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Microwave Chemistry in Silicon Carbide Reaction Vials: Separating Thermal from Nonthermal Effects

Microwave Chemistry in Silicon Carbide Reaction Vials: Separating Thermal from Nonthermal Effects. Figure. Heating rates for 3 mL samples of hexane (tand=0.02) ,[3] MeCN (tand=0.062) ,[3] EtOH (tand=0.941), [3] and 1-butyl-3-methylimidazolium

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Microwave Chemistry in Silicon Carbide Reaction Vials: Separating Thermal from Nonthermal Effects

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  1. Microwave Chemistry in Silicon Carbide Reaction Vials: Separating Thermal from Nonthermal Effects

  2. Figure. Heating rates for 3 mL samples of hexane (tand=0.02),[3] MeCN (tand=0.062),[3] EtOH (tand=0.941),[3] and 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6, tand>1)[8] at 130 W constant magnetron power in a 10 mL Pyrex vial (a), and in a custom-made SiC vial (b). Single-mode microwave irradiation, magnetic stirring, internal fiber-optic temperature measurement.[6]

  3. Figure. Comparison of heating rates for 3 mL samples of hexane (tan δ = 0.02), MeCN (tan δ =0.062),EtOH (tan δ = 0.941), and bmimPF6, tan δ >1) at 130 W constant microwave power in Pyrex and SiC vials. Single-mode microwave irradiation, magnetic stirring, internal fiber-optic temperature measurement (Monowave 300).

  4. Figure. Internal fiber-optic temperature profiles for the solvent-free synthesis of the ionic liquid [bmim]Br using Pyrex and SiC reaction vials. Experiments were performed using an IR-controlled set temperature of 1008C on a 10.6 mmol scale (1.02 equiv of BuBr)

  5. c) Newman-Kwart a) Mizoroki-Heck reaction d) Claisen rearrangement b) Alkylation of PPh3

  6. Newmqn-Kwart rearrangment

  7. Claisen rearrangment

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