Sentence examples for compounds with large from inspiring English sources

Compounds with large cation size mismatch (large rA/rB) are more susceptible to radiation damage and amorphize more easily than those with small mismatches.

The group is also pursuing new avenues in the design of multinuclear transition metal compounds with large spin and magnetic anisotropy, as well as mononuclear and multinuclear complexes of the 5f-elements.

Dissolution from the oil body was greatest for compounds with large effective solubilities (benzene) and with large degradation rates (toluene and o-xylene).

Polar compounds with large molecular weight have poor membrane permeability, liposomes can promote drugs to penetrate epidermis and remain or release at dermis.

We have carefully estimated ΔSM of the compounds with large thermal hysteresis from the Maxwell relation using the magnetization temperature curves.

Herein we reported the preparation of a new type of ferrocene-based compounds with large conjugated system containing symmetrical aromatic vinyl and Schiff base moieties and the study of their third-order nonlinear optical (NLO) properties.

The factors contributing to the reduced electrical resistivity in Cu3NMgx compounds with larger x values are discussed.

Characterization of the binding pocket by a grid-based surface calculation of the docking model revealed a large unfilled hydrophobic region near the central phenyl ring, suggesting that compounds with larger hydrophobic groups in this region would improve binding.

For lower molecular weight compounds, such as fluorene and DEP, inhalation is the main route of exposure; whereas, for compounds with larger log Koa values such as DEHP and DEHA, exposure to dust (dermal and ingestion) dominates.

This is by no means a highly quantitative relationship; for example, compounds with larger envelope violations can have smaller worst-fold affinity losses (AF-78 vs AF-69), particularly against a relatively small panel of mutants.

However, a significant improvement in activity against all resistant organisms (MIC, 2 to 8 μg/ml) was observed by simple methyl substitution of the aminomethyl side chain compound 6, and potent activity (MIC, 0.25 to 2 μg/ml) was observed for the dimethyl-substituted compound 7 and compounds with larger, single-alkyl substitutions, such as compounds 8 and 9.