152135-89-2

Basic information

• Product Name: Pd(1,10-phenanthroline){N(C₆H₅)C(O)N(C₆H₅)C(O)N(C₆H₅)}
• Synonyms: Pd(1,10-phenanthroline){N(C₆H₅)C(O)N(C₆H₅)C(O)N(C₆H₅)}
• CAS NO: 152135-89-2
• Molecular Weight: 615.987
• Mol File: 152135-89-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Pd(1,10-phenanthroline){N(C₆H₅)C(O)N(C₆H₅)C(O)N(C₆H₅)}(CAS DataBase Reference)
• NIST Chemistry Reference: Pd(1,10-phenanthroline){N(C₆H₅)C(O)N(C₆H₅)C(O)N(C₆H₅)}(152135-89-2)
• EPA Substance Registry System: Pd(1,10-phenanthroline){N(C₆H₅)C(O)N(C₆H₅)C(O)N(C₆H₅)}(152135-89-2)

Safety Data

• Hazardous Substances Data: 152135-89-2(Hazardous Substances Data)

Upstream product

• 56259-30-4 Pd(dibenzylideneacetone)(1,10-phenanthroline) 
• 103-71-9 phenyl isocyanate 
• 35679-81-3 (1,10-phenanthroline)-palladium(II) acetate 
• 66-71-7 1,10-Phenanthroline 
• 132140-99-9 (1,10-phenathroline)Pd(C(O)N(C₆H₅)OC(O)) 

Downstream Products

• 152135-91-6 (C₁₂H₈N₂)Pd(C₆H₅NCONC₆H₅)*CH₂Cl₂ 

Relevant articles and documents

Formation of six-membered palladacycles from phenanthroline Pd(II) bisacetate precursors and phenylisocyanate Dedicated to Professor John A. Osborn.

Phenylisocyanate reacts with palladium(II) bis-acetate phenanthroline complexes to give six-membered palladacycles in nearly quantitative yields. In this new reaction, the acetate ligands act as decarbonylating agents toward the isocyanate functionality by possibly forming the isolated palladacycles via an intramolecular rearrangement.