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   "text": "Bao, W. W. *et al.* Diketopyrrolopyrrole (DPP)-Based Materials and Its Applications: A Review. *Front. Chem.* **8**, 679 (2020).",
   "authors": "Bao, W. W.",
   "year": 2020,
   "journal": "Front. Chem.",
   "title": "*et al.* Diketopyrrolopyrrole (DPP)-Based Materials and Its Applications: A Review",
   "volume": "8",
   "pages": "679",
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    "doi_verificato": "10.3389/fchem.2020.00679",
    "url": "https://doi.org/10.3389/fchem.2020.00679",
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   "text": "Shaikh, S. A. L. *et al.* A minireview on diketopyrrolopyrrole chemistry: Historical perspective and recent developments. *Results Chem.* **4**, 100473 (2022).",
   "authors": "Shaikh, S. A. L.",
   "year": 2022,
   "journal": "Results Chem.",
   "title": "*et al.* A minireview on diketopyrrolopyrrole chemistry: Historical perspective and recent developments",
   "volume": "4",
   "pages": "100473",
   "doi": null,
   "url": null,
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    "doi_verificato": "10.1016/j.rechem.2022.100473",
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   "text": "Auwalu, M. A. & Cheng, S. Diketopyrrolopyrrole Fluorescent Probes, Photophysical and Biological Applications. *Chemosensors* **9**, 44 (2021).",
   "authors": "Auwalu, M. A. & Cheng, S.",
   "year": 2021,
   "journal": "Chemosensors",
   "title": "Diketopyrrolopyrrole Fluorescent Probes, Photophysical and Biological Applications",
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   "pages": "44",
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   "md_line": 1328,
   "text": "Zhang, B. *et al.* Diketopyrrolopyrrole-based fluorescent probe for visualizing over-expressed carboxylesterase in fever via ratiometric imaging. *Talanta* **266**, 124971 (2024).",
   "authors": "Zhang, B.",
   "year": 2024,
   "journal": "Talanta",
   "title": "*et al.* Diketopyrrolopyrrole-based fluorescent probe for visualizing over-expressed carboxylesterase in fever via ratiometric imaging",
   "volume": "266",
   "pages": "124971",
   "doi": null,
   "url": null,
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   "md_line": 1330,
   "text": "Iqbal, A. *et al.* The synthesis and properties of 1,4-diketo-pyrrolo[3,4-C]pyrroles. *Bull. Sociétés Chim. Belg.* **97**, 615–644 (1988).",
   "authors": "Iqbal, A.",
   "year": 1988,
   "journal": "Bull. Sociétés Chim. Belg.",
   "title": "*et al.* The synthesis and properties of 1,4-diketo-pyrrolo[3,4-C]pyrroles",
   "volume": "97",
   "pages": "615–644",
   "doi": null,
   "url": null,
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    "doi_verificato": "10.1002/bscb.19880970804",
    "url": "https://doi.org/10.1002/bscb.19880970804",
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   "anchor": "ref-6",
   "md_line": 1332,
   "text": "Sprake, J. M. & Watson, K. D. Addition products of 2-(N-arylformimidoyl)pyridines and carbanions, and their reduction to octahydroindolizine derivatives. *J. Chem. Soc. Perkin 1* 5 (1976) doi:10.1039/p19760000005.",
   "authors": "Sprake, J. M. & Watson, K. D.",
   "year": 1976,
   "journal": "J. Chem. Soc. Perkin 1",
   "title": "Addition products of 2-(N-arylformimidoyl)pyridines and carbanions, and their reduction to octahydroindolizine derivatives",
   "volume": null,
   "pages": null,
   "doi": "10.1039/p19760000005",
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    "doi_verificato": "10.1039/p19760000005",
    "url": "https://doi.org/10.1039/p19760000005",
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   "text": "Grzybowski, M. & Gryko, D. T. Diketopyrrolopyrroles: Synthesis, Reactivity, and Optical Properties. *Adv. Opt. Mater.* **3**, 280–320 (2015).",
   "authors": "Grzybowski, M. & Gryko, D. T.",
   "year": 2015,
   "journal": "Adv. Opt. Mater.",
   "title": "Diketopyrrolopyrroles: Synthesis, Reactivity, and Optical Properties",
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   "pages": "280–320",
   "doi": null,
   "url": null,
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    "doi_verificato": "10.1002/adom.201400559",
    "url": "https://doi.org/10.1002/adom.201400559",
    "oa_url": null,
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   "id": 8,
   "anchor": "ref-8",
   "md_line": 1336,
   "text": "Closs, F. & Gompper, R. 2,5-Diazapentalenes. *Angew. Chem. Int. Ed. Engl.* **26**, 552–554 (1987).",
   "authors": "Closs, F. & Gompper, R.",
   "year": 1987,
   "journal": "Angew. Chem. Int. Ed. Engl.",
   "title": "2,5-Diazapentalenes",
   "volume": "26",
   "pages": "552–554",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
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   "fonte": {
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    "stato": "verificata",
    "doi_verificato": "10.1002/anie.198705521",
    "url": "https://doi.org/10.1002/anie.198705521",
    "oa_url": null,
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   "id": 9,
   "anchor": "ref-9",
   "md_line": 1338,
   "text": "Stas, S., Sergeyev, S. & Geerts, Y. Synthesis of diketopyrrolopyrrole (DPP) derivatives comprising bithiophene moieties. *Tetrahedron* **66**, 1837–1845 (2010).",
   "authors": "Stas, S., Sergeyev, S. & Geerts, Y.",
   "year": 2010,
   "journal": "Tetrahedron",
   "title": "Synthesis of diketopyrrolopyrrole (DPP) derivatives comprising bithiophene moieties",
   "volume": "66",
   "pages": "1837–1845",
   "doi": null,
   "url": null,
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   ],
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   "fonte": {
    "file": "fonti/09-stas-2010.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.tet.2010.01.027",
    "url": "https://doi.org/10.1016/j.tet.2010.01.027",
    "oa_url": null,
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  },
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   "id": 10,
   "anchor": "ref-10",
   "md_line": 1340,
   "text": "Avcıbaşi, N. *et al.* Synthesis and in vitro evaluation of dioxopyrrolopyrroles as potential low-affinity fluorescent Ca<sup>2+</sup> indicators. *Int. J. Photoenergy* **6**, 159–167 (2004).",
   "authors": "Avcıbaşi, N.",
   "year": 2004,
   "journal": "Int. J. Photoenergy",
   "title": "*et al.* Synthesis and in vitro evaluation of dioxopyrrolopyrroles as potential low-affinity fluorescent Ca<sup>2+</sup> indicators",
