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davideandClaude Sonnet 5.5 480339b798 Allinea la wiki alla tesi aggiornata e riorganizza in hub e sottopagine
- rimappati righe, figure, tabelle e riferimenti; contenuti riscritti sui dati nuovi
- pagine spezzate per argomento (copolimeri, bottle brush, CV, fluorescenza, DPP, difetti)
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Bibliografia overview
bibliografia
2026-10-09 2026-10-15 r.1320-1446 true draft

Bibliografia

Elenco dei 63 riferimenti della tesi (text = testo originale). Ogni voce rimanda alla scheda in raw/fonti/ e alle righe/sezioni di raw/tesi.md in cui è citata. Difetti noti: difetti-noti.

N Riferimento (testo della tesi) Citato in (sezioni; righe) Scheda Stato DOI verificato Flag
1 Bao, W. W. et al. Diketopyrrolopyrrole (DPP)-Based Materials and Its Applications: A Review. Front. Chem. 8, 679 (2020). §1.1; r.77 01-bao-2020 verificata 10.3389/fchem.2020.00679 -
2 Shaikh, S. A. L. et al. A minireview on diketopyrrolopyrrole chemistry: Historical perspective and recent developments. Results Chem. 4, 100473 (2022). §1.1, 1.1.1, 1.1.2; r.81, 86, 90, 253 02-shaikh-2022 verificata 10.1016/j.rechem.2022.100473 -
3 Auwalu, M. A. & Cheng, S. Diketopyrrolopyrrole Fluorescent Probes, Photophysical and Biological Applications. Chemosensors 9, 44 (2021). §1.1; r.81 03-auwalu-2021 verificata 10.3390/chemosensors9030044 -
4 Zhang, B. et al. Diketopyrrolopyrrole-based fluorescent probe for visualizing over-expressed carboxylesterase in fever via ratiometric imaging. Talanta 266, 124971 (2024). §1.1; r.81 04-zhang-2024 verificata 10.1016/j.talanta.2023.124971 -
5 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). §1.1.1, 1.1.2, 4.1; r.94, 150, 168, 271, 734 05-iqbal-1988 verificata 10.1002/bscb.19880970804 -
6 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. §1.1.1; r.138, 174, 178 06-sprake-1976 verificata 10.1039/p19760000005 -
7 Grzybowski, M. & Gryko, D. T. Diketopyrrolopyrroles: Synthesis, Reactivity, and Optical Properties. Adv. Opt. Mater. 3, 280–320 (2015). §1.1.1, 1.1.2, 4.1; r.150, 247, 301, 305, 734, 740 07-grzybowski-2015 verificata 10.1002/adom.201400559 -
8 Closs, F. & Gompper, R. 2,5-Diazapentalenes. Angew. Chem. Int. Ed. Engl. 26, 552–554 (1987). §1.1.1; r.160 08-closs-1987 verificata 10.1002/anie.198705521 -
9 Stas, S., Sergeyev, S. & Geerts, Y. Synthesis of diketopyrrolopyrrole (DPP) derivatives comprising bithiophene moieties. Tetrahedron 66, 1837–1845 (2010). §1.1.1; r.180 09-stas-2010 verificata 10.1016/j.tet.2010.01.027 -
10 Avcıbaşi, N. et al. Synthesis and in vitro evaluation of dioxopyrrolopyrroles as potential low-affinity fluorescent Ca2+ indicators. Int. J. Photoenergy 6, 159–167 (2004). §1.1.1; r.180 10-avcbasi-2004 verificata 10.1155/s1110662x04000200 -
11 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). §1.1.1; r.180 11-riggs-2005 verificata 10.1016/j.tet.2005.09.005 -
12 Qian, G. & Wang, Z. Y. Near-Infrared Thermochromic Diazapentalene Dyes. Adv. Mater. 24, 1582–1588 (2012). §1.1.1; r.180 12-qian-2012 verificata 10.1002/adma.201104711 -
13 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). §1.1.1; r.182 13-langhals-1996 verificata 10.1002/jlac.199619960506 -
14 De Luca, L., Giacomelli, G. & Porcheddu, A. A Mild and Efficient Alternative to the Classical Swern Oxidation. J. Org. Chem. 66, 7907–7909 (2001). §1.1.1; r.184 14-de-luca-2001 verificata 10.1021/jo015935s -
15 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). §1.1.1; r.184 15-harris-1998 verificata 10.1021/jo972304i -
16 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). §1.1.2; r.205, 243 16-mizuguchi-1992 identificata_manualmente 10.1107/S0108768192003033 -
17 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). §1.1.2; r.205 17-david-2011 verificata 10.1016/j.dyepig.2010.10.001 -
