76124-48-6Relevant academic research and scientific papers
The synthesis, characterization and computional investigation of?new metalloporphyrazine containing 15-membered S4donor macrocyclic moieties
Y?ld?z, Burak,Baygu, Yasemin,Kara, ?zzet,Dal, Hakan,G?k, Ya?ar
, p. 6972 - 6981 (2016)
In this study, an improved synthesis of 1,5-bis(2-formylphenyl)-1,5-dithiapentane(3) has been performed according to the literature in a high yield. 1,5-Bis (2-benzyl alcohol)-1,5-dithia pentane (4) was prepared by the reduction reaction of precursor comp
Synthesis and physicochemical study of NiII complexes with tetradentate acyclic and macrocyclic N2S2 ligands as thiosalen analogs
Butin,Moiseeva,Beloglazkina,Chudinov,Chizhevskii,Mironov,Tarasevich,Lalov,Zyk
, p. 173 - 188 (2005)
N,N′-Polymethylenebis(thiosalicylidene)iminate and macrocyclic dithiadiazadibenzocycloalkadiene complexes of nickel(II) were synthesized and their electrochemical and spectroscopic properties were studied. Dithiadiazadibenzocycloalkadiene complexes contai
Facile and mild displacement of nitrite ions in electron-deficient nitroarenes by alkyl or aryl thiols in the presence of magnesium methoxide as a solid base catalyst
Naeimi, Hossein,Moradian, Mohsen
, p. 2223 - 2226 (2012/10/30)
The nucleophilic aromatic substitution reaction (Sr) between nitroarenes (having electron-withdrawing groups in the ortho or para position), and alkyl- or arylthiols using magnesium methoxide as a solid base catalyst is described. This method leads to the creation of a series of valuable compounds from arylsulfides via nucleophilic displacement of the nitro group with the sulfanyl moiety. This facile method is a synthetically useful process, and it is significant that the nucleophile is promoted effectively by magnesium methoxide as a base in N,N-dimethylformamide. The displacement of then nitrite ion occurred in the presence of a variety of functional groups that caused an electron-deficient ring such as aldehyde, ketone, ester, cyano, and nitro groups. Georg Thieme Verlag Stuttgart ? New York.
The structural and electrochemical consequences of hydrogenating copper N2S2 Schiff base macrocycles
Trotter, Katherine D.,Taylor, Michelle K.,Forgie, John C.,Reglinski, John,Berlouis, Leonard E.A.,Kennedy, Alan R.,Spickett, Corinne M.,Sowden, Rebecca J.
scheme or table, p. 1529 - 1538 (2010/08/05)
A series of cis and trans tetradentate copper macrocyclic complexes, of ring size 14-16, that employ amine and thioether donor groups are reported. Apart from 5,6,15,16-bisbenzo-8,13-diaza-1,4-dithia-cyclohexadecane copper(I) (cis-[Cu(H4Nb
Synthesis and electrochemical characterization of CoII, Ni II, and CuII complexes with organic N2S 2-type ligands derived from 2-thio-substituted benzaldehydes and aromatic amines
Beloglazkina,Shimorsky,Majouga,Moiseeva,Zyk
, p. 2189 - 2199 (2008/09/18)
Transition metal complexes (NiII, CoII, and Cu II) with tetradentate N2S2-type ligands (L), which are reaction products of 2-thio-substituted benzaldehydes with aromatic amines (3-aminopyridine or 2-a
