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This can be assigned to Cu in-diffusion from the Cu-related surface complexes observed in EPR spectra.
Spectra of collagen and parchment are similar, with few exceptions such as the absorption at 1031 cm−1 in parchment which is absent in collagen; this can be assigned to aromatic C C vibrational modes in tannins, and has been proposed as a marker for tannin-processing of parchment [66].
This can be assigned as trigonal bypyramidal equatorial-axial [Rh(H)(Ph-BPE)(CO 2], which has previously been detected by Vogt and Cornelissen under conventional hydroformylation conditions (Scheme 3).[ 9] In our view, this species is clinching evidence for a tandem decarbonylation/hydroformylation pathway for these reactions.
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(Note that when the CS is absent on a specific trial, this trial can be assigned unambiguously to the CS+ or CS − factor because this factor was blocked).
Therefore, this peak can be assigned to trimers.
This emission can be assigned more likely to defect states in the SRSO film.
This signal can be assigned to CO2− radicals, which were previously detected in MgO, NaHCO2, and KHCO2[17 19].
This decrease can be assigned to increasing magnetic interactions between neighboring wires caused by increasing side-pore length.
This change can be assigned to the synergism between Ru particles and Fe species on the surface of meso-TiO2 support.
Furthermore, this set can be assigned in such a way that the false rejection/acceptance rate is fixed and the false acceptance/rejection rate is minimized.
Specificity in this case can be assigned to the possibility of fragmentation reactions (MSn), which are supported by using an external standard for comparative purposes.
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