Photoelectrochemistryin Organic Synthesis
Transcript of Photoelectrochemistryin Organic Synthesis
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Photoelectrochemistry in Organic Synthesis
Reporter :Gao Shiquan (高师泉)Supervisor: Prof. Zhang Junliang
2020-12-25
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1. Introduction1.1 Synthetic Organic Electrochemistry
1.2 Visible-Light Photoredox Catalysis
1.3 Photoelectrochemical Organic Synthesis
2. Photoelectrochemical Organic Synthesis 2.1 Electromediated Reaction with Photoredox Catalysis
2.1.1 Oxidation Reaction2.1.2 Reduction Reaction2.1.3 Redox Neutral Reaction
2.2 Electromediated Reaction involving Photo-induced Radical
2.3 Interfacial Photoelectrochemistry
3. Summary and Prospection
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Contents
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1. Introduction1.1 Synthetic Organic Electrochemistry
1.2 Visible-Light Photoredox Catalysis
1.3 Photoelectrochemical Organic Synthesis
2. Photoelectrochemical Organic Synthesis 2.1 Electromediated Reaction with Photoredox Catalysis
2.1.1 Oxidation Reaction2.1.2 Reduction Reaction2.1.3 Redox Neutral Reaction
2.2 Electromediated Reaction involving Photo-induced Radical
2.3 Interfacial Photoelectrochemistry
3. Summary and Prospection
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Contents
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IntroductionSynthetic Organic Electrochemistry
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undivided cell divided cell (“H” cell)
workingelectrode
counterelectrode
power
constant current (cc)constant voltage (cv)
reference electrode
Electrochemical Cells
Modes of Operation
S. R. Waldvogel et al. Chem. Sci., 2020, 11, 12386.
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IntroductionSynthetic Organic Electrochemistry
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low surface area(graphite Pt)
high surface area(Ni foam RVC)
sacrificial anode (Zn Mg Al)
THF DCM Acetone Methanol MeCN DMA H2O8 9 21 33 38 38 80
more resistance less resistanceε
Electrodes
Solution
P. S. Baran et al. Acc. Chem. Res. 2020, 53, 72.
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- -
+ 2
+
- -
-
n+
- -
-+
Redox-neutralReaction
OxidativeReaction
ReductiveReaction
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Workingelectrode
Counterelectrode
Counterelectrode
Workingelectrode
Workingelectrode
Workingelectrode
IntroductionSynthetic Organic Electrochemistry
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R. D. Little et al. Chem. Soc. Rev., 2014, 43, 2492. 7
IntroductionSynthetic Organic Electrochemistry
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Mes-AcrIr[dFCF3ppy]2(bpy) Ru(bpy)3 4CzIPN Eosin Y
G. A. Molander et al. ACS Catal. 2017, 7, 2563. 8
Introduction
ReductiveReaction
OxidativeReaction
Redox NeutralReaction
Energy TransferReaction
Visible-Light Photoredox Catalysis
PC
*[PC]
PC-
Ox
Ox•-
sub
sub•+
PC
*[PC]
PC+
subb
suba
subb•-
suba•+
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• energy constrained• energy losses• equivalent oxidizing or reducing agent
• low conductivity of organic solvents • unselective redox processes• limited mediators potential
The limits of PRCThe limits of SOE
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IntroductionPhotoelectrochemical Organic Synthesis
High selectivity/energy efficiencyAtom efficient Large redox window
redox energyfrom
photoexcitation
redox energyfrom
electrochemistry
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J. P. Barham et al. Angew. Chem. Int. Ed. 2020, 59, 2. 10
IntroductionPhotoelectrochemical Organic Synthesis
NH
S
CN
CN9,10-dicyanoanthracene
(DCA)
phenothiazine (PTZ)
PTZ
PTZ +
*PTZ
MO-1
MO-2
MO-3
HOMO-4
MO-1
MO-2
HOMO-3
SOMO-4
SOMO-1
MO-2
MO-3
HOMO-4
SOMO-1
HOMO-2
SOMO-2
HOMO-1
LUMO-2
HOMO-1
1
1
1
E = +0.70 V
E = 2.23 eV
Imax = 514, 772,864 nm
-e-
h
*E = 2.9 V
DCA
DCA
*DCA
Imax = 450, 480,510 nm
