4792-88-5

Upstream product

• 106-54-7 p-Chlorothiophenol 

Downstream Products

• 37923-99-2 3-(4-Chlorphenylthio)-trifluormethansulfonanilid 
• 76542-10-4 S-(4-chlorophenyl) propanethioate 
• 52913-83-4 Ethyl (+/-)-2-[4-(4-chlorophenylthio)-phenoxy]-propionate 
• 59621-38-4 2-[4-(4-Chloro-benzenesulfonyl)-phenoxy]-propionic acid 
• 37950-17-7 3-(4-Chlorphenylsulfonyl)-trifluormethansulfonanilid 
• 37950-21-3 3-(4-Chlorphenylsulfinyl)-trifluormethansulfonanilid 
• 59621-39-5 2-[4-(4-Chloro-phenylsulfanyl)-phenoxy]-N-(2-hydroxy-ethyl)-2-methyl-propionamide 
• 57915-00-1 2-[4-(4-Chloro-benzenesulfonyl)-phenoxy]-2-methyl-propionic acid 
• 59621-35-1 2-{2-[4-(4-Chloro-phenylsulfanyl)-phenoxy]-2-methyl-propylamino}-ethanol 
• 57915-02-3 2-[4-(4-Chloro-benzenesulfinyl)-phenoxy]-2-methyl-propionic acid 
• 51338-02-4 2-[4-(4-Chloro-phenylsulfanyl)-phenoxy]-propionic acid 
• 57914-98-4 p-(p-chlorophenylthio)-phenoxy-isobutyric acid 

Relevant academic research and scientific papers

Electrical Conduction in Copper(I) Mercaptide Complexes of Aromatic and Heteroaromatic Mercaptans

Electrical conductivities of copper(I) mercaptide complexes of aromatic and heteroaromatic mercaptans have been measured and a conduction mechanism is discussed.The observed conductivities are highly substitution-dependent and vary in the range of 1E-4 to 1E-10 ohm-1 cm-1 at 25 deg C.The solid state absorption spectra and the pressure-induced colour change of the complexes indicate creation of mixed-valence Cu(I)-Cu(II) species which appear to be responsible for their relatively high conductivities.A model which assumes electron hopping assisted by Cu-S stretching frequency along the -Cu-S-Cu-S- conducting spine formed in the S-bridged polymeric structures of these complexes is suggested for the conduction process.