Provided are compounds of the following: ##STR00001##
wherein R.sub.1 is a saturated or unsaturated cyclic hydrocarbon optionally substituted with an alkyl and/or an OXO-ester, and R.sub.2 is a C.sub.4 to C.sub.14 hydrocarbyl, preferably the residue of a C.sub.4 to C.sub.14 OXO-alcohol. Also provided are processes for making the compounds and plasticized polymer compositions containing said compounds.

Provided are compounds of the following: ##STR00001##
wherein R.sub.1 is a saturated or unsaturated cyclic hydrocarbon optionally substituted with an alkyl and/or an OXO-ester, and R.sub.2 is a C.sub.4 to C.sub.14 hydrocarbyl, preferably the residue of a C.sub.4 to C.sub.14 OXO-alcohol. Also provided are processes for making the compounds and plasticized polymer compositions containing said compounds.

A method for the synthesis of a aryl compound of Formula (1). Formula (1)

UT-WR.sub.1).sub.n (1)

A method for the synthesis of a aryl compound of Formula (1). Formula (1)

UT-WR.sub.1).sub.n (1)

The present invention relates to a process for monitoring the catalytic activity of an ionic liquid. In step (a), providing an acidic ionic liquid; (b) providing an organic compound; (c) adding at least a portion of the organic compound to at least a portion of the ionic liquid; (d) recording an infrared spectrum of a mixture from step (c) to obtain at least one absorption peak. In step (e), repeating steps (c) and (d) until at least one absorption peak reaches a maximum value or a minimum value. In step (f), determining at the maximum value or minimum value of step (e): the total amount of the organic compound or the total amount of the ionic liquid added. In step (g), calculating the catalytic activity of the ionic liquid based on: the total amount of the organic compound or the total amount of ionic liquid, as determined in step (f).

The present invention relates to a process for monitoring the catalytic activity of an ionic liquid. In step (a), providing an acidic ionic liquid; (b) providing an organic compound; (c) adding at least a portion of the organic compound to at least a portion of the ionic liquid; (d) recording an infrared spectrum of a mixture from step (c) to obtain at least one absorption peak. In step (e), repeating steps (c) and (d) until at least one absorption peak reaches a maximum value or a minimum value. In step (f), determining at the maximum value or minimum value of step (e): the total amount of the organic compound or the total amount of the ionic liquid added. In step (g), calculating the catalytic activity of the ionic liquid based on: the total amount of the organic compound or the total amount of ionic liquid, as determined in step (f).

An alkylation process is described. The alkylation process includes contacting a feed comprising a paraffin or an aromatic with an olefin feed in the presence of a liquid Lewis acid catalyst in an alkylation reaction zone under alkylation conditions to form a reaction mixture comprising alkylation products and the liquid Lewis acid catalyst. The liquid Lewis acid catalyst is the liquid reaction product of a donor molecule and a metal halide. The alkylation products are separated from the liquid Lewis acid catalyst and recovered.

An alkylation process is described. The alkylation process includes contacting a feed comprising a paraffin or an aromatic with an olefin feed in the presence of a liquid Lewis acid catalyst in an alkylation reaction zone under alkylation conditions to form a reaction mixture comprising alkylation products and the liquid Lewis acid catalyst. The liquid Lewis acid catalyst is the liquid reaction product of a donor molecule and a metal halide. The alkylation products are separated from the liquid Lewis acid catalyst and recovered.

A functionalized magnetic nanoparticle including an organometallic sandwich compound and a magnetic metal oxide. The functionalized magnetic nanoparticle may be reacted with a metal precursor to form a catalyst for various CC bond forming reactions. The catalyst may be recovered with ease by attracting the catalyst with a magnet.

Provided are compounds of the following:

##STR00001##

wherein R.sub.1 is a saturated or unsaturated cyclic hydrocarbon optionally substituted with an alkyl and/or an OXO-ester, and R.sub.2 is a C.sub.4 to C.sub.14 hydrocarbyl, preferably the residue of a C.sub.4 to C.sub.14 OXO-alcohol. Also provided are processes for making the compounds and plasticized polymer compositions containing said compounds.