Relevant bibliographies by topics / Properties of cyanine dyes

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Properties of cyanine dyes'

Author: Grafiati
Published: 4 June 2025
Last updated: 15 July 2025

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Journal articles on the topic "Properties of cyanine dyes"

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H., A. Shindy. "Synthesis of different classes of five/six membered heterocyclic cyanine dyes: A review." Chemistry International 6, no. 2 (2020): 56–74. https://doi.org/10.5281/zenodo.3361022.

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In this review paper synthesis of different classes of five/six membered heterocyclic cyanine dyes have been reviewed. In this paper review detailed synthesis steps were represented via equations. The synthesis covers, monomethine cyanine dyes (simple cyanine dyes), dimethine cyanine dyes, trimethine cyanine dyes (carbocyanine dyes), styryl cyanine dyes (hemicyanine dyes), aza-styryl cyanine dyes (aza-hemicyanine dyes and/or aza-cyanine dyes), merocyanine dyes (acyclic merocyanine dyes and cyclic merocyanine dyes) and apocyanine dyes. Besides, in the introduction section of this review paper some light is focused on the uses, applications and properties of cyanine dyes. This review paper is informative, useful and very readable for synthetic dye chemists, researchers and students who look for the different methods in the synthesis and preparation of various classes of five/six membered heterocyclic cyanine dyes with special emphasize in the field of heterocyclic and/or cyanine dyes chemistry. This specific type of collective review in the synthesis of different classes of only five/six membered heterocyclic cyanine dyes has been paid little attention and has great importance in the chemistry literature.
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Pronkin, Pavel G., and Alexander S. Tatikolov. "Photonics of Trimethine Cyanine Dyes as Probes for Biomolecules." Molecules 27, no. 19 (2022): 6367. http://dx.doi.org/10.3390/molecules27196367.

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Cyanine dyes are widely used as fluorescent probes in biophysics and medical biochemistry due to their unique photophysical and photochemical properties (their photonics). This review is focused on a subclass of the most widespread and studied cyanine dyes—trimethine cyanines, which can serve as potential probes for biomolecules. The works devoted to the study of the noncovalent interaction of trimethine cyanine dyes with biomolecules and changing the properties of these dyes upon the interaction are reviewed. In addition to the spectral-fluorescent properties, elementary photochemical properties of trimethine cyanines are considered, including: photoisomerization and back isomerization of the photoisomer, generation and decay of the triplet state, and its quenching by oxygen and other quenchers. The influence of DNA and other nucleic acids, proteins, and other biomolecules on these properties is covered. The interaction of a monomer dye molecule with a biomolecule usually leads to a fluorescence growth, damping of photoisomerization (if any), and an increase in intersystem crossing to the triplet state. Sometimes aggregation of dye molecules on biomolecules is observed. Quenching of the dye triplet state in a complex with biomolecules by molecular oxygen usually occurs with a rate constant much lower than the diffusion limit with allowance for the spin-statistical factor 1/9. The practical application of trimethine cyanines in biophysics and (medical) biochemistry is also considered. In conclusion, the prospects for further studies on the cyanine dye–biomolecule system and the development of new effective dye probes (including probes of a new type) for biomolecules are discussed.
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Zhytniakivska, Olga, Uliana Tarabara, Pylyp Kuznietsov, Kateryna Vus, Valeriya Trusova, and Galyna Gorbenko. "Molecular Docking Study of the Interactions Between Cyanine Dyes And DNA." East European Journal of Physics, no. 2 (June 2, 2023): 335–40. http://dx.doi.org/10.26565/2312-4334-2023-2-39.

