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The novel hydrophilic pyridinium salt polymer was designed and synthesized containing the pyridinium salt for aqueous dissolution and thiophenes as the conjugation group to make the polymer/CNT composite film electrical connecting, therefore improving the thermoelectric performance.
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The polymers attach on the surface of CNTs through π-π conjugation interaction between conjugation groups and π-electrons of CNTs.
As with the immatures, GSTs were the most well expressed genes in the conjugation enzyme group.
Within the conjugation enzyme group, the GSTs were highly expressed in the immatures, especially the pupae, but not the eggs.
They included hydrolysis (A-ring), epoxidation (H-ring), oxidation (R-group aldehyde), reduction (R-group aldehyde and α, β-unsaturated carbon), and peptide conjugation (R-group α,β-unsaturated aldehyde).
The second step of the absorption edge in the transmission curve of films of polymer with amidic monomer inclusions became stronger for monomers with structures characterised by extended conjugation, meaning groups with a longer chain attached to the benzene ring (M4 and M7).
After BADGE conjugation, epoxide groups replace the amines and the ζ-potential decreased to −44.0 mV, indicating adequate particle stabilization was achieved sterically by the PEG and electrostatically by the 4-MBA's terminal carboxylic acid group.
Cross-conjugated molecules have been defined as containing three or more unsaturated groups, two of which are conjugated to the third but not directly to each other. 1 For example, in benzophenone the two phenyl groups share conjugation to the carbonyl group, but are not conjugated to each other.
These superior particles were prepared by thermal amide conjugation of COO− group of EDTA with NH2 group of chitosan employing spray-drying technique.
The 'protein modification by small protein conjugation or removal' group, which contains all mRNAs of the 'protein polyubiquitination' and 'protein ubiquitination' groups, shows the most significant p-value.
Chemical reaction and in vivo metabolism studies of the four most potent 6S derivatives showed that both α,β-unsaturated carbonyl entity and catechol moiety act as major active groups for conjugation with the sulfhydryl groups of the cysteine residues.
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