Polyphenylquinoxalines via aromatic nucleophilic displacement
AssigneeThe United States of America as represented by the Administrator of the National Aeronautics and Space Administration
InventorsPaul M. Hergenrother, John W. Connell
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Abstract
Polyphenylquinoxalines are prepared by the nucleophilic displacement reaction of di(hydroxyphenyl)quinoxaline monomers with activated aromatic dihalides or dinitro compounds. The reactions are carried out in polar aprotic solvents using alkali metal bases at elevated temperatures under nitrogen. The di(hydroxyphenyl)quinoxaline monomers are prepared either by reacting stoichiometric quantities of aromatic bis(o-diamines) with a hydroxybenzil or by reacting o-phenylenediamine with a dihydroxybenzil or bis(hydroxyphenylglyoxylyl)benzene.
Claims12
A poly(phenylquinoxaline) consisting of repeating units having the general structural formula ##STR20## wherein the substitution of oxygen is selected from the group consisting of meta-meta, para-para, and para-meta;
- wherein Ar is a radical selected from the group consisting of:
- ##STR21## wherein R is a bond or is selected from the group consisting of:
- O, S, C.dbd.O, SO.sub.2, CH.sub.2, C(CH.sub.3).sub.2, and C(CF.sub.3).sub.2 ;
- ##STR22## wherein Z is a substituent selected from the group consisting of:
- H, F, Cl, Br, CH.sub.3, CH.sub.2 CH.sub.3, OCH.sub.3, C.sub.6 H.sub.5, and C.sub.6 H.sub.5 O;
- wherein X is a radical selected from the group consisting of:
- ##STR23## and wherein n is an integer between 4 and 100.
A process for synthesizing polyphenylquinoxlines by aromatic nucleophilic displacement, which comprises reacting a di(hydroxyphenyl)quinoxaline having the general structure:
- ##STR29## wherein Ar is a radical selected from the group consisting of:
- ##STR30## wherein R is a bond or is selected from the group consisting of:
- O, S, C.dbd.O, SO.sub.2, CH.sub.2, C(CH.sub.3).sub.2, and C(CF.sub.3).sub.2 ;
- ##STR31## wherein Z is a substituent selected from the group consisting of:
- H, F, Cl, Br, CH.sub.3, CH.sub.2 CH.sub.3, OCH.sub.3, C.sub.6 H.sub.5, and C.sub.6 H.sub.5 O;
- with an activated aromatic dihalide or dinitro compound having the general structure:
- ##STR32## wherein X is a radical selected from the group consisting of:
- ##STR33## wherein Y is selected from the group consisting of:
- Cl, F, and NO.sub.2, and wherein said reaction is carried out in a polar aprotic solvent selected from the group consisting of N,N-dimethylacetamide, N-methylpyrrolidinone, sulfolane, diphenylsulfolane, N-cyclohexylpyrrolidinone, and dimethylsulfoxide;
- wherein said reaction is carried out in the presence of an alkali metal base selected from the group consisting of K.sub.2 CO.sub.3, Na.sub.2 CO.sub.3, KOH, and NaOH;
- and
- wherein said reaction is carried out with the application of heat.
Dependencies are inferred from the claim text.