CA2197303A1 - 2197303_ polymerization in carbon dioxide - Google Patents

Abstract

The present invention provides a method of carrying out the cationic polymerization of a monomer in carbon dioxide. The method includes the steps of (a) providing a reaction mixture comprising carbon dioxide, a monomer, a catalyst and a cationic polymerization initiator, wherein the cationic polymerization initiator is capable of initiating the cationic polymerization of the monomer; (b) polymerizing the monomer in the reaction mixture to form a polymer.

Description

- 21~7303 I
-CATIONIC POLYMERIZATION IN CARBON DIOXIDE

Related Al~plications This is a continuation-in-part application of - copending U.S. Application Serial No. 08/292,424, filed 18 August 1994.

sField of the Invention The present invention relates to the polymerization of a monomers, and more specifically relates to the cationic polymerization of monomers in carbon dioxide.

10Back~round of the Invention Prior to about 1984, cationic polymerizations which proceed through a carbenium ion were believed to be uncontrollable due to the high reactivity of the carbenium ion. Efforts have been expended to determine counteranion, temperature and solvent conditions which will permit the living polymerization of various monomer systems. The term "cationic" polymerization as used herein refers to a positively charged (cationic) polymer chain resulting from the reaction of an initiator with a monomer.
Proper selection of initiators for cationic polymerization is essential to the generation of polymers. The proper selection of the cationic polymerization initiator in turn depends upon the monomer to be polymerized. Kennedy et al., Polymer Bulletin 15:317 (1986), reported the cationic polymerization of 2~ 97303 ' isobutylene using an initiating system including boron trichloride with tertiary esters in chloromethane, methylene chloride, chloroethane, and mixtures of chlorinated solvents in n-hexane. Hagashimura et al., Macromolecules 22(3) :1009 (1989), proposes the cationic polymerization of vinyl ethers using a weak nucleophile and a Lewis base deactivator in a solution of n-hexane.
Nevertheless, there remains a need in the art for a method of cationically polymerizing a variety of monomers while controlling the characteristics of the polymer produced.
In view of the foregoing, it is a first object of the present invention to provide a method of cationically polymerizing monomers in an environmentally sound. solvent, while controlling the particle size and morphology of the polymer produced.

Summary of the Invention The present invention provides a method of carrying out the cationic polymerization of a monomer in carbon dioxide. The method includes the steps of (a) providing a reaction mixture comprising carbon dioxide, a monomer, a catalyst and a cationic polymerization initiator, wherein the cationic polymerization initiator is capable of initiating the cationic polymerization of the monomer; and (b) polymerizing the monomer in the reaction mixture to form a polymer.
Carbon dioxide as a polymerization solvent medium provides a number of significant advantages to polymerization systems. Traditionally, cationic polymerization were conducted in a dry, inert solution dispersing medium; typically an organic solvent or a chlorinated organic solvent. Herein we describe an environmentally sound solvent alternative for cationic polymerization, namely, carbon dioxide. In addition, the polymer can be easily isolated from the carbon dioxide -solvent (i.e. the continuous phase) at the termination of polymerization, as the carbon dioxide can simply be vented from the reaction vessel. Second, the density and viscosity of carbon dioxide can be tuned over a large range of conditions due to its compressibility, particularly in the supercritical phase, and thus the particle size and morphology of the polymer may be controlled.
U.S. Patent No. 5,312,882 to DeSimone et al.
discloses the use of supercritical carbon dioxide as a suitable solvent for heterogeneous polymerization of hydrophobic monomers. In addition, PCT Patent Application No. PCT/US93/01626 (W093-20116) discloses the use of supercritical carbon dioxide as a suitable solvent for the homogeneous polymerization of fluoromonomers as well.
The foregoing and other objects and aspects of the present invention are explained in detail in the specification set forth below.

Detailed Descril~tion of the Invention Cationic polymerizations of the present invention may take place heterogeneously or homogeneously. The term "heterogeneous polymerization"
as used herein refers to a polymerization carried out through the use of media that create at least two separate phases (i.e., a continuous phase and a dispersed phase). In contrast, the term "homogeneous polymerization" as used herein refers to a polymerization reaction carried out through the use of media which do not create more than one phase, and which are identified by being optically transparent. Heterogenous polymerizations include suspension polymerizations in which an initiator is solubilized in the dispersed phase, emulsion polymerizations in which an initiator is solubilized in the continuous phase, and dispersion and precipitation polymerizations which are initially .

homogeneous polymerization reactions but which nucleate particles precipitate out of solution to form a heterogeneous polymerization.
The present invention is directed to a method of carrying out the cationic polymerization of a variety of monomers in carbon dioxide. The method comprises (a) providing a reaction mixture comprising carbon dioxide, one or more monomers, a catalyst and a cationic polymerization initiator, wherein the cationic polymerization initiator is capable of initiating the cationic polymerization of the monomer(s), and (b) polymerizing the monomer(s) in the reaction mixture.
The carbon dioxide can be employed in a liquid, vapor, or supercritical phase. As used herein, "supercritical" means that a fluid medium is at a temperature that is sufficiently high that it cannot be liquified by pressure. The thermodynamic properties of carbon dioxide are reported in Hyatt, ~. Org. Chem.
49:5097 (1984); therein, it is stated that the critical temperature of carbon dioxide is about 31~C. If liquid carbon dioxide -is employed, the temperature of the reaction will be below 31~C. Preferably, the carbon dioxide is in a liquid phase. The reaction temperature should be chosen to provide sufficient heat energy to initiate and propagate the polymerization, without leading to unwanted side reactions. Preferably, the reaction temperature will be between -50~C and 200~C, and most preferably between -50~C and 31~C.
A wide variety of monomers may be employed in the method of the instant invention. The method may be employed for the polymerization of a single monomer or the copolymerization or block polymerization of two or more monomers. Monomers may be substituted or unsubstituted, saturated or unsaturated, linear or branched, cyclic or aromatic. The selection of monomer or monomers to be employed will affect the choice of '- 2197303 ~ appropriate cationic polymerization initiators, as discussed below.
Suitable monomers may be selected from a wide variety of monomers which are known to those skilled in the art as capable of undergoing cationic polymerization.
Some exemplary monomers include vinyl ether monomers, cyclic ether monomers, oxazoline monomers, hydrocarbon olefin monomers, cyclic carbonate monomers, and formaldehyde. In addition, diene comonomers may be employed in copolymerization systems.
Suitable vinyl ether monomers include alkyl vinyl ethers such as methyl vinyl ether and isobutyl vinyl - ether.
Suitable cyclic ether monomers include alkyl, alkoxy, and halo substituted cyclic ethers having a general formula selected from the group consisting of 2 0 Rl wherein R1.and R2 are independently selected from the group consisting of H, alkyl and preferably C1-C8 alkyl, haloalkylalkoxymethyl of the formula (CH20(cH2)mcxF2x~l) wherein m is 1-3 and x is 1-8, amine, amide, and alkylhaloamine of the formula (CH2)zNF2 wherein z is 1-3, and n is a number from 1 to 2 r and wherein R7 and R8 are indepdently selected from the group consisting of alkyl;
akloxy; haioalkylalkoxymethyl of the formula (CH2O (cH2) mcxF2x~l); azido of the formula CH2N3; alkylhalo of the formula CH2halo wherein halo is F~ Cl~ Br, or I;
alkylhydroxy; and alkylalkoxy. Suitable cyclic ether monomers for use in the instant invention include 3,3-(bisethoxymethyl)oxetane, 3-(1',1'-dihydroheptafluorobutoxymethyl)-3-methyloxetane, Substitute Page .

tetrahydrofuran, trioxane, ethylene oxide. Cyclic ethers have previously been cationically polymerized in nitromethane, methylene chloride, ethylene chloride, carbon tetrachloride, and halogenated aromatic hydrocarbons. See, U. S. Patent No. 4,393,199 to Manser, and E. Goethals, Makromol. Chem., Macromol. Symp 42/43 :51 Substitute Pago .

