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Faculty of Chemistry, Adam Mickiewicz University, Poznan, Poland 2012/2013 - lecture 7 "Molecular Photochemistry - how to study mechanisms of photochemical reactions ?" Bronislaw Marciniak Bronislaw Marciniak
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5. Examples illustrating the investigation 5. Examples illustrating the investigation of photoreaction mechanisms: photochemistry of 1,3,5,-trithianes in solution
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TT (1,3,5-trithiane) TMT (2,4,6-trimethyl-1,3,5-trithiane) ISOMER (cis-cis), ISOMER (cis–trans) TPT (2,4,6-triphenyl-1,3,5-trithiane) ISOMER (cis–cis), ISOMER (cis–trans)
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Trithiane structures TMT TPT TT
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Isomers of the trithianes -form (cis-trans) -form (cis-cis) R = CH 3, C 6 H 5
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Ground-state absorptions of trithianes in MeCN
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254 nm photolysis of TT in MeCN
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Stable products (GC, GCMS, HPLC, UV) For TT: primary product secondary product
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HPLC following 254 nm photolysis of TT in MeCN
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254 nm photolysis of TT in MeCN
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313 nm photolysis of TT in MeCN preirradiated at 254 nm for 12 minutes
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254 nm photolysis of -TMT in MeCN
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For -TMT: -TMT primary product secondary product Stable products (GC, GCMS, HPLC, UV)
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HPLC following 254 nm photolysis of -TMT in MeCN
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Extrapolation of to zero time
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Steady-state photolysis at 254 nm Laser flash photolysis at 266 nm 0.520.170.320.250.52 Thioester formation from laser flash photolysis 0.01 0.100.01– Isomer formation 0.440.140.320.220.49 Thioester formation 0.480.190.430.380.54 Trithiane disappearance -TPT -TPT -TMT -TMT TT Quantum yields
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266 nm laser flash of TT in MeCN
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266 nm laser flash of -TMT in MeCN
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Mechanism for Trithiane = TT, -TMT, or -TMT
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266 nm laser photolysis of -TPT in MeCN
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Laser-intensity dependence -TPT in MeCN
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Mechanism for Trithane = -TPT or -TPT
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Solvent effect
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Table: Quantum yields a of trithiane disappearance ( dis ) and dithioester formation ( prod ) in various solvents TrithianesSolvent dis prod TT CH 3 CN 0.540.51 CH 3 OH 0.510.085 -TMT CH 3 CN 0.390.22 CH 3 OH 0.260.01 -TMT CH 3 CN 0.430.32 CH 3 OH 0.200.04 -TPT CH 3 CN 0.48 0.46 b CH 3 OH 0.240.03 a All quantum yields were extrapolated to zero irradiation times; estimated error is equal to 10 %. b Sum of 0.34 + 0.12 for RC(=S)SCH(R)SCH 2 R and RC(=S)SCH 2 R, respectively.
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TrithianeSolvent decay ( s) growth ( s) k II (M 1 s 1 ) TT CH 3 CN 28 31 a CH 3 OH 3.8 b EtOEt 5761 1-BuOH20 13 c -TMT CH 3 CN 14 d 9d9d9d9d 8.4 × 10 4 CH 3 OH 0.13 b Cyclohexane1713 -TMT CH 3 CN 13 e CH 3 OH -- -TPT CH 3 CN 29 a 30 a 7.8 × 10 3 CH 3 OH 1.3 a Cyclohexane2023 a Previously measured [9]. b No growth observed. c Determined from a growth/decay fitting function d The decay lifetime of the shorter component of a biexponential decay. e Previously measured [6]. Decay time ( decay ) of intermediate I, growth time ( growth ) of the dithioesters absorbing at 310 nm, and rate constant (k II ) of I with CH 3 OH
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266 nm laser flash of in MeOH 266 nm laser flash of -TPT in MeOH 60 100 ns 600 700 ns 1.4 1.6 s 6 8 s
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= 1.3 s 266 nm laser flash of in MeOH 266 nm laser flash of -TPT in MeOH
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Initial spectra of 266-nm photolysis of -TPT in various solvents Open circles: CH 3 CN, filled circles: CH 3 OH, squares: cyclohexane
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Quenching of intermediate, I, by methanol, following 266-nm laser excitation of -TPT in acetonitrile k q II = 7.8 × 10 3 M 1 s 1
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