   "volume": "6",
   "pages": "159–167",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    180
   ],
   "cited_in_sections": [
    "1.1.1"
   ],
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   "fonte": {
    "file": "fonti/10-avcbasi-2004.md",
    "stato": "verificata",
    "doi_verificato": "10.1155/s1110662x04000200",
    "url": "https://doi.org/10.1155/s1110662x04000200",
    "oa_url": "https://downloads.hindawi.com/journals/ijp/2004/941913.pdf",
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   }
  },
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   "id": 11,
   "anchor": "ref-11",
   "md_line": 1342,
   "text": "Riggs, R. L. *et al.* Synthetic studies related to diketopyrrolopyrrole (DPP) pigments. Part 3: Syntheses of tri- and tetra-aryl DPPs. *Tetrahedron* **61**, 11230–11243 (2005).",
   "authors": "Riggs, R. L.",
   "year": 2005,
   "journal": "Tetrahedron",
   "title": "*et al.* Synthetic studies related to diketopyrrolopyrrole (DPP) pigments. Part 3: Syntheses of tri- and tetra-aryl DPPs",
   "volume": "61",
   "pages": "11230–11243",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    180
   ],
   "cited_in_sections": [
    "1.1.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/11-riggs-2005.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.tet.2005.09.005",
    "url": "https://doi.org/10.1016/j.tet.2005.09.005",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
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   "id": 12,
   "anchor": "ref-12",
   "md_line": 1344,
   "text": "Qian, G. & Wang, Z. Y. Near-Infrared Thermochromic Diazapentalene Dyes. *Adv. Mater.* **24**, 1582–1588 (2012).",
   "authors": "Qian, G. & Wang, Z. Y.",
   "year": 2012,
   "journal": "Adv. Mater.",
   "title": "Near-Infrared Thermochromic Diazapentalene Dyes",
   "volume": "24",
   "pages": "1582–1588",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    180
   ],
   "cited_in_sections": [
    "1.1.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/12-qian-2012.md",
    "stato": "verificata",
    "doi_verificato": "10.1002/adma.201104711",
    "url": "https://doi.org/10.1002/adma.201104711",
    "oa_url": null,
    "accesso": "closed",
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   "id": 13,
   "anchor": "ref-13",
   "md_line": 1346,
   "text": "Langhals, H., Grundei, T., Potrawa, T. & Polborn, K. Highly Photostable Organic Fluorescent Pigments – A Simple Synthesis of *N* -Arylpyrrolopyrrolediones (DPP). *Liebigs Ann.* **1996**, 679–682 (1996).",
   "authors": "Langhals, H., Grundei, T., Potrawa, T. & Polborn, K.",
   "year": 1996,
   "journal": "N",
   "title": "Highly Photostable Organic Fluorescent Pigments – A Simple Synthesis of",
   "volume": "1996",
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    182
   ],
   "cited_in_sections": [
    "1.1.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/13-langhals-1996.md",
    "stato": "verificata",
    "doi_verificato": "10.1002/jlac.199619960506",
    "url": "https://doi.org/10.1002/jlac.199619960506",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 14,
   "anchor": "ref-14",
   "md_line": 1348,
   "text": "De Luca, L., Giacomelli, G. & Porcheddu, A. A Mild and Efficient Alternative to the Classical Swern Oxidation. *J. Org. Chem.* **66**, 7907–7909 (2001).",
   "authors": "De Luca, L., Giacomelli, G. & Porcheddu, A.",
   "year": 2001,
   "journal": "J. Org. Chem.",
   "title": "A Mild and Efficient Alternative to the Classical Swern Oxidation",
   "volume": "66",
   "pages": "7907–7909",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    184
   ],
   "cited_in_sections": [
    "1.1.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/14-de-luca-2001.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/jo015935s",
    "url": "https://doi.org/10.1021/jo015935s",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
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   "id": 15,
   "anchor": "ref-15",
   "md_line": 1350,
   "text": "Harris, J. M., Liu, Y., Chai, S., Andrews, M. D. & Vederas, J. C. Modification of the Swern Oxidation: Use of a Soluble Polymer-Bound, Recyclable, and Odorless Sulfoxide. *J. Org. Chem.* **63**, 2407–2409 (1998).",
   "authors": "Harris, J. M., Liu, Y., Chai, S., Andrews, M. D. & Vederas, J. C.",
   "year": 1998,
   "journal": "J. Org. Chem.",
   "title": "Modification of the Swern Oxidation: Use of a Soluble Polymer-Bound, Recyclable, and Odorless Sulfoxide",
   "volume": "63",
   "pages": "2407–2409",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    184
   ],
   "cited_in_sections": [
    "1.1.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/15-harris-1998.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/jo972304i",
    "url": "https://doi.org/10.1021/jo972304i",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 16,
   "anchor": "ref-16",
   "md_line": 1352,
   "text": "Mizuguchi, J., Grubenmann, A., Wooden, G. & Rihs, G. Structures of 3,6-diphenylpyrrolo[3,4- *c* ]pyrrole-1,4-dione and 2,5-dimethyl-3,6-diphenylpyrrolo[3,4- *c* ]pyrrole-1,4-dione. *Acta Crystallogr. B* **48**, 696–700 (1992).",
   "authors": "Mizuguchi, J., Grubenmann, A., Wooden, G. & Rihs, G.",
   "year": 1992,
   "journal": "c",
   "title": "Structures of 3,6-diphenylpyrrolo[3,4-",
   "volume": "48",
   "pages": "696–700",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    205,
    243
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/16-mizuguchi-1992.md",
    "stato": "identificata_manualmente",
    "doi_verificato": "10.1107/S0108768192003033",
    "url": "https://doi.org/10.1107/S0108768192003033",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
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  },
  {
   "id": 17,
   "anchor": "ref-17",
   "md_line": 1354,
   "text": "David, J., Weiter, M., Vala, M., Vyňuchal, J. & Kučerík, J. Stability and structural aspects of diketopyrrolopyrrole pigment and its N-alkyl derivatives. *Dyes Pigments* **89**, 137–143 (2011).",
   "authors": "David, J., Weiter, M., Vala, M., Vyňuchal, J. & Kučerík, J.",
   "year": 2011,
   "journal": "Dyes Pigments",
   "title": "Stability and structural aspects of diketopyrrolopyrrole pigment and its N-alkyl derivatives",
   "volume": "89",
   "pages": "137–143",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    205
