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The results of 1H nuclear magnetic resonance indicate that the conjugation between the E7 and scaffolds was covalent.
The change of the oxidation potential was explained by considering the σ-π conjugation between the dimethylsilylene chain and the π unit.
Subsequently, Si-G-PANI composite was obtained through an in-situ polymerization, the PANI layer is tightly bounded to graphene owing to an enhancement of π conjugation between the PANI and graphene-grafted Si nanoparticles.
Raman spectra revealed that there were not only electrostatic interaction but also π π conjugation between the polyaniline nanofibers and carbon nanotubes, and also demonstrated that the formative polyaniline resulted in the more stable structure.
Density functional theory (DFT) calculations reveal that the remarkably enhanced performance of Pt2Pd/NPG originated from the robust conjugation between the Pt2Pd alloy nanoparticles and nitrogen-rich graphene nanopores, thereby leading to the synergistic effect of both interfaces.
Amino conjugation between the 4-amino-1,8-naphthalimide and the substituted moiety resulted in red shift of the absorption and fluorescence maximum wavelengths in the acetonitrile solution and in the net solid film.
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This not only enhanced the stability of the magnetic nanoparticles but also mediates the conjugation between nanoparticles and the antibodies for Dimer detection.
Electrochemical studies of polymer films exhibited one irreversible oxidation process at high potential consistent with a non-conjugation between the carbazole moities.
A degree of π-conjugation between the corannulene moiety and the iminonitroxide moiety has also been evaluated by UV Vis measurements.
The photophysical study revealed that there is no significant π-conjugation between the tridurylborane core and the oligoflourene endcaps due to the strong steric hindrance of bulky duryl groups.
The π-conjugation between the aromatic Fc and CN can be much enhanced by the covalent bond, thereby facilitating the bulk-to-surface charge transfer and separation as well as reversible photo-redox reactions during photocatalytic reactions.
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