(1991) the disclosure of which is incorporated herein by reference in its entirety. The cyclic ether monomers can be prepared using conventional methods known to those skilled in the art, such as the methods described in U.S.
Patent No. 5,210,153 to Manser et al., and H. Mark, et al., Encyclo~edia of Polymer Science and Enqineerinq, 2d ed. 10:654 (1985), the disclosures of which are incorporated herein by reference in their entirety.
Suitable oxazoline monomers include alkyl, alkoxy, and halo substituted oxazolines having a general formula <O

R~

wherein R3 and R4 are independently selected from the group consisting of H, alkyl and preferably C1-C8 alkyl, alkoxy and preferably C1-Cg alkoxy, haloalkylalkoxy of the formula (CH2O(CH2)mCXF2x~l) wherein m is 1-3 and x is 1-8, amine, amide, and alkylhaloamine of the formula (CH2)zNF2 wherein z is 1-3, and n is a number from 1 to 5.
Exemplary cyclic ether monomers for use in the instant invention include 2-ethyl oxazoline, 2-methyl oxazoline, 2-(1,1,2,2-tetrahydroperfluorooctane~ oxazoline.
Suitable hydrocarbon olefin monomers include substituted or unsubstituted styrene, such as p-methoxy styrene and alkylene monomers such as isobutylene and propene.
Suitable cyclic carbonate monomers include compounds having the formula - 2~ q7303 -o o l~ J
R5/ R~, wherein Rs and R6 are independently selected from the group consisting of H, alkyl and preferably C1-C8 alkyl, alkoxy and preferably C1-C9 alkoxy, and haloalkylalkoxy of the formula (CH2O(CH2)mCXF2x~l) wherein m is 1-3 and x is 1-8.
Suitable diene comonomers include butadiene, and isoprene.
The cationic polymerization is typically catalyzed by the addition of one or more cationic polymerization catalysts. The catalysts may be provided independently of the other reactants, or may be premixed or coupled with the initiator. Suitable catalysts will depend upon the particular polymerization system (i.e., monomer(s) and initiator) to be polymerization.
Suitable cationic polymerization catalysts for the polymerization of vinyl ether monomers include ethyl aluminum dichloride. According to one preferred embodiment, the ethyl aluminum dichloride catalyst and the initiator are provided in the reaction in the form of a catalyst/initiator couple. Preferably, the catalyst and initiator are premixed and coupled prior to reaction with the vinyl ether monomer.
Suitable cationic polymerization catalysts for the polymerization of cyclic ethers and oxazolines include boron trifluoride tetrahydrofuranoate.
Suitable cationic polymerization catalysts for the polymerization of hydrocarbon olefins include tin tetrachloride, titanium tetrachloride, boron trichloride, boron trifluoride.

- ?197303 . . ;
~ .

Suitable cationic polymerization catalysts for the polymerization of cyclic carbonates and formaldehyde include boron trifluoride.
The polymerization is initiated by the addition of a cationic polymerization initiator. The selection of a suitable cationic polymerization initiator will necessarily depend upon the monomer or monomers to be polymerized, and their compatibility with carbon dioxide.
The polymerization of vinyl ether monomers is typically initiated by the addition of a cationic polymerization initiator comprising an ester initiator and a Lewis base deactivator. The ester initiator comprises an adduct of - acetic acid and isobutyl vinyl ether. Suitable Lewis base deactivators include ethyl acetate.
The polymerization of cyclic ether monomers is typically initiated by the addition of a cationic polymerization initiator comprising a strong acid or a Lewis acid, and optionally also a preinitiator.
Exemplary strong acids for use in as cationic polymerization initiators of cyclic ethers include triflic acid. Suitable Lewis acid initiators include boron trifluoride. Suitable preinitiators include water, alcohols, ethers and esters. One preferred preinitiator is butanediol.
The polymerization of oxazoline monomers is typically initiated by the addition of a cationic polymerization initiator comprising a strong acid or a Lewis acid, and optionally also a preinitiator.
Exemplary strong acids and Lewis acids are described above. In addition, preinitiators such as those described above may be included.
The polymerization of hydrocarbon olefin monomers is typically polymerized by the catalyst described above together with a cationic polymerization initiator selected from the group consisting of l-chloro-1-phenyl ethane, 2-chloro-2,4,4-trimethylpentane, tertiary ethers, Lewis bases, or 2-methoxy-2-propyl benzene. Suitable Substitute Page - 2:1 97303 ;

