PL71075B1 - - Google Patents
Download PDFInfo
- Publication number
- PL71075B1 PL71075B1 PL1972157011A PL15701172A PL71075B1 PL 71075 B1 PL71075 B1 PL 71075B1 PL 1972157011 A PL1972157011 A PL 1972157011A PL 15701172 A PL15701172 A PL 15701172A PL 71075 B1 PL71075 B1 PL 71075B1
- Authority
- PL
- Poland
- Prior art keywords
- toluene
- mol
- pattern
- amorphous product
- product
- Prior art date
Links
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 27
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 238000004458 analytical method Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 claims description 7
- NFWSQSCIDYBUOU-UHFFFAOYSA-N methylcyclopentadiene Chemical compound CC1=CC=CC1 NFWSQSCIDYBUOU-UHFFFAOYSA-N 0.000 claims description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- -1 cyclic polyenes Chemical class 0.000 claims description 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 5
- 238000002441 X-ray diffraction Methods 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 239000011630 iodine Substances 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 238000004448 titration Methods 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 claims 2
- 238000007334 copolymerization reaction Methods 0.000 claims 2
- MWPIIMNHWGOFBL-UHFFFAOYSA-N dichloromethane;toluene Chemical compound ClCCl.CC1=CC=CC=C1 MWPIIMNHWGOFBL-UHFFFAOYSA-N 0.000 claims 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 claims 1
- 150000004291 polyenes Chemical class 0.000 claims 1
- CILQKUOYIAVYFK-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1.CC1=CC=CC=C1.CC1=CC=CC=C1.CC1=CC=CC=C1 CILQKUOYIAVYFK-UHFFFAOYSA-N 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 4
- DNJRKFKAFWSXSE-UHFFFAOYSA-N 1-chloro-2-ethenoxyethane Chemical compound ClCCOC=C DNJRKFKAFWSXSE-UHFFFAOYSA-N 0.000 description 2
- HECLRDQVFMWTQS-UHFFFAOYSA-N Dicyclopentadiene Chemical compound C1C2C3CC=CC3C1C=C2 HECLRDQVFMWTQS-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 238000004455 differential thermal analysis Methods 0.000 description 2
- NSWUXAUIAZVROT-UHFFFAOYSA-N 1-(2-cyclopenta-1,3-dien-1-ylpropan-2-yl)cyclopenta-1,3-diene Chemical compound C=1C=CCC=1C(C)(C)C1=CC=CC1 NSWUXAUIAZVROT-UHFFFAOYSA-N 0.000 description 1
- 229910003074 TiCl4 Inorganic materials 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cis-cyclohexene Natural products C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 150000005671 trienes Chemical class 0.000 description 1
Classifications
-
- 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
- C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F16/12—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT2701571 | 1971-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
PL71075B1 true PL71075B1 (en:Method) | 1974-04-30 |
Family
ID=11220771
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1972157011A PL71075B1 (en:Method) | 1971-07-31 | 1972-07-29 |
Country Status (21)
Country | Link |
---|---|
US (1) | US3853829A (en:Method) |
JP (1) | JPS5338313B2 (en:Method) |
AT (1) | AT332644B (en:Method) |
AU (1) | AU474224B2 (en:Method) |
BE (1) | BE786620A (en:Method) |
CA (1) | CA989541A (en:Method) |
CH (1) | CH551459A (en:Method) |
CS (1) | CS178874B2 (en:Method) |
DD (1) | DD99171A5 (en:Method) |
DE (1) | DE2237633C3 (en:Method) |
ES (1) | ES405821A1 (en:Method) |
FR (1) | FR2149110A5 (en:Method) |
GB (1) | GB1348213A (en:Method) |
HU (1) | HU165838B (en:Method) |
LU (1) | LU65792A1 (en:Method) |
NL (1) | NL152875B (en:Method) |
PL (1) | PL71075B1 (en:Method) |
RO (1) | RO63337A (en:Method) |
SE (1) | SE381470B (en:Method) |
TR (1) | TR16988A (en:Method) |
ZA (1) | ZA725070B (en:Method) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5146212A (ja) * | 1974-10-17 | 1976-04-20 | Fuji Kagaku Shikogyo | Chookingupeepaa |
CA3046464A1 (en) * | 2016-12-16 | 2018-06-21 | Novoset, Llc | Resin compositions |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3179717A (en) * | 1960-06-01 | 1965-04-20 | Edward J Dufek | Coating compositions comprising polymers of vinyl ethers of polyunsaturated fatty alcohols |
-
0
- BE BE786620D patent/BE786620A/xx unknown
-
1972
- 1972-07-11 AU AU44430/72A patent/AU474224B2/en not_active Expired
- 1972-07-14 RO RO7200071616A patent/RO63337A/ro unknown
- 1972-07-19 GB GB3385472A patent/GB1348213A/en not_active Expired
- 1972-07-24 CH CH1103572A patent/CH551459A/fr not_active IP Right Cessation
- 1972-07-24 ZA ZA725070A patent/ZA725070B/xx unknown
- 1972-07-24 CA CA147,811A patent/CA989541A/en not_active Expired
- 1972-07-25 TR TR16988A patent/TR16988A/xx unknown
- 1972-07-26 LU LU65792D patent/LU65792A1/xx unknown