+e-
h
*E = -3.2 V
1
1
1
E = 2.43 eV
E = -0.82 V
E E
electromediatedphotoredox calatlyst (e-PRC)
SOMO-HOMO inversion SOMO-HOMO inversion
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J.-C. Moutet, G. Reverdy. Tetrahedron Lett. 1979, 20, 2389. J.-C. Moutet, G. Reverdy. J. Chem. Soc. Chem. Commun. 1982, 654. 11
IntroductionPhotoelectrochemical Organic Synthesis
PhPh
Ph Ph
Ph
O
Ph Ph
Ph Ph
PTZ (6 mol%)LiClO4
Pt rotating disk voltammetry0.79 V vs SCE
Hg Lamp (<400 nm)MeCN
+
1:1.3 by HPLC
(DPE)NH
S
phenothiazine (PTZ)1 2
H2H+
e-
*TPPD•+
TPPD
TPPD•+
OH
OH OH O
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Contents
1. Introduction1.1 Synthetic Organic Electrochemistry
1.2 Visible-Light Photoredox Catalysis
1.3 Photoelectrochemical Organic Synthesis
2. Photoelectrochemical Organic Synthesis 2.1 Electromediated Reaction with Photoredox Catalysis
2.1.1 Oxidation Reaction2.1.2 Reduction Reaction2.1.3 Redox Neutral Reaction
2.2 Electromediated Reaction involving Photo-induced Radical
2.3 Interfacial Photoelectrochemistry
3. Summary and Prospection
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Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
B. Konig et al. Photochem. Photobiol. Sci., 2010, 9, 1367.B. Konig et al. Chem. Eur. J. 2008, 14, 1854.D. R. Carbery et al. Angew.Chem. Int.Ed. 2015, 54,8997.B. Konig et al. ChemCatChem. 2012, 4, 620.J. C. Gonzalez-Gomez et al. Organic Letters 2019 21 (5), 1368.
Flavin
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B. Konig et al. Chem. Eur. J. 2008, 14, 1854.S. Lin et al. Angew. Chem. Int. Ed. 2020, 59, 409.
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
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1a: E ≈ 1.5 V1b: E > 1.9 VRFT*: E = 1.67 V
Fluorescence quenching of RFT with 1a Fluorescence quenching of RFT with 1b
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S. Lin et al. Angew. Chem. Int. Ed. 2020, 59, 409.
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
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13C NMR of (A) TU-1-O2 (B) white precipitate (C) TU-1
Fluorescence quenching of RFT with TU-2
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S. Lin et al. Angew. Chem. Int. Ed. 2020, 59, 409. 16
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
OMe
Me
OMe
Me
1b (1 eq.), RFT (5 mol%)LiOTf (0.1 M CH3CN), H2O
C(+)/Pt(-), 2.5 Vblue LED, 22 °C, 1 h
OMe
Me
OMe
1b (1 eq.)RFT (5 mol%), TU-2 (10 mol%)
LiOTf (0.1 M CH3CN), H2OC(+)/Pt(-), 2.5 V
blue LED, 22 °C, 1 h
Me
Z:E = 6:1 71% recovered, Z:E = 10:1100% 1b recovered
75% recovered, Z:E = 1:100100% 1b recovered
Z:E = 6:1
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S. Lin et al. Angew. Chem. Int. Ed. 2020, 59, 409. 17
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
N
N
NH
N O
O
OAc
AcOOAc
OAc
Me
Me
RFT
Selected Substrates
H2
H+RFT-H2
RFTRFT*
RFT•-H
e-
OHtBu OtBu
NH
S
NH
R R
N
S
NH
R R
S
NHR
RNS NR
NHR
OHtBu
OHtBu
H2S +
E 0.8 V
NH
S
NH
R R
PhS
O O
Me
O
75%
O
Me Me
H
MeO
Me H
Me
H
H HO
O
96% 89%88%
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T. H. Lambert et al. Angew. Chem. Int. Ed. 2019, 58, 13318. 18
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
N N
CHO
N NN
N N
COOEt
Cl
Cl
Me
MeMe
Me
MeMe
Br
65% 42% 75% 71%
NN
COOEt
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T. H. Lambert et al. J. Am. Chem. Soc. 2020, 142, 1698. 19
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
*TAC2+
N
N N
Me MeMe
Me Me
Me
*
SO2Ph HNN
CHO
NBr
O NO
CHO
MeO
SO2Ph
89%72%40%80%
O NN
CHO
+ +
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H.-C. Xu et al. Angew. Chem. Int. Ed. 2019, 58,4592. 20
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
H2H+
e-
Mes-Acr•
*Mes-Acr+
Mes-Acr+
F3B Me
Me
Me
Me+ BF3
NH
Me
NH
Me
Me
Me
H+
Mes-Acr+ Mes-Acr•NH
Me
Me
2 mA
E = 2.06 VEp/2 = -1.19 V
Ep/2 = -0.57 V
Me
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H.-C. Xu et al. Angew. Chem. Int. Ed. 2020, 59, 10626. 21
