714975-01-6

Upstream product

• 108-91-8 cyclohexylamine 
• 1079-66-9 chloro-diphenylphosphine 

Downstream Products

• 1422761-39-4 dichloro[N-cyclohexylamine-N,N-bis(diphenylphosphino)]palladium(II) 

Relevant academic research and scientific papers

N-substituted diphosphinoamines: Toward rational ligand design for the efficient tetramerization of ethylene

Bis(diphenylphosphino)amine (PNP) ligands with different alkyl and cycloalkyl substituents attached to the N atom of the ligand backbone were synthesised and tested together with chromium as ethylene tetramerization catalysts. On activation with a methylaluminoxane-based activator, the catalysts displayed good activity and selectivity toward 1-octene and 1-hexene, with the best ligand systems containing cyclopentyl or cyclohexyl moieties. In addition, it was established that substitution at the 2 position of the cyclohexyl skeleton and, more importantly, an increase in steric bulk at that point, led to a drastic reduction of side product formation (i.e., methyl- and methylenecyclopentane). Interestingly, additional methyl substitution in the 6 position of the cyclohexyl ring changed the selectivity of the catalyst from predominantly tetramerization to a 1:1 mixture of 1-hexene and 1-octene. Structurally similar ligands, such as cyclohexylmethyl and cyclohexylethyl PNP, were also tested and were also found to yield efficient tetramerization catalysts. It was concluded that structural fine tuning of the N-alkyl moiety of the PNP ligand is essential for obtaining efficient tetramerization catalysts, with the best systems achieving combined selectivities as high as 88% (1-octene and 1-hexene) with exceptionally high activities exceeding 2,000,000 g/(g-Cr h).

Probing into the electrochemistry of four nickel(II) and cobalt(II) complexes with azadiphosphine ligands (PNP) and their catalysis on proton reduction

In this work, four complexes of Co(II) and Ni(II), [Co(L1)2(CH3CN)](ClO4)2 (1), [Ni(L1)2](ClO4)2 (2), [Co(L2)2(CH3CN)](ClO

METHOD OF OLIGOMERIZATION OF OLEFINS

?The present invention relates to a method of preparing α-olefins by oligomerization of C2-C4 olefins. The method is carried out by oligomerization of C2-C4 olefins in the presence of a catalyst system comprising a transition metal source, an activator, which is an alkylaluminoxane, and a compound of formula (I), Ar1Ar2P-N(R)-PAr3Ar4 [formula I], wherein Ar1-4 are the same or different and are selected from substituted or unsubstituted C6-C10 aryl, R is selected from linear or branched C1-C4 alkyl, substituted or unsubstituted C6-C10 aryl, and substituted or unsubstituted C3-C10 cycloalkyl, wherein the oligomerization is carried out in a solvent, which is a bicyclic compound or a mixture of bicyclic compounds, preferably decalin. The claimed method provides a significant increase in the activity of the catalyst during the oligomerization process and, as a consequence, a reduction in the catalyst unit consumption, as well a reduction in the formation of polymer by-product.

Catalytic activity of new PdII-complexes of bidentate PIII - N - PIII-ligands in Suzuki - Miyaura reaction

A reaction of readily available bis(diphenylphosphino)amines with (PhCN)2PdCl2 was used to synthesize PdII-complexes [Pd{Ph2PN(R)PPh2}Cl2] (R = Pr i, cyclo-C6H11

Catalyst composition for ethylene oligomerization and the use thereof

The present invention relates to a catalyst composition for ethylene oligomerization and the use thereof. Such catalyst composition includes chromium compound, ligand containing P and N, activator and accelerator; wherein the chromium compound is selected

Ethylene tetramerization: A new route to produce 1-octene in exceptionally high selectivities

Linear α-olefins, such as 1-hexene and 1-octene, are important comonomers in the production of linear low-density polyethylene (LLDPE). The conventional method of producing 1-hexene and 1-octene is by oligomerization of ethylene, which yields a wide spectrum of linear α-olefins (LAOs). While there exists several processes for producing 1-hexene via ethylene trimerization, a similar route for the selective production of 1-octene has so far been elusive. We now, for the first time, report an unprecedented ethylene tetramerization reaction that produces 1-octene in selectivities exceeding 70%, using an aluminoxane-activated chromium/((R2)2P)2NR1 catalyst system. Copyright