Relevant bibliographies by topics / Heterocyclic Dye

Contents

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

Academic literature on the topic 'Heterocyclic Dye'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Heterocyclic Dye"

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Abdel‐Hafiz, S. A., and Y. M. El‐Kholy. "Heterocyclic dye synthesis." Pigment & Resin Technology 24, no. 5 (1995): 13–16. http://dx.doi.org/10.1108/eb043153.

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Sparr, Christof, and Christian Fischer. "Configurationally Stable Atropisomeric Acridinium Fluorophores." Synlett 29, no. 16 (2018): 2176–80. http://dx.doi.org/10.1055/s-0037-1610233.

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Arylated heterocyclic fluorophores are particularly useful scaffolds for numerous applications, such as bioimaging or synthetic photochemistry. While variation of the substitution pattern at the heterocycle and aryl groups allows dye modulation, the bond rotational barriers are also strongly affected. Unsymmetrically substituted ring systems of rotationally restricted arylated heterocycles therefore lead to configurationally stable atropisomeric fluorophores. Herein, we describe these characteristics by determining the properties and configurational stability of atropisomeric, tri-ortho-substi
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Anita, Gour*1 Shirin Imam2 &. Niharika Shivhare3. "ANALYSIS AND PREPARATION OF AZO DISPERSE DYE C25H21N5O5." GLOBAL JOURNAL OF ENGINEERING SCIENCE AND RESEARCHES 4, no. 12 (2017): 129–32. https://doi.org/10.5281/zenodo.1133322.

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Disperse Dyes are aromatic heterocyclic organic compound. Advances over the last decade concerning the synthesis, properties and application of azo disperse dyes prepared from diazo components containing aromatic heterocycles are discussed here. Preparation of some novel disperse azo dyes synthesized by the coupling component of diazonium salt 1-(4-Aminophenyl)- 4 -(4-methoxy-3-methylphenyl)-5-((4-nitrophenylhydrazono)-2, 6-(1H)-Pyridinedione (29A)1to give the corresponding various azo disperse dyes (A-E). these dyes were applied to polyster fabric and their fastness properties were evaluated.
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Li, Qianqian, Zhongxing Jiang, Jingui Qin, and Zhen Li. "Heterocyclic-Functionalized Organic Dyes for Dye-Sensitized Solar Cells: Tuning Solar Cell Performance by Structural Modification." Australian Journal of Chemistry 65, no. 9 (2012): 1203. http://dx.doi.org/10.1071/ch12126.

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Due to their high conversion efficiency and low cost of production, dye-sensitized solar cells based on organic dyes have attracted considerable attention. By utilizing various heterocycles as construction blocks for organic dyes, the performance of solar cells was optimized to exhibit good light-harvesting features and suppress interfacial recombinations. The aim of this review is to highlight recent progress in the molecular design of heterocyclic-functionalized organic dyes for efficient dye-sensitized solar cells, and special attention has been paid to the relationship between chemical str
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B., R. MODI, B. D. MISTRY (MS.), and R. DESAI K. "Heterocyclic Dye Synthesis : Synthesis and Dyeing Performance of 4-Oxoquinazoline Dyes. Part-I." Journal of Indian Chemical Society Vol. 73, Aug 1996 (1996): 439–41. https://doi.org/10.5281/zenodo.5902171.

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Department of Chemistry, South Gujarat University, Surat-395 007 <em>Manuscript received 24 December 1993, revised 17 May 1994. accepted 27 January 1995</em> Heterocyclic Dye Synthesis : Synthesis and Dyeing Performance of 4-Oxoquinazoline Dyes. Part-I.
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Zhang, Yingtian, Huaiyan Ren, Huawei Zhou, et al. "Efficient CO2 Electrocarboxylation Using Dye-Sensitized Photovoltaics." Molecules 30, no. 1 (2024): 40. https://doi.org/10.3390/molecules30010040.

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This paper presents the solar-driven electrocarboxylation of 2-bromopyridine (2-BP) with CO2 into high-value-added chemicals 2-picolinic acid (2-PA) using dye-sensitized photovoltaics under simulated sunlight. Using three series-connected photovoltaic modules and an Ag electrode with excellent catalytic performance, a Faraday efficiency (FE) of 33.3% is obtained for 2-PA under mild conditions. The experimental results show that photovoltaics-driven systems for electrocarboxylation conversion of CO2 with heterocyclic halide to afford value-added heterocyclic carboxylic acid are feasible and eff
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Fernandes, Sara S. M., Maria Cidália R. Castro, Dzmitry Ivanou, Adélio Mendes, and Maria Manuela M. Raposo. "Push-Pull Heterocyclic Dyes Based on Pyrrole and Thiophene: Synthesis and Evaluation of Their Optical, Redox and Photovoltaic Properties." Coatings 12, no. 1 (2021): 34. http://dx.doi.org/10.3390/coatings12010034.

