반응 #456106

반응 방정식

norbornene

isobutylene

methylene chloride

THF

methylene chloride

methylene chloride

methanol

norbornene

→

5-norbornene-carboxylic acid

반응 조건

후처리

1. 1
   기타the solution was degassed under argon atmosphere
2. 2
   기타A 10 ml glass vial equipped with a Teflon® coated stir bar
3. 3
   기타The catalyst solution was prepared
4. 4
   기타Immediate precipitation of the silver chloride salt
5. 5
   여과which was filtered
6. 6
   기타to obtain a clear yellow solution
7. 7
   workup.ADDITIONThe active yellow catalyst solution was added to the monomer solution via a syringe at 50° C.
8. 8
   온도No appreciable increase in viscosity
9. 9
   여과the solution was filtered through a 0.5 μ
10. 10
    여과filter
11. 11
    농축concentrated
12. 12
    workup.DISSOLUTIONThe resulting viscous solution was dissolved in methanol
13. 13
    기타precipitated into methanol/water mixture
14. 14
    기타to obtain a white solid
15. 15
    기타yield (23%)
16. 16
    기타to be thermally stable to about 155° C.
17. 17
    기타by 290° C.

실험 절차

To a 25 ml glass vial equipped with a Teflon® coated stir bar was added 3.06 g (12.8 mmole) of pure of bicyclo[2.2.1]hept-5-ene-exo,exo-2,3-dicarboxylic acid diethyl ester, 2.5 g (12.8 mmole) of t-butylester of norbornene, followed by 15 ml of freshly distilled methylene chloride and 10 ml of methanol, and the solution was degassed under argon atmosphere. A 10 ml glass vial equipped with a Teflon® coated stir bar was charged with 0.0188 g (0.052 mmol) of allylpalladium chloride dimer (to give a monomer to catalyst ratio of 500/1) and 2 ml of methylene chloride. Into another 10 ml glass vial was charged with 0.0357 g (0.104 mmol) of silver hexafluoroantimonate and 2 ml of methylene chloride. The catalyst solution was prepared by mixing the allylpalladium chloride dimer solution with silver hexafluoroantimonate solution inside the dry box. Immediate precipitation of the silver chloride salt was observed, which was filtered, to obtain a clear yellow solution. The active yellow catalyst solution was added to the monomer solution via a syringe at 50° C. and the reaction mixture was allowed to stir for 16 hours at room temperature. No appreciable increase in viscosity was observed and the solution was filtered through a 0.5 μ filter, concentrated using a rotovap. The resulting viscous solution was dissolved in methanol and precipitated into methanol/water mixture to obtain a white solid yield (23%). The molecular weight was observed to be Mn=15,700 g/mole and Mw=32,100 g/mole (GPC in THF, polystyrene standards). 1H NMR indicates the presence of both methyl and t-butyl ester of norbornene. Thermogravimetric analysis (TGA) under nitrogen (heating rate 10° C./min.) showed the polymer to be thermally stable to about 155° C. and then to exhibit approximately 20 wt. % loss by 290° C. (indicating clean loss of the t-butyl groups as isobutylene to afford the homopolymer of 5-norbornene-carboxylic acid) and then degradation of the polymer at around 450° C.

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