WO1994010217A1 - Bis(diallylamino) silanes - Google Patents

Bis(diallylamino) silanes Download PDF

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Publication number
WO1994010217A1
WO1994010217A1 PCT/US1993/010025 US9310025W WO9410217A1 WO 1994010217 A1 WO1994010217 A1 WO 1994010217A1 US 9310025 W US9310025 W US 9310025W WO 9410217 A1 WO9410217 A1 WO 9410217A1
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Prior art keywords
bis
diallylamino
copolymer
flask
reaction
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PCT/US1993/010025
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French (fr)
Inventor
Steven E. Mulhall
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Aristech Chemical Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aristech Chemical Corporation filed Critical Aristech Chemical Corporation
Priority to EP93923952A priority Critical patent/EP0620831A4/en
Priority to JP6511142A priority patent/JPH07502565A/en
Priority to CA002125959A priority patent/CA2125959C/en
Publication of WO1994010217A1 publication Critical patent/WO1994010217A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/04—Monomers containing three or four carbon atoms
    • C08F210/06—Propene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
    • C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
    • C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon

Definitions

  • This invention relates to the use of bis(diallylamino) silanes of the general formula
  • R 1 and R2 are independently selected from alkyl and aryl groups having 1 to 6 carbon atoms as comonomers for lower olefins polymerized in highly active Ziegler-Natta catalyst systems.
  • Sivak et al propose the use of protected diallyl amine monomers for copolymerization with ethylene, propylene, and other lower alpha-olefins having up to 8 carbon atoms. Protection of the otherwise vulnerable amine group is provided by a silyl group having relatively bulky substituents, such as lower alkyl or phenyl groups. Diallyl amines are proposed and several examples are given of silyl-protected diallyl amines. However, bis-diallyl amines are not contemplated.
  • R 1 and R2 are independently selected from alkyl and aryl groups having 1 to 6 carbon atoms.
  • They may be used as cross-linking agents in polymers and find special utility as comonomers for lower olefins polymerized in highly active Ziegler-Natta catalyst systems.
  • the equipment used for the synthesis of bis(diallylamino)dimethylsilane was set up in the following manner.
  • a reflux condenser, mechanical stirrer and 125 ml addition funnel were placed on a 2000 ml 3-necked, round-bottomed flask.
  • An argon inlet was connected to the top of the reflux condenser and a heating mantle was placed on the flask.
  • the flask was flushed with argon (allowing the argon to exit the setup through the top of the addition funnel) until the atmosphere in the glassware was assured of being inert.
  • the reaction produces a large amount of salts (triethylamine hydrochloride and diallylamine hydrochloride) and twice during the reaction additional heptane had to be added (200 ml portions each time) in order to keep the slurry thinned to a stirrable consistency.
  • dichlorodimethyl- silane was complete, the mixture was heated to reflux for five hours. The flask was then allowed to cool to room temperature.
  • the salts were removed by filtration using a buchner funnel covered with a latex dam to keep exposure to the atmosphere to a minimum, the product was isolated from the filtrate by distillation.
  • the heptane and excess amines were removed at a vacuum of 40 mmHg with a temperature range from ambient to 43°C.
  • the product distilled at 72.6-74.6°C at 1 mmHg.
  • the glassware setup used for the preparation of bis(diallylamino)diphenylsilane was the same as the equipment used for the synthesis of bis(diallylamino)dimethylsilane above except that a 1000 ml flask was used instead of a 2000 ml flask.
  • the salts were removed by filtration using a sealed pressure filter under an inert atmosphere.
  • the product was isolated from the filtrate by distillation.
  • the heptane and excess amines were removed at a vacuum of 40 mmHg with a temperature range from ambient to 43°C.
  • the product distilled in a range from 160°/0.3 mmHg to 160°/0.1 mmHg.
  • My new monomers may be incorporated into chains of crystalline polypropylene and other lower olefin polymers as described in the above-mentioned Sivak et al patent. Thereafter, the silyl groups may be removed by hydrolysis or alcoholysis optionally promoted by acidic or basic catalysis and the remaining copolymers, which may be mildly cross-linked, will exhibit amine functionality or ammonium functionality in the presence of acids.
  • My monomers may be homopolymerized using Ziegler-Natta systems and/or copolymerized in amounts to yield copolymers having ratios of lower olefin to my monomer (m) of 0.1 mole % to 99.9 mole %.
  • BDMS bis(diallylamino) imethylsilane
  • BDPS bis(diallylamino)diphenylsilane
  • An apparatus consisting of a round bottom flask fitted with a side arm, magnetic stirring bar and a stopper was assembled hot from a drying oven and was then either evacuated and refilled with inert gas several times or (and) purged with inert gas for at least 15 minutes.
  • the flask was charged with a given amount of solvent, heptane or toluene, usually 125 mL.
  • the solvents were freshly distilled from sodium and triethyl-aluminum (TEA) over which they had been refluxed for at least 18 hours under an inert atmosphere.
  • an "external donor” which was diphenyldimethoxysilane. Phenyltrimethoxysilane may alternatively be used. Then the other comonomer was added. A given amount of alkyl aluminum co-catalyst, which was in the form of a heptane solution of about 25% by weight (0.715 g/mL in heptane), was also added to the flask.
  • the polymerization was initiated by the addition of the transition metal containing co-catalyst, which was a titanium tetrachloride on a magnesium chloride support. At this point the flask was lowered into a thermostated oil bath and magnetic stirring was begun.
  • the transition metal containing co-catalyst which was a titanium tetrachloride on a magnesium chloride support.
  • reaction was quenched by the addition of acidified alcohol (HC1 in iso-propanol, ethanol and/or methanol) .
  • acidified alcohol HC1 in iso-propanol, ethanol and/or methanol
  • the quenched reaction slurry was combined with the alcohol solution of volume at least twice the original volume of the inert reaction solvent.
  • the resultant slurry was stirred for at least 45 minutes and then filtered. This treatment not only stopped the reaction, it dissolved catalyst residues and removed silyl groups and thus regenerated the amino groups.
  • the slurry was combined with enough water to make the filtration proceed at a convenient rate.
  • the polymer was resuspended in alcohol, stirred, filtered and vacuum dried overnight. Boiling heptane soluble content was determined by standard methods.
  • This polymerization was done using the following quantities of reagents and reaction conditions with the general copolymerization procedure from above.
  • Polymer (5.8 g) was produced in this polymerization which is a yield of 55.5 g polymer/g catalyst which is approximately 25% of a comparable homopolymerization.
  • Copolymer (17.0 g) was produced by this copolymerization which corresponds to a yield of 145.3 g polymer/g catalyst. This is about 70% of what is produced in a comparable propylene homopolymerization. The fraction insoluble in boiling heptane was 91.8% of the tested sample.
  • a stock solution of dye was prepared by dissolving Acid Alizarin Blue BB dye (1.00 g) and ammonium acetate (7.0 g) in water to obtain 80 grams of solution.
  • Samples (200 mg) of the propylene homopolymer and each of the four propylene/amine copolymers produced in Examples 1-4 above were placed in test tubes and 10 mL of the stock dye solution was added. The samples were sealed and shaken to assure dispersion of the polymer powder in the dye and placed in a 60°C water bath. The temperature of the bath was increased to 100°C over a period of 30 minutes and held at that temperature for 1 hour and then cooled to room temperature.
  • the samples were filtered and rinsed repeatedly with water until the rinsings were clear and the color of the powder did not appear to change. The rinsings were then continued with an equivalent amount of water. The total amount of water used was about 500 ml. The samples were then suspended in boiling water for about one minute and then filtered and this hot wash was repeated two more times.
  • Example IV pale purple
  • Example V pale purple
  • Example VI reasonably intense purple/blue color

