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C–H activation: making diketopyrrolopyrrole derivatives ......the matrixes. Samples were prepared...
Transcript of C–H activation: making diketopyrrolopyrrole derivatives ......the matrixes. Samples were prepared...
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C–H activation: making diketopyrrolopyrrole derivatives easily accessible
Shi-Yong Liu,ab Min-Min Shi,*a Jia-Chi Huang,a Zheng-Neng Jin,ab Xiao-Lian Hu,a Jun-Ying Pan,a Han-Ying Li,a Alex K.-Y. Jen*ac and Hong-Zheng Chen*a
a MOE Key Laboratory of Macromolecular Synthesis and Functionalization, State Key Laboratory of Silicon Materials, & Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, P. R. China b Department of Pharmacy & Chemistry, Taizhou University, Taizhou 317000, P. R. China c Department of Materials Science and Engineering, University of Washington, Seattle, WA 98198, USA
Contents
1. Instruments and Materials........................................................................................S2
2. Synthetic route for the DPP 1a-1e and DPP 1-17...................................................S2
3. The comparison between our method and the reported methods.............................S8
4. Fluorescence spectra of DPP 1-17...........................................................................S9
5. 1H & 13C NMR and MALDI-TOF MS spectra......................................................S10
Electronic Supplementary Material (ESI) for Journal of Materials Chemistry AThis journal is © The Royal Society of Chemistry 2013
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1. Instruments and materials All 1H and 13C NMR spectra were obtained in chloroform-d, unless otherwise noted, with Bruker DMX-500 or
Bruker DMX-300. 13C NMR (126 MHz or 76 MHz) spectra were measured with a proton-decoupling pulse program. Chemical shifts for 1H and 13C NMR were referenced to residual signals from CDCl3 (1H NMR δ =7.26 ppm and 13C NMR δ =77.23 ppm). Matrix-assisted laser desorption/ionizationtime of flight mass spectrometry (MALDI-TOF MS MS) was performed on a Voyager DE STR using 2,5-Dihydroxybenzoicacid or α-Cyano-4-hydroxycinnamicacid as the matrixes. Samples were prepared by diluting the molecules in chloroform with the matrix. Elemental analyses were conducted on a Flash EA 1112 elemental analyzer. UV-visible absorption spectra were taken on a Shimadzu UV-2450 spectrophotometer. Cyclic voltammetry (CV) was done on a CHI 660C electrochemical workstation with Pt disk, Pt plate, and standard 10 calomel electrode (SCE) as working electrode, counter electrode, and reference electrode, respectively, in a 0.1 mol/L tetrabutylammonium hexafluorophosphate (Bu4NPF6) CH2Cl2 solution.
All starting organic compounds were purchased from Aldrich, Alfa Aesar, Alladin, Energy chemical, or TCI and used without further purification. The solvent toluene and dimethyl acetamide (DMA) are anhydrous.
2. Synthetic route for the DPP 1a-1e and DPP 1-17
Scheme S1. Synthetic route of parent DPP 1a-1c
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S3
Scheme S2. Synthetic route of parent DPP 1d and 1e
Scheme S3. Synthetic route of DPP 1
Scheme S4. Synthetic route of DPP 2
Electronic Supplementary Material (ESI) for Journal of Materials Chemistry AThis journal is © The Royal Society of Chemistry 2013
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S4
Scheme S5. Synthetic route of DPP 3
Scheme S6. Synthetic route of DPP 4
Scheme S7. Synthetic route of DPP 5
Scheme S8. Synthetic route of DPP 6
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S5
Scheme S9. Synthetic route of DPP 7
Scheme S10. Synthetic route of DPP 8
Scheme S11. Synthetic route of DPP 9
Scheme S12. Synthetic route of DPP 10
Electronic Supplementary Material (ESI) for Journal of Materials Chemistry AThis journal is © The Royal Society of Chemistry 2013
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Scheme S13. Synthetic route of DPP 11
Scheme S14. Synthetic route of DPP 12
Scheme S15. Synthetic route of DPP 13
Scheme S16. Synthetic route of DPP 14
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Scheme S17. Synthetic route of DPP 15
Scheme S18. Synthetic route of DPP 16
Scheme S19. Synthetic route of DPP 17
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S8
3. The comparison between our method and the reported methods
S N
N
O
O
R
R
S +S N
N
O
O
R
R
SBO
OO
LDA, -25 oC - rt
1 h, THFBO
O
BO
O SBr
NC
[Pd]
S N
N
O
O
R
R
S
S
S CN
NC
78% 40%
Two steps, Total Yield: 31 %
J. Org. Chem. 2011, 76, 2426.S N
N
O
O
R
R
SSNC Yield: 46 %,
one step
Our method:
Reported method:
N
N
O
O
R
R
ClCl
BO
OB
O
O
[Pd]
Dioxane, 4 h, 110 oC
N
N
O
O
R
R
BO
O
BO
O
63 %
Pd(OAc)2, 65 oC, THF
SPhos2.5 equ. K3PO4 22 h
I F
FF
FF
N
N
O
O
R
R
F
FF
FF
F
F F
FF
24 %
Two steps, Total Yield: 13 %
Reported method:
Our method:
N
N
O
O
R
R
BrBr
F
FF
FF
+
N
N
O
O
R
R
F
FF
FF
F
F F
FF
Yield: 95 %, one step
TM
S N
N
O
O
R
R
S Br
Br
+ (HO)2B CF3
Pd(PPh3)4
Toluene, 24h, 80 oC
S N
N
O
O
R
R
S CF3
F3C
69 %J. Mater . Chem. 2010, 20, 3626, Energy Environ. Sci., 2011, 4, 3617.
