GB1015501A - Organo-arsenical polymers - Google Patents
Organo-arsenical polymersInfo
- Publication number
- GB1015501A GB1015501A GB3403160A GB3403160A GB1015501A GB 1015501 A GB1015501 A GB 1015501A GB 3403160 A GB3403160 A GB 3403160A GB 3403160 A GB3403160 A GB 3403160A GB 1015501 A GB1015501 A GB 1015501A
- Authority
- GB
- United Kingdom
- Prior art keywords
- poly
- phenylene
- phenylarsinidene
- lithium
- organic
- 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
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
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
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)
Abstract
Linear phenylene-arsenical polymers built of units each of which contains one or two arsenic atoms and one or two phenylene or substituted phenylene groups, together, if desired, with an oxygen atom or an alkylene group are prepared either by (A) reacting n-butyl lithium (prepared by dissolving lithium metal in ethereal n-butyl bromide) at - 25 DEG C. with an organic dibromide to form the dilithium compound which is then reacted with a chloroarsine; or by (B) adding excess lithium to the organic dibromide in tetrahydrofuran containing some butyl bromide, removing excess lithium and converting butyl lithium into organic dilithium, and then reacting with chloroarsine. Examples describe the preparation of (I) poly - (p - phenylenephenylarsinidene [-C6H4-As(C6H5)-]n (II) Poly - (4,41 - diphenylether phenylarsinidene). (III) Poly-(m-2-methoxy-5-bromophenylene phenylaxinidene). (IV) Poly-(4,6-dimethoxy - m - phenylene phenylarsinidene). (V) Poly (9,10-anthracylene phenylarsinidene) [-C14H8-As(C6H5-]n (VI) Poly (p - phenylenearsanthrene - 5,10-diyl). (VII) Poly (p-phenylene-o-phenylene-di-arsinous acid anhydride-As, As1-diyl). <FORM:1015501/C3/1> (VIII) Poly (4,41 - diphenylene phenylarsinidene). (IX) Poly (p-phenylene-hydroxyarsinylidene) <FORM:1015501/C3/2> (X) Poly (p-phenylene - hydroxyarsinylidene-p-xylylenehydroxyarsinylidene). <FORM:1015501/C3/3> (XI) Poly (p - phenylene - hydroxyarsinylidene -ethylenehydroxyarsinylidene). <FORM:1015501/C3/4> Polyorganoarsinic acids may be useful as ion -exchange resins, or the arsenic acid groups may be reduced, e.g. with SO2 and HCl to give polychloroarsines which, reacted with a Grignard reagent or with an organic lithium compound, give organo-substituted polyarsines.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3403160A GB1015501A (en) | 1960-10-04 | 1960-10-04 | Organo-arsenical polymers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3403160A GB1015501A (en) | 1960-10-04 | 1960-10-04 | Organo-arsenical polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1015501A true GB1015501A (en) | 1966-01-05 |
Family
ID=10360503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3403160A Expired GB1015501A (en) | 1960-10-04 | 1960-10-04 | Organo-arsenical polymers |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1015501A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3442858A (en) * | 1967-10-05 | 1969-05-06 | Gen Electric | Products obtained by cleaving polyphenylene ethers |
-
1960
- 1960-10-04 GB GB3403160A patent/GB1015501A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3442858A (en) * | 1967-10-05 | 1969-05-06 | Gen Electric | Products obtained by cleaving polyphenylene ethers |
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