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16 results for “fluorescence yield”

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zenodo48/100

Experimental determination of the gadolinium L subshells fluorescence yields and Coster-Kronig transition probabilities

<p>Data associated with the two main tables of the publication &quot;Experimental determination of the gadolinium L subshells fluorescence yields and Coster-Kronig transition probabilities&quot;. There are two .txt files containing tabulator-separated&nbsp;values:</p> <p><em>tabl01_ck.txt: </em>Data associated with Table 1 of the publication. This file contains the L subshell Coster-Kronig (CK) factors and their respective uncertainties.</p> <p><em>tabl02_fy.txt: </em>Data associated with Table 2 of the publication. This file contains the experimentally determined Gd L subshell fluorescence yields in comparison to available literature sources and their respective uncertainties.</p> <p>For more details see the original Open Access publication:</p> <p>Kayser, Y.,&nbsp;H&ouml;nicke, P.,&nbsp;Wansleben, M.,&nbsp;W&auml;hlisch, A.,&nbsp;Beckhoff, B.,&nbsp;<em>X-Ray Spectrom</em>&nbsp;2022,&nbsp;1.&nbsp;<a href="https://doi.org/10.1002/xrs.3313">https://doi.org/10.1002/xrs.3313</a></p>

opencc-by-4.0Mar 2023View details →
dryad40/100

Dityrosine formation via reactive oxygen consumption yields increasingly recalcitrant humic-like fluorescent organic matter in the ocean

Open the record for dataset details and reuse information.

publicFeb 2020View details →
zenodo36/100

Source code of tables for the publication "K- and L-shell theoretical fluorescence yields for the Fe isonuclear sequence"

<p>In this work, we present K- and L- shell fluorescence yield values of the full isonuclear sequence of Fe ions, using a state-of-the-art multiconfiguration Dirac-Fock approach. These results may be of importance for spectral fitting and plasma modeling, both in laboratory and astrophysical studies, where Fe is an important benchmark element. The K-shell fluorescence yields were found to be very similar up to the removal of 14 electrons.</p>

opencc-by-4.0Oct 2024View details →
zenodo36/100

Data for "Shrinking gate fluorescence correlation spectroscopy yields equilibrium constants and separates photophysics from structural dynamics"

<p>We provide the raw data for the paper &quot;Shrinking gate fluorescence correlation spectroscopy yields equilibrium constants and separates photophysics from structural dynamics&quot;. The files hold time tagged and time resolved single photon data from experiments on immobilized structures as well on free diffusion structures. The files have PicoQuant&#39;s .ptu files-format.</p> <p>Additionally we provide the python scripts used to analyze these data sets.</p>

opencc-by-4.0Oct 2022View details →
zenodo32/100

Spatial and temporal drivers of in situ fluorescence quantum yield variability in the Southern Ocean

<p>The datasets in this repository are part of the manuscript entitled &quot;Spatial and temporal drivers of in situ fluorescence quantum yield variability in the Southern Ocean&quot;.</p>

opencc-by-4.0Mar 2022View details →
zenodo32/100

Fig. 5. A in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 5. A Reactivity of the α-alectoronic acid 18 and the α-collatolic acid 19 with K. B Structure of the perlatolic acid 20.

opennotspecifiedJun 2022View details →
zenodo32/100

Fig. 2 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 2. δ-keto ester-containing depsides considered in this study. 1 (Elix and Whitton, 1989); 2 (Elix et al., 1996; Elix and Wardlaw, 1997; Orange, 2014); 3 (Culberson et al., 1977; P´erez et al., 2016); 4 (Huneck et al., 1970).

opennotspecifiedJun 2022View details →
zenodo32/100

Fig. 9 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 9. KUV probe on extracts of P. cinereoatra C, P. speirea var speirea S, P. irriguaI I, P. macrocarpa Ma and P. platycarpoides P. Extracts were spotted and K was added (right) or not (left).

opennotspecifiedJun 2022View details →
zenodo32/100

Fig. 1 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 1. Molecular structures of glomelliferic acid 1 and glomellic acid 2 and their fluorescent behaviour upon addition of K. Key 2-oxoalkyl motif highlighted in blue. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedJun 2022View details →
zenodo32/100

Fig. 10. A in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 10. A. Direct application of the KUV probe on the medulla of P. cinereoatra; B. KUV probe on the eluted TLC (solvent G) of Porpidia cinereoatra C, P. tuberculosa T, P. speirea var speirea S, P. melinodes M, P. contraponenda Co, P. irrigua I and P. rugosa R.

opennotspecifiedJun 2022View details →
zenodo32/100

Fig. 8 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 8. Relaxed coordinate scans of simplified despides under A. neutral and B. basic conditions; C. Energy minimized structure of simplified depsidone under basic conditions; D. Manually adjusted dihedral angle to position the enolate close to the ester carbonyl group.

opennotspecifiedJun 2022View details →
zenodo28/100

Fig. 11 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 11. Structural data of compound s8 (NMR in acetone-d6).

opennotspecifiedJun 2022View details →
zenodo28/100

Fig. 4 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 4. Reactivity of the methyl, 2′-O-methylmicrophyllinate 4′ with K.

opennotspecifiedJun 2022View details →
zenodo28/100

Fig. 3 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 3. Reactivity of depsides with K.

opennotspecifiedJun 2022View details →
zenodo28/100

Fig. 7. A. Depsides rearrangement mechanisms with K in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 7. A. Depsides rearrangement mechanisms with K; B. MS fragmentation.

opennotspecifiedJun 2022View details →
zenodo28/100

Fig. 6 in Intramolecular transesterification of depsides yields fluorescent 1H-isochromen-1-ones: Application as a chemical probe for lichen determination

Fig. 6. UV and fluorescence spectra of the isochromen-1-ones 9 and 11.

opennotspecifiedJun 2022View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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Last verified 2026-04-29Open record

OpenNeuro

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Last verified 2026-04-29Open record