Reported method: Our method:
S N
N
O
O
R
R
SPd(OAc)2, 30 % PivOH
K2CO3 DMA, 110 oC, 4 h
TM
Yield: 92 %, one step
Br CF3
Ph2N
Br
BO
OB
O
O
[Pd]
Dioxane, 16 h, 85 oCPh2N
BO
O90 %
[Pd] P(o-toyl)3
DPP, 16h, 90 oCS N
N
O
O
R
R
S
Ph2NNPh2
50 %
Two steps, Total Yield: 45 %
S N
N
O
O
R
R
S Br
Br
B(OH)2[Pd] P(o-toyl)3
Toluene, 16h, 90 oC
+ S N
N
O
O
R
R
S
98 %
Adv. Mater . 2011, 23, 5359.
Adv. Mater . 2011, 23, 5359.
Reported method:Our method:
S N
N
O
O
R
R
S
Ph2N Br
4 h
TM
Yield: 95 %, one step
Reported method:
S N
N
O
O
R
R
S Pd(OAc)2, 30 % PivOH
Br
TM
Yield: 92 %, one step
Our method:
S N
N
O
O
R
R
S Br
BrS(Bu)3Sn
+
Pd(PPh3)2Cl2
THF, 22h, 70 oC S N
N
O
O
R
R
S
S
RS
RR
LDA, -78 oC, DMF
THF
S N
N
O
O
R
R
S
S
RS
R
CHO
HCO
19 % 45 %
Two steps, Total Yield: <10 %
Macromol. Rap. Commun. 2010, 31, 1554
Reported method:
S N
N
O
O
R
R
SS CH
OBr
Yield: 45 %, one step
Our method: TM
Case 1
Case 2
Case 3
Case 4
Case 5
Case 6
Eur. J. Org. Chem. 2012, 5282
BrBr
+
- HBr
- HBr
- HBr
- HBr
- HBr
- HBr
Pd(OAc)2, 110 oC, DMA
30 % (CH3)3C-COOH
K2CO3 DMA, 110 oC, 4 h
Pd(OAc)2, 30 % PivOH
K2CO3 DMA, 100 oC, 4 h
K2CO3 DMA, 100 oC, 4 h
Pd(OAc)2, 30 % PivOH
Pd(OAc)2, 30 % PivOH
K2CO3 DMA, 110 oC, 4 h
K2CO3
DPP 3
DPP 8
DPP 9
DPP 10
DPP 13
DPP 16
Scheme S20. The comparison between our method and the reported methods
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S9
4. Fluorescence spectra of DPP 1-17
Fig. S1. Fluorescence spectra of DPP 1-17 in CHCl3 (excitation at 467 nm)
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S10
5. 1H & 13C NMR and MALDI-TOF MS spectra
Fig. S2. 1H NMR for DPP 1a
Fig. S3. 1H NMR for DPP 1b
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S11
Fig. S4. 1H NMR for mono-bromo-DPP
Fig. S5. 1H NMR for DPP 1c
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S12
Fig. S6. 1H NMR for DPP 1d
Fig. S7. 1H NMR for DPP 1e
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S13
Fig. S8. 1H &13C NMR for DPP 1
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S14
Fig. S9. 1H &13C NMR for DPP 2
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S15
5 0 2 .0 5 8 3 .2 6 6 4 .4 7 4 5 .6 8 2 6 .8 9 0 8 .0M a s s (m /z )
0
6 .5 E+ 4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% I
nte
ns
ity
Voyager Spec #1[BP = 813.3, 65257]8 1 3 .3 8
8 1 5 .3 3
8 1 6 .2 9
8 1 7 .2 77 9 6 .2 2 8 3 5 .2 68 3 6 .2 77 9 7 .2 6
7 9 8 .2 6
Fig. S10. 1H &13C NMR and MALDI-TOF MS for DPP 3
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S16
Fig. S11. 1H &13C NMR for DPP 4
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S17
Fig. S12. 1H &13C NMR for DPP 5
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S18
5 20 .0 6 40 .2 7 60 .4 8 80 .6 1 00 0 .8 1 12 1 .0M a ss (m /z )
0
5 .6 E+4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 00
% I
nte
ns
ity
V oyager S pec #1[BP = 856.9, 56000]8 56 .9 5
8 57 .9 4
8 55 .9 3
8 58 .9 3
7 81 .0 0
7 79 .9 9 8 78 .8 97 82 .0 0
8 79 .9 0
8 80 .9 07 83 .0 0
Fig. S13. 1H &13C NMR and MALDI-TOF MS for DPP 6
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S19
