76124-46-4Relevant academic research and scientific papers
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
Macrocyclic [Cu(I/II)(bite)](+/2+) (bite = biphenyldiimino dithioether): An example of fully-gated electron transfer and its biological relevance
Flanagan, Scott,Dong, Jun,Haller, Kenneth,Wang, Shengke,Scheidt, W. Robert,Scott, Robert A.,Webb, Thomas R.,Stanbury, David M.,Wilson, Lon J.
, p. 8857 - 8868 (2007/10/03)
Template condensation of 2,2'-diaminobiphenyl, 1,4-bis(2-formylphenyl)-1,4-dithiabutane, and copper(II) tetrafluoroborate yields the new macrocyclic compound [Cu(I)(bite)l(BF4) (bite = biphenyldiimino dithioether). [Cu(I)(bite)]BF4 c
