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Advances in Functional Organic Dye Chemistry

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Colorants".

Deadline for manuscript submissions: 31 December 2024 | Viewed by 6715

Special Issue Editor


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Guest Editor
Italian National Research Council | CNR, Institute of Nanotechnology, Rome, Italy
Interests: organic dyes; organic emissive materials; organic semiconductors; open-shell organic conjugated materials; electrochromic organic materials; electrofluorochromic organic materials; self-assembly into organic materials
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Special Issue Information

Dear Colleagues,

Functional organic dyes are materials designed and synthesized with specific physicochemical properties to be key elements in several technological fields. These materials play a crucial role in various optoelectronic fields as well as in medical and biological research. Proof of the importance of functional organic dyes are the significant progresses in the fields  of light-emitting diodes (OLED), organic photovoltaics (OPV), electrochromic devices (ECD) and electrochromic devices (EFC), fluorescent probes for biodiagnostics, photodynamic therapy (PDT), and photonic organic crystals. Molecular design and organic synthesis represent a fundamental tool for the development of new functional organic dyes. This Special Issue entitled “Advances in Functional Organic Dye Chemistry” welcomes manuscripts (original research papers, short communications, or focus reviews) presenting results from current studies performed predominantly in the research areas pointed out by the keywords given below. However, other related topics are also welcome.

Dr. Agostina-Lina Capodilupo
Guest Editor

Manuscript Submission Information

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Keywords

  • organic dyes
  • organic semiconductors
  • photonic organic crystals
  • organic emissive materials
  • organic electrochromic materials
  • organic electrofluorochromic materials
  • molecular sensors

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Published Papers (5 papers)

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Research

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15 pages, 2759 KiB  
Article
Multicomponent Synthesis of New Fluorescent Boron Complexes Derived from 3-Hydroxy-1-phenyl-1H-pyrazole-4-carbaldehyde
by Viktorija Savickienė, Aurimas Bieliauskas, Sergey Belyakov, Eglė Arbačiauskienė and Algirdas Šačkus
Molecules 2024, 29(14), 3432; https://doi.org/10.3390/molecules29143432 - 22 Jul 2024
Viewed by 1220
Abstract
Novel fluorescent pyrazole-containing boron (III) complexes were synthesized employing a one-pot three-component reaction of 3-hydroxy-1-phenyl-1H-pyrazole-4-carbaldehyde, 2-aminobenzenecarboxylic acids, and boronic acids. The structures of the novel heterocyclic compounds were confirmed using 1H-, 13C-, 15N-, 19F-, and 11B-NMR, [...] Read more.
Novel fluorescent pyrazole-containing boron (III) complexes were synthesized employing a one-pot three-component reaction of 3-hydroxy-1-phenyl-1H-pyrazole-4-carbaldehyde, 2-aminobenzenecarboxylic acids, and boronic acids. The structures of the novel heterocyclic compounds were confirmed using 1H-, 13C-, 15N-, 19F-, and 11B-NMR, IR spectroscopy, HRMS, and single-crystal X-ray diffraction data. The photophysical properties of the obtained iminoboronates were investigated using spectroscopic techniques, such as UV–vis and fluorescence spectroscopies. Compounds display main UV–vis absorption maxima in the blue region, and fluorescence emission maxima are observed in the green region of the visible spectrum. It was revealed that compounds exhibit fluorescence quantum yield up to 4.3% in different solvents and demonstrate an aggregation-induced emission enhancement effect in mixed THF–water solutions. Full article
(This article belongs to the Special Issue Advances in Functional Organic Dye Chemistry)
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14 pages, 3799 KiB  
Article
Preparation of Dye Semiconductors via Coupling Polymerization Catalyzed by Two Catalysts and Application to Transistor
by Shiwei Ren, Wenqing Zhang, Zhuoer Wang, Abderrahim Yassar, Jinyang Chen, Minfeng Zeng and Zhengran Yi
Molecules 2024, 29(1), 71; https://doi.org/10.3390/molecules29010071 - 22 Dec 2023
Cited by 3 | Viewed by 1247
Abstract
Organic dye semiconductors have received increasing attention as the next generation of semiconductors, and one of their potential applications is as a core component of organic transistors. In this study, two novel diketopyrrolopyrrole (DPP) dye core-based materials were designed and separately prepared using [...] Read more.
Organic dye semiconductors have received increasing attention as the next generation of semiconductors, and one of their potential applications is as a core component of organic transistors. In this study, two novel diketopyrrolopyrrole (DPP) dye core-based materials were designed and separately prepared using Stille coupling reactions under different palladium catalyst conditions. The molecular weights and elemental compositions were tested to demonstrate that both catalysts could be used to successfully prepare materials of this structure, with the main differences being the weight-average molecular weight and the dispersion index. PDPP-2Py-2Tz I with a longer conjugation length exhibited better thermodynamic stability than the counterpart polymer PDPP-2Py-2Tz II. The intrinsic optical properties of the polymers were relatively similar, while the electrochemical tests showed small differences in their energy levels. The polymers obtained with different catalysts displayed similar and moderate electron mobility in transistor devices, while PDPP-2Py-2Tz I possessed a higher switching ratio. Our study provides a comparison of such dye materials under different catalytic conditions and also demonstrates the great potential of dye materials for optoelectronic applications. Full article
(This article belongs to the Special Issue Advances in Functional Organic Dye Chemistry)
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17 pages, 3202 KiB  
Article
Rational Design of Cost-Effective 4-Styrylcoumarin Fluorescent Derivatives for Biomolecule Labeling
by Raquel Eustáquio, João P. Prates Ramalho, Ana Teresa Caldeira and António Pereira
Molecules 2023, 28(19), 6822; https://doi.org/10.3390/molecules28196822 - 27 Sep 2023
Cited by 3 | Viewed by 1030
Abstract
Fluorescent labels are key tools in a wide range of modern scientific applications, such as fluorescence microscopy, flow cytometry, histochemistry, direct and indirect immunochemistry, and fluorescence in situ hybridization (FISH). Small fluorescent labels have important practical advantages as they allow maximizing the fluorescence [...] Read more.
Fluorescent labels are key tools in a wide range of modern scientific applications, such as fluorescence microscopy, flow cytometry, histochemistry, direct and indirect immunochemistry, and fluorescence in situ hybridization (FISH). Small fluorescent labels have important practical advantages as they allow maximizing the fluorescence signal by binding multiple fluorophores to a single biomolecule. At present, the most widely used fluorescent labels available present small Stokes shifts and are too costly to be used in routine applications. In this work we present four new coumarin derivatives, as promising and inexpensive fluorescent labels for biomolecules, obtained through a cost-effective, efficient, and straightforward synthetic strategy. Density functional theory and time-dependent density functional theory calculations of the electronic ground and lowest-lying singlet excited states were carried out in order to gain insights into the observed photophysical properties. Full article
(This article belongs to the Special Issue Advances in Functional Organic Dye Chemistry)
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Review