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/17-david-2011.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.dyepig.2010.10.001",
    "url": "https://doi.org/10.1016/j.dyepig.2010.10.001",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 18,
   "anchor": "ref-18",
   "md_line": 1356,
   "text": "Mizuguchi, J. & Wooden, G. A Large Bathochromic Shift from the Solution to the Solid State in 1,4-Diketo-3,6-Diphenyl-Pyrrolo-[3,4-c]-Pyrrole. *Berichte Bunsenges. Für Phys. Chem.* **95**, 1264–1274 (1991).",
   "authors": "Mizuguchi, J. & Wooden, G.",
   "year": 1991,
   "journal": "Berichte Bunsenges. Für Phys. Chem.",
   "title": "A Large Bathochromic Shift from the Solution to the Solid State in 1,4-Diketo-3,6-Diphenyl-Pyrrolo-[3,4-c]-Pyrrole",
   "volume": "95",
   "pages": "1264–1274",
   "doi": null,
   "url": null,
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    207
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   "fonte": {
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    "stato": "verificata",
    "doi_verificato": "10.1002/bbpc.19910951016",
    "url": "https://doi.org/10.1002/bbpc.19910951016",
    "oa_url": null,
    "accesso": "closed",
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   "id": 19,
   "anchor": "ref-19",
   "md_line": 1358,
   "text": "Luňák, S., Vyňuchal, J., Vala, M., Havel, L. & Hrdina, R. The synthesis, absorption and fluorescence of polar diketo-pyrrolo-pyrroles. *Dyes Pigments* **82**, 102–108 (2009).",
   "authors": "Luňák, S., Vyňuchal, J., Vala, M., Havel, L. & Hrdina, R.",
   "year": 2009,
   "journal": "Dyes Pigments",
   "title": "The synthesis, absorption and fluorescence of polar diketo-pyrrolo-pyrroles",
   "volume": "82",
   "pages": "102–108",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    215
   ],
   "cited_in_sections": [
    "1.1.2"
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   "fonte": {
    "file": "fonti/19-lunak-2009.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.dyepig.2008.12.001",
    "url": "https://doi.org/10.1016/j.dyepig.2008.12.001",
    "oa_url": null,
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  {
   "id": 20,
   "anchor": "ref-20",
   "md_line": 1360,
   "text": "Lenz, R. DPP chemistry- Continuous innovation.",
   "authors": "Lenz, R.",
   "year": null,
   "journal": null,
   "title": "DPP chemistry- Continuous innovation",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    219,
    233,
    239
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [
    "incomplete_in_source"
   ],
   "fonte": {
    "file": "fonti/20-lenz-2002.md",
    "stato": "verificata",
    "doi_verificato": "10.1007/bf02699738",
    "url": "https://doi.org/10.1007/bf02699738",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 21,
   "anchor": "ref-21",
   "md_line": 1362,
   "text": "Colonna, G., Pilati, T., Rusconi, F. & Zecchi, G. Synthesis and properties of some new N,N′-disubstituted 2,5-dihydro-1,4-dioxo-3,6-diphenylpyrrolo[3,4-c]pyrroles. *Dyes Pigments* **75**, 125–129 (2007).",
   "authors": "Colonna, G., Pilati, T., Rusconi, F. & Zecchi, G.",
   "year": 2007,
   "journal": "Dyes Pigments",
   "title": "Synthesis and properties of some new N,N′-disubstituted 2,5-dihydro-1,4-dioxo-3,6-diphenylpyrrolo[3,4-c]pyrroles",
   "volume": "75",
   "pages": "125–129",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    269
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/21-colonna-2007.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.dyepig.2006.05.024",
    "url": "https://doi.org/10.1016/j.dyepig.2006.05.024",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 22,
   "anchor": "ref-22",
   "md_line": 1364,
   "text": "Zambounis, J. S. & Iqbal, A. 54) PYRROLO(3,4-CIPYRROLES.",
   "authors": "Zambounis, J. S. & Iqbal, A.",
   "year": null,
   "journal": null,
   "title": "Pyrrolo(3,4-cipyrroles",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    273
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [
    "incomplete_in_source",
    "stray_text_in_source"
   ],
   "fonte": {
    "file": "fonti/22-zambounis-nd.md",
    "stato": "candidata",
    "doi_verificato": null,
    "url": "https://patents.google.com/patent/US5484943A/en",
    "oa_url": "https://patents.google.com/patent/US5484943A/en",
    "accesso": null,
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 23,
   "anchor": "ref-23",
   "md_line": 1366,
   "text": "Yue, W., Suraru, S., Bialas, D., Müller, M. & Würthner, F. Synthesis and Properties of a New Class of Fully Conjugated Azahexacene Analogues. *Angew. Chem. Int. Ed.* **53**, 6159–6162 (2014).",
   "authors": "Yue, W., Suraru, S., Bialas, D., Müller, M. & Würthner, F.",
   "year": 2014,
   "journal": "Angew. Chem. Int. Ed.",
   "title": "Synthesis and Properties of a New Class of Fully Conjugated Azahexacene Analogues",
   "volume": "53",
   "pages": "6159–6162",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    279,
    281
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/23-yue-2014.md",
    "stato": "verificata",
    "doi_verificato": "10.1002/anie.201403227",
    "url": "https://doi.org/10.1002/anie.201403227",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 24,
   "anchor": "ref-24",
   "md_line": 1368,
   "text": "Zambounis, J. S., Hao, Z. & Iqbal, A. Latent pigments activated by heat. *Nature* **388**, 131–132 (1997).",
   "authors": "Zambounis, J. S., Hao, Z. & Iqbal, A.",
   "year": 1997,
   "journal": "Nature",
   "title": "Latent pigments activated by heat",
   "volume": "388",
   "pages": "131–132",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    279
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/24-zambounis-1997.md",
    "stato": "verificata",
    "doi_verificato": "10.1038/40532",
    "url": "https://doi.org/10.1038/40532",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 25,
   "anchor": "ref-25",
   "md_line": 1370,
   "text": "Tieke, B., Rabindranath, A. R., Zhang, K. & Zhu, Y. Conjugated polymers containing diketopyrrolopyrrole units in the main chain. *Beilstein J. Org. Chem.* **6**, 830–845 (2010).",
   "authors": "Tieke, B., Rabindranath, A. R., Zhang, K. & Zhu, Y.",
   "year": 2010,
   "journal": "Beilstein J. Org. Chem.",
   "title": "Conjugated polymers containing diketopyrrolopyrrole units in the main chain",
   "volume": "6",
   "pages": "830–845",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    327
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/25-tieke-2010.md",
