Dimethyl Sulfoxide → HCID 86603851, compound
Reaction equation
[CH3:1][S:2]([CH3:4])=[O:3].[CH3:5][C:6](=[O:12])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].C[Si](C)(OC(=O)C)OC(=O)C>C([O-])(=O)C.C[N+](C)(C)C.N#N>[CH3:5][C:6](=[O:12])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[CH3:1][S:2]([CH3:4])=[O:3]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 125 °C
Procedure
0.0126 g tetramethylammonium acetate (Aldrich Chemical Company, Milwaukee, Wis. 53201), were added to 1.247 g dimethylsulfoxide, the mix was stirred until dissolution, then 44.24 g of 2-heptanone (Ultra Pure Solutions Inc., Castroville, Calif. 85012), and 4.49 g of dimethyldiacetoxysilane (Gelest, Tullytone, Pa. 19007) were added in a 60 ml particle free high density polyethylene bottle. The solution was mixed vigorously for one minute. After mixing, the diluted precursor was hand filtered to 0.1 μm using a teflon filter. Approximately 2.0-3.0 ml of The formulation was deposited onto an 8″ etched (C4F8; 20 s.) & ashed (plasma O2; 20 s.) carbon depleted porous SiCOH film (˜4000 Å thick NANOGLASS-E®). After deposition, the wafer was spun at 2500 rpm for 30 seconds to form a film. The films were heated at elevated temperatures for 1 min. each at 125° C., 200° C. and 350° C. in N2. The following results were observed:
Workup
- additionThe solution was mixed vigorously for one minute
- additionAfter mixing
- filtrationfiltered to 0.1 μm
- filtrationfilter
- custometched (C4F8; 20 s.) & ashed (plasma O2; 20 s.) carbon depleted porous SiCOH film (˜4000 Å thick NANOGLASS-E®)
- customto form a film
- customThe following results
Sources & evidence
- ORD record
- ord-84b89b041cb9464eb15351cf3eff46f9
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07915159B2
Reaction notes
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