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Bis(diallylamino) silanes of formula (I) where R?1 and R2¿ are lower alkyl or phenyl groups are copolymerized with lower olefins and desilylated to exhibit amine functionality; they are receptive to dyes.

Description

BIS(DIALLYLAMINO) SILANES
Related Application
This is a continuation-in-part of my co-pending application Serial No. 894,970, filed June 8, 1992.
Technical Field
This invention relates to the use of bis(diallylamino) silanes of the general formula
R1
I (CH2=CH-CH2)2N-Si-N(CH2-CH=CH2)2
I R2
where R 1 and R2 are independently selected from alkyl and aryl groups having 1 to 6 carbon atoms as comonomers for lower olefins polymerized in highly active Ziegler-Natta catalyst systems.
Background Art
In European Patent Publication 0423438, Sivak et al propose the use of protected diallyl amine monomers for copolymerization with ethylene, propylene, and other lower alpha-olefins having up to 8 carbon atoms. Protection of the otherwise vulnerable amine group is provided by a silyl group having relatively bulky substituents, such as lower alkyl or phenyl groups. Diallyl amines are proposed and several examples are given of silyl-protected diallyl amines. However, bis-diallyl amines are not contemplated.
Summary of Invention
I have invented new compounds of the general formula
R1
I (CH2=CH-CH2)2N-Si-N(CH2-CH=CH2)2
I R2
where R 1 and R2 are independently selected from alkyl and aryl groups having 1 to 6 carbon atoms.
They may be used as cross-linking agents in polymers and find special utility as comonomers for lower olefins polymerized in highly active Ziegler-Natta catalyst systems.
Detailed Description of the Invention
My invention will be described with respect to two paradigms, namely bis(diallylamino)dimethylsilane and bis(diallylamino)diphenylsilane. EXAMPLE I
Bis(diallylamino)dimethylsilane
The equipment used for the synthesis of bis(diallylamino)dimethylsilane was set up in the following manner. A reflux condenser, mechanical stirrer and 125 ml addition funnel were placed on a 2000 ml 3-necked, round-bottomed flask. An argon inlet was connected to the top of the reflux condenser and a heating mantle was placed on the flask. The flask was flushed with argon (allowing the argon to exit the setup through the top of the addition funnel) until the atmosphere in the glassware was assured of being inert.
Heptane (400 ml), triethylamine (136.62 g, 1.350 moles, 188 ml) and diallylamine (98.36 g, 1.012 moles, 125 ml) were charged into the reaction flask. Dichlorodimethylsilane (43.55 g, 0.3375 moles, 41 ml) was placed in the addition funnel and added to the reaction mixture in the flask over a period of 70 minutes. The temperature of the reaction mixture reached 37.5°C (as measured by a thermocouple between the flask and heating mantle).
The reaction produces a large amount of salts (triethylamine hydrochloride and diallylamine hydrochloride) and twice during the reaction additional heptane had to be added (200 ml portions each time) in order to keep the slurry thinned to a stirrable consistency. After the addition of dichlorodimethyl- silane was complete, the mixture was heated to reflux for five hours. The flask was then allowed to cool to room temperature.
The salts were removed by filtration using a buchner funnel covered with a latex dam to keep exposure to the atmosphere to a minimum, the product was isolated from the filtrate by distillation. The heptane and excess amines were removed at a vacuum of 40 mmHg with a temperature range from ambient to 43°C. The product distilled at 72.6-74.6°C at 1 mmHg.
61.2 g of bis(diallylamino)dimethylsilane was isolated by this technique which corresponds to a yield of 72% of theoretical after distillation.
EXAMPLE II
Bis(diallylamino)diphenylsilane
The glassware setup used for the preparation of bis(diallylamino)diphenylsilane was the same as the equipment used for the synthesis of bis(diallylamino)dimethylsilane above except that a 1000 ml flask was used instead of a 2000 ml flask.
After the system was flushed with argon, triethylamine (159.84 g, 1.580 moles, 220.2 ml), diallylamine (84.48 g, 0.8699 moles, 107.3 ml) and toluene (200 ml) were added to the reaction flask. Dichlorodiphenylsilane (100.75 g, 0.3980 moles, 83.7 ml) was charged into the addition funnel and added to the reaction mixture in the flask over a period of 15 minutes, the temperature rose to 60°C. A large amount of solid precipitated from the mixture. Toluene (100 ml) was added to the flask through the addition funnel to rinse out the remaining silane and make the reaction mixture more stirrable and the mixture was heated to reflux for two hours, then cooled to room temperature.
