Exact(1)
An additional benefit of alginate is that it is able to form both ionic and acidic gels.
Similar(59)
In addition, LDH can accommodate both ionic and non-ionic anticancer drugs [43] at high distribution and sustained release [24].
Zwitterionic detergents combine properties of both ionic and nonionic detergents and in general, are milder than ionic detergents.
Both ionic liquids without acidic protons do not react with metallic lithium; on the other hand, the formation of carbene species when BMITFSI was exposed to Li was confirmed by 1H and 13C nuclear magnetic resonance (NMR) and gas chromatography mass spectrometry (GC MS).
The Hammett acidity of these conventional acids and acidic ionic liquids were also assessed using UV visible spectroscopy.
Moreover, the enhanced interaction between prolinamide and acidic ionic liquid facilitated the recoverability and reusability of organocatalyst.
The electrochemical behaviour of basic and acidic ionic liquids (x 1-butyl-1-methyl-pyrrolidinium chloride-(1 − x 1-butyl-1-methyl-pyrrolidinium.40 was investigated over the temperature range 90–160 °C in respect to the electrochemical deposition of niobium.
In continuation of our previous work on the application of task-specific and acidic phosphonium ionic liquids (PIL) for EDS, tri-n-butyl- 2-hydroxyethyl phosphonium bromide ([tri-n-butyl- 2-hydroxyethyl phosphoniumEDS performance of itri-n-butyl- 2-hydroxyethyl phosphoniumty, tri-n-butyl- 2-hydroxyethyl phosphonium
In recent years, there has been an increasing interest in polyoxometalates (POMs) as catalysts due to their composition, size, shape, photochemical response, ionic charge, acidic properties and tunable redox properties (Zhang et al. 2013).
Interaction between polyamines and acidic phospholipids is an ionic one such that the strongest interaction is between the polyamine with the highest positive charges and the phospholipid with the highest content of negative groups [ 68].
Importantly, the H4 K16 side chain forms several hydrogen bonds and ionic interactions with acidic Sir3 side chains, offering a molecular mechanism for the observed loss of Sir3 binding upon H4 K16 acetylation.
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