ES262203A1 - Un procedimiento para preparar polimeros lineales de peso molecular elevado - Google Patents
Un procedimiento para preparar polimeros lineales de peso molecular elevadoInfo
- Publication number
- ES262203A1 ES262203A1 ES0262203A ES262203A ES262203A1 ES 262203 A1 ES262203 A1 ES 262203A1 ES 0262203 A ES0262203 A ES 0262203A ES 262203 A ES262203 A ES 262203A ES 262203 A1 ES262203 A1 ES 262203A1
- Authority
- ES
- Spain
- Prior art keywords
- acyl
- alkoxy
- integer
- group
- aldehydes
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical class CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 abstract 3
- 150000001299 aldehydes Chemical class 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- YGHRJJRRZDOVPD-UHFFFAOYSA-N 3-methylbutanal Chemical compound CC(C)CC=O YGHRJJRRZDOVPD-UHFFFAOYSA-N 0.000 abstract 2
- YGCZTXZTJXYWCO-UHFFFAOYSA-N 3-phenylpropanal Chemical compound O=CCCC1=CC=CC=C1 YGCZTXZTJXYWCO-UHFFFAOYSA-N 0.000 abstract 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052760 oxygen Chemical group 0.000 abstract 2
- 239000001301 oxygen Chemical group 0.000 abstract 2
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 abstract 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 2
- MYHGOWDLVRDUFA-UHFFFAOYSA-N 3-phenylbutanal Chemical compound O=CCC(C)C1=CC=CC=C1 MYHGOWDLVRDUFA-UHFFFAOYSA-N 0.000 abstract 1
- 229910015900 BF3 Inorganic materials 0.000 abstract 1
- 239000002841 Lewis acid Substances 0.000 abstract 1
- 239000002879 Lewis base Substances 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- -1 acyl titanium halide Chemical class 0.000 abstract 1
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 238000010494 dissociation reaction Methods 0.000 abstract 1
- 230000005593 dissociations Effects 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Chemical group 0.000 abstract 1
- 239000001257 hydrogen Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 150000007517 lewis acids Chemical class 0.000 abstract 1
- 150000007527 lewis bases Chemical class 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 229940100595 phenylacetaldehyde Drugs 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000010936 titanium Substances 0.000 abstract 1
- 229910052719 titanium Inorganic materials 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 239000011592 zinc chloride Substances 0.000 abstract 1
- 235000005074 zinc chloride Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/06—Catalysts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/14—Polymerisation of single aldehydes not provided for in groups C08G2/08 - C08G2/12
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/18—Copolymerisation of aldehydes or ketones
- C08G2/20—Copolymerisation of aldehydes or ketones with other aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/28—Post-polymerisation treatments
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/30—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1849759 | 1959-11-06 | ||
| IT2097659 | 1959-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES262203A1 true ES262203A1 (es) | 1961-04-16 |
Family
ID=26326999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0262203A Expired ES262203A1 (es) | 1959-11-06 | 1960-11-05 | Un procedimiento para preparar polimeros lineales de peso molecular elevado |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE596750A (en)) |
| DE (1) | DE1162563B (en)) |
| ES (1) | ES262203A1 (en)) |
| GB (1) | GB946832A (en)) |
| NL (1) | NL257300A (en)) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3183210A (en) | 1959-11-06 | 1965-05-11 | Zh Nihon Kagaku Seni Kenkyusho | Polymerization of aldehyde by organometallic compound |
| IT649605A (en)) | 1960-04-16 | |||
| BE603088A (en)) * | 1960-04-26 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL196512A (en)) * | 1954-04-16 |
-
0
- NL NL257300D patent/NL257300A/xx unknown
- BE BE596750D patent/BE596750A/xx unknown
-
1960
- 1960-09-26 GB GB3303160A patent/GB946832A/en not_active Expired
- 1960-11-02 DE DEM47003A patent/DE1162563B/de active Pending
- 1960-11-05 ES ES0262203A patent/ES262203A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL257300A (en)) | |
| DE1162563B (de) | 1964-02-06 |
| GB946832A (en) | 1964-01-15 |
| BE596750A (en)) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1058159A (en) | Organosilicon polymers | |
| GB1441726A (en) | Dielectric films | |
| ES262203A1 (es) | Un procedimiento para preparar polimeros lineales de peso molecular elevado | |
| US3013002A (en) | Polymerization of ethylene with dicyclopentadienyl chromium-metal alkylcatalysts | |
| US3470220A (en) | Germanium and tin compounds | |
| ES410782A1 (es) | Procedimiento para la obtencion de ceras atasticas de poli-olefinas. | |
| Maher et al. | 1047. Proton magnetic resonance spectra of thallium trialkyls, chemical exchange, and the formation of a mixed tri (methyl, vinyl)-thallium | |
| GB870425A (en) | Improvements in and relating to organic phosphorus compounds | |
| GB1378446A (en) | Process for the manufacture of dicyanovinyl compounds | |
| GB1081835A (en) | A method of producing organoaluminium compounds | |
| US2917543A (en) | Process of producing substituted borazoles | |
| US3300503A (en) | Nitrogen-containing fluoro-phosphoranes | |
| US3030398A (en) | Complex bimetallic cyclopentadienyl organometallic compounds | |
| Harmon et al. | Carbonium Ion Salts. II. Reaction of Cycloheptatriene with Inorganic Halides; Tropenium CHLOROBORATE1 | |
| US3579481A (en) | Catalyst system for polymerizing saturated, aliphatic aldehydes | |
| GB978594A (en) | Process for polymerizing ª-mono-olefines | |
| US3086983A (en) | Tetrakis (triphenyl or trialkyl) siloxyvanadium | |
| US3201464A (en) | Boron compounds | |
| Pattison et al. | Reactions between oximes and organo-derivatives of Group III elements. Part II. Pyridine-2-carbaldehyde oxime | |
| ES254936A1 (es) | Un procedimiento para preparar complejos organometalicos cristalizables | |
| US3751446A (en) | Preparation of aryl-substituted acetylenic compounds | |
| US2543341A (en) | Aroylacetamidine | |
| US3652623A (en) | Organic aluminum compounds | |
| US3350379A (en) | Bis-triphenylphosphine cadmium halide, aluminum powder, mercuric dihalide reaction product and trialkyl aluminum catalyst for the polymerization of butadiene-1, 3 | |
| GB959320A (en) | A method for polymerizing aldehydes |