Lewis bases include dimethyl sulfoxide, acetamide, or ethyl acetate. The Substitute Page -initiator may also comprise a deactivator, such as tetrabutylammonium chloride or the like. Accordingly to one preferred embodiment, styrene is cationically polymerized using 1-chloro-1-phenyl ethane and tetrabutylammonium chloride as the initiator. According to a second preferred embodiment, isobutylene is cationically polymerized using 2-chloro-2,4,4-trimethylpentane as the initiator.
The polymerization of cyclic carbonate monomers is typically initiated by the addition of a cationic polymerization initiator comprising methyl triflate, methyl iodide, or benzyl bromide. The use of these initiators in the cationic polymerization of cyclic carbonate monomers in methylene chloride was previously reported in T. Endo, et al., J. of Poly. Sci. :Part A:Poly. Chem., 31:581 (1993) the disclosure of which is incorporated herein by reference in its entirety.
The polymerization of formaldehyde is typically initiated by the addition of a cationic polymerization initiator comprising strong acids or Lewis acids and a preinitiator. One suitable strong acid is hydrochloric acid. A suitable Lewis acid is boron trifluoride. A
suitable preinitiator is water. The use of this initiator system was previously reported in M. Stevens PolYmer ChemistrY, 2nd ed., Oxford University Press, 355-366 (1990), the disclosure of which is incorporated herein by reference in its entirety for the polymerization of formaldehyde in hydrocarbon solvents.
The reaction mixture may be homogeneous or heterogeneous depending upon the monomer or monomers to be polymerized. In some cases, the polymerization is a dispersion polymerization meaning that the reaction mixture may initially be homogeneous and becomes heterogeneous as the polymer nucleates a particle which is not soluble in the solvent.
The polymerization reaction mixture may include other additives and reactants known to those skilled in 21 973~3 ' the art. For example in one preferred embodiment, the process of the invention includes the addition of surfactant for stabilizing the monomer and polymer in the polymerization medium. The surfactant should be one that is surface active in carbon dioxide and thus partitions itself at the carbon dioxide-monomer interface. Suitable surfactants are described in detail in U.S. Patent No.
5,312,882 to DeSimone et al., the disclosure of which is incorporated herein by reference in its entirety. Such a surfactant should lower the interfacial tension between the carbon dioxide polymerization medium and the polymer, and thus create a dispersed phase. The surfactant is generally present in the reaction mixture in a concentration of from about 0.001 up to about 30 percent by weight. The surfactants can be nonreactive in the polymerization or can react with and thereby be included with the forming polymer. See, e. g., U . S . Pat. Nos.
4,592,933 and 4,429,666 for exemplary reactive surfactants.
The surfactant should contain a segment that is soluble or interfacially active in carbon dioxide ("CO2-philic"). Exemplary CO2-philic segments include a fluorine-containing segment, such as can be found in fluoropolymers or copolymers of fluoropolymers, or a siloxane-containing segment, such as can be found in siloxane polymers or copolymers of siloxane polymers. As used herein, a "fluoropolymer" has its conventional meaning in the art. Exemplary fluoropolymers are those formed from: fluoroacrylate monomers such as 2-(N-ethylperfluorooctanesulfonamido) ethyl acrylate ("Et-FOSEA"), 2-(N-ethylperfluorooctanesulfonamido) ethyl m e t h a c r y l a t e ( " E t F O S E M A " ) , 2 - ( N -methylperfluorooctanesulfonamido) ethyl acrylate ("MeFOSEA"),2-(N-methylperfluorooctanesulfonamido) ethyl methacrylate ("MeFOSEMA"), 1,1-Dihydroperfluorooctyl acrylate ("FOA"), 1,1-dihydroheptafluorobutoxy methyl oxetane (p(FOX7)), and 1,1-Dihydroperfluorooctyl acrylate ' 2 1 97303 ("FOMA"); fluoroolefin monomers such as tetrafluoroethylene, fluorostyrene monomers such as a-fluorostyrene, ,B-fluorostyrene, cY, ,B-difluorostyrene 9, ~"B-difluorostyrenes, ~x"B,,B-trifluorostyrenes, a-5 trifluoromethylstyrenes, 2, 4, 6 -Tris ( -trifluoromethyl)styrene, 2,3,4,5,6-pentafluorostyrene, 2,3,4,5,6-pentafluoro-~-methylstyrene, and 2,3,4,5,6-pentafluoro-~-methylstyrene; fluoroalkylene oxide monomers such as perfluoropropylene oxide and 10 perfluorocyclohexene oxide; fluorinated vinyl alkyl ether monomers; and the copolymers thereof with suitable comonomers, wherein the comonomers are fluorinated or unfluorinated. Exemplary siloxane-containing compounds include alkyl, fluoroalkyl, and chloroalkyl siloxanes.
More preferably, the surfactant comprises a "CO2-phobic" group along with a CO2-soluble group, such as a fluoropolymer. The CO2-phobic group may be a hydrophobic group, such as a polystyrene group, or a hydrophillic group such as carboxylic acid. Such 20 copolymers can take many forms; exemplary forms are graft copolymers, random copolymers, and block copolymers.
Other suitable surfactants that are surface active in carbon dioxide include CF3--(CF2)~--(CF2h--CF3 CF3--(CF2)~--(CF2h--OH

CF3--(CF2~--CH=CH--(CF~b,--CF3 OH
CF3--(CF2~--CH2--CH--CH2OH
CF3 1~
CF3--(CF2)~--O--CF--C~--Cl~

CF3--(CF2)~--C--OH

lc~
CF3--(CF2~--R--(C~C~h -C~C~CH3 [~

where x=1-30 and y=1 to 30. The x and y values are chosen to adjust the balance between "CO2-philic~ and "CO2-phobic" to tailor the surface activity of the reagents.
Exemplary silicone-containing surfactants (i.e., siloxane polymers cr copolymers) include CH3 lcii i3u--(CH2 -CH~--(Si-Oh -Sl-Ci~i3 CH3 Ci-i3 CH3 CH3 IcH3 CH3--(Cl~ (Si-O~-Si CH--CH2ci'i3 CH3 CHs wherein x and y are varied to adjust to "CO2-philic" and "CO2-phobic" balance.
The polymerizing step of the present invention can be carried out by polymerization methods using apparatus and conditions known to those skilled in this art. For example, the polymerization reaction is carried out in a suitable high pressure reaction vessel of about 24 mL and capable of withstanding pressures on the order of up to about 8000 psi. The reaction vessel typically includes a cooling system. Additional features of the reaction vessel used in accordance with the invention include heating means such as an electric heating furnace to heat the reaction mixture and mixing means, i.e., stirrers such as paddle stirrers, impeller stirrers, or multistage impulse countercurrent agitators, blades, and .

' the like. Typically, the reaction begins by cooling the reaction vessel to a temperature below about 31~C. The initiator, monomer or monomers, and carbon dioxide are added to the vessel. Typically the mixture is allowed to polymerize for between about 2 and 24 hours, and preferably is stirred as the reaction proceeds. At the conclusion of the reaction, the polymer can be collected by methods such as venting of the carbon dioxide or by fractionation. After separation, the polymer can be collected by conventional means. In addition, the polymers of the present invention may be retained in the carbon dioxide, and sprayed onto a surface. After the carbon dioxide and solvent evaporate, the polymer forms a coating on the surface.
The polymer formed by the present invention can also be used to form molded articles, such as valves and bottles, films, fibers, resins, and matrices for composite materials.
The present invention is explained in greater detail in the following examples. As used herein, "M"
means molar concentration, "NMR" means nuclear magnetic resonance, "MHz" means megahertz, "GPC" means gas phase chromatography, ~A~ means angstroms, " W " means ultraviolet, "g" means grams, "mol" means moles, "mL"
means milliliters, "C" means degrees Centigrade, "S"
means seconds, "h" means hours, "psig" means pounds per square inch (gauge), IIMnl' means number average molecular weight, "MWD" means molecular weight distribution, "f"
means functionality, "ppm" means parts per million, IITgl' means glass transition temperature, "nm~' means nanometers, "mg" means milligrams, "rpm~' means revolutions per minute, "mm Hg" means millimeters of mercury, and "psi" means pounds per square inch. These Examples are illustrative and are not to be taken as limiting of the invention.

