Sentence examples for more negative reduction from inspiring English sources

Ortho compounds exhibit more negative reduction potentials compared to the other isomers, in the same chemical class.

The more negative reduction potential of the conduction band of solid solutions would allow for more efficient hydrogen generation than CdS.

Noteworthy is that aryl chlorides, which have more negative reduction potential than aryl bromides and iodides, exhibited high reactivity in the reaction, and the corresponding five-membered and six-membered cyclized products were obtained in good to high yields.

The single addition of FEC was insufficient to prevent the decomposition of the electrolyte and damage of graphite electrode, due to FEC's more negative reduction potential compared to PC, leading to serious irreversible charge loss during the 1st charge-discharge process.

Although a system of more negative reduction potential (E′) should reduce one with a less negative, zero or positive E′, there exists a hierarchy of oxidants.

Gly143Asp, Pro146Leu, and Pro159Leu mutations in the Pro loop resulted in a shift of about 50 100 mV toward more negative reduction potentials, mostly due to distortion in the Fe S environment and changes in the H-bond network around it.

The mutant BCO shows a similar structure compared to the wild-type enzyme and retains catalytic activity (both the oxidation and the isomerisation reaction) but with a 35-fold decrease in turnover number, a 100 mV more negative midpoint reduction potential, and a significant lower stability to denaturant agents and temperature than the covalent counterpart [ 6- 8].

The CB flatband potential of TiO2 is −0.5 V (vs. normal hydrogen electrode (NHE), pH = 7) [57], which is more negative than the reduction potential of CO2/CH4 (−0.24 V vs. NHE, pH = 7) [58] acts as a donor.

If the lower limit of the potential scan was more negative than the reduction potential of the molybdenum oxide film (∼−0.6 V), the oxidation peaks of these species occurred at the potentials near their formal potentials.

Considering that the peaks occurred far more negative than Mn reduction, at −170, −270, and −600 mV for borate buffer, and −200, −300, and −630 mV for buffer with 10 ppm Mn, we believe they would not interfere with the stripping process of manganese oxide in CSV.

When electron-donor properties of the substituent at the para position to the ethylenic double bond increased, it would make the reduction potential of nitro group more negative, meaning that the reduction of the nitro group requires more energy to be triggered.