18 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). §1.1.2; r.207 18-mizuguchi-1991 verificata 10.1002/bbpc.19910951016 -
19 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). §1.1.2; r.215 19-lunak-2009 verificata 10.1016/j.dyepig.2008.12.001 -
20 Lenz, R. DPP chemistry- Continuous innovation. §1.1.2; r.219, 233, 239 20-lenz-2002 verificata 10.1007/bf02699738 incomplete_in_source
21 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). §1.1.2; r.269 21-colonna-2007 verificata 10.1016/j.dyepig.2006.05.024 -
22 Zambounis, J. S. & Iqbal, A. 54) PYRROLO(3,4-CIPYRROLES. §1.1.2; r.273 22-zambounis-nd candidata - incomplete_in_source, stray_text_in_source
23 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). §1.1.2; r.279, 281 23-yue-2014 verificata 10.1002/anie.201403227 -
24 Zambounis, J. S., Hao, Z. & Iqbal, A. Latent pigments activated by heat. Nature 388, 131–132 (1997). §1.1.2; r.279 24-zambounis-1997 verificata 10.1038/40532 -
25 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). §1.1.2; r.327 25-tieke-2010 verificata 10.3762/bjoc.6.92 -
26 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). §1.1.2; r.327 26-li-2013 verificata 10.1039/c3ee00015j -
27 McGlacken, G. P. & Bateman, L. M. Recent advances in aryl–aryl bond formation by direct arylation. Chem. Soc. Rev. 38, 2447 (2009). §1.1.2; r.331, 333 27-mcglacken-2009 verificata 10.1039/b805701j -
28 Han, W. & Ofial, A. No Detours: Palladium-Catalyzed Oxidative C-H/C-H Cross-Couplings of Heteroarenes. Synlett 2011, 1951–1955 (2011). §1.1.2; r.331, 347 28-ofial-2011 verificata 10.1055/s-0030-1260941 -
29 Liu, S.-Y. et al. C–H activation: making diketopyrrolopyrrole derivatives easily accessible. J. Mater. Chem. A 1, 2795 (2013). §1.1.2; r.339 29-liu-2013 verificata 10.1039/c2ta01318e -
30 Hong, W. et al. A conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors. Chem. Commun. 48, 8413 (2012). §1.1.2; r.363 30-hong-2012 verificata 10.1039/c2cc33998f -
31 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). §1.1.2; r.363 31-burckstummer-2011 verificata 10.1021/jo2003117 -
32 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). §1.1.2; r.363 32-hu-2012 verificata 10.1039/c2jm31700a -
33 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). §1.2; r.380 33-valeur-2011 verificata 10.1021/ed100182h -
34 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. §1.2, 1.2.2, 1.2.3; r.386, 413, 445, 474 34-lakowicz-1999 verificata 10.1007/978-1-4757-3061-6_1 -
35 Kasha, M. Characterization of electronic transitions in complex molecules. Discuss. Faraday Soc. 9, 14 (1950). §1.2; r.398 35-kasha-1950 verificata 10.1039/df9500900014 -
36 On the Change of Refrangibility of Light. §1.2.1; r.420 36-stokes-1852 identificata_manualmente 10.1098/rstl.1852.0022 incomplete_in_source, authors_unparsed
37 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). §1.2.1; r.424 37-prodi-2011 verificata_con_correzioni 10.1007/978-94-007-2042-8_5 -
38 Brouwer, A. M. Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report). Pure Appl. Chem. 83, 2213–2228 (2011). §1.2.2; r.445 38-brouwer-2011 verificata 10.1351/pac-rep-10-09-31 -
39 Weber, G. & Teale, F. W. J. Determination of the absolute quantum yield of fluorescent solutions. Trans. Faraday Soc. 53, 646 (1957). §1.2.2; r.445 39-weber-1957 verificata 10.1039/tf9575300646 -
40 Stoddart, J. F. Chapter 12. Host–guest chemistry. Annu. Rep. Sect. B Org. Chem. 85, 353–386 (1988). §1.3; r.491 40-stoddart-1988 verificata 10.1039/oc9888500353 -
41 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). §1.3; r.491 41-valdes-1996 verificata 10.1002/chem.19960020814 -
42 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). §1.3; r.493 42-wang-2015 verificata 10.1002/pola.27531 -