5 0 1 6 4 9 7 9 7 9 4 5 1 0 9 3 1 2 4 1M a s s (m /z )
0
5 .5 E+ 4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% I
nte
ns
ity
Voyager Spec #1[BP = 1011.1, 55180]1 0 1 1 .1 2 6 1
1 0 1 2 .1 1 9 4
1 0 1 3 .1 0 7 6
1 0 1 4 .0 9 5 21 0 3 4 .1 0 2 8
1 0 3 5 .1 0 5 75 2 4 .1 4 1 2 7 6 8 .0 8 1 7 1 0 1 5 .0 8 0 95 2 5 .1 2 4 7 7 6 9 .0 8 3 7 9 0 6 .5 6 2 5
1 0 0 9 .1 3 5 7 1 0 4 9 .0 6 6 48 5 8 .0 8 5 97 7 0 .0 8 5 45 4 0 .3 2 6 0 9 1 0 .9 9 3 07 0 1 .1 1 2 2 1 0 9 0 .0 2 7 0
Fig. S14. 1H &13C NMR and MALDI-TOF MS for DPP 7
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S20
Fig. S15. 1H &13C NMR for DPP 8
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S21
1 0 1 7 .0 1 1 5 4 .8 1 2 9 2 .6 1 4 3 0 .4 1 5 6 8 .2 1 7 0 6 .0M a s s (m /z )
0
5 .1 E+ 4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% I
nte
ns
ity
Voyager Spec #1[BP = 1477.0, 51118]1 4 7 7 .0 4
1 4 7 8 .0 3
1 4 7 5 .0 3
1 4 7 9 .0 0
1 4 7 9 .9 9
1 4 9 8 .9 51 4 9 7 .9 5
1 4 8 0 .9 71 1 9 8 .9 51 2 2 0 .9 2
Fig. S16. 1H &13C NMR and MALDI-TOF MS for DPP 9
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S22
Fig. S17. 1H &13C NMR for DPP 10
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S23
6 5 3 7 2 3 7 9 3 8 6 3 9 3 3 1 0 0 3M a s s (m /z )
0
3 .9 E+ 4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% I
nte
ns
ity
Voyager Spec #1[BP = 832.8, 38648]8 3 2 .8 2
8 3 1 .8 28 3 3 .8 2
8 3 4 .8 2
8 5 4 .8 0
8 3 5 .8 1 8 5 5 .8 1
8 5 6 .8 1
8 3 6 .8 1 8 5 7 .8 0
Fig. S18. 1H &13C NMR and MALDI-TOF MS for DPP 11
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S24
4 9 9 .0 5 9 9 .4 6 9 9 .8 8 0 0 .2 9 0 0 .6 1 0 0 1 .0M a s s (m /z )
0
1 7 3 3
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% I
nte
ns
ity
Voyager Spec #1[BP = 943.8, 1733]9 4 3 .8 2
9 4 4 .8 3
9 4 5 .8 4
9 4 6 .8 5
9 4 7 .8 5
9 4 8 .8 6 9 6 6 .8 4
Fig. S19. 1H &13C NMR and MALDI-TOF MS for DPP 12
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S25
Fig. S20. 1H &13C NMR for DPP 13
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S26
Fig. S21. 1H &13C NMR for DPP 14
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S27
Fig. S22. 1H &13C NMR for DPP 15
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S28
8 3 3 .0 9 3 2 .6 1 0 3 2 .2 1 1 3 1 .8 1 2 3 1 .4 1 3 3 1 .0M a s s (m /z )
0
1 .8 E+ 4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% In
te
ns
ity
Voyager Spec #1[BP = 1069.2, 18208]1 0 6 9 .2 7
1 0 7 0 .2 7
1 0 9 1 .2 3
1 0 7 1 .2 7 1 0 9 2 .2 4
1 0 6 8 .2 5
1 0 9 3 .2 51 0 7 2 .3 0
Fig. S23. 1H &13C NMR and MALDI-TOF MS for DPP 16
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S29
7 5 4 .0 1 0 6 1 .4 1 3 6 8 .8 1 6 7 6 .2 1 9 8 3 .6 2 2 9 1 .0M a s s (m /z )
0
5 .0 E+ 4
0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
% In
te
ns
ity
Voyager Spec #1[BP = 1710.3, 50296]1 7 1 0 .3 9
1 7 3 2 .1 9
1 7 0 8 .4 4
1 7 3 4 .1 8
1 6 0 4 .8 5
1 7 1 4 .2 41 7 3 6 .1 71 5 9 8 .2 0
1 6 9 2 .3 11 5 8 7 .3 2
Fig. S24. 1H &13C NMR and MALDI-TOF MS for DPP 17
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