123746-54-3

Upstream product

• 107-15-3 ethylenediamine 
• 65924-65-4 2-(tert-butylthio)benzaldehyde 

Downstream Products

• 125009-32-7 N,N'-bis(o-tert-butylthiobenzyl)ethylenediamine 
• 226383-42-2 N,N'-bis(2-(tert-butylthio)benzyl)ethane-1,2-diamine 
• 226383-43-3 N,N'-bis(2-t-butylthiobenzyl)ethylenediamine-N,N'-diacetic acid, di-t-butyl ester 
• 226383-45-5 N,N'-bis(2-t-butylthiobenzyl)ethylenediamine-N,N'-diacetic acid 

Relevant academic research and scientific papers

Syntheses and Structures of NiS2N2 Compounds. nickel(II), Ni(tsalen), and nickel(II), Ni(ebmba)

The syntheses, structures, absorption spectra, and redox potentials of Ni(tsalen), H2tsalen=N,N'-bis(o-mercaptobenzyliden)ethylenediamine, and Ni(ebmba), H2ebmba=N,N'-bis(o-mercaptobenzyl)ethylenediamine, are described.Ni(tsalen) was prepared directly fro

HYDROGENATION OF ESTERS OR CARBONYL GROUPS WITH TETRADENTATE AMINO/IMINO-THIOETHER BASED RUTHENIUM COMPLEXES

The present invention relates to the field of catalytic hydrogenation and, more particularly, to the use of specific ruthenium catalysts, or pre-catalysts, in hydrogenation processes for the reduction of ketones and/or aldehydes into the corresponding alcohol respectively. Said catalysts are ruthenium complexes comprising a tetradentate ligand (L4) coordinating the ruthenium with: two nitrogen atoms, each in the form of a primary or secondary amine (i.e. a NH2 or NH group) or N-alkyl imine functional groups (i.e. a C═N group), and two sulfur atoms, each in the form of thioether functional groups.

A New Synthetic Route and the Structural Analysis of Ni(tsalen). (N,N'-Ethylenebis(thiosalicylidenaminato))nickel(II)

A simple route to the nickel complex of thiosalen, Ni(tsalen), which is the correspondent of the classical salen compound, was developed.The molecular structure of Ni(tsalen) was studied also.