The salts were removed by filtration using a sealed pressure filter under an inert atmosphere. The product was isolated from the filtrate by distillation. The heptane and excess amines were removed at a vacuum of 40 mmHg with a temperature range from ambient to 43°C. The product distilled in a range from 160°/0.3 mmHg to 160°/0.1 mmHg.
101.5 g of bis(diallylamino)diphenylsilane was isolated by this technique which corresponds to a yield of 68% of theoretical after distillation.
Similar preparations may be made for the diethyl, dipropyl, dibutyl, dipentyl, dihexyl and methylphenyl variants.
My new monomers may be incorporated into chains of crystalline polypropylene and other lower olefin polymers as described in the above-mentioned Sivak et al patent. Thereafter, the silyl groups may be removed by hydrolysis or alcoholysis optionally promoted by acidic or basic catalysis and the remaining copolymers, which may be mildly cross-linked, will exhibit amine functionality or ammonium functionality in the presence of acids.
My monomers may be homopolymerized using Ziegler-Natta systems and/or copolymerized in amounts to yield copolymers having ratios of lower olefin to my monomer (m) of 0.1 mole % to 99.9 mole %. Following are examples of propylene copolymerizations with bis(diallylamino) imethylsilane ("BDMS") and bis(diallylamino)diphenylsilane ("BDPS") .
General Copolymerization Procedure
Standard inert atmosphere techniques were used to exclude moisture and oxygen throughout the manipulations.
An apparatus consisting of a round bottom flask fitted with a side arm, magnetic stirring bar and a stopper was assembled hot from a drying oven and was then either evacuated and refilled with inert gas several times or (and) purged with inert gas for at least 15 minutes. The flask was charged with a given amount of solvent, heptane or toluene, usually 125 mL. The solvents were freshly distilled from sodium and triethyl-aluminum (TEA) over which they had been refluxed for at least 18 hours under an inert atmosphere.
At this point the inert gas atmosphere in the flask was replaced with the gaseous comonomer by a minimum of three cycles of evacuation and refilling back to atmospheric pressure with the comonomer. After the third cycle the solution was stirred for at least ten minutes (usually longer) to allow the solvent to become saturated with the comonomer. Pressure was maintained at one atmosphere via a bubbler.
Next was added an "external donor", which was diphenyldimethoxysilane. Phenyltrimethoxysilane may alternatively be used. Then the other comonomer was added. A given amount of alkyl aluminum co-catalyst, which was in the form of a heptane solution of about 25% by weight (0.715 g/mL in heptane), was also added to the flask.
The polymerization was initiated by the addition of the transition metal containing co-catalyst, which was a titanium tetrachloride on a magnesium chloride support. At this point the flask was lowered into a thermostated oil bath and magnetic stirring was begun.
An excess of gaseous comonomer was passed into the flask in order to replace any that was consumed. Excess gaseous comonomer was allowed to pass from the reaction vessel via a bubbler, maintaining a pressure in the flask of one atmosphere.
After a specified period of time the reaction was quenched by the addition of acidified alcohol (HC1 in iso-propanol, ethanol and/or methanol) . The quenched reaction slurry was combined with the alcohol solution of volume at least twice the original volume of the inert reaction solvent. The resultant slurry was stirred for at least 45 minutes and then filtered. This treatment not only stopped the reaction, it dissolved catalyst residues and removed silyl groups and thus regenerated the amino groups.
If the filtration proceeded very slowly, the slurry was combined with enough water to make the filtration proceed at a convenient rate.
The polymer was resuspended in alcohol, stirred, filtered and vacuum dried overnight. Boiling heptane soluble content was determined by standard methods.
