9-Vinylanthracene → Anthracene

To a 100-mL three-necked round bottom flask fitted with a condenser/nitrogen inlet and two stoppers was added divinyltetramethyldisiloxane (4.43 g, 23.8 mmole), divinyltetraethoxydisiloxane (0.38 g, 1.24 mmoles), and tetrakis(dimethylsiloxy)silane (12.33 g, 37.5 mmoles). A solution of 9-vinylanthracene (0.0442 g, 0.525 mmole) in toluene (20 mL) was then added and the mixture stirred at RT. Karstedt's catalyst (21 microliters) was added using an automatic pipette. The mixture was stirred for 1 h then the flask was immersed in an oil bath which was heated to 50° C. overnight. The reaction mixture was cooled then transferred to a single necked round bottom flask and solvent removed on a rotary evaporator. The residue was washed with acetonitrile (4×30 mL), devolatilized using a rotary evaporator at 30° C., followed by devolatization using a Kugelrohr distillation apparatus at 80° C. at full vacuum for 30 mins. The resultant material was a water-white clear liquid (12.85 g, ˜75%). A sample was diluted in methylene chloride and analyzed by UV-Vis spectroscopy. Bands indicative of anthracene were present indicating that the 9-vinylanthracene was incorporated into the polymer.

1. customTo a 100-mL three-necked round bottom flask fitted with a condenser/nitrogen inlet
2. stirringThe mixture was stirred for 1 h
3. customthe flask was immersed in an oil bath
4. temperaturewhich was heated to 50° C. overnight
5. temperatureThe reaction mixture was cooled
6. customthen transferred to a single necked round bottom flask
7. customsolvent removed on a rotary evaporator
8. washThe residue was washed with acetonitrile (4×30 mL)
9. customa rotary evaporator at 30° C.
10. distillationa Kugelrohr distillation apparatus at 80° C. at full vacuum for 30 mins
11. additionA sample was diluted in methylene chloride

ORD record

ord-7830b2a548e94561ac4d19924a5a364b

Source dataset

uspto-grants-2014_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08791222B2