Sentence examples for more amine groups from inspiring English sources

More amine groups were detected on the surface and the hydrophilicity of the films was obviously improved by annealing the films in water.

All results of FTIR, XPS and Raman indicate that there are more amine groups from allylamine monomer on the 20/80 film fabricated by 20% duty cycle.

This process can generate the cation radical at the surface and then more amine groups on surface of the plasma-polymerized film during plasma treatment using DBD process in N2 environment than the low plasma power.

Compared to 1,1-bis(4-dimethylaminophenyl)-ethylene(BDMA-DPE), 4-dimethylaminophenyl -ethyleneuced into polymer chain end when 1-(4-dimethylaminophenyl -ethyleneethylene (DMA-DPE) units were employed in this system.

However, as the pH increases (pH = 6), more amine groups become available in the chitosan chain for dative bonding (electron donor) with zinc divalent cations, thus reducing the electrostatic repulsion (Zn2+ ↔ NH3+) and favouring the stabilisation of the ZnS nanocrystals at smaller dimensions due to the increase of the number of nucleation sites.

Polyamines, cationic compounds having two or more amine groups, are low molecular weight organic molecules present in most of the organisms with diverse functions due to the diversity in number and position of amino groups [ 8].

For example, the chemical class 'aminopyridine' is defined as 'Compounds containing a pyridine skeleton substituted by one or more amine groups', while an example of a role based class is 'antiviral drug', which groups together chemical entities that are used as antiviral drugs, regardless of their chemical structure.

It had been demonstrated that the sorbents impregnated with more unprotonated amine groups and higher Mw or EO/PO showed larger CO2 capture capacities and good stabilities over multiple adsorption desorption cycles.

Surprisingly, PMs with a 1 1 molar ratio showed a smaller change in size than PMs with a 2 1 molar ratio, perhaps reflecting the high hydrophilicity conferred by pArg (there are more primary amine groups on PEI, which are readily conjugated by pArg).

This conjugate exerted a higher negative amount of surface charge due to the involvement of more HSA amine groups in bonding with the linker.

It was rapidly found that the pyridyl group at the R position of the molecule was less important in contributing to the binding affinity than the core and R groups, so this R could be replaced with a more basic amine group with the aim of lowering the log  D and improving the ADME and physical properties of the compounds.