- 1972-07-26 FR FR7226807A patent/FR2149110A5/fr not_active Expired
- 1972-07-28 US US00275935A patent/US3853829A/en not_active Expired - Lifetime
- 1972-07-28 DD DD164741A patent/DD99171A5/xx unknown
- 1972-07-28 HU HUSA2383A patent/HU165838B/hu unknown
- 1972-07-29 PL PL1972157011A patent/PL71075B1/pl unknown
- 1972-07-31 DE DE2237633A patent/DE2237633C3/de not_active Expired
- 1972-07-31 SE SE7209974A patent/SE381470B/xx unknown
- 1972-07-31 CS CS7200005353A patent/CS178874B2/cs unknown
- 1972-07-31 AT AT661572A patent/AT332644B/de not_active IP Right Cessation
- 1972-07-31 NL NL727210510A patent/NL152875B/xx unknown
- 1972-07-31 ES ES405821A patent/ES405821A1/es not_active Expired
- 1972-07-31 JP JP7605372A patent/JPS5338313B2/ja not_active Expired
Also Published As
Publication number | Publication date |
---|---|
AU474224B2 (en) | 1976-07-15 |
FR2149110A5 (en:Method) | 1973-03-23 |
HU165838B (en:Method) | 1974-11-28 |
CS178874B2 (en) | 1977-10-31 |
DE2237633A1 (de) | 1973-02-15 |
DE2237633C3 (de) | 1978-08-17 |
BE786620A (fr) | 1973-01-24 |
ATA661572A (de) | 1976-01-15 |
ES405821A1 (es) | 1975-07-16 |
US3853829A (en) | 1974-12-10 |
AU4443072A (en) | 1974-01-17 |
NL7210510A (en:Method) | 1973-02-02 |
JPS5338313B2 (en:Method) | 1978-10-14 |
SE381470B (sv) | 1975-12-08 |
DD99171A5 (en:Method) | 1973-07-20 |
TR16988A (tr) | 1974-03-06 |
AT332644B (de) | 1976-10-11 |
NL152875B (nl) | 1977-04-15 |
DE2237633B2 (de) | 1977-12-01 |
LU65792A1 (en:Method) | 1972-11-28 |
ZA725070B (en) | 1973-04-25 |
GB1348213A (en) | 1974-03-13 |
RO63337A (fr) | 1978-09-15 |
CH551459A (fr) | 1974-07-15 |
CA989541A (en) | 1976-05-18 |
JPS4825088A (en:Method) | 1973-04-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Chung | Synthesis of polyalcohols via Ziegler-Natta polymerization | |
Ivan et al. | Living carbocationic polymerization. XXX. One‐pot synthesis of allyl‐terminated linear and tri‐arm star polyisobutylenes, and epoxy‐and hydroxy‐telechelics therefrom | |
Kricheldorf et al. | Polymers of carbonic acid. 11. Reactions and polymerizations of aliphatic cyclocarbonates with boron halogenides | |
Hazer et al. | Preparation of block copolymers using a new polymeric peroxycarbamate | |
Weilandt et al. | Synthesis and ring‐opening polymerization of 2‐acetoxymethyl‐2‐alkyltrimethylene carbonates and of 2‐methoxycarbonyl‐2‐methyltrimethylene carbonate; a comparison with the polymerization of 2, 2‐dimethyltrimethylene carbonate | |
Abu‐Surrah et al. | Ultrahigh molecular weight alternating propene/ethene/carbon monoxide terpolymers with elastic properties | |
Lee et al. | Enhancement of self-healing property by introducing ethylene glycol group into thermally reversible Diels-Alder reaction based self-healable materials | |
US3488332A (en) | Process for preparation of living polymer | |
PL71075B1 (en:Method) | ||
Matyjaszewski | Cationic polymerization of 1, 4, 6‐trioxaspiro [4, 4]‐nonane | |
Mallakpour et al. | Modification of polymers via electrophilic aromatic substitution | |
Kagiya et al. | Copolymerization of Carbon Dioxide and N-Phenylethylenimine | |
US3225120A (en) | Thermoplastic copolymer of vinyl monomer and sulfur | |
Cesca et al. | The cationic polymerization of “endo”‐dicyclopentadiene, 1, 2–dihydro‐“endo”‐dicyclopentadiene and 9, 10–dihydro‐“endo”‐dicyclopentadiene | |
Ogawa et al. | Living cationic polymerization of cyclic unsaturated ethers | |
Kricheldorf et al. | Polymers of Carbonic Acid. 15. Polymerization of Cyclotrimethylene Carbonate with TiCl4 or SbCl5 as Initiator | |
US3884891A (en) | Method for preparing branched copolymers by ethylene with unsaturated silicone monomers | |
Shih et al. | Poly [(2‐chloroethyl) oxirane], poly [(3‐chloropropyl)‐oxirane] and poly [(4‐chlorobutyl) oxirane]: New polyether elastomers of improved chemical reactivity | |
Ji et al. | Novel hyperbranched predominantly alternating copolymers made from a charge transfer complex monomer pair of p-(chloromethyl) styrene and acrylonitrile via controlled living radical copolymerization | |
Shimidzu et al. | Synthesis of poly (3‐vinyl‐1, 4‐butyrolactone‐co‐acrylonitrile) | |
US3770661A (en) | Aryleneisopropylidene copolymers | |
Yamashita et al. | Random and block copolymers of 1.3‐dioxolane, styrene and 3.3‐bis (chloromethyl) oxacyclobutane | |
Carbonaro et al. | Isotactic polyvinylethylsilane. A polymer containing active bonds Si—H in its side groups | |
Danusso et al. | Polymers and copolymers of N-acryloyl-N′-phenyl-piperazine | |
Tanaka et al. | Self‐crosslinkable polymers. I. Copolymerization of glycidyl methacrylate with 2‐vinylpyridine and 2‐vinyl‐5‐ethylpyridine |