, -ExDerilllentdl Procedures and Materials Monomers of isobutyl vinyl ether, styrene, and 3, 3 ~ -bisethoxymethyl oxetane were provided by Dr. Gerald Manser of Aerojet Corporation. Bisethoxymethyl oxetane (BEMO) was vacuum distilled at 5 X 10-2 mm Hg, with the fraction distilling at 54~C to 57~C being collected.
Styrene was vacuum distilled from calcium hydride at 5 x 10-2 mm Hg and 50~C. Isobutyl vinyl ether was distilled twice from calcium hydride under an argon atmosphere at about atmospheric pressure and a temperature of 82 ~C .
Lewis acid catalysts ethyl aluminum dichloride ( 1. 0 M in hexanes, obtained from Aldrich) and tin tetrachloride (obtained from Aldrich) were used without further purification. Lewis acid catalyst boron trifluoride tetrahydrofuranoate (BF3-THF) was prepared by stirring boron trifluoride diethyletherate (obtained from Aldrich) with prechilled tetrahydrofuran (obtained from Mallinckrodt) for two hours at 25~C. BFCl-THF was purified by distillation at 100~ under argon to remove volatiles, followed by vacuum distillation with the fraction distilling at 70~C being isolated. The acetic acid/isobutyl vinyl ether adduct was prepared as described by T. Hagashimura et al. Macromolecules 22 (3):
1009 (1989). Isobutyl vinyl ether (IBVE) was treated with acetic acid for three hours at 60~C and atmospheric pressure, then the adduct was distilled twice under vacuum at 5 X 10-2 mm Hg with the middle fraction, which is distilled over at about 60~C, being collected both 3 0 times to prepare the ester initiator .
Initiators 1, 4-butanediol, 2, 2, 2-trifluoroethanol, and 1-phenyl-1-chloroethane (obtained from Aldrich) were used without further purification.
The deactivator, ethyl acetate was obtained from Aldrich and was distilled twice from calcium hydride under an argon atmosphere. Cyclohexane was obtained from Phillips Petroleum and was stirred over concentrated sulfuric acid 2 1 q7303 for two weeks, decanted, and distilled from sodium metal under an argon atmosphere. Methylene chloride was obtained from Mallinckrodt, and, was distilled twice from calcium hydride under an argon atmosphere. Carbon dioxide was obtained from Matheson, 99.99~ was passed through copper oxide catalyst column to remove trace amounts of oxygen and then through a 3A molecular sieve column to remove trace amounts of moisture. The high pressure reactor was constructed from Hastelloy C-22, having a volume of 24 mL and a pressure capacity of up to about 8000 psi and was obtained from Haynes International.

PolY",e,iLdlion in CYclohexane in the Absence of Ester Initiator Before running polymerization in supercritical carbon dioxide, a series of polymerization were conducted in cyclohexane. The monomer employed was isobutyl vinyl ether.
A 300 mL round-bottom glass flask equipped with a teflon stirring bar and sealed with a rubber septa, is flame dried under an argon atmosphere. IBVE (10 mL, 7.68 g), ethyl acetate (10 mL), and cyclohexane (30 mL) were combined in the flask. The temperature of the flask is maintained near 40~C using a water bath, and stirring is achieved using a stir plate. Ethyl aluminum dichloride (EtAlCl2) (0.38 mL, 0.38 mmol) is added via syringe to catalyze the polymerization, with trace amounts of water being added as the initiator. The reaction proceeds for twelve hours at which time a solution of sodium ethoxide in ethanol is added to the flask to terminate the reaction. The resulting polymer is precipitated into methanol, filtered, and dried in vacuum overnight. The polymerization conditions, yields and molecular weight data are summarized in Table 1.

-' 21 97303 Sample feed ratio Mw Mn MWD Yield monomer ethyl acetate EtAlCl, solvent (x 103) (x 10 3) (9l (mL) (mmol)~ (mL) mrcA137 3.072 4 0.31 12 165 107 l.S --mrcB137 7.68 10 0.38 30 134 80 1.7 --both polymerizations are run at 40~C

Pohl",e,i~d~iGn of IsobutYI vinYI ether (IBVE) in S~l er~ ical Carbon Dioxide in the Absence of Ester Initiator Ethyl acetate (3 mL) and EtAlCl2 (0.46 mL, 0.46 mmol) are added to the high pressure cell via syringe under an argon atmosphere. The cell is equipped with a teflon coated stir bar and heated to 40~C. Carbon dioxide is added to the cell using a high pressure syringe to achieve a cell pressure of 4500 psi. IBVE (3 mL, 2.304 g) is added to the cell using a high pressure syringe. The reaction continued for fourteen (14) hours and was accompanied by a pressure drop, to a final pressure of 3683 psi. During the course of the reaction, polymer could be seen forming and precipitating from the carbon dioxide fluid.
At the end of the polymerization, carbon dioxide -is vented slowly to leave the polymer in the cell. The reaction is terminated using a solution of sodium ethoxide in ethanol. The polymer is then dissolved in cyclohexane or a solution of cyclohexane/tetrahydrofuran, precipitated into a large excess of methanol, filtered and dried in vacuum overnight. Poly(isobutyl vinyl ether) (1.997 g) was recovered. (Yield = 87%).
Characterizations: 1H NMR spectra show the expected patterns, without vinyl proton peaks of the monomer and without any indication of incorporation of carbon dioxide into the polymer backbone. The FTIR

spectrum are consistent with the corresponding homopolymer made in cyclohexane, with no carbonyl peak present. Gel permeation chromatography (GPC) analysis show Mn = 1.51 x 105, Mw = 5.99 x 105, and MWD = 4.o.

Pol~",e,i~dtion of IsobutYI vinYI ether (IBVE) in Su~ercritical Carbon Dioxide in the Absence of Ester Initiator Ethyl acetate (4 mL) and ethyl aluminum dichloride (0.25 mL, 0.25 mmol) are added to the high pressure cell. Following the same procedure in Example 3, carbon dioxide and isobutyl vinyl ether (4 mL, 3.702 g) are added for a final pressure of 4200 psi. The reaction proceeds for twenty-two hours at 40~C, during which time pressure within the cell decreases to 3860 psi. Poly(IBVE) (2.211 g) is recovered. (Yield = 72~).
Characterization: 1H NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates MN = 8.0 x 104, Mw = 5.2 x 105, and MWD = 6.5.

EXAMPLE ~
PolY",eli~dlion of IsobutYI viml ether (IBVE) in SuDe~ ical Carbon Dioxide in the Absence of Ester Initiator Ethyl acetate (4 mL) and ethyl aluminum dichloride (0.5 mL, 0.5 mmol) are added to the high pressure cell. Following the same procedure as described in Example 3, carbon dioxide and IBVE (4 mL, 3.072 g) are added for a final pressure of 4200 psi. The reaction proceeds for 23 hours at 40~C. Poly(IBVE) (1.277 g) is recovered. (Yield = 44~).
Characterizations: lH NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates Mn = 5.2 x 104, Mw = 2.8 x 105, and MWD = 5.4.

