64:
454:"Design and Synthesis of N -Phenylcarbazole-Substituted Diketopyrrolopyrrole-Based Monomers and Dimers: A Comparative Study: Design and Synthesis of N -Phenylcarbazole-Substituted Diketopyrrolopyrrole-Based Monomers and Dimers: A Comparative Study"
806:
Jin, Yi; Xu, Yanbin; Liu, Yinling; Wang, Lingyun; Jiang, Huanfeng; Li, Xianjie; Cao, Derong (2011). "Synthesis of Novel
Diketopyrrolopyrrole-Based Luminophores Showing Crystallization-Induced Emission Enhancement Properties".
686:
Jin, Yi; Xu, Yanbin; Qiao, Zhi; Peng, Junbiao; Wang, Baozheng; Cao, Derong (2010). "Enhancement of
Electroluminescence Properties of Red Diketopyrrolopyrrole-Doped Copolymers by Oxadiazole and Carbazole Units as Pendants".
742:
Xu, Yanbin; Jin, Yi; Lin, Weihong; Peng, Junbiao; Jiang, Huanfeng; Cao, Derong (2010). "Syntheses and
Electroluminescence Properties of Red Emitting Copolymers with Different Lengths of Diketopyrrolopyrrole Units".
714:
Qiao, Zhi; Peng, Junbiao; Jin, Yi; Liu, Qilin; Weng, Jiena; He, Zhicai; Han, Shaohu; Cao, Derong (2010). "Synthesis and
Electroluminescence Properties of Fluorene-co-Diketopyrrolopyrrole-co-Phenothiazine Polymers".
770:
Xu, Yanbin; Jin, Yi; Peng, Junbiao; Wang, Baozheng; Cao, Derong (2010). "Syntheses and
Characterization of 4-Octyloxybenzyl Substituted Diketopyrrolopyrrole-Based Red Emitting Copolymers with Low Turn-on Voltage".
75:. 2,5-Dihydropyrrolopyrrole-1,4-dione is a basic body of Diketopyrrolopyrrole dye. DPP pigments are an important class of high-performance pigments used in inks, paints and plastic. More recently their
1063:"Small molecule carbazole-based diketopyrrolopyrroles with tetracyanobutadiene acceptor unit as a non-fullerene acceptor for bulk heterojunction organic solar cells"
360:"Formation of Highly Efficient, Long‐Lived Charge Separated States in Star‐Shaped Ferrocene‐Diketopyrrolopyrrole‐Triphenylamine Donor–Acceptor–Donor Conjugates"
1305:
1235:"Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells"
1149:"1,1,4,4-Tetracyanobuta-1,3-diene Substituted Diketopyrrolopyrroles: An Acceptor for Solution Processable Organic Bulk Heterojunction Solar Cells"
260:
Choi, Dong Hoon; Kaur, Matinder (2014-12-08). "Diketopyrrolopyrrole: brilliant red pigment dye-based fluorescent probes and their applications".
305:"Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl)diketopyrrolopyrrole Bridged Donor‐TCBD Push‐Pull System"
836:"Rational molecular design towards NIR absorption: efficient diketopyrrolopyrrole derivatives for organic solar cells and photothermal therapy"
670:
35:
2,5-dihydropyrrolopyrrole-1,4-dione, widely used in optoelectronics. DPPs were initially used as pigments in the painting industry (e.g. in
660:
593:
111:, and expanding of the conjugated system increase the emission wavelength. DPP is also developed as a red emitting group in pure
1188:"D–A–D–π–D–A–D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cells"
1315:
179:
Grzybowski, Marek; Gryko, Daniel T. (2015). "Diketopyrrolopyrroles: Synthesis, Reactivity, and
Optical Properties".
1310:
985:"Diketopyrrolopyrrole-Based and Tetracyano-Bridged Small Molecules for Bulk Heterojunction Organic Solar Cells"
883:"Metal Functionalized Diketopyrrolopyrroles: A Promising Class of Materials for Optoelectronic Applications"
532:"Tuning of the HOMO-LUMO Gap of Symmetrical and Unsymmetrical Ferrocenyl-Substituted Diketopyrrolopyrroles"
217:
Tian, He; Qu, Sanyin (2012-02-27). "Diketopyrrolopyrrole (DPP)-based materials for organic photovoltaics".
