davideandClaude Sonnet 5.5
60aaca3418
Una scheda per fonte in fonti/ (metadati verificati con Crossref/OpenAlex/ Europe PMC, DOI e link, abstract, riassunto del contenuto per le fonti ad accesso aperto lette, citazioni nella tesi, bibliografia della fonte). bibliografia.json: campo fonte per ogni voce; CLAUDE.md aggiornato. Co-Authored-By: Claude Sonnet 5.5 <noreply@anthropic.com>
134 lines
7.8 KiB
Markdown
134 lines
7.8 KiB
Markdown
---
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id: 30
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anchor: ref-30
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stato: verificata
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doi: 10.1039/c2cc33998f
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url: https://doi.org/10.1039/c2cc33998f
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anno: 2012
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rivista: "Chemical Communications"
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volume: "48"
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pagine: "8413"
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editore: "Royal Society of Chemistry (RSC)"
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tipo: journal-article
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autori: ["Wei Liang Hong", "Bin Xiang Sun", "Hany Aziz", "Won‐Tae Park", "Yong‐Young Noh", "Yuning Li"]
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accesso: closed
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licenza: null
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pmcid: null
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citata_da: 99
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argomenti: ["Organic Electronics and Photovoltaics", "Conducting polymers and applications", "Organic Light-Emitting Diodes Research"]
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parole_chiave: ["diketopyrrolopyrrole", "polyazines", "conjugated polymers", "polycondensation", "electron mobility", "hole mobility", "organic semiconductors"]
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contenuto_letto: solo_abstract
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tags: [fonte, bibliografia]
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cited_in_sections: [1.1.2]
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---
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# [30] Hong (2012) - A conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors
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## Come è scritta nella tesi
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Hong, W. *et al.* A conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors. *Chem. Commun.* **48**, 8413 (2012).
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## Scheda bibliografica
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**Citazione completa:** Hong, W.; Sun, B.; Aziz, H.; Park, W. T.; Noh, Y. Y.; Li, Y. A conjugated polyazine containing diketopyrrolopyrrole for ambipolar organic thin film transistors. *Chemical Communications* **2012**, 48 (67), 8413. https://doi.org/10.1039/c2cc33998f
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- **Pubblicato in:** Chemical Communications, vol. 48, n. 67, pp. 8413 (2012)
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- **Editore:** Royal Society of Chemistry (RSC) · tipo: journal-article
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- **ISSN:** 1359-7345, 1364-548X
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- **Data di pubblicazione:** 2012-01-01
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- **Lingua:** en
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### Autori e affiliazioni
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- Wei Liang Hong ([ORCID](https://orcid.org/0000-0003-2509-7614)) - University of Waterloo
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- Bin Xiang Sun ([ORCID](https://orcid.org/0000-0002-8233-0999)) - University of Waterloo
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- Hany Aziz ([ORCID](https://orcid.org/0000-0002-5973-4979)) - University of Waterloo
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- Won‐Tae Park ([ORCID](https://orcid.org/0000-0002-7646-1204)) - Hanbat National University
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- Yong‐Young Noh ([ORCID](https://orcid.org/0000-0001-7222-2401)) - Hanbat National University
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- Yuning Li ([ORCID](https://orcid.org/0000-0003-3679-8133)) - University of Waterloo
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## Stato della verifica
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**Verificata (Crossref/OpenAlex)** - fonte dati: Crossref + OpenAlex
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## Dove trovarla
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- **DOI:** https://doi.org/10.1039/c2cc33998f
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- **PubMed:** https://pubmed.ncbi.nlm.nih.gov/22801409/
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- **OpenAlex:** https://openalex.org/W2040469312
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- **Accesso:** closed - il testo completo richiede un abbonamento dell'editore o l'acquisto
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## Abstract
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A π-conjugated polyazine containing diketopyrrolopyrrole (DPP) moiety, PDBTAZ, is synthesized through a simple condensation polymerization. PDBTAZ is found to be a high-performance ambipolar semiconductor in organic thin film transistors (OTFTs), showing an electron mobility of up to 0.41 cm(2) V(-1) s(-1) and a hole mobility of up to 0.36 cm(2) V(-1) s(-1).
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*(Fonte: Europe PMC. Non è il testo integrale dell'articolo.)*
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## Argomenti e parole chiave
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- **Argomenti (OpenAlex):** Organic Electronics and Photovoltaics (Electrical and Electronic Engineering); Conducting polymers and applications (Polymers and Plastics); Organic Light-Emitting Diodes Research (Electrical and Electronic Engineering)
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- **Parole chiave:** diketopyrrolopyrrole, polyazines, conjugated polymers, polycondensation, electron mobility, hole mobility, organic semiconductors
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- **Concetti:** Ambipolar diffusion, Conjugated system, Materials science, Thin-film transistor, Transistor, Optoelectronics, Organic semiconductor, Nanotechnology
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## Contenuto in sintesi
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Il testo completo non è ad accesso aperto e non è stato consultato: sono disponibili solo i metadati e l'abstract riportati sopra. Per approfondire, aprire la fonte dal DOI (o tramite biblioteca/abbonamento).
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## Come è citata nella tesi
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- **Sez. 1.1.2 Struttura e reattività** (`tesi.md` r. 363): N-formilpiperidina o DMF) genera la dialdeide 43[30].
