Sentence examples for bonding preference from inspiring English sources

For monolayer SiGe, Zhou et al. found the same bonding preference as us, and they believed this bonding preference facilitates the synthesis of one-side semihydrogenated SiGe with chair configuration [45].

The influence of the C60 molecule incident energy upon the bonding preference, i.e. sp3, sp2, sp or s is investigated.

In each case of semihydrogenated monolayer SiGe, SiC, and GeC with chair configuration, formation energies are different when hydrogen atoms are bonded with different group-IV atoms, indicating a bonding preference of hydrogen to different group-IV elements.

As McBride [44] predicted, the bonding preference of trace metal chemisorption was Cd2+ > Zn2+ in accordance with the electronegativity of trace metal.

Thus, hydrogen atoms have higher bonding preference to silicon atoms than to germanium atoms in monolayer SiGe and have higher preference to carbon atoms than to silicon (germanium) atoms in monolayer SiC (GeC), i.e., hydrogen atoms prefer to bond with the lighter element in the monolayer group-IV binary compound.

The properties of a solid can usually be predicted from the valence and bonding preferences of its constituent atoms.

Tilting also significantly changes the coordination environments of the A-site cations which lead to a 4-coordinate square-planar environment for Cu and a 12-coordinate icosahedral environment for Ca. It is the mismatch in size and the bonding preferences of these two ions and the titanium that drive the large octahedral tilting distortion.

Many protectionist efforts by individual states, including favoritism in tax treatment of local industries, have fallen because of this interpretation, which the Kentucky Court of Appeals relied on in striking down the state's municipal bond preference.

Similarly, chemically distinct molecules with identical H-bond functions may form different HBSs, leading to the question of how molecular structure and H-bond preferences are correlated with one another.

The conservation of a hydrophobic subsitesite provides a likely explanation why M13 peptidases from distantly related organisms retain the ability to cleave similar substrates, whereas the range of side chains found at the subsitesite might determine the different peptide bond preferences seen between enzymes [ 2, 4, 25, 30].

FTIR shows that the decomposition occurs through initial cleavage of P O C bonds in preference to other covalent bonds, which allows dehydration and subsequent charring and/or chain scission.