Pyrrole → HCID 86673204, compound
Reaction equation
[CH:1]1[C:14]2[C:15]3=[C:16]4[C:11](=[CH:12][CH:13]=2)[CH:10]=[CH:9][CH:8]=[C:7]4[CH:6]=[CH:5][C:4]3=[CH:3][CH:2]=1.[NH:17]1[CH:21]=[CH:20][CH:19]=[CH:18]1>N#N>[CH:8]1[C:7]2[C:16]3=[C:15]4[C:4](=[CH:5][CH:6]=2)[CH:3]=[CH:2][CH:1]=[C:14]4[CH:13]=[CH:12][C:11]3=[CH:10][CH:9]=1.[NH:17]1[CH:21]=[CH:20][CH:19]=[CH:18]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
FIG. 15 shows the thermal stability results of the copolymers in TG analysis, and Table 4 shows the thermal decomposition temperatures and char yields. All tested copolymers exhibit high thermal stability, including initial decomposition temperature of above 350° C., and the temperature at the maximal weight-loss rate (i.e. thermal decomposition temperature) of above 560° C. The char yields of all tested copolymers at 1000° C. in N2 are above 83%. As the pyrene feed content increases from 0% to 100%, the char yield of the resulting polymers increases at first and slightly declines, with the maximum char yield found as 87.6% for copolymer 95/5. The maximum char yield is much higher than that of conventional carbon precursors and aromatic polymers, and is much higher than the theoretical carbon content of pyrrole monomer of 71.5% and close to the theoretical carbon content of pyrene monomer of 95.1%. The high thermal stability and very high char yields of these copolymers can be ascribed to their high aromaticity.
Workup
- customresults of the copolymers in TG analysis, and Table 4
- customyields
- customat the maximal weight-loss rate (i.e. thermal decomposition temperature) of above 560° C
- temperaturethe char yield of the resulting polymers increases at first and slightly declines
- customwith the maximum char yield
- customThe maximum char yield
- customThe high thermal stability and very high char yields of these copolymers
Sources & evidence
- ORD record
- ord-6dc82f6e3e244797a6b3010d4d456fb7
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08907015B2
Reaction notes
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