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Among the various fluorescent probes currently used for biomedical and biochemical studies, significant attention attracts cyanine dyes possessing advantageous properties upon their complexation with biomolecules, particularly nucleic acids. Given the wide range of cyanine applications in DNA studies, a better understanding of their binding mode and intermolecular interactions governing dye-DNA complexation would facilitate the synthesis of new molecular probes of the cyanine family with optimized properties and would be led to the development of new cyanine-based strategies for nucleic acid detection and characterization. In the present study molecular docking techniques have been employed to evaluate the mode of interaction between one representative of monomethines (AK12-17), three trimethines (AK3-1, AK3-3, AK3-5), three pentamethines (AK5-1, AK5-3, AK5-9) and one heptamethine (AK7-6) cyanine dyes and B–DNA dodecamer d(CGCGAATTCGCG)2 (PDB ID: 1BNA). The molecular docking studies indicate that: i) all cyanines under study (excepting AK5-9 and AK7-6) form the most stable dye-DNA complexes with the minor groove of double-stranded DNA; ii) cyanines AK5-9 and AK7-6 interact with the major groove of the DNA on the basis of their more extended structure and higher lipophilicity in comparison with other dyes; iii) cyanine dye binding is governed by the hydrophobic and Van der Waals interactions presumably with the nucleotide residues C9A, G10A (excepts AK3-1, AK3-5), A17B (excepts AK3-5, AK5-3) and A18B in the minor groove and the major groove residues С16B, A17B, A18B, C3A, G4A, A5A, A6A (AK5-9 and AK7-6); iv) all dyes under study (except AK3-1, AK3-5 and AK5-39 possess an affinity to adenine and cytosine residues, whereas AK3-1, AK3-5 and AK5-3 also interact with thymine residues of the double-stranded DNA.
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Yu, Lijia, Yansong Zhang, Chunguang Ding, and Xiaodong Shi. "Disassembly of Dimeric Cyanine Dye Supramolecular Assembly by Tetramolecular G-quadruplex Dependence on Linker Length and Layers of G-quartet." Molecules 24, no. 10 (2019): 2015. http://dx.doi.org/10.3390/molecules24102015.

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Cyanine dyes have been widely applied in various biological systems owing to their specific photochemical properties. Assembly and disassembly process of cyanine dyes were constructed and regulated by special biomolecules. In this paper, dimeric cyanine dyes with different repeat units (oligo-oxyethylene) in linker (TC-Pn) (n = 3–6) were found to form H-aggregates or mixture aggregates in PBS. These aggregates could be disassembled into dimer and/or monomer by (TGnT) tetramolecular G-quadruplexes (n = 3–6, 8), which were affected by the linker length of dimeric cyanine dyes and layers of G-quartets. The 1H-NMR titration results suggest that the binding mode of dimeric cyanine dye with TGnT might be on both ends—stacking like a clip. This binding mode could clearly explain that matching structures between dimeric cyanine dyes and TGnT quadruplexes could regulate the disassembly properties of aggregates. These results could provide clues for the development of highly specific G-quadruplex probes.
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Janeková, Hana, Marina Russo, and Peter Štacko. "Cyanine Renaissance: Tailoring the Properties to Applications." CHIMIA 76, no. 9 (2022): 763. http://dx.doi.org/10.2533/chimia.2022.763.

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In this account, we provide an overview of the applications that arose from the recently developed synthetic methodology that delivers heptamethine cyanines (Cy7) substituted at the central chain. The ability to easily introduce and manipulate various substituents in different substitution patterns along the cyanine chain enabled rational tailoring of the photophysical and photochemical properties. Exercising this control over the structure–property relationship proved to have a substantial impact in the field of cyanine dyes and was swiftly harnessed in a number of emerging applications in distinct areas, including fluorescent probes, biosensors, dye-sensitized upconversion nanoparticles, phototruncation of cyanines and photocages. While this method unlocked a number of new avenues, many synthetic challenges remain to be conquered in order to fully capitalize on the potential of cyanines, and we provide a short perspective that summarizes them at the end of this manuscript.
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Maia, Ana, Cathy Ventura, Adriana O. Santos, et al. "A New Demand for Improved Selectivity and Potency of Cyanine Dyes as Antiproliferative Agents Against Colorectal Cancer Cells." Molecules 29, no. 23 (2024): 5581. http://dx.doi.org/10.3390/molecules29235581.