- 2~ 9~303 ComParative Exam~le: PolYmerization in CYclohexane in the Presence of Ester Inidator A 300 mL round-bottom glass flask equipped with a teflon stirring bar and sealed with a rubber septa, is flame dried under an argon atmosphere. IBVE (10 mL, 7.68 g), ethyl acetate (9.8 mL), the ester initiator (0.06 mL, 0.31 mmol), and cyclohexane (100 mL~ are combined in the flask. The temperature of the flask is maintained near 40~C using a water bath and stirring is achieved with a stir plate. Ethyl aluminum dichloride (EtAlCl2) (0.40 mL, ~ 0.40 mmol) is added via syringe to catalyze the polymerization. The reaction proceeds for twenty-four hours at which time a solution of sodium ethoxide in ethanol is added to the flask to terminate the reaction.
The resulting polymer is precipitated into methanol, filtered, and dried in vacuum overnight. Poly(IBVE) (3.35 g) is recovered. (Yield = 44%).
Characterization: GPC indicates Mn = 7.0 x 103, Mw = 8.1 x 103, MWD = 1.15.

PolY,ne,i~dLion of IsobutYI viml ether (IBVE) in SuDercritical Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (2.4 mL), EtAlCl2 (0.2 mL, 0.2 mmol), and the ester initiator (0.04 mL, 0.23 mmol) are combined in the cell. Following the procedure as described in Exa~ple 3, carbon dioxide and IBVE ( 3 ml, 2.304) are added to achieve a pressure of 4800 psi. The reaction proceeds for thirteen hours at 40~C, during which time the pressure within the cell drops to 3800 psi. Poly(IBVE) (2.11 g) is recovered. (Yield = 91%).
Characterization: 1H NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates Mn = 6.7 x 103, Mw = 1.2 x 1o4, and MWD = 1.8.

.~

Pol~1llleliLd~ion of IsobutYI vinYI ether (IBVÉ) in Su~ele, Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (2.4 mL), EtAlCl2 (0.2 ml, 0.2 mmol), and the ester initiator (0.01 mL, 0.06 mmol) are combined in the cell. Following the same procedure as described in Example 3, carbon dioxide and IBVE (3 ml, 2.304) are added to achieve a pressure of 5000 psi. The reaction proceeds for twelve hours, during which time the pressure drops to 4041 psi.
Characterization: 1H NMR and FTIR spectra are ~ consistent with those of the homopolymer made in cyclohexane.

15POIYIIIel iLd~iOI) of IsobutYI viml ether (IBVE) in Liauid Grbon Dioxide in the Presence of Ester Initiator Ethyl acetate (2.4 mL), EtAlCl2 (0.2 mL, 0.2 mmol), and the ester initiator (0.04 mL, 0.23 mmol) are combined in the cell. Following the same procedure described in Example 3, carbon dioxide and IBVE (3 mL, 2.304 g) are added to a pressure of 5200 psi. The reaction proceeds for twelve hours at 30~C, during which time the pressure drops to 3236 psi.
Characterization: 1H NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC lndicates Mn = 1.4 x 104, Mw = 2.0 x 104, MWD = 1.4.

PolY",e,iLd~ion of IsobutYI viml ether (IBVE) in SuPer~ icdl 30Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (2.4 mL), EtAlC12 (0.2 mL, 0.2 mmol), and the ester initiator (0.04 mL, 0.23 mmol) are combined in the cell. Following the same procedure - 219~3~3 described in Ex~ple 3, carbon dioxide and IBVE (3 mL, 2.304 g) are added to a pressure of 5000 psi. The reaction proceeds for twelve hours at 60~C, during which time the pressure drops to 4200 psi. Poly(IBVE) (2.043 g) is recovered. (Yield = 92~).
- Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates Mn = 1.4 x 104, Mw .= 2.0 x 104, MWD = 1 .4 .

o EXAMPLE 11 Pol~.l.e-i~dLion of IsobutYI viml ether (IBVE) in Su~ercritical Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (1.2 mL), EtAlC12 (0.2 mL, 0.2 mmol), and the ester initiator (0.04 mL, 0.23 mmol) are combined in the cell. Following the same procedure described in Example 3, carbon dioxide and IBVE (3 mL, 2.304 g) are added. The reaction proceeds for twelve hours at 40~C. Poly(IBVE) (1.994 g) is recovered.
(Yield = 87~).
Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates Mn = 2.3 x 104, Mw = 8.7 x 104, MWD = 3.9.

25 PolY.. ,e,i~d~ion of IsobutYI vinyl ether (IBVE) in Su~,e,~ ical Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (4.8 mL), EtAlC12 (0.2 mL, 0.2 mmol), and the ester initiator (0.04 mL, 0.23 mmol) are combined in the cell. Following the same procedure described in Example 3, carbon dioxide and IBVE (3 mL, 2.304 g) are added to the cell to a pressure of 5000 psi.
The reaction proceeds for twelve hours at 40~C, during which time the pressure drops to 4050 psi. Poly(IBVE) (1.063 g) is recovered. (Yield = 46~).

-' 2 1 97303 -Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC lndicates Mn = 3.4 x 10~, Mw = 4.8 x 103, MWD = 1.4.

PolY",~ d~ion of IsobutYI viml ether (IBVE) in SuDel.,iLical Carbon Dioxide in the Presence of Ester Initiator EtAlCl2 (0.2 mL, 0.2 mmol), and the ester initiator (0.04 mL, 0.23 mmol) are combined in the cell.
Following the same procedure described in Example 3, ~ carbon dioxide and IBVE (3 mL, 2.304 g) are added to the cell to a pressure of 5000 psi. The reaction proceeds for twelve hours at 40~C, during which time the pressure drops to 3300 psi. Poly(IBVE) (1.614 g) is recovered.
(Yield = 70%).
Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates Mn = 1.3 x 104, Mw = 3.9 x 104 MWD = 2.9.

PolY",~,iLdliGn of IsobutYI vinYI ether (IBVE) in Su~e~ ical Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (2.4 mL), EtAlCl2 (0.2 mL, 0.2 mmol), and the ester initiator (0.02 mL, 0.12 mmol) are combined in the cell. Following the same procedure described in Example 3, carbon dioxide and IBVE (3 mL, 2.304 g) are added to the cell to a pressure of 4500 psi.
The reaction proceeds for twelve hours at 40~C.
Poly(IBVE) (2.245 g) is recovered. (Yield = 93~).
Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates Mn = 1.4 x 104, Mw = 2.0 x 104, MWD = 1.4.

EXAMPLE t 5 Pol~,l,leli~dLion of Isobutyl vinYI ether (IBVE) in SuPercritical Carbon Dioxide in the Presence of Ester Initiator Ethyl acetate (2.0 mL), EtAlCl2 (0.2 mL, 0.2 mmol), and the ester initiator (0.02 mL, 0.12 mmol) are combined in the cell. Following the same procedure described in Example 3, carbon dioxide and IBVE (3 mL, 2. 304 g) are added to the cell to a pressure of 4955 psi.
The reaction proceeds for twelve hours at 60OC, during which time the pressure had dropped to 3957 psi.
Characterization: lH NMR and FTI~ spectra are consistent with those of the homopolymer made in cyclohexane. GPC indicates a bimodal molecular weight distribution.