    "stato": "verificata",
    "doi_verificato": "10.3762/bjoc.6.92",
    "url": "https://doi.org/10.3762/bjoc.6.92",
    "oa_url": "https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-6-92.pdf",
    "accesso": "diamond",
    "contenuto_letto": "full_text"
   }
  },
  {
   "id": 26,
   "anchor": "ref-26",
   "md_line": 1372,
   "text": "Li, Y., Sonar, P., Murphy, L. & Hong, W. High mobility diketopyrrolopyrrole (DPP)-based organic semiconductor materials for organic thin film transistors and photovoltaics. *Energy Environ. Sci.* **6**, 1684 (2013).",
   "authors": "Li, Y., Sonar, P., Murphy, L. & Hong, W.",
   "year": 2013,
   "journal": "Energy Environ. Sci.",
   "title": "High mobility diketopyrrolopyrrole (DPP)-based organic semiconductor materials for organic thin film transistors and photovoltaics",
   "volume": "6",
   "pages": "1684",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    327
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/26-li-2013.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/c3ee00015j",
    "url": "https://doi.org/10.1039/c3ee00015j",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 27,
   "anchor": "ref-27",
   "md_line": 1374,
   "text": "McGlacken, G. P. & Bateman, L. M. Recent advances in aryl–aryl bond formation by direct arylation. *Chem. Soc. Rev.* **38**, 2447 (2009).",
   "authors": "McGlacken, G. P. & Bateman, L. M.",
   "year": 2009,
   "journal": "Chem. Soc. Rev.",
   "title": "Recent advances in aryl–aryl bond formation by direct arylation",
   "volume": "38",
   "pages": "2447",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    331,
    333
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/27-mcglacken-2009.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/b805701j",
    "url": "https://doi.org/10.1039/b805701j",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 28,
   "anchor": "ref-28",
   "md_line": 1376,
   "text": "Han, W. & Ofial, A. No Detours: Palladium-Catalyzed Oxidative C-H/C-H Cross-Couplings of Heteroarenes. *Synlett* **2011**, 1951–1955 (2011).",
   "authors": "Han, W. & Ofial, A.",
   "year": 2011,
   "journal": "Synlett",
   "title": "No Detours: Palladium-Catalyzed Oxidative C-H/C-H Cross-Couplings of Heteroarenes",
   "volume": "2011",
   "pages": "1951–1955",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    331,
    347
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/28-ofial-2011.md",
    "stato": "verificata",
    "doi_verificato": "10.1055/s-0030-1260941",
    "url": "https://doi.org/10.1055/s-0030-1260941",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 29,
   "anchor": "ref-29",
   "md_line": 1378,
   "text": "Liu, S.-Y. *et al.* C–H activation: making diketopyrrolopyrrole derivatives easily accessible. *J. Mater. Chem. A* **1**, 2795 (2013).",
   "authors": "Liu, S.-Y.",
   "year": 2013,
   "journal": "J. Mater. Chem. A",
   "title": "*et al.* C–H activation: making diketopyrrolopyrrole derivatives easily accessible",
   "volume": "1",
   "pages": "2795",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    339
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/29-liu-2013.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/c2ta01318e",
    "url": "https://doi.org/10.1039/c2ta01318e",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 30,
   "anchor": "ref-30",
   "md_line": 1380,
   "text": "Hong, W. *et al.* A conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors. *Chem. Commun.* **48**, 8413 (2012).",
   "authors": "Hong, W.",
   "year": 2012,
   "journal": "Chem. Commun.",
   "title": "*et al.* A conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors",
   "volume": "48",
   "pages": "8413",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    363
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/30-hong-2012.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/c2cc33998f",
    "url": "https://doi.org/10.1039/c2cc33998f",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 31,
   "anchor": "ref-31",
   "md_line": 1382,
   "text": "Bürckstümmer, H., Weissenstein, A., Bialas, D. & Würthner, F. Synthesis and Characterization of Optical and Redox Properties of Bithiophene-Functionalized Diketopyrrolopyrrole Chromophores. *J. Org. Chem.* **76**, 2426–2432 (2011).",
   "authors": "Bürckstümmer, H., Weissenstein, A., Bialas, D. & Würthner, F.",
   "year": 2011,
   "journal": "J. Org. Chem.",
   "title": "Synthesis and Characterization of Optical and Redox Properties of Bithiophene-Functionalized Diketopyrrolopyrrole Chromophores",
   "volume": "76",
   "pages": "2426–2432",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    363
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/31-burckstummer-2011.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/jo2003117",
    "url": "https://doi.org/10.1021/jo2003117",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 32,
   "anchor": "ref-32",
   "md_line": 1384,
   "text": "Hu, X. *et al.* Incorporation of ester groups into low band-gap diketopyrrolopyrrole containing polymers for solar cell applications. *J. Mater. Chem.* **22**, 15710 (2012).",
   "authors": "Hu, X.",
   "year": 2012,
   "journal": "J. Mater. Chem.",
   "title": "*et al.* Incorporation of ester groups into low band-gap diketopyrrolopyrrole containing polymers for solar cell applications",
   "volume": "22",
   "pages": "15710",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    363
   ],
   "cited_in_sections": [
    "1.1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/32-hu-2012.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/c2jm31700a",
    "url": "https://doi.org/10.1039/c2jm31700a",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 33,
   "anchor": "ref-33",
   "md_line": 1386,
   "text": "Valeur, B. & Berberan-Santos, M. N. A Brief History of Fluorescence and Phosphorescence before the Emergence of Quantum Theory. *J. Chem. Educ.* **88**, 731–738 (2011).",
   "authors": "Valeur, B. & Berberan-Santos, M. N.",
   "year": 2011,
   "journal": "J. Chem. Educ.",
   "title": "A Brief History of Fluorescence and Phosphorescence before the Emergence of Quantum Theory",
   "volume": "88",
   "pages": "731–738",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    380
   ],
   "cited_in_sections": [
    "1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/33-valeur-2011.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/ed100182h",