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Cancer treatment remains a significant challenge, with chemotherapy still being one of the most common therapeutic approaches. Based on our initial studies of symmetric monomethine cyanine dyes, which showed potential against colorectal cancer, this study explored several asymmetric cyanines, aiming to develop more potent and selective antitumor agents, particularly against colorectal cancer. In pursuit of this goal, we have designed, synthesized, and structurally characterized twelve new cyanine dyes. Their antiproliferative effects were then investigated in vitro against both tumor and non-tumor cell lines. Notably, the two most promising dyes in terms of potency and selectivity against Caco-2 colorectal cancer cells were derived from the combination of N-methylbenzoxazole and N-methylquinoline (dye 5), as well as N-ethylbenzothiazole and N-ethyl-6-nitrobenzothiazole (dye 10). The potential mechanisms behind their antiproliferative action were also explored, revealing that both dyes penetrate cells and localize within the cytoplasm and nucleus. Furthermore, dye 5 was found to slightly induce apoptosis without causing significant cell cycle arrest, in contrast to dye 10, which increased the number of cells in the G0/G1 phase. Interestingly, both dyes exhibited marked topoisomerase II inhibitory effects, particularly cyanine 5, which may further explain their antiproliferative activity. Additionally, drug-likeness properties were predicted for both dyes. Overall, cyanine 5 emerged as the most promising candidate for further investigation as a potential treatment for colorectal cancer.
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Hassan, Abazied Shindy, Abdallah El-Maghraby Mohamed, Mubark Goma Maha, and Abdelrahman Harb Nemat. "Dicarbocyanine and tricarbocyanine dyes: Novel synthetic approaches, photosensitization evaluation and antimicrobial screening." Chemistry International 6, no. 1 (2020): 30–41. https://doi.org/10.5281/zenodo.2631739.

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Novel dicarbocyanine dyes (pentamethine cyanine dyes), bis dicarbocyanine dyes (bis pentamethine cyanine dyes), tricarbocyanine dyes (heptamethine cyanine dyes) and bis tricarbocyanine dyes (bis heptamethine cyanine dyes) derived from the nucleus of furo[(3,2-d)pyrazole; (3&#39;,2&#39;-d)oxazole] were prepared using novel synthetic approaches. The electronic visible absorption spectra were investigated in 95% ethanol to evaluate the photosensitization properties. The cyanine dyes were better photosensitizers in visible light to initiate the electronic transitions at higher wavelength bands (bathochromic shifted and/or red shifted dyes). Consequently, the photosensitization of the cyanine dyes decreases in visible light to initiate the electronic transitions at lower wavelength bands (hypsochromic shifted and/or blue shifted dyes). Antimicrobial activity of ten selected compounds was tested against four bacterial strains (<em>Bacillus subtilis, Escherichia coli, Pseudomona aeruginosa</em> and <em>Staphylococcus aureus</em>). The compounds were thought to be better antimicrobial active when they give higher inhibition zone against the tested strains. Consequently, the antimicrobial activity was promising and variable among all synthesized compounds against tested strains. Structural characterization and confirmations were determined by elemental analysis, visible, mass, IR and <sup>1</sup>H NMR spectral data.
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Fabijanić, Ivana, Atanas Kurutos, Ana Tomašić Paić, et al. "Selenium-Substituted Monomethine Cyanine Dyes as Selective G-Quadruplex Spectroscopic Probes with Theranostic Potential." Biomolecules 13, no. 1 (2023): 128. http://dx.doi.org/10.3390/biom13010128.

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The binding interactions of six ligands, neutral and monocationic asymmetric monomethine cyanine dyes comprising benzoselenazolyl moiety with duplex DNA and RNA and G-quadruplex structures were evaluated using fluorescence, UV/Vis (thermal melting) and circular dichroism (CD) spectroscopy. The main objective was to assess the impact of different substituents (methyl vs. sulfopropyl vs. thiopropyl/thioethyl) on the nitrogen atom of the benzothiazolyl chromophore on various nucleic acid structures. The monomethine cyanine dyes with methyl substituents showed a 100-fold selectivity for G-quadruplex versus duplex DNA. Study results indicate that cyanines bind with G-quadruplex via end π-π stacking interactions and possible additional interactions with nucleobases/phosphate backbone of grooves or loop bases. Cyanine with thioethyl substituent distinguishes duplex DNA and RNA and G-quadruplex structures by distinctly varying ICD signals. Furthermore, cell viability assay reveals the submicromolar activity of cyanines with methyl substituents against all tested human cancer cell lines. Confocal microscopy analysis shows preferential accumulation of cyanines with sulfopropyl and thioethyl substituents in mitochondria and indicates localization of cyanines with methyl in nucleus, particularly nucleolus. This confirms the potential of examined cyanines as theranostic agents, possessing both fluorescent properties and cell viability inhibitory effect.
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Hassan, Abazied Shindy, Abdallah El-Maghraby Mohamed, Mubark Goma Maha, and Abdelrahman Harb Nemat. "Novel styryl and aza-styryl cyanine dyes: Synthesis and spectral sensitization evaluation." Chemistry International 5, no. 2 (2019): 117–25. https://doi.org/10.5281/zenodo.1475414.