Homopolymerization of propylene under these conditions produces polypropylene with yields in the range of 200-220- g polymer/g titanium-containing catalyst. The extent of reduction in polymer yield in the copolymerizations relative to this homopolymer yield is used as a rough guide to the utility of the comonomers in the copolymerization systems.
Copolymerizations of Propylene with Bis(diallylamino) dimethylsilane (BDMS)
Example III
The general copolymerization procedure above was followed using the following quantities of reagents and reaction conditions in the polymerization.
Solvent heptane 100 mL
External Donor DPMS 75 μL
Comonomer BDMS 3.85 g Cocatalyst triethylaluminum 4.3 mL (25 wt %)
TiC14/MgCl2 Catalyst 91 mg
Reaction Temperature 50°C
Reaction Time 2 hr
Alcohol Used in Work Up iso-propanol
The polymerization yielded 8.3 g of polymer which is a yield of 91.2 g polymer/g catalyst. This corresponds to about 40% of the yield of a homopolymerization of propylene under these conditions. Example IV
This polymerization was done using the following quantities of reagents and reaction conditions with the general copolymerization procedure from above.
Solvent heptane 75 mL
External Donor DPMS 225 μL
Comonomer BDMS 11.12 g Cocatalyst triethylaluminum 12.9 mL (25 wt %)
TiC14/MgC12 Catalyst 104 mg
Reaction Temperature 50°C
Reaction Time 2 hr
Alcohol Used in Work Up iso-propanol
Polymer (5.8 g) was produced in this polymerization which is a yield of 55.5 g polymer/g catalyst which is approximately 25% of a comparable homopolymerization.
Copolymerizations of Propylene with Bis(diallylamino) diphenylsilane (BDPS)
Example V
The following quantities of reagents and reaction conditions were used with the general copolymerization procedure.
Solvent heptane 100 mL
External Donor DPMS 220 μL
Comonomer BDPS 18.19 g Cocatalyst triethylaluminum 12.5 mL (25 wt %)
TiC14/MgC12 Catalyst 137 mg
Reaction Temperature 50°C
Reaction Time 2 hr
Alcohol Used in Work Up iso-propanol The polymerization yielded 15.4 g of polymer which is a yield of 112.4 g polymer/g catalyst which is in the range of 51-57% of a comparable propylene homopolymerization. 98.4% of a tested sample was insoluble in boiling heptane.
Example VI
The following quantities of reagents and reaction conditions were used with the general copolymerization procedure.
Solvent heptane 50 mL
External Donor DPMS 400 μL
Comonomer BDPS 31.97 g Cocatalyst triethylaluminum 23.5 mL (25 wt %)
TiC14/MgC12 Catalyst 117 mg
Reaction Temperature 50°C
Reaction Time 2 hr
Alcohol Used in Work Up iso-propanol
Copolymer (17.0 g) was produced by this copolymerization which corresponds to a yield of 145.3 g polymer/g catalyst. This is about 70% of what is produced in a comparable propylene homopolymerization. The fraction insoluble in boiling heptane was 91.8% of the tested sample.
Uptake of an Acid Dye by Polymer
Samples as a Test for Amine Incorporation
Example VII
A sample of propylene homopolymer was prepared using the general polymerization conditions given above and used as a blank in the dye uptake experiments described below.
A stock solution of dye was prepared by dissolving Acid Alizarin Blue BB dye (1.00 g) and ammonium acetate (7.0 g) in water to obtain 80 grams of solution. Samples (200 mg) of the propylene homopolymer and each of the four propylene/amine copolymers produced in Examples 1-4 above were placed in test tubes and 10 mL of the stock dye solution was added. The samples were sealed and shaken to assure dispersion of the polymer powder in the dye and placed in a 60°C water bath. The temperature of the bath was increased to 100°C over a period of 30 minutes and held at that temperature for 1 hour and then cooled to room temperature.
The samples were filtered and rinsed repeatedly with water until the rinsings were clear and the color of the powder did not appear to change. The rinsings were then continued with an equivalent amount of water. The total amount of water used was about 500 ml. The samples were then suspended in boiling water for about one minute and then filtered and this hot wash was repeated two more times.
After the samples were dried, their color intensities were compared and are described in Table 1 below.
Table 1 Dyed Propylene/Amine Copolymers Sample Color
Propylene homopolymer very pale pink/ purple color
Example III slightly more intense purple than propylene homopolymer
Example IV pale purple Example V pale purple Example VI reasonably intense purple/blue color

