C08F4/60

STABILIZED UV ACTIVE ORGANOPALLADIUM COMPOUNDS AS VINYL ADDITON CATALYSTS

Embodiments in accordance with the present invention encompass compositions comprising a long shelf stabilized organopalladium compound of formula (I) as described herein. The composition further contains a photoacid generator, a photosensitizer and one or more olefinic monomers as described herein. The shelf life of the compositions can further be extended by employing a stabilizer, such as for example, a hindered amine. The composition undergoes vinyl addition polymerization when it is exposed to a suitable actinic radiation to form a substantially transparent film or a three dimensional object. More specifically, the compositions of this invention are stable at room temperature for several days to several months and can also be stored at higher temperatures from about 40° C. to 60° C. for several days and undergo mass polymerization only when subjected to suitable actinic radiation. The monomers employed therein have a range of optical and mechanical properties, and thus these compositions can be tailored to form films and/or three dimensional objects having various opto-electronic properties. Accordingly, compositions of this invention are useful in various applications, including as coatings, encapsulants, fillers, leveling agents, sealants, adhesives, among others.

ATTENUATED POST-METALLOCENE CATALYSTS

A method of making an attenuated-light-off post-metallocene catalyst, the method comprising combining a faster-light-off catalyst with an effective amount of a kinetics modifier compound of formula (A.sup.1), (B.sup.1), or (C.sup.1): R5-C≡C—R.sup.6 (A.sup.1), (R.sup.5).sub.2C═C═C(R.sup.6).sub.2 (B.sup.1), or (R.sup.5)(R.sup.7)C═C(R.sup.6)(R.sup.7) (C.sup.1) as defined herein under effective reaction conditions to give an attenuated post-metallocene catalyst that exhibits an attenuated light-off monomer uptake profile (relative to that of the faster-light-off catalyst); wherein the faster-light-off catalyst has been made by activating a post-metallocene precatalyst of structural formula (I) as defined herein; and related methods, compositions and uses.

Stabilized UV active organopalladium compounds as vinyl addition catalysts
11667731 · 2023-06-06 · ·

Embodiments in accordance with the present invention encompass compositions comprising a long shelf stabilized organopalladium compound of formula (I) as described herein. The composition further contains a photoacid generator, a photosensitizer and one or more olefinic monomers as described herein. The shelf life of the compositions can further be extended by employing a stabilizer, such as for example, a hindered amine. The composition undergoes vinyl addition polymerization when it is exposed to a suitable actinic radiation to form a substantially transparent film or a three dimensional object. More specifically, the compositions of this invention are stable at room temperature for several days to several months and can also be stored at higher temperatures from about 40° C. to 60° C. for several days and undergo mass polymerization only when subjected to suitable actinic radiation. The monomers employed therein have a range of optical and mechanical properties, and thus these compositions can be tailored to form films and/or three dimensional objects having various opto-electronic properties. Accordingly, compositions of this invention are useful in various applications, including as coatings, encapsulants, fillers, leveling agents, sealants, adhesives, among others.

TWO-DIMENSIONAL COORDINATION POLYMERS
20220306566 · 2022-09-29 ·

Octaaminonaphthalene and a method of synthesizing octaaminonaphthalene are described. A two-dimensional coordination polymer and a method of synthesizing the two-dimensional coordination polymer are described. The two-dimensional coordination polymer includes ligands including anchorage sites, and metal linkers, each metal linker including a metal and an organic moiety. Each metal linker is coupled to two ligands via the anchorage sites. Synthesizing the two-dimensional coordination polymer includes contacting a first liquid precursor with a second liquid precursor at an interface, reacting the metal linker and the water-soluble ligand to yield a two-dimensional coordination polymer at the interface, and removing the two-dimensional coordination polymer from the interface.

Catalyst Composition, Cleaning Liquid Composition Containing the Same, and Method of Cleaning Polymerization Apparatus Using the Cleaning Liquid Composition
20220162351 · 2022-05-26 · ·

The present invention relates to a catalyst composition containing: one or more selected from the group consisting of a transition metal compound represented by Formula 1 and a transition metal compound represented by Formula 3, and dialkyl L-tartrate; a cleaning liquid composition containing the catalyst composition; and a method of cleaning a polymerization apparatus using the cleaning liquid composition,

##STR00001## wherein all the variables are described herein.