43 Lee, J.-K. et al. Light-emitting properties of PMMA-based new side chain polymers. Synth. Met. 111–112, 489–491 (2000). §1.3; r.495 43-lee-2000 verificata 10.1016/s0379-6779(99)00425-7 -
44 Bao, W. W. et al. Diketopyrrolopyrrole (DPP)-Based Materials and Its Applications: A Review. Front. Chem. 8, 679 (2020). §1.4; r.504, 532 44-bao-2020 verificata 10.3389/fchem.2020.00679 duplicate_entry
45 Ostroverkhova, O. Organic Optoelectronic Materials: Mechanisms and Applications. Chem. Rev. 116, 13279–13412 (2016). §1.4; r.512, 532, 538 45-ostroverkhova-2016 verificata 10.1021/acs.chemrev.6b00127 -
46 Nowsherwan, G. A. et al. Advances in Organic Materials for Next-Generation Optoelectronics: Potential and Challenges. Organics 5, 520–560 (2024). §1.4; r.514 46-nowsherwan-2024 verificata 10.3390/org5040028 -
47 Li, Y. Diketopyrrolopyrrole-Based Conjugated Polymers for Organic Electronics. https://doi.org/10.1021/ar500252u (2014) doi:10.1021/ar500252u. §1.4; r.516 47-li-2014 non_risolta - -
48 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. §1.4; r.516 48-kroon-2008 verificata_con_correzioni 10.1080/15583720802231833 -
49 Hendriks, K. H. Diketopyrrolopyrrole-Based Polymers for High-Efficiency Organic Solar Cells. https://doi.org/10.1039/c3ta11429c (2013) doi:10.1039/c3ta11429c. §1.4; r.516, 518 49-hendriks-2013 non_risolta - -
50 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). §3.4; r.706 50-cardona-2011 verificata 10.1002/adma.201004554 -
51 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). §4.1; r.722 51-scurti-2026 verificata 10.1016/j.dyepig.2025.113288 -
52 Wang, L. et al. Robust singlet fission process in strong absorption π-expanded diketopyrrolopyrroles. Chem. Sci. 13, 13907–13913 (2022). §4.1; r.808 52-wang-2022 verificata 10.1039/d2sc05580e -
53 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). §4.2; r.842 53-abdel-aziz-2025 verificata 10.1039/d5mh00096c -
54 Paganin, D. L., Bizzarri, P. C. & Lanzi, D. M. SSIINNTTEESSII EE PPRROOPPRRIIEETTÀÀ DDII NNUUOOVVII PPOOLLIIMMEERRII TTIIOOFFEENNIICCII PPEERR AAPPPPLLIICCAAZZIIOONNII OOPPTTOO--EELLEETTTTRROONNIICCHHEE. §4.2; r.850 54-paganin-nd non_risolta - incomplete_in_source, ocr_doubled_letters_in_source
55 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 -. §4.2; r.934, 936 55-chelora-2017 verificata 10.1088/1361-6528/aa744c raw_ris_in_source
56 Odian, G. G. Principles of Polymerization. (Wiley-Interscience, Hoboken, N.J, 2004). §4.2; r.957 56-odian-2004 identificata_manualmente 10.1002/047147875x -
57 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). §4.2; r.971 57-chen-1995 verificata 10.1021/ja00106a027 -
58 Woodruff, M. A. & Hutmacher, D. W. The return of a forgotten polymer—Polycaprolactone in the 21st century. Prog. Polym. Sci. 35, 1217–1256 (2010). §4.3; r.988 58-woodruff-2010 verificata 10.1016/j.progpolymsci.2010.04.002 -
59 Labet, M. & Thielemans, W. Synthesis of polycaprolactone: a review. Chem. Soc. Rev. 38, 3484 (2009). §4.3; r.990 59-labet-2009 verificata 10.1039/b820162p -
60 Floyd, T. G. et al. Cationic Bottlebrush Copolymers from Partially Hydrolyzed Poly(oxazoline)s. Macromolecules 54, 9461–9473 (2021). §4.3; r.1079 60-floyd-2021 verificata 10.1021/acs.macromol.1c01458 -
61 Kepska, K. et al. Spectroelectrochemistry of poly(3-hexylthiophenes) in solution. Chem. Pap. 72, 251–259 (2018). §4.4.3; r.1240 61-kepska-2018 verificata 10.1007/s11696-017-0277-6 -
62 Kasha, M., Rawls, H. R. & Ashraf El-Bayoumi, M. The exciton model in molecular spectroscopy. Pure Appl. Chem. 11, 371–392 (1965). §4.5; r.1277 62-kasha-1965 verificata 10.1351/pac196511030371 -
63 Spano, F. C. & Silva, C. H- and J-Aggregate Behavior in Polymeric Semiconductors. Annu. Rev. Phys. Chem. 65, 477–500 (2014). §4.5; r.1279 63-spano-2014 verificata 10.1146/annurev-physchem-040513-103639 -

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