ComDarative ExamDle: PolYIlleli~ n of 3.3'-bisethoxymethYI oxetane in MethYlene Chloride Polymers of 3,3'-(bisethoxymethyl)oxetane (BEMO) are prepared in methylene chloride. A 300 mL
round-bottom glass flask equipped with a teflon stirring bar and sealed with a rubber septa, was flame dried under an argon atmosphere. BEMO (4 mL, 3.99 g), and methylene chloride (20 mL) are combined in the flask. If no external proton source (i.e., initiator) is added, adventitious water was employed as the proton source.
The temperature of the flask is maintained near 10~C
using an ice bath and stirring is achieved with a stir plate. The catalyst boron trifluoride tetrahydrofuranoate (BF3-THF) (0.06 mL, 0.58 mmol) is added via syringe to catalyze the polymerization, with trace amounts of water being added as the initiator. The reaction proceeds for four hours at which time a solution of aqueous sodium hydroxide is added to the flask to terminate the reaction. The resulting polymer is precipitated into methanol, filtered, and dried in vacuum overnight. Table 2 summarizes the results obtained in methylene chloride.

Table 2 S~mple feed r~tio Mw Mn MWD ~ield monomer proton source BF3-THF solvent (x 103) (x io-3) (g) (mmol) (mL) mcllO9~B 3.99 -- O.58 20 19.9 35.9 1.8 61~
mclll94 3.99 -- 0.58 20 17.6 34.9 1.9 70S
mcBF3A 3.99 -- 0.58 20 29.3 63.7 2.2 77~
mcBOOA 3.99 BOO 1.16 20 17.9 30.5 1.7 37S
mcS494 3.99 CF3CH20H 0.58 20 33.2 72.4 2.2 79 1 O mcSl094 3.99 CF3CH20H 2.32 20 28.0 55.6 1.7 64 mc51894 3.99 CF3CH20H 2.32 20 28.1 57.1 2.0 76 PolY",e,i~dlion of 3,3'-(bisethoxYmethYI)oxetdne (BEMO) in Liauid Cdrbon Dioxide I5 The high pressure cell is equipped with a Hastelloy C-22 dish to allow both monomer and catalysts to be added to the cell before the carbon dioxide and not premix. BEMO (4.8 mL, 4.8 g) is added to the body of the high pressure cell via syringe under an argon atmosphere.
BF3-THF (0.28 mL, 0.69 mmol) is added to the Hastelloy dish via syringe under an argon atmosphere. The cell is equipped with a stir bar and the temperature is maintained near -lO~C using a sodium chloride/ice bath.
Carbon dioxide is added to the cell using an ISCO~ high pressure syringe pump to a pressure of 4300 psi. The reaction proceeds for four hours, during which time the pressure drops to 3500 psi. Carbon dioxide is slowly vented and the reaction is terminated using an aqueous ; solution of sodium hydroxide. The polymer is dissolved in tetrahydrofuran and precipitated -in methanol, filtered, washed with dilute hydrochloric acid and water, .' 2197303 -then dried overnight in a vacuum. Poly(BEMO) (3.210 g) is recovered. (Yield = 67~) Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer prepared in methylene chloride. GPC indicates Mn = 8.1 x 103, Mw =
2.2 x 104, MWD = 2.7.

PolYIlleli~d~Gn of 3.3'-(bisethoxYmethYI)oxetdne (BEMO) in Liauid Grbon Dioxide Reaction is conducted as described in Example ~ 17. Carbon dioxide is added to a pressure of 4800 psi.
Poly(BEMO) (1.484 g) is recovered. (Yield = 31~).
Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in methylene chloride. GPC indicates Mn = 9.0 x 103, Mw =
2.8 x 104, MWD = 3.1.

PolYmeliLdliGIl of 3,3'-(bisethoxYmethYI)oxetdne (BEMO) in Liauid Cdrbon Dioxide BEMO (4.8 mL, 4.8 g) and 1,4-butanediol (0.06 mL, 0.69 mmol) are added to the cell. Following the same procedure described in Example 17, BF3-THF (0.15 mL, 1.38 mmol) is added to the cell. Carbon dioxide is added to an initial pressure of 4800 psi. Poly(BEMO) (2.08 g) is recovered. (Yield = 43~).
Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in methylene chloride. GPC indicates Mn = 7.3 x 103, Mw =
1.2 x 104, MWD = 1.6.

' Pol~ime,i~dtion of 3.3'-(bisethoxYmethYl)oxetane (BEMO) in Liquid Carbon Dioxide Reaction is conducted as described in Ex~mple 18, except the initial pressure of carbon dioxide is 3000 psi. Poly(BEMO) (0.74 g) is recovered. (Yield = 16~).
Characterization: lH NMR and FTIR spectra are - consistent with those of the homopolymer made in methylene chloride. GPC indicates Mn = 1.0 x 104, Mw =
1.6 x 104, MWD = 1.6.

PolYIneli~d~ion of 3,3'-(bisethox~nnethYl)oxetane (BEMO) in Liauid Carbon Dioxide Reaction is conducted as described in Example 19, except that 1,4-butanediol is premixed with BF3-THF
and then injected into the reactor dish. BEMO (4.8 mL, 4.8 g) is added to the body of the cell. BDo/BF3-THF
solution (0.22 mL, 0.69 mmol) is injected into the dish within the cell. Carbon dioxide is added to a pressure of 4200 psi. Poly(BEMO) (0.840 g) is recovered.
(Yield = 18%).
Characterization: lH NMR and FTIR spectra are consistent with those of the homopolymer made in methylene chloride. GPC indicates Mn = 1.2 x 104, Mw =
2.0 x 104, MWD = 1.7.

ComDarative Exam~le: PolYIlle.iLdLiGn of StYrene in MethYlene Chloride Polymers of styrene are prepared in methylene chloride using a method outlined by T. Higashimura et al., Macromolecules 26:744 (1993).
A 300 mL round-bottom glass flask equipped with a teflon stirring bar and sealed with a rubber septa, is flame dried under an argon atmosphere. Styrene (4.0 mL, -3.64 g), the initiator, l-chloro-1-phenyl ethane (0.5-mL, 0.70 mmol), the deactivator, tetrabutyl ammonium chloride (2.4 mL, 1.40 mmol), and methylene chloride (20 mL) are added to the flask via syringe. The temperature of the flask is maintained near -10~C using an ice bath and stirring is achieved with a stir plate. The catalyst, tin tetrachloride (0.7 mL, 3.49 mmol) is added to the cell via syringe. The reaction proceeds for 3 hours at -10~C, at which time the reaction is terminated by the addition of a solution of sodium methoxide and methanol.
The polymer is precipitated into methanol, filtered, and dried overnight under vacuum. Poly(styrene) (2.813 g) is recovered. (Yield = 77~).
Characterization: GPC indicates Mn = 4.2 x 103, Mw = 4.9 x 103, MWD = 1.17.