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35 pages, 20847 KiB  
Review
The ATTO 565 Dye and Its Applications in Microscopy
by Yuheng Wu and René M. Williams
Molecules 2024, 29(17), 4243; https://doi.org/10.3390/molecules29174243 - 6 Sep 2024
Viewed by 708
Abstract
ATTO 565, a Rhodamine-type dye, has garnered significant attention due to its remarkable optical properties, such as a high fluorescence quantum yield, and the fact that it is a relatively stable structure and has low biotoxicity. ATTO 565 has found extensive applications in [...] Read more.
ATTO 565, a Rhodamine-type dye, has garnered significant attention due to its remarkable optical properties, such as a high fluorescence quantum yield, and the fact that it is a relatively stable structure and has low biotoxicity. ATTO 565 has found extensive applications in combination with microscopy technology. In this review, the chemical and optical properties of ATTO 565 are introduced, along with the principles behind them. The functionality of ATTO 565 in confocal microscopy, stimulated emission depletion (STED) microscopy, single-molecule tracking (SMT) techniques, two-photon excitation–stimulated emission depletion microscopy (TPE-STED) and fluorescence correlation spectroscopy (FCS) is discussed. These studies demonstrate that ATTO 565 plays a crucial role in areas such as biological imaging and single-molecule localization, thus warranting further in-depth investigations. Finally, we present some prospects and concepts for the future applications of ATTO 565 in the fields of biocompatibility and metal ion detection. This review does not include theoretical calculations for the ATTO 565 molecule. Full article
(This article belongs to the Special Issue Advances in Functional Organic Dye Chemistry)
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20 pages, 8078 KiB  
Review
Advances in Organic Fluorescent Probes for Intracellular Zn2+ Detection and Bioimaging
by Yi Chen
Molecules 2024, 29(11), 2542; https://doi.org/10.3390/molecules29112542 - 28 May 2024
Cited by 2 | Viewed by 1153
Abstract
Zinc ions (Zn2+) play a key role in maintaining and regulating protein structures and functions. To better understand the intracellular Zn2+ homeostasis and signaling role, various fluorescent sensors have been developed that allow the monitoring of Zn2+ concentrations and [...] Read more.
Zinc ions (Zn2+) play a key role in maintaining and regulating protein structures and functions. To better understand the intracellular Zn2+ homeostasis and signaling role, various fluorescent sensors have been developed that allow the monitoring of Zn2+ concentrations and bioimaging in live cells in real time. This review highlights the recent development of organic fluorescent probes for the detection and imaging of intracellular Zn2+, including the design and construction of the probes, fluorescent response mechanisms, and their applications to intracellular Zn2+ detection and imaging on-site. Finally, the current challenges and prospects are discussed. Full article
(This article belongs to the Special Issue Advances in Functional Organic Dye Chemistry)
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