    "url": "https://doi.org/10.1021/ed100182h",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 34,
   "anchor": "ref-34",
   "md_line": 1388,
   "text": "Lakowicz, J. R. Introduction to Fluorescence. in *Principles of Fluorescence Spectroscopy* (ed. Lakowicz, J. R.) 1–23 (Springer US, Boston, MA, 1999). doi:10.1007/978-1-4757-3061-6_1.",
   "authors": "Lakowicz, J. R.",
   "year": 1999,
   "journal": "Principles of Fluorescence Spectroscopy",
   "title": "Introduction to Fluorescence",
   "volume": null,
   "pages": null,
   "doi": "10.1007/978-1-4757-3061-6_1",
   "url": null,
   "cited_in_md_lines": [
    386,
    413,
    445,
    474
   ],
   "cited_in_sections": [
    "1.2",
    "1.2.2",
    "1.2.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/34-lakowicz-1999.md",
    "stato": "verificata",
    "doi_verificato": "10.1007/978-1-4757-3061-6_1",
    "url": "https://doi.org/10.1007/978-1-4757-3061-6_1",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 35,
   "anchor": "ref-35",
   "md_line": 1390,
   "text": "Kasha, M. Characterization of electronic transitions in complex molecules. *Discuss. Faraday Soc.* **9**, 14 (1950).",
   "authors": "Kasha, M.",
   "year": 1950,
   "journal": "Discuss. Faraday Soc.",
   "title": "Characterization of electronic transitions in complex molecules",
   "volume": "9",
   "pages": "14",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    398
   ],
   "cited_in_sections": [
    "1.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/35-kasha-1950.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/df9500900014",
    "url": "https://doi.org/10.1039/df9500900014",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 36,
   "anchor": "ref-36",
   "md_line": 1392,
   "text": "On the Change of Refrangibility of Light.",
   "authors": null,
   "year": null,
   "journal": null,
   "title": "On the Change of Refrangibility of Light",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    420
   ],
   "cited_in_sections": [
    "1.2.1"
   ],
   "quality_flags": [
    "incomplete_in_source",
    "authors_unparsed"
   ],
   "fonte": {
    "file": "fonti/36-stokes-1852.md",
    "stato": "identificata_manualmente",
    "doi_verificato": "10.1098/rstl.1852.0022",
    "url": "https://doi.org/10.1098/rstl.1852.0022",
    "oa_url": "https://www.archive.org/download/jstor-108550/108550.pdf",
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 37,
   "anchor": "ref-37",
   "md_line": 1394,
   "text": "Prodi, L. & Credi, A. Spectrofluorimetry. in *The Exploration of Supramolecular Systems and Nanostructures by Photochemical Techniques* (ed. Ceroni, P.) vol. 78 97–129 (Springer Netherlands, Dordrecht, 2012).",
   "authors": "Prodi, L. & Credi, A.",
   "year": 2012,
   "journal": "The Exploration of Supramolecular Systems and Nanostructures by Photochemical Techniques",
   "title": "Spectrofluorimetry",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    424
   ],
   "cited_in_sections": [
    "1.2.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/37-prodi-2011.md",
    "stato": "verificata_con_correzioni",
    "doi_verificato": "10.1007/978-94-007-2042-8_5",
    "url": "https://doi.org/10.1007/978-94-007-2042-8_5",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 38,
   "anchor": "ref-38",
   "md_line": 1396,
   "text": "Brouwer, A. M. Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report). *Pure Appl. Chem.* **83**, 2213–2228 (2011).",
   "authors": "Brouwer, A. M.",
   "year": 2011,
   "journal": "Pure Appl. Chem.",
   "title": "Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report)",
   "volume": "83",
   "pages": "2213–2228",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    445
   ],
   "cited_in_sections": [
    "1.2.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/38-brouwer-2011.md",
    "stato": "verificata",
    "doi_verificato": "10.1351/pac-rep-10-09-31",
    "url": "https://doi.org/10.1351/pac-rep-10-09-31",
    "oa_url": "https://www.degruyter.com/document/doi/10.1351/PAC-REP-10-09-31/pdf",
    "accesso": "bronze",
    "contenuto_letto": "full_text"
   }
  },
  {
   "id": 39,
   "anchor": "ref-39",
   "md_line": 1398,
   "text": "Weber, G. & Teale, F. W. J. Determination of the absolute quantum yield of fluorescent solutions. *Trans. Faraday Soc.* **53**, 646 (1957).",
   "authors": "Weber, G. & Teale, F. W. J.",
   "year": 1957,
   "journal": "Trans. Faraday Soc.",
   "title": "Determination of the absolute quantum yield of fluorescent solutions",
   "volume": "53",
   "pages": "646",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    445
   ],
   "cited_in_sections": [
    "1.2.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/39-weber-1957.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/tf9575300646",
    "url": "https://doi.org/10.1039/tf9575300646",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 40,
   "anchor": "ref-40",
   "md_line": 1400,
   "text": "Stoddart, J. F. Chapter 12. Host–guest chemistry. *Annu. Rep. Sect. B Org. Chem.* **85**, 353–386 (1988).",
   "authors": "Stoddart, J. F.",
   "year": 1988,
   "journal": "Annu. Rep. Sect. B Org. Chem.",
   "title": "Chapter 12. Host–guest chemistry",
   "volume": "85",
   "pages": "353–386",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    491
   ],
   "cited_in_sections": [
    "1.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/40-stoddart-1988.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/oc9888500353",
    "url": "https://doi.org/10.1039/oc9888500353",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 41,
   "anchor": "ref-41",
   "md_line": 1402,
   "text": "Valdés, C., Toledo, L. M., Spitz, U. & Rebek, J. Structure and Selectivity of a Small Dimeric Encapsulating Assembly. *Chem. – Eur. J.* **2**, 989–991 (1996).",
   "authors": "Valdés, C., Toledo, L. M., Spitz, U. & Rebek, J.",
   "year": 1996,
   "journal": "Chem. – Eur. J.",
   "title": "Structure and Selectivity of a Small Dimeric Encapsulating Assembly",
   "volume": "2",
   "pages": "989–991",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    491
   ],
   "cited_in_sections": [
    "1.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/41-valdes-1996.md",
    "stato": "verificata",
    "doi_verificato": "10.1002/chem.19960020814",
    "url": "https://doi.org/10.1002/chem.19960020814",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 42,
   "anchor": "ref-42",
   "md_line": 1404,