PolYIlle~ iGn of St~rene in Liquid Carbon Dioxide The high pressure cell is equipped with a Hastelloy C-22 dish to allow both monomer and catalysts to be added to the cell before the carbon dioxide without pre~'xlng. Styrene (5.0 mL, 4.55 g), 1-chloro-1-phenyl ethane (0.1 mL, 0.87 mmol), and tetrabutylammonium chloride (1.9 mL, 1.7 mmol) are added to the body of the high pressure cell via syringe under an argon atmosphere.
Tin tetrachloride (0.9 mL, 4.41 mmol) is added to the Hastelloy dish via syringe under an argon atmosphere.
The cell is equipped wlth a stir bar and temperature is maintained near 0~C using a NESL~3~ circulating bath equipped with a refrigeration unit and a solution of water and ethylene glycol as the coolant. Carbon dioxide is added to the cell using an ISC0~ high pressure syringe pump to a pressure of 4500 psi. Within minutes, polymer can be seen forming and precipitating out of solution in the reactor. The polymerization proceeds for 3 hours near 0~C, during which time the pressure drops to approximately 4000 psi. The carbon dioxide is then 2 1 973~3 slowly vented off and the reaction is terminated by the addition of a solution of sodium methoxide and methanol.
The polymer is dissolved in tetrahydrofuran, precipitated into methanol, filtered, and dried under vacuum overnight. Poly(styrene) (2.3838 g) is recovered.
(Yield = 52~).
Characterization: lH NMR and FTIR spectra are consistent with that of the homopolymer prepared in methylene chloride. GPC indicates Mn = 4.4 x 103, Mw =
0 1 .1 X 103, MWD = 2.58.

PolYIlleli~dliGn of StYrene in Liauid Carbon Dioxide The reaction is conducted following the same procedure described in Example 23, with the following changes. No tetrabutylammonium chloride is added. The 1-chloro-1-phenyl ethane is added to the Hastelloy C-22 dish instead of the body of the cell to allow it to premix with the tin tetrachloride. Poly(styrene) (1.9903 g) is recovered. (Yield = 44~).
Characterization: 1H NMR and FTIR spectra are consistent with that of the homopolymer prepared in methylene chloride. GPC indicates Mn = 2.8 x 103, Mw =

5.3 x 103, MWD = 1.9.

Catatonic PolYn~el i~dLiGn of IsobutYlene in Liauid Carbon Dioxide Isobutylene is polymerized with an initiator system including 2-chloro-2,4,4-trimethylpentane (TMPCl)/titanium tetrachloride (TiC14)/Lewis bases, where the Lewis base include dimethyl sulfoxide, acetamide, or ethyl acetate, in liquid and supercritical carbon dioxide using the procedure of Example 23 above. This monomer has previously been polymerized in liquid solvents, such -as methyl chloride. See, M. Sawamoto, Prog. Polym, Sci.
16:111 (1991).

Cationic Co~olY,l,eri~d~ion of StYrene and IsobutYlene s in Carbon Dioxide Styrene is copolymerized with isobutylene using 2-methoxy-2-propyl benzene and titanium tetrachloride in ~ the presence of di-t-butyl pyridine using the method - described in Example 23 above with one change. The second monomer (styrene) is added to the cell using a ~ hign pressure syringe once the isobutylene has been consumed in the reaction. It is known that these two monomers can form copolymers cationically in the mixed solvent system methyl chloride/methyl cyclohexane. See, J. Kennedy, et al. Makromol. Chem., Macromol. Symp.
51:1269 (1991).

Block CoPolY,ne,iLd~iGn of IsobutYlene and MethYI VinYI Ether Isobutylene is cationically block copolymerized with methyl vinyl ether using the TMPC1/TiC14 initiating system described in Example 25 in the presence of tetrabutylammonium chloride in liquid and supercritical carbon dioxide using the procedure described in Example 26, where methyl vinyl ether is the second monomer. It is known that these monomers can form block copolymers cationically in mixed solvent systems such as methyl chloride/n-hexane or methylene chloride/n-hexane. See, J. Kennedy, et al., Macromolecules 25:1642 (1992).

Cationic Cowl~l",eriL~tion of IsobutYlene and Iso~rene Isobutylene is cationically block copolymerized with isoprene using cumyl acetate or boron trichloride in ' 2~ 97303 liquid and supercritical carbon dioxide using the procedure described in Example 26. Isoprene is the - second monomer. It is known that these monomers can form block copolymers cationically in methyl chloride. See, J. Kennedy, et al. Macromolecules 25:1771 (1992).

Cationic PolY",eli~dLion of CYCIjC Carbonates Cyclic carbonates are polymerized cationically using methyl triflate, methyl iodide, or benzyl bromide in liquid or supercritical carbon dioxide according to the method described in Example 17 above.

Cationic PolY.IleliLdlion of Oxetanes in Carbon Dioxide Oxetanes are polymerized cationically using strong acids or Lewis acids and preinitiators such as alcohols, ethers, and esters in liquid and supercritical carbon dioxide as described in Exampl- 17 above.

Cadonic CoDolY,.,eli~d~ion of Oxetanes ' and CYCIjC Carbonates Oxetanes, are copolymerized cationically with cyclic carbonates using methyl triflate or boron trifluoride diethyl etherate in liquid and supercritical carbon dioxide as described in Example 17 above, with one exception. The oxetane and the cyclic carbonate are added simultaneously to the cell. The initial cell temperature is held at 0~C until the oxetane monomer is consumed. The temperature is then raised to 30~C while the cyclic carbonate monomer is consumed. It has been previously known that these monomers could be copolymerized in methylene chloride and deuterated chloroform. See, T. Endo, et al ., Macromolecules 26 :7106 (1993).

Cationic CoPolY,neriLdlion of Other CYCIjC Monomers Cyclic monomers, such as oxiranes, tetrahydrofuran, trioxane, and oxazolines are polymerized cationically using: (1) triflic acid or (2) Lewis acids and some proton source such as water or alcohols, in liquid and supercritical carbon dioxide as described in Example 17 above. It has been known that these monomers could be cationically polymerized in solvents such as nitromethane, methylene chloride, and carbon tetrachloride. See, E. Goethals, Makromol. Chem., - Macromol . Symp. 42/43:51 (1991).

PolY"~e,iLdtion of FormaldehYde in Carbon Dioxide Formaldehyde is polymerized cationically using hydrochloric acid or Lewis acids such as boron trifluoride and water in liquid and supercritical carbon dioxide as described in Example 17 above.

pol~llleli~d~ion of 3,3'-bisethoxymethYI oxetane (BEMO) in Liauid Carbon Dioxide in the Presence of Surfactant The high pressure cell is equipped with a hastelloy C-22 dish to allow both monomer and catalyst to be added to the cell before the carbon dioxide while avoiding premix. Poly(l,l dihydroheptafluorobutoxy methyl oxetane) (p(FOX7)) (0.9902 g) is added to the cell. BEMO (4.8 mL, 4.8 g) is added to the body of the cell via syringe under an argon atmosphere. Boron trifluoride tetrahydrofuranate (BF3-THF) (0.28 mL, 0.69 mmol) is added to the hastelloy dish via syringe under an argon atmosphere. The cell is equipped with a mechanical stirrer to allow the contents to be agitated during the reaction and temperature is maintained near 5OC using a circulating cold bath and a cooling coil around the cell.

-Carbon dioxide is added to the cell using an ISCO high pressure syringe pump, to achieve a pressure of 4267 psi.
The reaction proceeds for six hours during which time the solution changes from clear to an opaque, "milky"
dispersion. The reaction is terminated by venting the dispersion into deoxygenated, deionized water and injecting 2 mL of water into the cell. The polymer is collected and dried overnight under vacuum. Poly(BEMO) (3.1731 g) is recovered. (Yleld = 66%).
Characterization: GPC indicates Mn = 1.7 x 103 g/mol, Mw = 5.4 x 103 g/mol, and MWD = 3.1.

PolY"~ a~ion of 3.3'-bisethoxYmethYI oxeLdne (BEMO) in Liquid Dioxide in the Presence of Surfactdnt Reaction is set up as described in Example 34, except poly(1,1-dihydroperfluorooctyl acrylate) (p(FOA)) is used as the surfactant instead of poly(FOX7). Carbon dioxide is added to a pressure of 4200 psi. Stirring is halted after 4 hours, 25 minutes has elapsed. The "milky" dispersion described in Example 34 did not precipitate after termination of stirring. Reaction is terminated after a total reaction time of 4 hours, 35 minutes by venting into deoxygenated methanol and addition of 4 mL of deoxygenated methanol to the depressurized cell. Poly(BEMO) (3.043 g) is recovered.
(Yield = 63%).
Characterization: GPC indicates Mn = 1.4 x 104 g/mol, Mw = 4.6 x 104 g/mol, and MWD = 3.3 polylll~ d~ion of IsobutYlene in Liauid Cdrbon Dioxide in the Presence of Su, rdc~dnt p(FOA) (0.8403 g) is added to the high pressure reactor. Tin tetrachloride (0.05 mL, .43 mmoles) is added to the cell via syringe under an argon atmosphere.

Carbon dioxide is added as described in Example 34 to a pressure of 1285 psi. Cell temperature was 1.2~C.
Isobutylene (3.4 g, 0.06 moles) is added slowly using a high pressure syringe pump to a final cell pressure of 4150 psi. The reaction began clear, but became increasingly cloudy as the reaction proceeds. Reaction proceeded for twenty-two hours at which time it is terminatedby depressurization of the cell contents into deoxygenated methanol and injection of 3 mL of deoxygenated methanol into the cell. The product polymer with surfactant can be redispersed in Freon-113 as a stable suspension. Poly(isobutylene) (0.57 g) is recovered, (17~ yield).
Characterization: GPC indicated a product of bimodal molecular weight, with peak molecular weights of 1.8 x 103 g/mol and 3.9 x 103 g/mol.
The foregoing is illustrative of the present invention and is not to be construed as limiting thereof.
The invention is defined by the following claims, with equivalents of the claims to be included therein.

Claims

That Which Is Claimed Is:

1. A method of carrying out the cationic polymerization of a monomer in carbon dioxide, the method comprising:
(a) providing a reaction mixture comprising carbon dioxide, a monomer selected from the group consisting of cyclic ether monomers, oxazoline monomers, and cyclic carbonate monomers; a catalyst; and a cationic polymerization initiator, wherein said cationic polymerization initiator is capable of initiating the cationic polymerization of said monomer;
(b) polymerizing said monomer in said reaction mixture to form a polymer.

2. The method according to Claim 1, wherein the reaction mixture comprises a heterogeneous reaction mixture.

3. The method according to Claim 1, wherein the reaction mixture comprises a homogeneous reaction mixture.

5. The method according to Claim 1, wherein said carbon dioxide is liquid carbon dioxide.

6. The method according to Claim 1, wherein said carbon dioxide is supercritical carbon dioxide.

7. The method according to Claim 1, further comprising separating said polymer from said solution following the polymerization step.

8. The method according to Claim 1, further comprising collecting said polymer from said solution following the separating step.

9. A reaction mixture useful for the cationic polymerization of a monomer in carbon dioxide, said mixture comprising:
(a) at least one monomer selected from the group consisting of cyclic ether monomers, oxazoline monomers, cyclic carbonate monomers;
(b) carbon dioxide;
(c) a catalyst; and (d) a cationic polymerization initiator capable of initiating the cationic polymerization of said monomer.

11. The reaction mixture according to Claim 9, wherein said carbon dioxide is liquid carbon dioxide.

12. The reaction mixture according to Claim 9, wherein said carbon dioxide is supercritical carbon dioxide.

13. A cationic polymerization reaction mixture produced from the cationic polymerization of a monomer in carbon dioxide, wherein the monomer is selected from the group consisting of cyclic ether monomers, oxazoline monomers, cyclic carbonate monomers, said reaction mixture comprising:
(a) at least one cationic polymerization polymer;
(b) carbon dioxide; and (c) a catalyst.

15. The reaction mixture according to Claim 13, wherein said carbon dioxide is liquid carbon dioxide.

16. The reaction mixture according to Claim 13, wherein said carbon dioxide is supercritical carbon dioxide.

18. The method according to Claim 1, wherein said polymerizing step is carried out in the presence of a surfactant.

19. The reaction mixture according to Claim 9 further comprising a surfactant.

20. The reaction mixture according to Claim 13 further comprising a surfactant.

21. A method for carrying out the cationic polymerization of a monomer in carbon dioxide, the method comprising:
(a) providing a reaction mixture comprising carbon dioxide, a monomer, a catalyst, a cationic polymerization initiator capable of initiating the cationic polymerization of said monomer;
and a surfactant containing a CO2-phillic segment; and (b) polymerizing said monomer in said reaction mixture to form a polymer.

22. The method according to claim 21, wherein said monomer is selected from the group consisting of substituted and unsubstituted vinyl ether monomers, cyclic ether monomers, oxazoline monomers, hydrocarbon olefin monomers, cyclic carbonate monomers,and formaldehyde.

23. A reaction mixture useful for the cationic polymerization of a monomer capable of cationic polymerization in carbon dioxide, said mixture comprising:
(a) at least one monomer capable of cationic polymerization;
(b) carbon dioxide;
(c) a catalyst;
(d) a cationic polymerization initiator capable of initiating the cationic polymerization of said monomer; and (e) a surfactant containing a CO2-phillic segment.

24. The reaction mixture according to claim 23, wherein said monomer is selected from the group consisting of substituted and unsubstituted vinyl ether monomers, cyclic ether monomers, oxazoline monomers, hydrocarbon olefin monomers, cyclic carbonate monomers, and formaldehyde.

25. A cationic polymerization reaction mixture produced from the cationic polymerization of a monomer capable of cationic polymerization in carbon dioxide, said reaction mixture comprising:
(a) at least one cationic polymerization polymer;
(b) carbon dioxide;
(c) a catalyst; and (d) a surfactant containing a CO2-phillic segment.

26. The reaction mixture according to claim 25, wherein said monomer is selected from the group consisting of substituted and unsubstituted vinyl ether monomers, cyclic ether monomers, oxazoline monomers, hydrocarbon olefin monomers, cyclic carbonate monomers, and formaldehyde.