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The solution spectrum of the 12-DOXYL is dominated by the spin exchange narrowing expected for concentrated assemblies of the 12-DOXYL molecules, such as a micelle or bilayer.
The spectrum of reduced FAD was recovered from the difference spectrum by adding to it the conventionally determined solution spectrum of the stable oxidized form of the redox couple.
It is sometimes assumed that any solution spectrum which changes as a function of polarity of the solvent is of CTTS nature.
The λmax extracted from the solution spectrum of 5,5′ -BZ at 525 nm is smaller compared to the λmax of 550 nm of the solution spectrum of 5,5′ -BT.
Figure 3a shows the allowable solution spectrum for each EM, where the spectrum for each EMC contains 146 data points.
In fact, the λmax extracted from the solution spectrum of 5,5′ -BZ is comparable to that of 5,5′ -Br.
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Thin films exhibit an intense PL emission with a slightly red-shifted maximum at 532 nm compared to that in the solution spectra.
Figure 8 shows the normalized UV visible absorption spectra of the Pt clusters hydrosol measured at 0.2 mM concentration of Pt0 and precursor solution spectra (Pt4+ ions) was measured at 1.0 mM concentration.
Previously, although existence of a feature was calculated at 12.3 μm for longaxis polarization, it was not found in solution spectra and in stretched polyethylene spectra, and finally it was not assigned (Radziszewski and Michl, 1985).
Solution spectra of peptides were made in deuterated 10 mM phosphate buffer, pD 7.4 (pD = pH+0.4) and in structure promoting mixed solvent-buffer solutions (trifluoroethanol (TFE) or hexafluoroisopropanol (HFIP) at a sample concentration of 1 mM.
Solution spectra of peptides were made in deuterated 10 mM phosphate buffer, pD = 7.4 (pD = pH+0.4) and in structure promoting mixed solvent-buffer solutions (trifluoroethanol (TFE) or hexafluoroiso propanol (HFIP).
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