Claims

Claims
1. A copolymer of about 0.1% to about 99.9% lower alpha-olefin having 2 to 8 carbon atoms and a bis(diallylamino) silane of the formula
R1
I (CH2=CH-CH2)2N-Si-N(CH2-CH=CH2)2
I R2
where R 1 and R2 are independently selected from alkyl and aryl groups having 1 to 6 carbon atoms.
2. Copolymer of claim 1 wherein the alpha-olefin is propylene.
3. Copolymer of claim 1 wherein the silane is bis(diallylamino) dimethylsilane.
4. Copolymer of claim 1 wherein the silane is bis(diallylamino) diphenylsilane.
5. A desilanated copolymer of claim 1.
6. A desilanated copolymer of claim 2.
7. A desilanated copolymer of claim 3.
8. A desilanated copolymer of claim 4.
9. A dyed copolymer of claim 5.
10. A dyed copolymer of claim 6.
11. A dyed copolymer of claim 7.
12. A dyed copolymer of claim 8.
13. Bis(diallylamino) silanes of the formula
R1
(CH2=CH-CH2)2N-Si- (CH2-CH=CH2)2
I R2
where R 1 and R2 are independently selected from alkyl and aryl groups having 1 to 6 carbon atoms.
14. A silane of claim 13 wherein R 1 and R2 are CH.,.
15. A silane of claim 13 wherein R 1 and R2 are phenyl groups.
PCT/US1993/010025 1992-10-23 1993-10-21 Bis(diallylamino) silanes WO1994010217A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP93923952A EP0620831A4 (en) 1992-10-23 1993-10-21 Bis(diallylamino) silanes.
JP6511142A JPH07502565A (en) 1992-10-23 1993-10-21 Bis(diallylamino)silane
CA002125959A CA2125959C (en) 1992-10-23 1993-10-21 Bis(diallylamino) silanes

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US96532092A 1992-10-23 1992-10-23
US965,320 1992-10-23

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US7956207B2 (en) * 2006-09-28 2011-06-07 Praxair Technology, Inc. Heteroleptic organometallic compounds
JP2011256120A (en) * 2010-06-07 2011-12-22 Toho Titanium Co Ltd Process for producing organoaminosilane compound

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0423438A2 (en) * 1989-10-16 1991-04-24 Aristech Chemical Corporation Amine/propylene copolymers

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0423438A2 (en) * 1989-10-16 1991-04-24 Aristech Chemical Corporation Amine/propylene copolymers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0620831A4 *

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CA2125959A1 (en) 1994-05-11
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CA2125959C (en) 2000-02-22
JPH07502565A (en) 1995-03-16

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