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US5102971A Expired / Lapsed US ⏱️ 0.0 years remaining

Soluble polyaromatic compounds

Assignee: Bayer AG
•
Filing: 1990-09-14
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Granted: 1992-04-07
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Expires: 2010-09-14
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Abstract

Abstract Process for the preparation of polyaromatic compounds in which an aromatic dichloro compound, optionally in the presence of an anhydrous aprotic solvent, is reacted with metallic zinc, manganese or magnesium in the presence of a catalyst system of (1) from 0.1 to 25 mol-% (based on the dihalogen compound) of a nickel salt, nickel complex salt or nickel complex, (2) from 2 to 100 mol per mol of nickel in (1) of a triarylphosphine and optionally (3) from 0.1 to 10 mol per mol of nickel (1) of a halide, sulphate or phosphate of an alkali metal, alkaline earth metal, zinc, magnesium or manganese.

Inventors

  • 👤 Thomas Himmler
  • 👤 Rudolf Braden
  • 👤 Joachim Genz
  • 👤 Karsten-Josef Idel
  • 👤 Ralf Pakull

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 10:42
CPC Classifications
C; C08; C08G; C08G61/00; C08G61/12; C08G61/122; C08G61/123; C07; C07C; C07C1/00; C07C1/26; C07C43/00; C07C43/02; C07C43/20; C07C43/225; C07C43/257; C07C43/29; C07C45/00; C07C45/61; C07C45/67; C07C45/68; C07C45/72; C07D; C07D333/00; C07D333/02; C07D333/04; C07D333/26; C07D333/28; C08G61/02; C08G61/10; C07C2527/00; C07C2527/02; C07C2527/053; C07C2527/06; C07C2527/08; C07C2527/14; C07C2527/16; C07C2527/167; C07C2531/00; C07C2531/16; C07C2531/22; C07C2531/24

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 225 words
Polyaromatic polyphenylene compounds corresponding to the formula --A--.sub.n (I) wherein n stands for a number from 3 to 1000 and A denotes an aromatic group of the formula ##STR17## in which one to three CH units in each of the aromatic rings can be replaced by nitrogen atoms; C represents: COO-C 1 -C 18 -alkyl or -cycloalkyl or COO-C 6 -C 10 -aryl, each of which may be unsubstituted or mono or multi substituted by halogen; substituted or unsubstituted phenoxy; C 2 -C 16 -dialkylamino; C 6 -C 12 -diarylamino; diacetylamino; formyl; cyano; CO-C 1 -C 6 -alkyl, CO-C 6 -C 10 -aryl, OCO-C 1 -C 18 -alkyl or OCOC 6 -C 10 -aryl, each of which may be unsubstituted or mono- or multisubstituted by halogen; CONR 5 R 6 wherein R 5 and R 6 denote, independently of one another, C 1 -C 18 -alkyl or C 6 -C 10 -aryl; C 1 -C 18 -alkylsulphinyl, C 6 -C 10 -arylsulphinyl, C 1 -C 18 -alkylsulphonyl or C 6 -C 10 -arylsulphonyl, each of which may be unsubstituted or mono- or multisubstituted by halogen; and m represents the number 1 or 2 and if m represents the number 2, the two groups C together denote --OCH 2 O or --OCH 2 CH 2 O, which may be unsubstituted or mono or multisubstituted by halogen.
Claim 2
Dependent Claim 225 words
Polyaromatic polyphenylene compounds corresponding to the formula --A--.sub.n (I) wherein n stands for a number from 3 to 1000 and A denotes an aromatic group of the formula ##STR17## in which one to three CH units in each of the aromatic rings can be replaced by nitrogen atoms; C represents: COO-C 1 -C 18 -alkyl or -cycloalkyl or COO-C 6 -C 10 -aryl, each of which may be unsubstituted or mono or multi substituted by halogen; substituted or unsubstituted phenoxy; C 2 -C 16 -dialkylamino; C 6 -C 12 -diarylamino; diacetylamino; formyl; cyano; CO-C 1 -C 6 -alkyl, CO-C 6 -C 10 -aryl, OCO-C 1 -C 18 -alkyl or OCOC 6 -C 10 -aryl, each of which may be unsubstituted or mono- or multisubstituted by halogen; CONR 5 R 6 wherein R 5 and R 6 denote, independently of one another, C 1 -C 18 -alkyl or C 6 -C 10 -aryl; C 1 -C 18 -alkylsulphinyl, C 6 -C 10 -arylsulphinyl, C 1 -C 18 -alkylsulphonyl or C 6 -C 10 -arylsulphonyl, each of which may be unsubstituted or mono- or multisubstituted by halogen; and m represents the number 1 or 2 and if m represents the number 2, the two groups C together denote --OCH 2 O or --OCH 2 CH 2 O, which may be unsubstituted or mono or multisubstituted by halogen.

References Cited (Backward Citations)

EP0012201A2 Cited
EP0131936A1 Cited
US4326989A Cited
US4400499A Cited
US4521589A Cited
US4870153A Cited

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