949084-46-2

Basic information

• Product Name: N₃,N₃'-bis(diphenylphosphino)-2,2'-bipyridine-3,3'-diamine
• Synonyms: N₃,N₃'-bis(diphenylphosphino)-2,2'-bipyridine-3,3'-diamine
• CAS NO: 949084-46-2
• Molecular Weight: 554.571
• Mol File: 949084-46-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N₃,N₃'-bis(diphenylphosphino)-2,2'-bipyridine-3,3'-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N₃,N₃'-bis(diphenylphosphino)-2,2'-bipyridine-3,3'-diamine(949084-46-2)
• EPA Substance Registry System: N₃,N₃'-bis(diphenylphosphino)-2,2'-bipyridine-3,3'-diamine(949084-46-2)

Safety Data

• Hazardous Substances Data: 949084-46-2(Hazardous Substances Data)

Upstream product

• 1079-66-9 chloro-diphenylphosphine 
• 75449-26-2 2,2'-bipyridine-3,3'-diamine 
• 1024-94-8 3,3’-dinitro-2,2’-bipyridine 
• 5470-18-8 2-Chloro-3-nitropyridine 

Downstream Products

• 1407482-92-1 [C₁₀H₆N₂{PPh₂NHRh(cod)Cl}₂] 
• 1407482-93-2 [C₁₀H₆N₂{NHPPh₂Ir(η⁵-C₅Me₅)Cl₂}₂] 
• 1178867-16-7 [(N3,N3'-bis(diphenylphopshino)-2,2'-bipyridine-3,3'-diamine)(Ru(η6-p-cymene)Cl2)2] 

Relevant articles and documents

Applications of transition metal complexes containing 3,3′- bis(diphenylphosphinoamine)-2,2′-bipyridine ligand to transfer hydrogenation of ketones

Hydrogen transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity. 3,3′-bis(diphenylphosphinoamine)-2,2′-bipyridine, (Ph 2PNH)2C10H6N2, was prepared through a single step reaction of 3,3′-diamino-2,2′- bipyridine with diphenylchlorophosphine. Reaction of (Ph2PNH) 2C10H6N2 with [Ru(η6- benzene)(μ-Cl)Cl]2, [Rh(μ-Cl)(cod)]2 or [Ir(η5-C5Me5)(μ-Cl)Cl]2 gave a range of new bridged dinuclear complexes [C10H6N 2{NHPPh2Ru(η6-benzene)Cl2} 2], 1, [C10H6N2{PPh 2NHRh(cod)Cl}2], 2 and [C10H6N 2{NHPPh2Ir(η5-C5Me 5)Cl2}2], 3, respectively. All new complexes have been fully characterized by analytical and spectroscopic methods. 1H31P-{1H} NMR, 1H13C HETCOR or 1H1H COSY correlation experiments were used to confirm the spectral assignments. 1, 2 and 3 are suitable catalyst precursors for the transfer hydrogenation of acetophenone derivatives. Notably [Ru((Ph 2PNH)2C10H6N2) (η6-benzene)Cl2], 1 acts as an excellent catalyst, giving the corresponding alcohols in 98-99% yields in 10 min at 82 °C (TOF ≤600 h-1) for the transfer hydrogenation reaction in comparison to analogous rhodium or iridium complexes. This transfer hydrogenation is characterized by low reversibility under these conditions.