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
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L. Ackermann. et al. Chem. Eur. J. 2020, 26, 3241. 22
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
Me Me
Me
CF3
79%with [Mes-Acr]ClO4
iPr
iPr
CF3
67%with [Ru(bpy)3](PF6)2
OMeCF3
MeO2C
71%with [Ru(bpy)3](PF6)2
SnBu
CF312
64% (1:2 = 14:1)with [Mes-Acr]ClO4
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A.-W. Lei et al. J. Am. Chem. Soc. 2020, 142, 17693. 23
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
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S. Lin et al. J. Am. Chem. Soc. 2020,142, 2087. 24
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
CN
CNDCA
DCA
*DCA•-
DCA•-
Cl
MeO
MeO
B2pin2Bpin
MeO
E = -3.2 V
Zn2+
E = -1.0 Ve-
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T. H. Lambert et al. Angew. Chem. Int. Ed. 2020, 59, 658. 25
Photoelectrochemical Organic Synthesis Electromediated Reaction with Photoredox Catalysis
Selected Substrates
ONC
NC
Cl
ClO
DDQ
Cl
e-
*DDQ
DDQ•-
DDQ
F
Cl
Cl
F
NHN
CHOH+
Cl
Cl
F-
E = 3.18 V
FNN
CHO
FNN
CHO N N
CHO
E = 1.5 V
DDQ•-
DDQ
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H.-C. Xu et al. Angew. Chem. Int. Ed. 2020, 59, 10626. 26
Electromediated Reaction involving Photo-induced RadicalPhotoelectrochemical Organic Synthesis
Selected Substrates
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H.-C. Xu et al. Angew. Chem. Int. Ed. 2020, 59, 14275. 27
Electromediated Reaction involving Photo-induced RadicalPhotoelectrochemical Organic Synthesis
Selected Substrates
N
HCl (6 eq.)Et4NCl (0.3 eq.)C(+) Pt(-), 2 mAblue LED (10 W)
MeCN N
C(sp3)
+ H C(sp3)R1 R1
H
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S. Stahl et al. Angew. Chem. Int. Ed. 2019, 58, 6385. 28
Electromediated Reaction involving Photo-induced RadicalPhotoelectrochemical Organic Synthesis
Selected Substrates
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X.-L. Hu et al. Nat. Catal. 2019, 2, 366.
Interfacial Photoelectrochemistry
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Photoelectrochemical Organic Synthesis
Selected Substrates
CB
VBh+
e-
photoanode(semiconductor)
h
e-
sub
sub•+
VB:valence bandCB:conduction bandh:hole conduction
H2H+
e-
OMeNHN
OMe
•-H+
OMe
•
OMe -e-
-H+NN
OMe
H H
HN
N N
N
N NH
E = 0.73 V
OMe
MeO CO2Me
N N
N
Cl
OOEt
O
Me Me
87%(P1:P2=3:1)
1
2
82%
N
NNOMe
77%o:p = 6:1
NNOMe
58%o:p = 14:1
Cl
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C. P. Berlinguette et al. Nat. Commun. 2017, 8, 390. 30
Interfacial PhotoelectrochemistryPhotoelectrochemical Organic Synthesis
NO O
OH
(NHS)
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Contents
1. Introduction1.1 Synthetic Organic Electrochemistry
1.2 Visible-Light Photoredox Catalysis
1.3 Photoelectrochemical Organic Synthesis
2. Photoelectrochemical Organic Synthesis 2.1 Electromediated Reaction with Photoredox Catalysis
2.1.1 Oxidation Reaction2.1.2 Reduction Reaction2.1.3 Redox Neutral Reaction
2.2 Electromediated Reaction involving Photo-induced Radical
2.3 Interfacial Photoelectrochemistry
3. Summary and Prospection
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Summary and Prospection
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OxidativeNMe
Me
Me Me
ONC
NC
Cl
ClO
Reductive
HAT
4czIPN
4czIPN
TAC Mes-Acr
DDQ
DCA
RFT TAC
NN
Ru
N
N
NN
Ru(bpy)3
ONC
NC
Cl
ClO
DDQ
9-fluorenone
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• Rigorous control experiments• Interelectrode ohmic drop• Mass transfer
Summary and Prospection
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The limits of Photoelectrochemistry
a
b
c
d
pump
e-
reactants
products
a:borosilicate glass coverb:working electrode platewith groove channelsc:ion-exchange membraned:counter electrode plate
New reaction ?New mediator ?Chiral reaction ?
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Thanks for your kind attention
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