free acetonitrile solutions, the complexes display dual fluorescence due to intense ligand-centered triplet emission.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]


Exploiting a Dual-Fluorescence Process in Fluorene,Dibenzothiophene- S,S -dioxideCo-Polymers to Give Efficient Single Polymer LEDs with Broadened Emission

ADVANCED FUNCTIONAL MATERIALS, Issue 4 2009
Simon M. King
Abstract A description of the synthesis of random (9,9-dioctylfluorene-2,7-diyl),(dibenzothiophene- S,S -dioxide-3,7-diyl) co-polymers (p(F-S)x) by palladium-catalyzed Suzuki cross-coupling polymerization where the feed ratio of the latter is varied from 2 to 30,mol % (i.e., x,=,2,30) is given. Polymer light emitting devices are fabricated with the configuration indium tin oxide/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid)/p(F,S)x/Ba/Al. The device external quantum efficiency increased as the ratio of the S co-monomer was increased, up to a maximum of 1.3% at 100,mA cm,2 for p(F-S)30 and a brightness of 3 770,cd m,2 (at 10,V). The S units impart improved electron injection, more balanced mobilities, and markedly improved device performance compared to poly(9,9-dioctylfluorene) under similar conditions. These co-polymers display broad emission, observed as greenish-white light, which arises from dual fluorescence, viz. both local excited states and charge transfer states. Utilizing dual emission can reduce problems associated with Förster energy transfer from high-energy to-low energy excited states. [source]


Fluorescence and photoisomerization studies of p -nitrophenyl-substituted ethenylindoles

JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 1 2006
Anil K. Singh
Abstract The synthesis, electronic absorption, fluorescence (,f, ,ex, ,f, ,f) and photoisomerization (,t,c, photostationary state composition) properties of 3-(4-nitrophenylethenyl- E)-NH-indole (1), 3-(4-nitrophenylethenyl- E)- N -ethylindole (2) and 3-(4-nitrophenyl ethenyl- E)- N -benzenesulfonylindole (3) in organic solvents of varying polarity are reported. The absorption maximum of these compounds undergoes a moderate red shift with increasing solvent polarity. However, the fluorescence maximum becomes highly red shifted with increasing solvent polarity. Whereas 1 and 2 show broad fluorescence bands, 3 exhibits dual fluorescence. Further, 1 and 2 fluoresce much more efficiently than 3. Correlation of the Stokes shift with solvent polarity parameters such as ,f and ET(30) and excited-state dipole moment indicate a highly polar excited state for 1,3. Time-resolved fluorescence studies show that the fluorescence decays are single- and multi-exponential type, depending on the solvent polarity. Further, 1 and 2 do not show photoisomerization on irradiation. However, 3 is photoactive and shows efficient photoisomerization in non-polar heptane. The sensitivity (,) of the photoreaction is determined in various solvent in terms of the Hammett plot, which showed that the excited states involved are electron deficient in nature and consequently stabilized more by an electron sufficient polar solvent and electron donating substituent. These results led us to suggest the existence of three types of excited states, namely the locally excited state, the intramolecular charge-transfer excited state and the conformationally relaxed intramolecular charge-transfer excited state in the photoprocesses of these compounds. Copyright © 2005 John Wiley & Sons, Ltd. [source]


Qualitative aspects of sperm stock in males and females from Eupelmus orientalis and Dinarmus basalis (Hymenoptera: Chalcidoidea) as revealed by dual fluorescence

PHYSIOLOGICAL ENTOMOLOGY, Issue 2 2002
David Damiens
Abstract The quality of a sperm population can be characterized physiologically and its fecundity predicted by its viable : non-viable sperm ratio. To improve the knowledge of reproductive strategies in two ectoparasitoid hymenopteran species, Eupelmus orientalis Crawford (Hymenoptera: Eupelmidae) and Dinarmus basalis Rondani (Hymenoptera: Pteromalidae), the assessment of sperm viability using the dual fluorescence staining procedure SYBR-14 : propidium iodide was developed. The aim of the study was to provide a comparative test in vitro applicable to both sexes to study the evolution of sperm quality at various stages of the reproductive processes. The reliability of propidium iodide to detect non-viable sperm (stained in red) was confirmed in both species on the basis of two stress tests (ethanol and Triton X-100) but our study also revealed that propidium iodide concentrations must be adequately adjusted for each single species. This experiment also demonstrated the physiological heterogeneity of sperm populations in E. orientalis and D. basalis males and females. In both species, 40% of the sperm in the seminal vesicles was found to be non-viable. By contrast with E. orientalis, the populations of non-viable sperm estimated from the seminal vesicles of D. basalis were found to be strongly different from those observed in the spermatheca. From the present results, the population of viable sperm detected in the spermatheca of females from both species proved a reliable predictor of fertilization achieved in ovipositing females. [source]


Pressure-Induced Emission Enhancement of a Series of Dicyanovinyl-Substituted Aromatics: Pressure Tuning of the Molecular Population with Different Conformations

CHEMPHYSCHEM, Issue 8 2008
Qian Wang Dr.
Abstract A series of dicyanovinyl-substituted aromatic compounds (Ar-DCV; Ar=9-anthracenyl, 1-naphthyl, 1-pyrenyl) with dual fluorescence are prepared, and their emission properties,when molecularly dispersed in a polymer medium,are investigated under pressure perturbation. The total emission intensity is enhanced drastically from ambient pressure up to 70 kbar. Emission 30,107 times more intense than that at ambient pressure is observed at higher pressure. In dual emission, the enhancement of the local excited state (LE state) is significantly different from that of the intramolecular charge-transfer state (ICT state). The intensity of the ICT emission increases faster (30,370 times) than that of the LE emission (less than 20 times). In accordance with spectroscopic data, emission dynamics at different pressures, and computational studies on the molecular conformations of these compounds, a kinetic model is proposed to explain the effect of pressure on the emissive properties of the Ar-DCV compounds from the point of view of pressure-dependent populations of the species in the ground state. [source]