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Novel styryl cyanine dyes and aza-styryl cyanine dyes having the nucleus of furo[(3,2-d)pyrazole;(3&#39;,2&#39;-d)oxazole] iodide salt were prepared. Spectral sensitization evaluation for all the synthesized styryl and aza-styryl cyanine dyes was carried out through investigating their electronic visible absorption spectra in 95% ethanol solution. The dyes were thought to be better spectral sensitizers when they absorb light at longer wavelength bands (bathochromic shifted and/or red shifted dyes). Consequently the spectral sensitization of the dyes decreased when they absorb light at shorter wavelength bands (hypsochromic shifted and/or blue shifted dyes). The results discussed in this study revealed that the spectral sensitization properties of the examined dyes is highly effected by the type of the X substituted in the phenyl ring system for the styryl cyanine dyes and by the type of the phenyl and/or the naphthyl ring system for the aza-styryl cyanine dyes. Structural confirmations were identified by elemental analysis, visible spectra, IR and 1H NMR spectroscopic data.
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Chapman, Gala, Maged Henary, and Gabor Patonay. "The Effect of Varying Short-Chain Alkyl Substitution on the Molar Absorptivity and Quantum Yield of Cyanine Dyes." Analytical Chemistry Insights 6 (January 2011): ACI.S6568. http://dx.doi.org/10.4137/aci.s6568.

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The effect of varying short-chain alkyl substitution of the indole nitrogens on the spectroscopic properties of cyanine dyes was examined. Molar absorptivities and fluorescence quantum yields were determined for a set of pentamethine dyes and a set of heptamethine dyes for which the substitution of the indole nitrogen was varied. For both sets of dyes, increasing alkyl chain length resulted in no significant change in quantum yield or molar absorptivity. These results may be useful in designing new cyanine dyes for analytical applications and predicting their spectroscopic properties.
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Dissertations / Theses on the topic "Properties of cyanine dyes"

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Fernando, Nilmi T. "Novel Near-Infrared Cyanine Dyes for Fluorescence Imaging in Biological Systems." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_diss/57.

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Heptamethine cyanine dyes are attractive compounds for imaging purposes in biomedical applications because of their chemical and photophysical properties exhibited in the near-infrared region. A series of meso amino-substituted heptamethine cyanine dyes with indolenine, benz[e]indolenine and benz[c,d]indolenine heterocyclic moieties were synthesized and their spectral properties including fluorescence quntum yield were investigated in ethanol and ethanol/water mixture. Upon substitution with amines, the absorption maxima of the dyes shifted to the lower wavelength region (~600 nm), showed larger Stokes shifts and stronger fluorescence which can be attributed to an excited state intramolecular charge transfer (ICT). High quantum yields were observed for primary amine derivatives and lower quantum yields were observed for secondary amine derivatives. Fluorescence quantum yields are greater for dyes with 3H-indolenine terminal moieties than for dyes with benz[e]indolenine end groups. Benz[c,d]indolenine based heptamethine cyanine dyes exhibited the lowest quantum yield due to aggregation in solution. In general, the benz[e]indolenine hepatemethine cyanines showed high Stokes shifts compared to indolenine dyes. For the meso-chloro dyes, the absorption maxima for the dyes shifted bathochromically in the order of indolenine, benz[e]indolenine and benz[c,d]indolenine.
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Eisele, Dörthe Melitta. "Optical, structural and redox properties of nanotubular j-aggregates of amphiphilic cyanine dyes." Aachen Shaker, 2009. http://d-nb.info/1002585198/04.

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Eisele, Dörthe M. [Verfasser]. "Optical, Structural and Redox Properties of Nanotubular J-aggregates of Amphiphilic Cyanine Dyes / Dörthe M Eisele." Aachen : Shaker, 2010. http://d-nb.info/1120864127/34.

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Yau, C. M. Simon. "The synthesis and properties of cyanine dye rotaxanes." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540266.

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Gragg, Jamie Loretta. "Synthesis of Near-Infrared Heptamethine Cyanine Dyes." Digital Archive @ GSU, 2010. http://digitalarchive.gsu.edu/chemistry_theses/28.

