2018
DOI: 10.1016/j.radphyschem.2018.06.007
|View full text |Cite
|
Sign up to set email alerts
|

Protein fouling of modified microporous PET track-etched membranes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
20
0
1

Year Published

2020
2020
2024
2024

Publication Types

Select...
5
1
1

Relationship

0
7

Authors

Journals

citations
Cited by 31 publications
(22 citation statements)
references
References 46 publications
1
20
0
1
Order By: Relevance
“…The CS of carbons of C=O groups are shielded in substituted imidazolinone rings in average up to 2.0 ppm (2a-e), and for compounds 2f, g with electron-acceptor substituents (-NO, -СОCН 3 ) the carbonyl signals shift to the high-field region by 8.9 ppm. The observed effect of strong shielding of the C=O group in compounds 2f, g is explained by the circulation of electron-acceptor substituents' electrons due to the presence of π-bonds, which leads to the appearance of a field additionally strengthening the external [23; 183] or «anisotropy cone» [24]. This effect is similar for 2,6-N-disubstituted compounds 5e-h and is shown in Figure 4.…”
Section: T a B L E 1 сHemical Shifts Of N-monosubstituted Glycolurilssupporting
confidence: 54%
See 3 more Smart Citations
“…The CS of carbons of C=O groups are shielded in substituted imidazolinone rings in average up to 2.0 ppm (2a-e), and for compounds 2f, g with electron-acceptor substituents (-NO, -СОCН 3 ) the carbonyl signals shift to the high-field region by 8.9 ppm. The observed effect of strong shielding of the C=O group in compounds 2f, g is explained by the circulation of electron-acceptor substituents' electrons due to the presence of π-bonds, which leads to the appearance of a field additionally strengthening the external [23; 183] or «anisotropy cone» [24]. This effect is similar for 2,6-N-disubstituted compounds 5e-h and is shown in Figure 4.…”
Section: T a B L E 1 сHemical Shifts Of N-monosubstituted Glycolurilssupporting
confidence: 54%
“…Aminacid derivatives of fullerenes. The synthesis of water-soluble derivatives of C60 fullerene with sodium salts of aminobutyric and ε-aminocaproic acids, as well as hybrid structures based on the fullerene derivative with proline and carnosine (β-alanyl-L-histidine) are described [19][20][21][22][23]24]. The considered derivatives possessed antioxidant activity.…”
Section: Main Partmentioning
confidence: 99%
See 2 more Smart Citations
“…There has been a significant amount of interest for track-etched membrane (TeMs) in MD. A unique feature of TeMs is the control of the number of pores per unit area [20][21][22][23][24][25], which significantly expands fields of application in sensing [26], catalysis [27][28][29][30][31], lithium-ion batteries [32,33], template synthesis of nanostructures [34][35][36][37][38]. At the present time various types of polymers are known, intended as a material for TeMs.…”
Section: Introductionmentioning
confidence: 99%