Reference of 1,2-DiphenyldisulfaneIn 2020 ,《C-N, C-S and S-S Bond Cleavage by Rhodium PCcarbeneP Pincer Complexes》 was published in Chemistry – An Asian Journal. The article was written by Tinnermann, Hendrik; Young, Rowan D.. The article contains the following contents:
Rhodium carbene pincer complexes I·BArF4 [1-L, L = PPh3, PPh2(C6F5)] react with isothiocyanate, carbodiimide and disulfide to enable C-S, C-N and S-S bond cleavage. The cleaved mols. are sequestered by the metal center and the pincer alkylidene linkage, forming η2-coordinated sulfide or imide centered pincer complexes. When a C-S or S-S bond is cleaved, the resulting complexes can bridge two rhodium centers through sulfur forming dimeric complexes and eliminating a monodentate phosphine ligand. In the part of experimental materials, we found many familiar compounds, such as 1,2-Diphenyldisulfane(cas: 882-33-7Reference of 1,2-Diphenyldisulfane)
1,2-Diphenyldisulfane(cas: 882-33-7) belongs to ethers.Ethers do have nonbonding electron pairs on their oxygen atoms, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Reference of 1,2-Diphenyldisulfane The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem