Let`s talk about compounds: 14481-08-4

In addition to the literature in the link below, there is a lot of literature about this compound(Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)nickel(II))Computed Properties of C22H38NiO4, illustrating the importance and wide applicability of this compound(14481-08-4).

Foulds, Gary A.; Bennett, Alison M.; Thornton, David A.; Brown, Stephen J.; Clutterbuck, Linda M.; Hinton, Cassandra; Humphreys, Geoffrey B.; Masters, Anthony F. published the article 《Ligand donor atom and substituent effects in olefin oligomerization and isomerization catalyzed by nickel-based catalyst systems》. Keywords: olefin isomerization oligomerization catalyst; nickel based catalyst.They researched the compound: Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)nickel(II)( cas:14481-08-4 ).Computed Properties of C22H38NiO4. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:14481-08-4) here.

The olefin oligomerization and isomerization catalytic activities and selectivities of catalysts generated by combining [Ni(RC(X)CHC(Y)R)2]n (R = Me, X = Y = O, n = 3; X = O, Y = NH, n = 1; X = O, Y = S, n = 1; X = Y = S, n = 1; and R = tert-Bu, n = 1, X = Y = O; X = O, Y = S; X = Y = S) and [Ni(CH3C(S)CHC(S)CH3)(PR3)Cl] (R = alkyl, aryl) precursors with [Et6-xAl2Clx] (x = 0, 2, 3, 4, 6) co-catalysis have been compared. All catalysts exhibit some olefin isomerization activity, but only those generated from precursors containing oxygen-donor ligands exhibit olefin oligomerization activity. Olefin oligomerization is also favored by the use of [EtAlCl2]2 as a co-catalyst. Almost no activity for either olefin oligomerization or isomerization was observed when using [Ni(CH3C(S)CHC(S)CH3)2] as a catalyst precursor. However, extremely active olefin oligomerization and isomerization catalysts could be generated from [Ni(CH3C(S)CHC(S)CH3)(PBu3)Cl] and appropriate co-catalysts. The mol.-weight of the products could be controlled in these systems by varying the co-catalyst. The catalysts with the most sustained high activity were those generated from [Ni(CH3C(S)CHC(S)CH3)(PBu3)Cl].

In addition to the literature in the link below, there is a lot of literature about this compound(Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)nickel(II))Computed Properties of C22H38NiO4, illustrating the importance and wide applicability of this compound(14481-08-4).

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics