Nickel → HCID 136378371, compound
Reaction equation
[Ni:1].[OH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[S:10][C:11]2[N:12]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[OH:23])[S:14][C:15]=2[N:16]=1>>[Ni:1].[OH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[S:10][C:11]2[N:12]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[OH:23])[S:14][C:15]=2[N:16]=1Participants
4
Procedure
Dressler and coworkers dyed polypropylene yellow by treating polypropylene containing nickel with 2,5-bis(o-hydroxyphenyl)thiazolo[5,4-d]thiazole. The yellow color resulted from the formation of a nickel/2,5-bis(o-hydroxyphenyl)thiazolo[5,4-d]thiazole coordination compound (see Dressler, H. et al. U.S. Pat. No. 3,326,627).
Sources & evidence
- ORD record
- ord-7be92ce4392a426cb234ca63c8997bd5
- Source dataset
- uspto-grants-1994_09
- Patent number
- US05350857
Reaction notes
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