Hydroquinone, quinone, and amine functionalized polyolefins

Macromolecules

Volumn 31, Issue 6, 1998, Pages 1999-2001

  Patil, Abhimanyu O ^a   Zushma, Stephen ^a  

^a EXXONMOBIL UPSTREAM RESEARCH COMPANY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITIVES; ALKYLATION; AMINES; AROMATIC COMPOUNDS; CHEMICAL BONDS; KETONES; LUBRICANTS; MOLECULAR WEIGHT; POLYETHYLENES; POLYPROPYLENES; REFRACTIVE INDEX; SOLUBILITY;

BENZOQUINONE; HYDROQUINONE; MANNICH BASE DISPERSANTS;

COPOLYMERS;

EID: 0032028250     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma971564z     Document Type: Article

References (24)

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19. n 870, 0.057 mol) with 95% vinylidene terminal double bonds was then added showly to the aforementioned solution, and the mixture was refluxed for 6 h under nitrogen. The reaction mixture was then filtered, and the filtrate was evaporated on rotary evaporator to obtain the product.
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21. There are several reports on quinone-amine chemistry, see Erhan, S. J. The Polymeric Materials Encyclopedia: Synthesis, Properties and Applications; CRC: Boca Raton, 1996; p 7311. Nikles, D. E.; Cain, J. L.; Chacko, A. P.; Liang, J.; Webb, R. I. The Polymeric Materials Encyclopedia: Synthesis, Properties and Applications; CRC: Boca Raton, 1996; p 7303.
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23. -3 mol) of diethylenetriamine (DETA) was added. The solution was stirred at room temperature for 72 h. The product was diluted with 50 mL of heptane and filtered. The solvent was removed initially by nitrogen stripping and then by high vacuum.
24. Patil, A. O. U.S. Patent 5,576,274, November 19, 1996.