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Carbocyanine dyes are organic compounds containing chains of conjugated methine groups with electron-donating and electron-withdrawing substituents at the terminal heterocycles of the general formula [R1-(CH)n-R2]+X-. The synthetic methodology and optical properties of carbocyanines will be discussed. This thesis consists of two parts: (A) synthesis and optical properties of novel carbocyanine dyes substituted with various amines and the synthesis of unsymmetrical carbocyanine dyes containing monofunctional groups for bioconjugation. (B) synthesis of heptamethine carbocyanine dyes to be used for image-guided surgery. In part A, the synthesis of carbocyanine dyes functionalized with various amines and studies of their optical properties with respect to absorbance, fluorescence, quantum yield and extinction coefficient will be presented. These property studies will aid in designing efficient dyes for future biomedical applications. Part A will also include a one pot synthesis of unsymmetrical carbocyanine dyes functionalized with mono carboxylic acid chains, useful for biomolecule (i.e. proteins, amino acids, etc.) conjugation. Part B will describe the synthesis of novel carbocyanine dyes to be used for cancer image-guided surgery. Cancers are thus far incurable diseases, i.e. there are no drugs currently available to cure cancer; however, by designing a dye to visualize tumor cells will greatly increase the efficiency of cancer removal and hopefully increase the survival rate of cancer patients. The dyes reported in this thesis are superior to commercially available dyes used to visualize and identify various tumors invisible to the naked eye of surgeons with regards to biodistribution and clearance through kidney filtration.
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Hake, Jennifer Louise. "Solid-phase synthesis and applications of cyanine dyes." Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613994.

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Fegan, Adrian. "Cyanine dyes : synthesis and applications as nucleic acid labels." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611861.

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Mason, Stephen John. "Studies on the solid-phase synthesis of cyanine dyes." Thesis, University of Cambridge, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620058.

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Paranjpe, Shirish. "Synthesis of Novel Fluorescent Benzothiazole Cyanine Dyes as Potential Imaging Agents." Digital Archive @ GSU, 2012. http://digitalarchive.gsu.edu/chemistry_theses/55.

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Near-infrared (NIR) fluorescence imaging has emerged as an attractive non-invasive approach for direct visualization of diseases which depends on the development of stable, highly specific and sensitive optical probes. The NIR region of the electronic spectrum offers a reduction in the background autofluorescence and an increase in the tissue penetration depth. Cyanine dyes have often been considered promising contrast optic agents owing to their photophysical properties. Herein the synthesis of various penta- and heptamethine benzothiazole cyanine dyes has been described and their in vivo imaging efficacy was determined. Varying functionalities on the benzothiazole aromatic ring and changing substituents on the benzothiazolium nitrogen atom reflected subsequent changes in the imaging pattern and have resulted in the development of promising brain targeting agents.
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Osedach, Timothy. "Colloidal Quantum Dots and J-Aggregating Cyanine Dyes for Infrared Photodetection." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10088.

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The emergence of nanostructured semiconducting materials enables new approaches toward the realization of photodetectors that operate in the technologically important near- and short-wave infrared (NIR and SWIR) spectral ranges. In particular, organic semiconductors and colloidal quantum dots (QDs) possess numerous advantages over conventional crystalline semiconductors including highly tunable optical and electronic characteristics, the prospect for low-temperature processing, and compatibility with inexpensive and exible substrates. Photodetectors based on such materials may lead to low-cost IR focal plane arrays for night-vision imaging as well as a multitude of novel applications in biological and chemical sensing. This thesis describes the development and detailed characterization of several photodetectors that incorporate colloidal QD and organic semiconductor thin films as active layers. The electronic properties of PbS QDs are thoroughly investigated in a field effect transistor (FET) geometry and several QD-based photoconductive structures exhibiting SWIR photosensitivity are demonstrated. We describe a novel QD-sensitized lateral heterojunction photoconductor in which the functions of optical absorption and charge transport are dissociated into different physical layers that can be independently optimized. This structure is advantageous because it obviates the need for aggressive chemical treatments to the QD film that may compromise the quality of QD surface passivation. Photovoltaic device architectures are addressed, noting their advantages of being operable without an external applied bias and at fast response speeds. We present detailed experimental and theoretical characterization of a photovoltaic structure that is sensitized at NIR wavelengths by a J-aggregating cyanine dye. The high absorption coefficient of the J-aggregate film, combined with the use of a reflective anode and optical spacer layer, enables an external quantum efficiency (EQE) of \(16.1\pm0.1\%(\lambda = 756 nm)\) to be achieved at zero-bias in a device that incorporates an \(8.1\pm0.3 nm\)-thick dye film. The merits and drawbacks of the various device architectures and nanostructured material systems are discussed and the outlook for nanostructured photodetectors that exhibit infrared sensitivity is presented.<br>Engineering and Applied Sciences
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Books on the topic "Properties of cyanine dyes"

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Ferreira, L. F. Vieira. Photophysics of cyanine dyes adsorbed onto surfaces. Rutherford Appleton Laboratory, 1998.