Catalyst Composition, Cleaning Liquid Composition Containing the Same, and Method of Cleaning Polymerization Apparatus Using the Cleaning Liquid Composition
20220162351 · 2022-05-26 · ·

The present invention relates to a catalyst composition containing: one or more selected from the group consisting of a transition metal compound represented by Formula 1 and a transition metal compound represented by Formula 3, and dialkyl L-tartrate; a cleaning liquid composition containing the catalyst composition; and a method of cleaning a polymerization apparatus using the cleaning liquid composition,

##STR00001## wherein all the variables are described herein.

BLOCK COPOLYMER AND METHOD FOR PREPARING THE SAME
20220144976 · 2022-05-12 ·

A block copolymer is disclosed. The block copolymer has a structure of formula (V) below:


[D].sub.x-[E].sub.y-[F].sub.z  (V) wherein D, E, and F are each independently a compound of formula (VI) below, and D, E, and F are different from each other; and x, y, and z are each independently an integer from 1 to 40;

##STR00001## wherein A.sub.2 is O or S; R.sub.7 is H or a C.sub.1-6 alkyl; and R.sub.8 is a C.sub.1-12 alkyl, (CH.sub.2).sub.qN(R.sub.11).sub.2, CH.sub.2(CH.sub.2OCH.sub.2).sub.rCH.sub.2N(R.sub.12).sub.2, or CH.sub.2(CH.sub.2OCH.sub.2).sub.sCH.sub.2OR.sub.13, wherein R.sub.11, R.sub.12, and R.sub.13 are each independently a C.sub.1-6 alkyl; and q, r, and s are each independently an integer from 1 to 10.

BLOCK COPOLYMER AND METHOD FOR PREPARING THE SAME
20220144976 · 2022-05-12 ·

A block copolymer is disclosed. The block copolymer has a structure of formula (V) below:


[D].sub.x-[E].sub.y-[F].sub.z  (V) wherein D, E, and F are each independently a compound of formula (VI) below, and D, E, and F are different from each other; and x, y, and z are each independently an integer from 1 to 40;

##STR00001## wherein A.sub.2 is O or S; R.sub.7 is H or a C.sub.1-6 alkyl; and R.sub.8 is a C.sub.1-12 alkyl, (CH.sub.2).sub.qN(R.sub.11).sub.2, CH.sub.2(CH.sub.2OCH.sub.2).sub.rCH.sub.2N(R.sub.12).sub.2, or CH.sub.2(CH.sub.2OCH.sub.2).sub.sCH.sub.2OR.sub.13, wherein R.sub.11, R.sub.12, and R.sub.13 are each independently a C.sub.1-6 alkyl; and q, r, and s are each independently an integer from 1 to 10.

Ziegler-Natta catalyst systems and methods of controlling particle size

A colloidal suspension includes an organic phase and a complex of Formula I as precursor for Ziegler-Natta catalyst synthesis:
XTiCl.sub.p(OR.sup.1).sub.4−p.Math.YMg(OR.sup.2).sub.q(OR.sup.3).sub.t  (I).
In Formula I, a molar ratio of X to Y (X/Y) is from 0.2 to 5.0, p is 0 or 1, 0<q<2, 0<t<2, the sum of q and t is 2, R.sup.1, R.sup.2, and R.sup.3 are each independently a linear or branched alkyl, a linear or branched heteroalkyl, a cycloalkyl, a substituted cycloalkyl, a substituted heterocycloalkyl, a substituted aryl, or a (heteroaryl)alkyl; and R.sup.2 is not the same as R.sup.3.

Ziegler-Natta catalyst systems and methods of controlling particle size

A colloidal suspension includes an organic phase and a complex of Formula I as precursor for Ziegler-Natta catalyst synthesis:
XTiCl.sub.p(OR.sup.1).sub.4−p.Math.YMg(OR.sup.2).sub.q(OR.sup.3).sub.t  (I).
In Formula I, a molar ratio of X to Y (X/Y) is from 0.2 to 5.0, p is 0 or 1, 0<q<2, 0<t<2, the sum of q and t is 2, R.sup.1, R.sup.2, and R.sup.3 are each independently a linear or branched alkyl, a linear or branched heteroalkyl, a cycloalkyl, a substituted cycloalkyl, a substituted heterocycloalkyl, a substituted aryl, or a (heteroaryl)alkyl; and R.sup.2 is not the same as R.sup.3.