HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290791Generated: October 30, 2026
Azobisisobutyronitrile → HCID 17937502, compound
https://huagongshe.com/reaction/2290791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 2-ethenyl-9H-fluorene | HCID 11041607 | — |
| Reactant | 2VF phenyl vinyl ketone | HCID 131714938 | — |
| Reactant | 2VF phenyl isopropenyl ketone | HCID 131714939 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 17937502 | HCID 17937502 | — |
Reaction Steps
Concentrated solution polymerizations of three runs P1, P2 and P3, respectively, 2-vinyl fluorene (2VF), 2VF+phenyl vinyl ketone (PVK) and 2VF+phenyl isopropenyl ketone (PIPK) were carried out. In each case the procedure was the same: the monomer(s) was placed in a 6 mm diameter tube, approximately 0.25% azobisisobutyronitrile (AIBN) initiator was added in toluene so as to give a final monomer/solvent ratio of approximately 1/1. The tubes were then flushed with nitrogen and vacuum pumped five times before being left capped under nitrogen. After a variable raction time at 75° C., as shown in Table I the tubes were opened and the polymer was dissolved in toluene; dropwise addition of this solution to methyl alcohol gave a precipitate that was filtered and vacuum dried. Details are given in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04618566 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-122ba2e7f496486dbbde714225d682a2 |
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| Source note | uspto-grants-1986_10 |
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