In the first process two genes, CYB17A1 and CYB5, are involved in this synthesis [ 16].
Various parameters in this synthesis have been comprehensively investigated.
In this synthesis process, no any organic solvents or fluorine-containing surfactants were added.
Two intermediate species, adsorbed formate species and alkyl formate species, were formed in this synthesis process.
In this synthesis, a solution comprising liquid polysiloxanes is used as the Si-containing precursor.
In this synthesis, hexadecyltrimethylammonium bromide (CTAB) was self-assembled onto MWCNTs to provide adsorption sites for PdCl42− ions.
In this synthesis process, free-standing mesoporous precursor flakes are deposited on Ni foams by an electrochemical method.
In this synthesis, the fluorescent precursors with carbamate groups were locally restricted to the shell of prepared spheres.
The effect of citric acid to metal ion ratio in this synthesis has been studied and optimized.
Based on an extensive search in the Web of Science, 19 articles were included in this synthesis.
In this synthesis method, sodium ascorbate acts as a reducing agent, sodium dodecyl sulphate as a capping agent, and sodium hydroxide was used to form Cu(OH 4 2−, which was then reduced to produce Cu2O seeds.