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Klaus, Hunger, ed. Industrial dyes: Chemistry, properties, applications. Wiley-VCH, 2003.

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Nikolaĭ, Ti͡u︡i͡u︡lkov, ed. Polymethine dyes: Structure and properties. St. Kliment Ohridski University Press, 1991.

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Lucjan, Strękowski, ed. Heterocyclic polymethine dyes: Synthesis, properties and applications. Springer, 2008.

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Todd, Richard Samuel Joseph. The optical properties of triazinylaniline dyes in homogeneous and organized media. TheAuthor], 1987.

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Zollinger, Heinrich. Color chemistry: Syntheses, properties, and applications of organic dyes and pigments. 2nd ed. VCH, 1991.

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Zollinger, Heinrich. Color chemistry: Syntheses, properties and applications of organic dyes and pigments. VCH, 1987.

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Zollinger, Heinrich. Color chemistry: Syntheses, properties, and applications of organic dyes and pigments. VCH, 1987.

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Owen, Hywel Leroy. Physical properties of organosiloxane ferroelectric liquid crystals and fluorescent dyes for electro-optic device applications. University of Manchester, 1995.

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Hamer, Frances M. Cyanine Dyes and Related Compounds. Wiley & Sons, Incorporated, John, 2009.

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Book chapters on the topic "Properties of cyanine dyes"

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Sturmer, David M. "Syntheses and Properties of Cyanine and Related Dyes." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187005.ch8.

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Kocheshev, Igor A., Vladyslava B. Kovalska, and Sergiy M. Yarmoluk. "Spectral properties of novel cyanine homodimere dyes as possible fluorescent probes for nucleic acids detection." In Spectroscopy of Biological Molecules: New Directions. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4479-7_281.

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Matsuoka, Masaru. "Cyanine Dyes." In Infrared Absorbing Dyes. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2046-1_3.

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Henrie, Robert N., Thomas Cullen, Benjamin Dugan, et al. "Discovery of Insecticidal Cyanine Dyes." In ACS Symposium Series. American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0948.ch007.

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Larivé, Henri, and René Dennilauler. "Cyanine Dyes Derived from Thiazolium Salts." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187074.ch2.

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Rettig, W., K. Rurack, and M. Sczepan. "From Cyanines to Styryl Bases — Photophysical Properties, Photochemical Mechanisms, and Cation Sensing Abilities of Charged and Neutral Polymethinic Dyes." In New Trends in Fluorescence Spectroscopy. Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-56853-4_7.

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Tolmachev, A. I., Yu L. Slominskii, and A. A. Ishchenko. "New Cyanine Dyes Absorbing in the NIR Region." In Near-Infrared Dyes for High Technology Applications. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5102-3_19.

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Jung, Michael E., Wan-Joong Kim, Nuraly K. Avliyakulov, Merve Oztug, and Michael J. Haykinson. "Synthesis and Validation of Cyanine-Based Dyes for DIGE." In Methods in Molecular Biology. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-573-2_6.

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Deligeorgiev, Todor G. "Molecular Probes Based on Cyanine Dyes for Nucleic Acid Research." In Near-Infrared Dyes for High Technology Applications. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5102-3_6.

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Bricks, Yu L., and N. N. Romanov. "Near-Infrared Cyanine Dyes: A New Approach to an Old Problem." In Near-Infrared Dyes for High Technology Applications. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5102-3_20.

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Conference papers on the topic "Properties of cyanine dyes"

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Ogoshi, Kunizoh, Fumio Matsui, Tsutomu Suzuki, and Takeo Yamamoto. "An Optical Recording Disk Using an Organic Dye Medium." In Optical Data Storage. Optica Publishing Group, 1985. http://dx.doi.org/10.1364/ods.1985.wdd2.

