Sentence examples for weak stabilization from inspiring English sources

All σ to σ* transitions involving C C bonds correspond to the weak stabilization energies in the range of ~2.53 4.58 kcal/mol.

The alloy, wherein a weak stabilization of austenite with respect to the subsequent forward γ-α transformation was observed, has been investigated to reveal the evolution of the structure refinement.

The alloy, in which a weak stabilization of austenite with respect to the subsequent direct γ-α transformation was observed, was investigated to reveal the evolution of the structure refinement.

In E. coli, poor induction of the RpoS regulon in the ppGpp-null mutant likely results from lower induction of the rpoS gene, weak stabilization of RpoS by IraP, and poor competition of core RNAP for RpoS (Traxler et al. 2008).

Moreover, the weak stabilization of actin filaments at high concentrations of cucurbitacin I is qualitatively different from the effects of phallacidin: the initiation of depolymerization is delayed but once depolymerization begins, it appears to do so at the same rate as the control.

Compound 2 exhibited weak stabilization for all G-quadruplex targets; 3 displayed very good stabilization (matching or surpassing 1 in most cases); strikingly, octamer 4 stabilized all G-quadruplex targets (maximal Δ Tm at 1 μ m compound; Table 1).

All these findings indicate that the reduced enzyme turnover observed with GPLRP2-Δβ9 results from a weaker stabilization of the acyl enzyme intermediate due to a loss of hydrophobic interactions.

This is generally attributed to the weaker stabilization capacity of these two cations, due to their smaller ionic radius [ 47- 49].

Geosynthetics placed at the base subgrade interface function more as weak subgrade stabilization than as base layer reinforcement in this study.

28 Much weaker charge transfer (between 2.2 and 4.2 kJ mol−1, Table 2) and no BCP are found for the vicinal fluorohydrins, suggesting that in these cases, this intramolecular OH⋅⋅⋅F interaction probably represents more a weak electrostatic stabilization than a typical H-bond.

Interestingly, the bonds between the carbene center and the Cipso(Ph) carbon atoms are not contracted and the two phenyl rings are significantly twisted from the carbene plane, implying a very weak π-stabilization of the carbene by these substituents.