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## Bibliografia della fonte
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La fonte cita 31 riferimenti:
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- Curtius J. Prakt. Chem. 1891 44 176
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- Zimmerman J. Am. Chem. Soc. 1936 58 948 https://doi.org/10.1021/ja01297a032
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- Pastravanu Eur. Polym. J. 1981 17 197 https://doi.org/10.1016/0014-3057(81)90055-0
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- Hauer J. Am. Chem. Soc. 1987 109 5760 https://doi.org/10.1021/ja00253a031
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- Cao J. Chem. Soc., Chem. Commun. 1988 937 https://doi.org/10.1039/c39880000937
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- Thakur Macromolecules 1988 21 661 https://doi.org/10.1021/ma00181a021
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- Euler Chem. Mater. 1990 2 209 https://doi.org/10.1021/cm00008a027
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- Dudis J. Am. Chem. Soc. 1993 115 8770 https://doi.org/10.1021/ja00072a033
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- Euler Chem. Mater. 1996 8 554 https://doi.org/10.1021/cm9504394
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- Ng J. Mater. Sci. Lett. 1997 16 841 https://doi.org/10.1023/A:1018594812116
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- Nalwa Adv. Mater. 1993 5 341 https://doi.org/10.1002/adma.19930050504
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- Nalwa J. Appl. Phys. 1993 73 4743 https://doi.org/10.1063/1.353837
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- Nalwa Synth. Met. 1993 55–57 3901 https://doi.org/10.1016/0379-6779(93)90532-2
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- Destri J. Opt. Soc. Am. B 2007 24 1505 https://doi.org/10.1364/JOSAB.24.001505
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- Faccinetto ChemPhysChem 2008 9 2028 https://doi.org/10.1002/cphc.200800240
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- Anthopoulos Adv. Mater. 2004 16 2174 https://doi.org/10.1002/adma.200400309
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- Anthopoulos Appl. Phys. Lett. 2004 85 4205 https://doi.org/10.1063/1.1812577
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- Baeg J. Polym. Sci., Part B: Polym. Phys. 2011 49 62 https://doi.org/10.1002/polb.22148
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- Baeg ACS Appl. Mater. Interfaces 2011 3 3205 https://doi.org/10.1021/am200705j
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- Bürgi Adv. Mater. 2008 20 2217 https://doi.org/10.1002/adma.200702775
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- Bijleveld J. Am. Chem. Soc. 2009 131 16616 https://doi.org/10.1021/ja907506r
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- Chen Adv. Mater. 2012 24 647 https://doi.org/10.1002/adma.201102786
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- Li Adv. Mater. 2010 22 4862 https://doi.org/10.1002/adma.201002313
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- Sonar Adv. Mater. 2010 22 5409 https://doi.org/10.1002/adma.201002973
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- Li J. Am. Chem. Soc. 2011 133 2198 https://doi.org/10.1021/ja1085996
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- Sonar Energy Environ. Sci. 2011 4 2288 https://doi.org/10.1039/c1ee01213d
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- Ha J. Am. Chem. Soc. 2011 133 10364 https://doi.org/10.1021/ja203189h
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- Chen Adv. Mater. 2012 24 647 https://doi.org/10.1002/adma.201102786
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- Yuen J. Am. Chem. Soc. 2011 133 20799 https://doi.org/10.1021/ja205566w
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- Ortiz Materials 2010 3 1533 https://doi.org/10.3390/ma3031533
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- Bürgi Adv. Mater. 2008 20 2217 https://doi.org/10.1002/adma.200702775
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## Lavori correlati (OpenAlex)
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- Recent Advances in Ambipolar Transistors for Functional Applications (2019) - https://doi.org/10.1002/adfm.201902105 - citato 232 volte
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- Ambipolar organic field-effect transistors based on rubrene single crystals (2006) - https://doi.org/10.1063/1.2166698 - citato 157 volte
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- Poly(arylenethynyl-thienoacenes) as candidates for organic semiconducting materials. A DFT insight (2012) - https://doi.org/10.1016/j.orgel.2012.09.029 - citato 28 volte
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- Majority carrier type conversion in solution-processed organic transistors and flexible complementary logic circuits (2010) - https://doi.org/10.1063/1.3310025 - citato 50 volte
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- Carrier‐Selective Traps: A New Approach for Fabricating Circuit Elements with Ambipolar Organic Semiconductors (2017) - https://doi.org/10.1002/aelm.201600537 - citato 16 volte
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- Tuning polarity and improving charge transport in organic semiconductors (2013) - https://doi.org/10.1117/12.2023157 - citato 0 volte
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- F4CuPc based ambipolar organic thin-film transistors (2007) - https://doi.org/10.1109/iwpsd.2007.4472577 - citato 0 volte
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- Organic Semiconductors: Carrier‐Selective Traps: A New Approach for Fabricating Circuit Elements with Ambipolar Organic Semiconductors (Adv. Electron. Mater. 3/2017) (2017) - https://doi.org/10.1002/aelm.201770015 - citato 0 volte
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## Metriche
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- Citata **99** volte (OpenAlex); riferimenti nella fonte: 30
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- Citazioni per anno: 2026: 1, 2025: 2, 2024: 5, 2023: 4, 2022: 5, 2021: 4
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[Torna alla bibliografia della tesi](../tesi.md#ref-30) · Generata dal catalogo `bibliografia.json` e da Crossref, OpenAlex, Europe PMC.
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