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Many organic dyes have been proposed as a recording media for Optical Digital Data Disks. It was found that a water-insoluble cyanine dye has excellent properties as an optical recording medium. Some of the properties of the cyanine dye for that purpose are as follows.
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Salaeh, Salsabila, Wei Lim Chong, Supaporn Dokmaisrijan, et al. "Theoretical structures and binding energies of RNA-RNA/cyanine dyes and spectroscopic properties of cyanine dyes." In 3RD INTERNATIONAL CONFERENCE ON FUNDAMENTAL AND APPLIED SCIENCES (ICFAS 2014): Innovative Research in Applied Sciences for a Sustainable Future. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898453.

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Starovoytov, A. A., V. I. Belotitskii, Yu A. Kumzerov, and A. A. Sysoeva. "Optical properties of cyanine dyes in the nanoporous chrysotile asbestos." In 2016 International Conference Laser Optics (LO). IEEE, 2016. http://dx.doi.org/10.1109/lo.2016.7549923.

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Starovoytov, Anton A., Tigran A. Vartanyan, Vladimir I. Belotitskii, Yuri A. Kumzerov, and Anna A. Sysoeva. "Optical properties of cyanine dyes in nanotubes of chrysotile asbestos." In Nanophotonic Materials XIV, edited by Stefano Cabrini, Gilles Lérondel, Adam M. Schwartzberg, and Taleb Mokari. SPIE, 2017. http://dx.doi.org/10.1117/12.2274721.

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Kawabe, Yutaka, Sho Kato, Mayuko Honda, and Junichi Yoshida. "Effects of DNA on the optical properties of cyanine dyes." In SPIE NanoScience + Engineering, edited by Norihisa Kobayashi, Fahima Ouchen, and Ileana Rau. SPIE, 2010. http://dx.doi.org/10.1117/12.858846.

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Toropov, Nikita A., Anton A. Starovoytov, Nikita B. Leonov, Elena N. Kaliteevskaya, and Tigran A. Vartanyan. "Optical properties of silver nanoparticles coated by cyanine dyes molecular overlayers." In SPIE Microtechnologies, edited by Rainer Adelung. SPIE, 2013. http://dx.doi.org/10.1117/12.2017137.

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He, Xuemei, Junyi Yang, Yu Fang, Feng Zhou, and Yinglin Song. "The third-order nonlinear optical properties of unsymmetrical trimethine cyanine dyes." In Applied Optics and Photonics China (AOPC2015), edited by Shibin Jiang, Lijun Wang, Chun Tang, and Yong Cheng. SPIE, 2015. http://dx.doi.org/10.1117/12.2202964.

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Bjornholm, T., K. B. Simonsen, J. Becher, J. C. Petersen, and T. Geisler. "Nonlinear optical properties of cyanine-like dyes derived from bis-dithioles." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835736.

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Ibrayev, N. Kh, E. Seliverstova, D. Afanasyev, A. Nurmakhanova, N. A. Davidenko, and A. A. Ishchenko. "Photonics of cyanine dyes of different ionicity in matrices of halogen-containing derivatives of PEPC." In 2017 IEEE 7th International Conference "Nanomaterials: Application & Properties" (NAP). IEEE, 2017. http://dx.doi.org/10.1109/nap.2017.8190246.

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Tsukruk, V. V., A. Liebmann, Foster, et al. "Composite Molecular Films From Cyanine Dye Single Crystals Grown On Lipid Monolayers." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.19.

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Abstract:
Cyanine dyes can be used for formation of composite molecular Langmuir- Blodgett (LB) films with interesting photosensitive properties and prospects of non-linear optical applications1. For water-soluble cyanine dye molecules the possibility of epitaxial single crystal growth by adsorption of dye molecules onto the surface of oppositely charged lipid monolayers was demonstrated recently2. X-ray analysis, electron diffraction and fluorescence microscopy give information about unit cell parameters, average thickness of these composite LB films, and their morphology on a micron scale2,3 Data about surface morphology and roughness on a submicron scale and details of the molecular packing in these films have not yet been obtained. Here we discuss the results of atomic force microscopy (AFM) and quantitative X-ray reflectivity studies of the molecular structures of these composite molecular films.
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Reports on the topic "Properties of cyanine dyes"

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Bird, G., P. Panayotatos, R. Sauers, and J. Potenza. Photovoltaic p-n junction cells employing new organic dyes having high stability and designed molecular properties: Final subcontract report. Office of Scientific and Technical Information (OSTI), 1986. http://dx.doi.org/10.2172/7228960.

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