890526-06-4

Upstream product

• 10025-99-7 potassium tetrachloroplatinate(II) 
• 124411-23-0 2-(phenylazo)pyrimidine 

Downstream Products

• 890526-12-2 [Pt(II)(papm-N-C₆H₄-Me-p)Cl] 
• 890526-09-7 chloro[(2-(8-imidophenyl)phenylazo)pyrimidine-N,N',N'']platinum(II) 
• 890526-11-1 [Pt(II)(papm-N-C₆H₄-Me-m)Cl] 

Relevant academic research and scientific papers

Coupling of arylamine with coordinated arylazopyrimidine in platinum(II) complexes. Single crystal X-ray structure, spectra and electrochemistry

2-(Arylazo)pyrimidine (p-R-C6H4-N{double bond, long}N-C4H3N2, aapm, R = H (papm, 3a), Me (tapm, 3b), Cl (Clpapm, 3c)) are N,N′-chelating ligands. Platinum(II) complexes, Pt(aapm)Cl2 (4) have been synthesized by the reaction of K2PtCl4 and aapm in MeCN-water under refluxing condition. The reaction of Pt(aapm)Cl2 with ArNH2 in MeCN has synthesized C-N coupled product, Pt(aapm-N-Ar)Cl (5-10). The single crystal X-ray structure determination of one of the compounds has suggested the coupling of ArNH2 at ortho-C-H of the pendant aryl part of aapm in the chelated complex. The stereochemistry and the bonding are described by 1H NMR data. The solution electronic spectra of Pt(aapm-N-Ar)Cl exhibit multiple transition at Vis-NIR region (500-1250 nm) which are absent in Pt(aapm)Cl2. Cyclic voltammograms show two quasireversible azo reductions of Pt(aapm)Cl2; Pt(aapm-N-Ar)Cl exhibit four successive redox couples, one of them (positive to SCE) is oxidative in nature and other (negative to SCE) are ligand reductions.