1024:"Ferrocene-diketopyrrolopyrrole based non-fullerene acceptors for bulk heterojunction polymer solar cells"
594:"Recent Advances in the Development of Semiconducting DPP-Containing Polymers for Transistor Applications"
72:
63:
492:
1234:
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1101:
1062:
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is adjustable by change the aromatic group at 3 and 6 positions. Both electron donor group, such as
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788:
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395:
340:
161:
1102:"Ferrocene-diketopyrrolopyrrole based small molecule donors for bulk heterojunction solar cells"
563:"Design and Synthesis of Low HOMO-LUMO Gap N- Phenylcarbazole-Substituted Diketopyrrolopyrroles"
115:. Some DPP derivatives show aggregation induced emission and were used as effective fluorescent
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Popli, Charu; Jang, Youngwoo; Patil, Yuvraj; Misra, Rajneesh; D'Souza, Francis (2020-11-26).
304:
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Khan, Faizal; Jang, Youngwoo; Patil, Yuvraj; Misra, Rajneesh; D'Souza, Francis (2021-09-06).
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Patil, Yuvraj; Misra, Rajneesh; Singh, Manish Kumar; Sharma, Ganesh D. (2017-03-08).
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Patil, Yuvraj; Jadhav, Thaksen; Dhokale, Bhausaheb; Misra, Rajneesh (February 2016).
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Patil, Yuvraj; Jadhav, Thaksen; Dhokale, Bhausaheb; Misra, Rajneesh (August 2016).
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Patil, Yuvraj; Misra, Rajneesh; Sharma, Abhishek; Sharma, Ganesh D. (2016-06-22).
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Patil, Yuvraj; Misra, Rajneesh; Keshtov, M. L.; Sharma, Ganesh D. (2016-03-31).
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Patil, Yuvraj; Misra, Rajneesh; Keshtov, M. L.; Sharma, Ganesh D. (2017-02-14).
1022:
Patil, Yuvraj; Misra, Rajneesh; Singhal, Rahul; Sharma, Ganesh D. (2017-07-04).
44:
136:
Wallquist, O.; Lenz, R. (2002-03-01). "DPP chemistry — continuous innovation".
104:
96:
48:
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Patil, Yuvraj; Misra, Rajneesh; Chen, F. C.; Sharma, Ganesh D. (2016-08-17).
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662:
Encyclopedia of
Interfacial Chemistry: Surface Science and Electrochemistry
638:
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578:
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469:
415:"Near-infrared absorbing tetracyanobutadiene-bridged diketopyrrolopyrroles"
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375:
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898:
43:. More recently, DPP derivatives have been also investigated as promising
28:
1250:
1203:
1117:
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1039:
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430:
273:
230:
149:
116:
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of amide groups improves the solubility. The modified DDP shows high
32:
493:"Near-infrared absorbing metal functionalized diketopyrrolopyrroles"
938:"Small Molecule Based Non-Fullerene Acceptors: A Comparative Study"
592:
Nielsen, Christian B.; Turbiez, Mathieu; McCulloch, Iain (2013).
112:
92:
24:
491:
Patil, Yuvraj; Shinde, Jivan; Misra, Rajneesh (2017-12-01).
138:
Surface
Coatings International Part B: Coatings Transactions
51:
applications, as well as components of materials for use in
452:
Popli, Charu; Patil, Yuvraj; Misra, Rajneesh (2018-12-13).
413:
Patil, Yuvraj; Popli, Charu; Misra, Rajneesh (2018-02-26).
71:
DPP dyes are based on the bicyclic heterocyclic compound
91:
DPP has high stability to heat but not very well to
936:Patil, Yuvraj; Misra, Rajneesh (September 2018).
983:Patil, Yuvraj; Misra, Rajneesh (2018-02-02).
834:Patil, Yuvraj; Misra, Rajneesh (2019-10-31).
8:
881:Patil, Yuvraj; Misra, Rajneesh (June 2020).
773:J. Macromol. Sci., Part A: Pure Appl. Chem
620:
62:
309:Angewandte Chemie International Edition
128:
536:European Journal of Organic Chemistry
458:European Journal of Organic Chemistry
7:
212:
210:
1306:Heterocyclic compounds with 2 rings
1239:Physical Chemistry Chemical Physics
1192:Physical Chemistry Chemical Physics
1153:The Journal of Physical Chemistry C
1106:Physical Chemistry Chemical Physics
497:Journal of Organometallic Chemistry
567:Asian Journal of Organic Chemistry
39:) due to their high resistance to
14:
1067:Journal of Materials Chemistry A
1028:Journal of Materials Chemistry A
840:Journal of Materials Chemistry C
509:10.1016/j.jorganchem.2017.10.014
83:applications and related uses.