   "text": "Wang, K. *et al.* Highly fluorescent polycaprolactones decorated with di(thiophene-2-yl)-diketopyrrolopyrrole: A covalent strategy of tuning fluorescence properties in solid states. *J. Polym. Sci. Part Polym. Chem.* **53**, 1032–1042 (2015).",
   "authors": "Wang, K.",
   "year": 2015,
   "journal": "J. Polym. Sci. Part Polym. Chem.",
   "title": "*et al.* Highly fluorescent polycaprolactones decorated with di(thiophene-2-yl)-diketopyrrolopyrrole: A covalent strategy of tuning fluorescence properties in solid states",
   "volume": "53",
   "pages": "1032–1042",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    493
   ],
   "cited_in_sections": [
    "1.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/42-wang-2015.md",
    "stato": "verificata",
    "doi_verificato": "10.1002/pola.27531",
    "url": "https://doi.org/10.1002/pola.27531",
    "oa_url": "https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/pola.27531",
    "accesso": "bronze",
    "contenuto_letto": "abstract_only"
   }
  },
  {
   "id": 43,
   "anchor": "ref-43",
   "md_line": 1406,
   "text": "Lee, J.-K. *et al.* Light-emitting properties of PMMA-based new side chain polymers. *Synth. Met.* **111–112**, 489–491 (2000).",
   "authors": "Lee, J.-K.",
   "year": 2000,
   "journal": "Synth. Met.",
   "title": "*et al.* Light-emitting properties of PMMA-based new side chain polymers",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    495
   ],
   "cited_in_sections": [
    "1.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/43-lee-2000.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/s0379-6779(99)00425-7",
    "url": "https://doi.org/10.1016/s0379-6779(99)00425-7",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "no"
   }
  },
  {
   "id": 44,
   "anchor": "ref-44",
   "md_line": 1408,
   "text": "Bao, W. W. *et al.* Diketopyrrolopyrrole (DPP)-Based Materials and Its Applications: A Review. *Front. Chem.* **8**, 679 (2020).",
   "authors": "Bao, W. W.",
   "year": 2020,
   "journal": "Front. Chem.",
   "title": "*et al.* Diketopyrrolopyrrole (DPP)-Based Materials and Its Applications: A Review",
   "volume": "8",
   "pages": "679",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    504,
    532
   ],
   "cited_in_sections": [
    "1.4"
   ],
   "quality_flags": [
    "duplicate_entry"
   ],
   "duplicate_of": 1,
   "fonte": {
    "file": "fonti/44-bao-2020.md",
    "stato": "verificata",
    "doi_verificato": "10.3389/fchem.2020.00679",
    "url": "https://doi.org/10.3389/fchem.2020.00679",
    "oa_url": "https://www.frontiersin.org/articles/10.3389/fchem.2020.00679/pdf",
    "accesso": "gold",
    "contenuto_letto": "full_text"
   }
  },
  {
   "id": 45,
   "anchor": "ref-45",
   "md_line": 1410,
   "text": "Ostroverkhova, O. Organic Optoelectronic Materials: Mechanisms and Applications. *Chem. Rev.* **116**, 13279–13412 (2016).",
   "authors": "Ostroverkhova, O.",
   "year": 2016,
   "journal": "Chem. Rev.",
   "title": "Organic Optoelectronic Materials: Mechanisms and Applications",
   "volume": "116",
   "pages": "13279–13412",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    512,
    532,
    538
   ],
   "cited_in_sections": [
    "1.4"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/45-ostroverkhova-2016.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/acs.chemrev.6b00127",
    "url": "https://doi.org/10.1021/acs.chemrev.6b00127",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 46,
   "anchor": "ref-46",
   "md_line": 1412,
   "text": "Nowsherwan, G. A. *et al.* Advances in Organic Materials for Next-Generation Optoelectronics: Potential and Challenges. *Organics* **5**, 520–560 (2024).",
   "authors": "Nowsherwan, G. A.",
   "year": 2024,
   "journal": "Organics",
   "title": "*et al.* Advances in Organic Materials for Next-Generation Optoelectronics: Potential and Challenges",
   "volume": "5",
   "pages": "520–560",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    514
   ],
   "cited_in_sections": [
    "1.4"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/46-nowsherwan-2024.md",
    "stato": "verificata",
    "doi_verificato": "10.3390/org5040028",
    "url": "https://doi.org/10.3390/org5040028",
    "oa_url": "https://doi.org/10.3390/org5040028",
    "accesso": "gold",
    "contenuto_letto": "abstract_only"
   }
  },
  {
   "id": 47,
   "anchor": "ref-47",
   "md_line": 1414,
   "text": "Li, Y. Diketopyrrolopyrrole-Based Conjugated Polymers for Organic Electronics. https://doi.org/10.1021/ar500252u (2014) doi:10.1021/ar500252u.",
   "authors": "Li, Y.",
   "year": 2014,
   "journal": null,
   "title": "Diketopyrrolopyrrole-Based Conjugated Polymers for Organic Electronics",
   "volume": null,
   "pages": null,
   "doi": "10.1021/ar500252u",
   "url": "https://doi.org/10.1021/ar500252u",
   "cited_in_md_lines": [
    516
   ],
   "cited_in_sections": [
    "1.4"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/47-li-2014.md",
    "stato": "non_risolta",
    "doi_verificato": null,
    "url": null,
    "oa_url": null,
    "accesso": null,
    "contenuto_letto": "no"
   }
  },
  {
   "id": 48,
   "anchor": "ref-48",
   "md_line": 1416,
   "text": "Kroon, R. Small Bandgap Polymers for Organic Solar Cells (Polymer Material Development in the Last 5 Years). https://doi.org/10.1080/15583724.2015.1121853 doi:10.1080/15583724.2015.1121853.",
   "authors": "Kroon, R.",
   "year": null,
   "journal": null,
   "title": "Small Bandgap Polymers for Organic Solar Cells (Polymer Material Development in the Last 5 Years)",
   "volume": null,
   "pages": null,
   "doi": "10.1080/15583724.2015.1121853",
   "url": "https://doi.org/10.1080/15583724.2015.1121853",
   "cited_in_md_lines": [
    516
   ],
   "cited_in_sections": [
    "1.4"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/48-kroon-2008.md",
    "stato": "verificata_con_correzioni",
    "doi_verificato": "10.1080/15583720802231833",
    "url": "https://doi.org/10.1080/15583720802231833",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 49,
   "anchor": "ref-49",
   "md_line": 1418,
   "text": "Hendriks, K. H. Diketopyrrolopyrrole-Based Polymers for High-Efficiency Organic Solar Cells. https://doi.org/10.1039/c3ta11429c (2013) doi:10.1039/c3ta11429c.",
   "authors": "Hendriks, K. H.",
   "year": 2013,
   "journal": null,
   "title": "Diketopyrrolopyrrole-Based Polymers for High-Efficiency Organic Solar Cells",
   "volume": null,
