Evidence map›Paper›PMID 35244293›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2022

Novel Thienyl DPP derivatives Functionalized with Terminal Electron-Acceptor Groups: Synthesis, Optical Properties and OFET Performance.

Sandra Fusco, Mario Barra, Lorenzo Gontrani, Matteo Bonomo, Federico Chianese, Simone Galliano, Roberto Centore, Antonio Cassinese, Marilena Carbone, Antonio Carella

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Synthesis and structure of 2,4-bis-(2,6-dimethyl-4Acta crystallographica. Section E, Crystallographic communications · 2026
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  6. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sandra FuscoDipartimento di Scienze Chimiche, Università degli Studi di Napoli 'Federico II', Complesso Universitario Monte Sant'Angelo, Via Cintia 21, 80126, Napoli, Italy.ORCID http://orcid.org/0000-0002-1347-7241
Mario BarraDipartimento di Fisica "Ettore Pancini" CNR-SPIN, P.le Tecchio, 80, 80125, Napoli, Italy.ORCID http://orcid.org/0000-0002-1990-0119
Lorenzo GontraniDipartimento di Chimica, Università di Roma "La Sapienza", Piazzale Aldo Moro 5, 00185, Roma, Italy.ORCID http://orcid.org/0000-0001-8212-7029
Matteo BonomoDipartimento di Chimica, Università di Roma "La Sapienza", Piazzale Aldo Moro 5, 00185, Roma, Italy.ORCID http://orcid.org/0000-0002-1944-2664
Federico ChianeseDipartimento di Fisica "Ettore Pancini" CNR-SPIN, P.le Tecchio, 80, 80125, Napoli, Italy.ORCID http://orcid.org/0000-0001-6895-2137
Simone GallianoDepartment of Chemistry and NIS Interdepartmental Centre, University of Torino, Via Pietro Giuria 7, 10125, Torino, Italy.ORCID http://orcid.org/0000-0002-0381-5809
Roberto CentoreDipartimento di Scienze Chimiche, Università degli Studi di Napoli 'Federico II', Complesso Universitario Monte Sant'Angelo, Via Cintia 21, 80126, Napoli, Italy.ORCID http://orcid.org/0000-0002-2797-0117
Antonio CassineseDipartimento di Fisica "Ettore Pancini" CNR-SPIN, P.le Tecchio, 80, 80125, Napoli, Italy.ORCID http://orcid.org/0000-0002-5866-223X
Marilena CarboneDipartimento di Scienze e Tecnologie Chimiche, Università di Roma "Tor Vergata", Via della ricerca scientifica 1, 00133, Roma, Italy.ORCID http://orcid.org/0000-0002-4224-1393
Antonio CarellaDipartimento di Scienze Chimiche, Università degli Studi di Napoli 'Federico II', Complesso Universitario Monte Sant'Angelo, Via Cintia 21, 80126, Napoli, Italy.ORCID http://orcid.org/0000-0003-2761-0426

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca ARS01_01158Università degli Studi di Napoli Federico II FRA_Centore_Roberto_20200910935
6 · The paper itself

Abstract

Three novel diketopyrrolopyrrole (DPP) based small molecules have been synthesized and characterized in terms of their chemical-physical, electrochemical and electrical properties. All the molecules consist of a central DPP electron acceptor core symmetrically functionalized with donor bi-thienyl moieties and flanked in the terminal positions by three different auxiliary electron-acceptor groups. This kind of molecular structure, characterized by an alternation of electron acceptor and donor groups, was purposely designed to provide a significant absorption at the longer wavelengths of the visible spectrum: when analysed as thin films, in fact, the dyes absorb well over 800 nm and exhibit a narrow optical bandgap down to 1.28 eV. A detailed DFT analysis provides useful information on the electronic structure of the dyes and on the features of the main optical transitions. Organic field-effect transistors (OFETs) have been fabricated by depositing the DPP dyes as active layers from solution: the different end-functionalization of the dyes had an effect on the charge-transport properties with two of the dyes acting as n-type semiconductors (electron mobility up to 4.4 ⋅ 10

Indexed as

diketopyrrolopyrroledyes/pigmentsNIR absorptionsemiconductorssynthesis

Identifiers

PMID35244293
PMCPMC9314809

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.