79:performance was discovered for
757:10.1016/j.synthmet.2010.07.044
1:
729:10.1016/j.polymer.2009.12.044
701:10.1016/j.polymer.2010.09.046
364:Chemistry: A European Journal
113:polymer light emitting diodes
821:10.1016/j.dyepig.2011.01.005
785:10.1080/10601325.2010.511091
989:Chemistry: An Asian Journal
1332:
181:Advanced Optical Materials
119:, in organic solar cells.
31:based on the heterocyclic
1165:10.1021/acs.jpcc.5b12307
665:. Elsevier. 2018-03-29.
419:New Journal of Chemistry
262:Chemical Society Reviews
219:Chemical Communications
1001:10.1002/asia.201701493
613:10.1002/adma.201201795
579:10.1002/ajoc.201600194
548:10.1002/ejoc.201501123
470:10.1002/ejoc.201801072
376:10.1002/chem.202002851
321:10.1002/anie.202108293
193:10.1002/adom.201400559
68:
1283:Chem. Commun., 2012,
954:10.1002/tcr.201800037
899:10.1002/tcr.201900061
66:
17:Diketopyrrolopyrroles
751:(19–20): 2135–2142.
73:diketopyrrolopyrrole
1316:Organic electronics
1245:(33): 22999–23005.
1198:(25): 16950–16957.
1034:(26): 13625–13633.
942:The Chemical Record
887:The Chemical Record
846:(42): 13020–13031.
370:(66): 15109–15115.
315:(37): 20518–20527.
53:organic electronics
1251:10.1039/C6CP03767D
1204:10.1039/C6CP02700H
1118:10.1039/C7CP00231A
1079:10.1039/C6TA09607G
1040:10.1039/C7TA03322B
852:10.1039/C9TC03640G
601:Advanced Materials
431:10.1039/C7NJ05162J
274:10.1039/C4CS00248B
231:10.1039/C2CC17886A
150:10.1007/BF02699738
87:Optical properties
77:optical-electronic
69:
1159:(12): 6324–6335.
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779:(11): 1059–1068.
695:(24): 5726–5733.
672:978-0-12-809894-3
607:(13): 1859–1880.
464:(46): 6474–6481.
225:(25): 3039–3051.
103:and the emission
37:automotive paints
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1311:Fluorescent dyes
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101:fluorescence
90:
81:photovoltaic
70:
67:nomenclature
20:
16:
15:
1287:, 3039–3051
1295:Categories
123:References
105:wavelength
97:alkylation
49:bioimaging
1259:1463-9084
1212:1463-9084
1173:1932-7447
1126:1463-9084
1087:2050-7496
1048:2050-7496
923:209340212
907:1527-8999
868:203513134
860:2050-7534
809:Dyes Pigm
631:1521-4095
517:0022-328X
503:: 48–53.
478:105757956
439:1369-9261
400:220075391
384:0947-6539
345:235820925
329:1433-7851
282:1460-4744
239:1364-548X
201:2195-1071
158:1476-4865
109:thiophene
59:Structure
1267:27489031
1220:27292157
1134:28239736
1009:29219247
970:47012825
962:29888443
915:31833617
793:97899350
647:10575133
639:23008141
392:32589288
337:34258866
290:25186723
247:22343975
166:98773045
33:dilactam
29:pigments
1301:Lactams
717:Polymer
689:Polymer
117:sensors
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966:S2CID
919:S2CID
864:S2CID
789:S2CID
643:S2CID
597:(PDF)
474:S2CID
396:S2CID
341:S2CID
162:S2CID
1263:PMID
1255:ISSN
1216:PMID
1208:ISSN
1169:ISSN
1130:PMID
1122:ISSN
1083:ISSN
1044:ISSN
1005:PMID
958:PMID
911:PMID
903:ISSN
856:ISSN
667:ISBN
635:PMID
627:ISSN
540:2016
513:ISSN
462:2018
435:ISSN
388:PMID
380:ISSN
333:PMID
325:ISSN
286:PMID
278:ISSN
243:PMID
235:ISSN
197:ISSN
154:ISSN
93:acid
47:for
27:and
25:dyes
1247:doi
1200:doi
1161:doi
1157:120
1114:doi
1075:doi
1036:doi
997:doi
950:doi
895:doi
848:doi
817:doi
781:doi
753:doi
749:160
725:doi
697:doi
617:hdl
609:doi
575:doi
544:doi
505:doi
501:852
466:doi
427:doi
372:doi
317:doi
270:doi
227:doi
189:doi
146:doi
21:DPP
1297::
1285:48
1261:.
1253:.
1243:18
1241:.
1237:.
1214:.
1206:.
1196:18
1194:.
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