   "pages": null,
   "doi": "10.1039/c3ta11429c",
   "url": "https://doi.org/10.1039/c3ta11429c",
   "cited_in_md_lines": [
    516,
    518
   ],
   "cited_in_sections": [
    "1.4"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/49-hendriks-2013.md",
    "stato": "non_risolta",
    "doi_verificato": null,
    "url": null,
    "oa_url": null,
    "accesso": null,
    "contenuto_letto": "no"
   }
  },
  {
   "id": 50,
   "anchor": "ref-50",
   "md_line": 1420,
   "text": "Cardona, C. M., Li, W., Kaifer, A. E., Stockdale, D. & Bazan, G. C. Electrochemical Considerations for Determining Absolute Frontier Orbital Energy Levels of Conjugated Polymers for Solar Cell Applications. *Adv. Mater.* **23**, 2367–2371 (2011).",
   "authors": "Cardona, C. M., Li, W., Kaifer, A. E., Stockdale, D. & Bazan, G. C.",
   "year": 2011,
   "journal": "Adv. Mater.",
   "title": "Electrochemical Considerations for Determining Absolute Frontier Orbital Energy Levels of Conjugated Polymers for Solar Cell Applications",
   "volume": "23",
   "pages": "2367–2371",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    706
   ],
   "cited_in_sections": [
    "3.4"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/50-cardona-2011.md",
    "stato": "verificata",
    "doi_verificato": "10.1002/adma.201004554",
    "url": "https://doi.org/10.1002/adma.201004554",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 51,
   "anchor": "ref-51",
   "md_line": 1422,
   "text": "Scurti, S. *et al.* Symmetric azobenzene-substituted diketopyrrolopyrroles dyes as acid-base switchable molecular-probe for colorimetric paper-based sensors. *Dyes Pigments* **245**, 113288 (2026).",
   "authors": "Scurti, S.",
   "year": 2026,
   "journal": "Dyes Pigments",
   "title": "Symmetric azobenzene-substituted diketopyrrolopyrroles dyes as acid-base switchable molecular-probe for colorimetric paper-based sensors",
   "volume": "245",
   "pages": "113288",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    722
   ],
   "cited_in_sections": [
    "4.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/51-scurti-2026.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.dyepig.2025.113288",
    "url": "https://doi.org/10.1016/j.dyepig.2025.113288",
    "oa_url": "https://doi.org/10.1016/j.dyepig.2025.113288",
    "accesso": "hybrid",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 52,
   "anchor": "ref-52",
   "md_line": 1424,
   "text": "Wang, L. *et al.* Robust singlet fission process in strong absorption π-expanded diketopyrrolopyrroles. *Chem. Sci.* **13**, 13907–13913 (2022).",
   "authors": "Wang, L.",
   "year": 2022,
   "journal": "Chem. Sci.",
   "title": "*et al.* Robust singlet fission process in strong absorption π-expanded diketopyrrolopyrroles",
   "volume": "13",
   "pages": "13907–13913",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    808
   ],
   "cited_in_sections": [
    "4.1"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/52-wang-2022.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/d2sc05580e",
    "url": "https://doi.org/10.1039/d2sc05580e",
    "oa_url": "https://pubs.rsc.org/en/content/articlepdf/2022/sc/d2sc05580e",
    "accesso": "diamond",
    "contenuto_letto": "full_text"
   }
  },
  {
   "id": 53,
   "anchor": "ref-53",
   "md_line": 1426,
   "text": "Abdel Aziz, I., Tullii, G., Antognazza, M. R. & Criado-Gonzalez, M. Poly(3-hexylthiophene) as a versatile semiconducting polymer for cutting-edge bioelectronics. *Mater. Horiz.* **12**, 5570–5593 (2025).",
   "authors": "Abdel Aziz, I., Tullii, G., Antognazza, M. R. & Criado-Gonzalez, M.",
   "year": 2025,
   "journal": "Mater. Horiz.",
   "title": "Poly(3-hexylthiophene) as a versatile semiconducting polymer for cutting-edge bioelectronics",
   "volume": "12",
   "pages": "5570–5593",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    842
   ],
   "cited_in_sections": [
    "4.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/53-abdel-aziz-2025.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/d5mh00096c",
    "url": "https://doi.org/10.1039/d5mh00096c",
    "oa_url": "https://pubs.rsc.org/en/content/articlepdf/2025/mh/d5mh00096c",
    "accesso": "hybrid",
    "contenuto_letto": "full_text"
   }
  },
  {
   "id": 54,
   "anchor": "ref-54",
   "md_line": 1428,
   "text": "Paganin, D. L., Bizzarri, P. C. & Lanzi, D. M. SSIINNTTEESSII EE PPRROOPPRRIIEETTÀÀ DDII NNUUOOVVII PPOOLLIIMMEERRII TTIIOOFFEENNIICCII PPEERR AAPPPPLLIICCAAZZIIOONNII OOPPTTOO--EELLEETTTTRROONNIICCHHEE.",
   "authors": "Paganin, D. L., Bizzarri, P. C. & Lanzi, D. M.",
   "year": null,
   "journal": null,
   "title": "SSIINNTTEESSII EE PPRROOPPRRIIEETTÀÀ DDII NNUUOOVVII PPOOLLIIMMEERRII TTIIOOFFEENNIICCII PPEERR AAPPPPLLIICCAAZZIIOONNII OOPPTTOO--EELLEETTTTRROONNIICCHHEE",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    850
   ],
   "cited_in_sections": [
    "4.2"
   ],
   "quality_flags": [
    "incomplete_in_source",
    "ocr_doubled_letters_in_source"
   ],
   "fonte": {
    "file": "fonti/54-paganin-nd.md",
    "stato": "non_risolta",
    "doi_verificato": null,
    "url": null,
    "oa_url": null,
    "accesso": null,
    "contenuto_letto": "no"
   }
  },
  {
   "id": 55,
   "anchor": "ref-55",
   "md_line": 1430,
   "text": "TY - JOUR AU - Chelora, Jipsa AU - Chen, Rui AU - Rishi, Hrisheekesh AU - Lee, Chun-Sing PY - 2017/06/19 SP - 285102 T1 - Highly stable red-emitting polymer dots for cellular imaging VL - 28 DO - 10.1088/1361-6528/aa744c JO - Nanotechnology ER -.",
   "authors": "Chelora, J.",
   "year": 2017,
   "journal": "Nanotechnology",
   "title": "Highly stable red-emitting polymer dots for cellular imaging",
   "volume": "28",
   "pages": "285102",
   "doi": "10.1088/1361-6528/aa744c",
   "url": null,
   "cited_in_md_lines": [
    934,
    936
   ],
   "cited_in_sections": [
    "4.2"
   ],
   "quality_flags": [
    "raw_ris_in_source"
   ],
   "fonte": {
    "file": "fonti/55-chelora-2017.md",
    "stato": "verificata",
    "doi_verificato": "10.1088/1361-6528/aa744c",
    "url": "https://doi.org/10.1088/1361-6528/aa744c",
    "oa_url": null,
    "accesso": null,
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 56,
   "anchor": "ref-56",
   "md_line": 1432,
   "text": "Odian, G. G. *Principles of Polymerization*. (Wiley-Interscience, Hoboken, N.J, 2004).",
   "authors": "Odian, G. G.",
   "year": 2004,
   "journal": "Principles of Polymerization",
   "title": "",
