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A new kind of host compound, 2,5-bis(diphenylmethyl)hydroquinone is designed and prepared.
Clathrates are formed when a host compound encloses guest molecules without using strong ionic interactions or covalent bonds.
The metallic nature of the host compound is retained in its delithiated phase which confirms that the bands crossing E F are from valence electrons of Ti.
Mass losses of 2.44% in TGA of solvate-I suggest 0.5 mole of isopropyl alcohol per mole of the host compound.
In the partial DOS of LiTiS3 given in Fig. 4b, the maximum number of electronic states at the energy −2.5 eV is increased compared to that of the host compound which might be due to the removal of electrons from host compound due to delithiation.
Thus, it is clearly evident that the distribution of electronic states at E F for the host compound is almost similar to its delithiated phase which implies that the transition metal atom is not affected by Li+ extraction.
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The new host compounds also showed good film morphology and bipolar charge transport properties.
Unfortunately, the host compounds are usually quite heavy and thus possess a low gravimetric storage density.
The importance of phosphonates in the composition of host compounds (53 63% of total host phosphorus compounds) was highlighted for the first time, and the response of coral and CZ phosphorus composition to ambient phosphorus pools was established.
Porous spherical γ-aluminas (1860 µm and 71 µm mean particle diameter) were used in this work as host compounds.
Chiral recognition properties of these host compounds towards L- and D-threonine were studied by UV-Vis spectroscopy.
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