The influence of catalyst in reaction 3411-48-1

After consulting a lot of data, we found that this compound(3411-48-1)Computed Properties of C30H21P can be used in many types of reactions. And in most cases, this compound has more advantages.

Computed Properties of C30H21P. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Tri(naphthalen-1-yl)phosphine, is researched, Molecular C30H21P, CAS is 3411-48-1, about Selective hydroformylation of 1-hexene to branched aldehydes using rhodium complex of modified bulky phosphine and phosphite ligands.

The selective hydroformylation of 1-hexene to branched aldehydes was investigated using rhodium complex of tri-1-naphthylphosphine PNp3 and tri-1-naphthylphosphite P(ONp)3. The PNp3 and P(ONp)3 ligands having more steric nature than PPh3 enhanced the formation of branched aldehydes at 110 °C and 4.0 MPa syngas pressure. The branched aldehyde selectivity increased remarkably (82%) by adding P(ONp)3 as auxiliary ligand in Rh/PNp3 catalyzed hydroformylation of 1-hexene. The high selectivity for the branched aldehydes is due to rapid alkene isomerization producing internal alkenes followed by hydroformylation to yield branched aldehydes.

After consulting a lot of data, we found that this compound(3411-48-1)Computed Properties of C30H21P can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis