Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Polymers from only ethylenic monomers or processes of...
Utility Patent
1998-07-06
2001-01-02
Wu, David W. (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Polymers from only ethylenic monomers or processes of...
C526S329100, C526S249000
Utility Patent
active
06169153
ABSTRACT:
The present invention relates to a process for preparing polymers of cyclopentadiene using a palladium catalyst, to palladium complexes which are suitable as catalyst and to the hydrogenation of the polymers obtained.
It is known that the cationic polymerization of cyclopentadiene proceeds with retention of the five-membered ring and a double bond of the cyclic diene, see Encycl. Polym. Sci. Engng., Volume 4, p. 538, Wiley Interscience, New York (1985). The polymerization over various catalysts which make possible the ationic polymerization leads to polycyclopentadiene having the following structure:
which in many cases is partially gelated.
Suitable cationic catalysts, eg. Lewis acid halides, alkylaluminum halides and titanium-, tungsten-, vanadium- and molybdenum-containing catalysts, are disclosed, for example, in U.S. Pat. No. 3,328,372, DE-A 12 50 128, U.S. Pat. No. 3,387,046, U.S. Pat. No. 3,498,961, JP 80 104 307 and JP 72 436 333. The proportion of 1,2 and 1,4 linkages of the cyclopentene rings in the polymer depends on the solvent used in the polymerization of the cyclopentadiene (J. Polym. Sci. 5 (1968), 1175) and on the cationic catalyst (J. Polym. Sci. 6 (1968), 1163). Typical values are from 40 to 50% of 1,2 linkages. The solubility of the polymer in solvents such as toluene, cyclohexane, chloroform and tetrahydrofuran is increased by a higher proportion of 1,4 linkages. However, owing to the partial gelation of the polymer, it is generally relatively low.
The double bdnd can easily be functionalized, for example by reaction with butyllithium and addition of chlorinated derivatives or hydrogenation. This enables functionalized polymers or graft copolymers having a polycyclopentadiene backbone to be obtained. Polymers of cyclopentadiene are used, for example, after hydrogenation as resins in adhesives. However, a prerequisite for this functionalization is sufficient solubility of the polycyclopentadiene in solvents which are inert under the conditions of the functionalization. The solubility of the polycyclopentadienes obtainable using previously known catalysts is, however, not satisfactory.
The use of palladium complexes as catalysts for the cationic copolymerization of cyclopentadiene with CO is known from J. Polym. Sci., 31 (1993), 309. Palladium compounds have also been used for the copolymerization of CO with a series of olefins under mild conditions by Sen et al., J. Am. Chem. Soc., 104 10 (1982), 3520 and Organometallics, 3 (1984), 866. However, in the homopolymerization of cyclopentadiene, the use of these Pd catalysts also leads to a partially crosslinked product and to a correspondingly increased proportion of 1,2 linkages.
WO 96/23010 describes palladium complexes containing bidentate ligands coordinated via N for the polymerization of monoolefins. However, these complexes are not suitable for the polymerization of conjugated dienes whose presence is even expressly excluded.
It is an object of the present invention to provide a process for preparing cyclopentadiene polymers which have a low proportion of 1,2 linkages and therefore have better solubility in many solvents.
We have found that this object is achieved by use of certain, cationic palladium catalysts to prepare polymers of cyclopentadiene having a low proportion of 1,2 linkages.
The present invention accordingly provides a process for preparing cyclopentadiene homopolymers using a palladium catalyst which comprises a palladium complex of the formula
[Pd(R
1
—CN)
4
]
2+
(A)
2
—
where R
1
is a C
1
-C
8
-alkyl group and A is a stable anion.
The palladium catalysts of the present invention lead to polycyclopentadiene of the above formula having a high number average molecular weight of Mn>10,000, in particular>30,000 (determined by means of gel permeation chromatography in chlorobenzene on Polymer Standards Service columns (10 &mgr;m, SDV linear, 60 cm), detection: differential refractometer (Waters R
401
), polystyrene standards). The upper limit of the molecular
45
weight is generally 1,000,000, preferably 300,000. The polymer has <35%, in particular <30% and preferably <25%, of 1,2 linkages and is soluble in many organic solvents such as chloroform, toluene, cyclohexane, etc. It can, for example, advantageously be hydrogenated in a manner known per se using H
2
or chemical H-transferring agents. Formation of other derivatives is also readily possible since the polycyclopentadiene obtainable according to the present invention is essentially uncrosslinked and thus virtually all double bonds are still available.
The monomer cyclopentadiene is advantageously prepared by thermal cracking of the dimer at about 175° C. immediately before the polymerization in the process of the present invention. Cracking is advantageously carried out under dry nitrogen as protective gas. The cyclopentadiene can be stored at −20° C. in a dry atmosphere.
The palladium catalysts [Pd(R
1
—CN)
4
]
2+
(A)
2
−
of the present invention can be prepared by methods known to those skilled in the art. Stable anions A which are suitable according to the present invention are those which are not nucleophilic. Preference is given to BF
4
−
, Sbx
6
−
, PX
6
−
, AsX
6
−
BiX
6
−
, where X is Cl or F, and/or B(Ar)
4
−
, where Ar is phenyl which bears 1, 2, 3, 4 or 5 substituents which are, independently of one another, selected from the group consisting of F, Cl and CF
3
, eg. C
6
F
5
or 3,5-di-CF
3
-C
6
H
3
. Suitable radicals R
1
are C
1
-C
8
-alkyl groups, preferably C
1
-C
4
-alkyl groups and in particular methyl or ethyl groups.
Particular preference is given to complexes of these catalysts with palladium-coordinating agents, in particular olefins or diolefins. Suitable palladium-complexing agents are, for example, C
1
-C
12
-olefins such as ethylene, propylene or 1,2-butene, etc., cycloolefins such as cyclopentene or cyclohexene, C
4
-C
8
-diolefins such as butadiene, isoprene, 1,4-pentadiene or 1,5-hexadiene and cyclic diolefins such as norbornadiene or cyclooctadiene. Another suitable olefin ligand is the allyl radical (&pgr;-allyl). Preferred olefins or diolefins are selected from dicyclopentadiene, cyclopentene, norbornadienes, &pgr;-allyl, and/or cyclooctadiene. Accordingly, slight contamination of the monomer cyclopentadiene by the corresponding dimer dicyclopentadiene does not interfere with the polymerization, but according to the present invention is even advantageous. The addition of Pd-complexing agents enables the reaction times or reaction temperatures and the molecular weight to be controlled (the activity of the catalyst is reduced under the reaction conditions). Gel formation of the polymer, ie. crosslinking, is prevented and the solubility of the catalyst is improved.
The reaction temperature in the polymerization process of the present invention is advantageously in the range from about −100 to +100° C., preferably from −80 to +80° C. and in particular from −50 to +50° C. The reaction times are typically from 2 minutes to 168 hours, preferably from 15 minutes to 48 hours.
According to the present invention, the polymerization of cyclopentadiene advantageously takes place in an inert organic solvent in which the palladium catalyst is soluble. Examples of suitable solvents are halogenated or nonhalogenated alkanes such as pentane, hexane, dichloromethane, chloroform, carbon tetrachloride or dichloroethane; cycloalkanes such as cyclohexane; substituted or unsubstituted aromatic hydrocarbons such as toluene, benzene, xylene and chlorobenzene and/or nitroalkanes or nitroaromatics such as nitrobenzene or nitromethane or mixtures thereof. Preferred organic solvents are selected from dichloromethane, chloroform, carbon tetrachloride, dichloroethane, cyclohexane, toluene, chlorobenzene, nitrobenzene or nitromethane or a mixture thereof. When nitromethane is used as solvent for the polymerization, precipitation of the polymer occurs. Alternatively, the polymer may be precipitated using me
Connor Eric
Mehler Christof
Risse Wilhelm
BASF - Aktiengesellschaft
Keil & Weinkauf
Wu David W.
Zalukaeva Tanya
LandOfFree
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