Hemilabile ligands can release a free coordination site "on demand" of an incoming nucleophilic substrate while occupying it otherwise. This is believed to increase the thermal stability and activity of catalytic systems and therefore prevent decomposition via free coordination sites. In this investigation chelating pyridinyl-alcoholato ligands were identified as possible hemilabile ligands for...

The isolation and characterization of a strain of Pseudomonas oleovorans which epoxidates 1-octene at a rate nine times that of the original strain are described. In addition, it has been confirmed that a greater amount of the mono-epoxide product is formed from 1,7-octadiene than is formed from 1-octene. 1,7-octadiene will not support growth, but will induce the enzymes required for epoxidation.

Biphasic hydroformylation of 1-octene was performed using rhodium sulfoxantphos catalyst dissolved in [BuPy][BF4] ionic liquid. Preliminary experiments proved this system to retain the catalytic complex within the ionic liquid phase and to maintain a high selectivity towards the linear aldehyde (n:iso ratio of 30) over several cycles. Process parameter investigation showed a first order depende...

Complexes of the type [Cu(H-dpa)(olefin)]BF4 for ethylene (1), propylene (2), 1-butene (3), 1-hexene (4), 1-octene (5), cis-2-octene (6), trans-2-octene (7), cis-3-octene (8), trans-3-octene (9), 2-norbornylene (10), 1,5-cyclooctadiene (11), styrene (12), cis-stilbene (13), trans-stilbene (14), and Ph2C=CH2 (15) have been prepared and characterized by 1H and 13C NMR, FTIR, and TGA. The crystal ...

alkylation of biphenyl with 1-octene was investigated using ((al+c3h7cl)+c2h4) catalysts. the catalytic activity of ((al+c3h7cl)+c2h4) for the alkylation was studied at different temperatures, mol ratios of biphenyl to 1-octene, reaction times and catalyst concentrations. it was shown that using this catalyst has more advantagous than another catalysts. experiments show that by increasing tempe...

The insertion, elimination and isomerisation of octenes with di-n-octylaluminium hydride [HAl(Oct)2], tri-n-octylaluminium [Al(Oct)3] and sec-octylaluminium species have been studied as individual steps in a putative aluminium based contrathermodynamic olefin isomerisation process. While elimination of 1-octene from [Al(Oct)3] is energetically unfavourable, the process is driven by high tempera...

The insertion of internal olefins (hydroalumination) and chain walking isomerisation at di-n-octylaluminium hydride [Al(Oct)2H], promoted by zirconocene dichloride [Cp2ZrCl2] has been studied. The reaction between [Cp2ZrCl2] and [Al(Oct)2H] in non-polar solvents leads to clusters containing bridging hydride ligands between Zr and Al. This system promotes hydroalumination of 1-octene but is larg...

In the presence of rat liver microsomes and NADPH n-loctene, n-4-octene and 3-ethyl-2-pentene were converted to the glycols with no trace of epoxides. Increased substitution of ethylenic hydxogen atoms by alkyl groups was found to retard. the rate of biological oxid.ation but to enhance that of epoxidation by perbenzoic acid. in chloroform. Microsomes without cofactors hydrolyzed the monosubsti...