   "volume": null,
   "pages": null,
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    957
   ],
   "cited_in_sections": [
    "4.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/56-odian-2004.md",
    "stato": "identificata_manualmente",
    "doi_verificato": "10.1002/047147875x",
    "url": "https://doi.org/10.1002/047147875x",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 57,
   "anchor": "ref-57",
   "md_line": 1434,
   "text": "Chen, T.-A., Wu, X. & Rieke, R. D. Regiocontrolled Synthesis of Poly(3-alkylthiophenes) Mediated by Rieke Zinc: Their Characterization and Solid-State Properties. *J. Am. Chem. Soc.* **117**, 233–244 (1995).",
   "authors": "Chen, T.-A., Wu, X. & Rieke, R. D.",
   "year": 1995,
   "journal": "J. Am. Chem. Soc.",
   "title": "Regiocontrolled Synthesis of Poly(3-alkylthiophenes) Mediated by Rieke Zinc: Their Characterization and Solid-State Properties",
   "volume": "117",
   "pages": "233–244",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    971
   ],
   "cited_in_sections": [
    "4.2"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/57-chen-1995.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/ja00106a027",
    "url": "https://doi.org/10.1021/ja00106a027",
    "oa_url": null,
    "accesso": null,
    "contenuto_letto": "no"
   }
  },
  {
   "id": 58,
   "anchor": "ref-58",
   "md_line": 1436,
   "text": "Woodruff, M. A. & Hutmacher, D. W. The return of a forgotten polymer—Polycaprolactone in the 21st century. *Prog. Polym. Sci.* **35**, 1217–1256 (2010).",
   "authors": "Woodruff, M. A. & Hutmacher, D. W.",
   "year": 2010,
   "journal": "Prog. Polym. Sci.",
   "title": "The return of a forgotten polymer—Polycaprolactone in the 21st century",
   "volume": "35",
   "pages": "1217–1256",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    988
   ],
   "cited_in_sections": [
    "4.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/58-woodruff-2010.md",
    "stato": "verificata",
    "doi_verificato": "10.1016/j.progpolymsci.2010.04.002",
    "url": "https://doi.org/10.1016/j.progpolymsci.2010.04.002",
    "oa_url": "https://eprints.qut.edu.au/32270/1/c32270.pdf",
    "accesso": "green",
    "contenuto_letto": "partial"
   }
  },
  {
   "id": 59,
   "anchor": "ref-59",
   "md_line": 1438,
   "text": "Labet, M. & Thielemans, W. Synthesis of polycaprolactone: a review. *Chem. Soc. Rev.* **38**, 3484 (2009).",
   "authors": "Labet, M. & Thielemans, W.",
   "year": 2009,
   "journal": "Chem. Soc. Rev.",
   "title": "Synthesis of polycaprolactone: a review",
   "volume": "38",
   "pages": "3484",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    990
   ],
   "cited_in_sections": [
    "4.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/59-labet-2009.md",
    "stato": "verificata",
    "doi_verificato": "10.1039/b820162p",
    "url": "https://doi.org/10.1039/b820162p",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 60,
   "anchor": "ref-60",
   "md_line": 1440,
   "text": "Floyd, T. G. *et al.* Cationic Bottlebrush Copolymers from Partially Hydrolyzed Poly(oxazoline)s. *Macromolecules* **54**, 9461–9473 (2021).",
   "authors": "Floyd, T. G.",
   "year": 2021,
   "journal": "Macromolecules",
   "title": "*et al.* Cationic Bottlebrush Copolymers from Partially Hydrolyzed Poly(oxazoline)s",
   "volume": "54",
   "pages": "9461–9473",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    1079
   ],
   "cited_in_sections": [
    "4.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/60-floyd-2021.md",
    "stato": "verificata",
    "doi_verificato": "10.1021/acs.macromol.1c01458",
    "url": "https://doi.org/10.1021/acs.macromol.1c01458",
    "oa_url": null,
    "accesso": "closed",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 61,
   "anchor": "ref-61",
   "md_line": 1442,
   "text": "Kepska, K. *et al.* Spectroelectrochemistry of poly(3-hexylthiophenes) in solution. *Chem. Pap.* **72**, 251–259 (2018).",
   "authors": "Kepska, K.",
   "year": 2018,
   "journal": "Chem. Pap.",
   "title": "Spectroelectrochemistry of poly(3-hexylthiophenes) in solution",
   "volume": "72",
   "pages": "251–259",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    1240
   ],
   "cited_in_sections": [
    "4.4.3"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/61-kepska-2018.md",
    "stato": "verificata",
    "doi_verificato": "10.1007/s11696-017-0277-6",
    "url": "https://doi.org/10.1007/s11696-017-0277-6",
    "oa_url": "https://link.springer.com/content/pdf/10.1007%2Fs11696-017-0277-6.pdf",
    "accesso": "hybrid",
    "contenuto_letto": "solo_abstract"
   }
  },
  {
   "id": 62,
   "anchor": "ref-62",
   "md_line": 1444,
   "text": "Kasha, M., Rawls, H. R. & Ashraf El-Bayoumi, M. The exciton model in molecular spectroscopy. *Pure Appl. Chem.* **11**, 371–392 (1965).",
   "authors": "Kasha, M., Rawls, H. R. & Ashraf El-Bayoumi, M.",
   "year": 1965,
   "journal": "Pure Appl. Chem.",
   "title": "The exciton model in molecular spectroscopy",
   "volume": "11",
   "pages": "371–392",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    1277
   ],
   "cited_in_sections": [
    "4.5"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/62-kasha-1965.md",
    "stato": "verificata",
    "doi_verificato": "10.1351/pac196511030371",
    "url": "https://doi.org/10.1351/pac196511030371",
    "oa_url": "https://www.degruyter.com/document/doi/10.1351/pac196511030371/pdf",
    "accesso": "bronze",
    "contenuto_letto": "abstract_only"
   }
  },
  {
   "id": 63,
   "anchor": "ref-63",
   "md_line": 1446,
   "text": "Spano, F. C. & Silva, C. H- and J-Aggregate Behavior in Polymeric Semiconductors. *Annu. Rev. Phys. Chem.* **65**, 477–500 (2014).",
   "authors": "Spano, F. C. & Silva, C.",
   "year": 2014,
   "journal": "Annu. Rev. Phys. Chem.",
   "title": "H- and J-Aggregate Behavior in Polymeric Semiconductors",
   "volume": "65",
   "pages": "477–500",
   "doi": null,
   "url": null,
   "cited_in_md_lines": [
    1279
   ],
   "cited_in_sections": [
    "4.5"
   ],
   "quality_flags": [],
   "fonte": {
    "file": "fonti/63-spano-2014.md",
    "stato": "verificata",
    "doi_verificato": "10.1146/annurev-physchem-040513-103639",
    "url": "https://doi.org/10.1146/annurev-physchem-040513-103639",
    "oa_url": "https://www.annualreviews.org/doi/pdf/10.1146/annurev-physchem-040513-103639",
    "accesso": "bronze",
    "contenuto_letto": "abstract_only"
   }
  }
 ]
}