Welcome to LookChem.com Sign In|Join Free
  • or
Naphthylen-(1,5)-bis-diphenylphosphin, also known as 1,5-naphthylen-bis(diphenylphosphine) or 1,5-bis(diphenylphosphino)naphthalene, is a phosphine-based ligand with the chemical formula C34H26P2. It is a white crystalline solid that is soluble in common organic solvents. Naphthylen-(1,5)-bis-diphenylphosphin is characterized by its naphthalene core with two diphenylphosphino groups attached at the 1 and 5 positions, forming a bidentate ligand. It is widely used in homogeneous catalysis, particularly in transition metal complexes, due to its ability to stabilize metal centers and facilitate various chemical reactions. The electronic and steric properties of naphthylen-(1,5)-bis-diphenylphosphin make it a valuable ligand in the synthesis of catalysts for applications such as hydrogenation, hydroformylation, and olefin polymerization.

1260-72-6

Post Buying Request

1260-72-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1260-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1260-72-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,6 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1260-72:
(6*1)+(5*2)+(4*6)+(3*0)+(2*7)+(1*2)=56
56 % 10 = 6
So 1260-72-6 is a valid CAS Registry Number.

1260-72-6Downstream Products

1260-72-6Relevant academic research and scientific papers

Multi-Stage Redox Systems Based on Dicationic P-Containing Polycyclic Aromatic Hydrocarbons

Bouit, Pierre-Antoine,Caytan, Elsa,Delouche, Thomas,Hissler, Muriel,Jacquemin, Denis,Le Guennic, Boris,Roisnel, Thierry,Vacher, Antoine

, (2020)

We report the straightforward synthesis of unprecedented electron-acceptors based on dicationic P-containing PAHs (Polycyclic Aromatic Hydrocarbons) based on copper mediated radical approach. In these systems, two phosphoniums are connected through various PAHs backbones. The impact of π-extension on both the optical and redox properties is investigated using a joint experimental (UV/Vis absorption, fluorescence and cyclic voltammetry) and theoretical approach (TD-DFT calculations). Finally, (spectro)-electrochemical studies prove that these compounds possess three redox states and EPR studies confirm the in situ formation of an organic radical delocalized on the PAH backbone.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1260-72-6