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Three heterocyclic dyes were synthesized having in mind the changes in the photovoltaic, optical and redox properties by functionalization of 5-aryl-thieno[3,2-b]thiophene, 5-arylthiophene and bis-methylpyrrolylthiophene π-bridges with different donor, acceptor/anchoring groups. Knoevenagel condensation of the aldehyde precursors with 2-cyanoacetic acid was used to prepare the donor-acceptor functionalized heterocyclic molecules. These organic metal-free dyes are constituted by thieno[3,2-b]thiophene, arylthiophene, bis-methylpyrrolylthiophene, spacers and one or two cyanoacetic acid acceptor
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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 s
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Rana, Rashmi, and Anam Ansari. "Synthesis of 7-Membered Heterocyclic Compounds and Their Biological Activity." Journal of Physics: Conference Series 2603, no. 1 (2023): 012058. http://dx.doi.org/10.1088/1742-6596/2603/1/012058.

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Abstract Heterocyclic compounds are an important class of organic compound. Owing to their usefulness in synthetic processes, numerous heterocyclic compounds are currently known, and this number is growing quickly. The uses of heterocyclic compounds are numerous. They are mostly used as veterinary goods, agricultural chemicals, and medications. Additionally, they are used as sanitizers, cleansers, antioxidants, corrosion inhibitors, co-polymers, and dye ingredients. The ring of a heterocyclic compound contains at least two unique components as members. On such a cyclic ring, the frequent heter
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Geiger, Thomas, Iuliia Schoger, Daniel Rentsch, et al. "Unsymmetrical Heptamethine Dyes for NIR Dye-Sensitized Solar Cells." International Journal of Photoenergy 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/258984.

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Seven unsymmetrical heptamethine dyes with carboxylic acid functionality were synthesized and characterized. These near-infrared dyes exhibit outstanding photophysical properties depending on their heterocyclic moieties and molecular structure. As proof of principle, the dyes were used as photosensitizers in dye-sensitized solar cells. Using the most promising dye, an overall conversion efficiency of 1.22% and an almost colorless solar cell were achieved.
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Dissertations / Theses on the topic "Heterocyclic Dye"

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Clemence, Nathan C. "Pyrolytic syntheses of 6,5,5 heterocyclic systems as novel magenta dye couplers." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/14577.

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Heterocyclic ring systems of the 6,5,5 azoloindole type have been found to have potential applications in colour photography as magenta dye couplers. The work described here has involved using flash vacuum pyrolysis (FVP) as a novel synthetic route to these tricyclic systems and structurally related tetracyclics. With new disconnections involving a key FVP stage, synthesis of complex ring systems can be reduced to as little as two or three steps, giving a significant advantage over more conventional synthetic routes. In this case FVP of substituted 2-(azolo)nitrobenzene and related heterocycli
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Walker, Philip Anthony. "Synthesis of functionalised benzothiophenes and novel heterocyclic dyes." Thesis, Bangor University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278813.

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Boyle, Kevin J. "Synthesis and properties of new heterocyclic metallised dyes." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/12580.

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Various 3-substituted isoquinolin-4-ols have been successfully synthesised by two different methodologies. Treatment of isoquinoline <i>N</i>-oxide with <i>p</i>-toluenesulfonyl chloride, provided 4-(<i>p</i>-toluenesulfonyloxy) isoquinoline in 30% yield and high purity <i>via </i>rearrangement of an intermediate <i>N</i>-(<i>p</i>-toluenesulfonyloxy) compound. Isoquinolin-4-ol was then obtained, after acid hydrolysis of 4-(<i>p</i>-toluenesulfonyloxy) isoquinoline. 3-Methylisoquinolin-4-ol has been synthesised in a similar manner and yield, from 3-methylisoquinoline <i>N</i>-oxide <i>via </i>
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Burrows, Kenneth Dvid. "The chemistry of some heterocyclic analogues of triphenylmethane dyes." Thesis, University of Central Lancashire, 1985. http://clok.uclan.ac.uk/20234/.

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A comprehensive series of triphenylmethane dyes has been synthesised in which the phenyl ring of Malachite Green has been replaced by a 5- or 6- membered heterocycle containing nitrogen, oxygen or sulphur as hetetâacoins. The visible absorption spectra of the dyes have been correlated with the electronic and structural features of the molecules. Novel analogues of Malachite Green have been prepared containing terminal pyrrolidine and N-methylpiperazine groups. Differences in the electronic absorption spectra of the parent dyes have been compared with those of related systems and the difference
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Iannarelli, Paul M. "Routes to novel azo compounds." Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/3492.

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Routes to novel heterocyclic azo compounds and components of use as potential inkjet dyes were investigated. A new route to fluorenones from biphenyl acid chlorides using FVP (Flash Vacuum Pyrolysis) has been discovered. Fluorenone and 4-methylfluoren-9-one were prepared by FVP of 2-phenylbenzoyl chloride and 2-methylbiphenyl-2-carbonyl chloride respectively. Xanthen-9-one and thioxanthen-9-one were also prepared by FVP from the corresponding acid chlorides. 9-Phenanthrol could also be prepared via the FVP of biphenylacetyl choride and the application of this method to a heterocylic thiophene
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Bender, Christoph. "Stereoselektive Synthese neuartiger 1,2-Dihydroisochinoline als Vorstufen für die Alkaloidsynthese." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2008. http://dx.doi.org/10.18452/15728.

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Ausgangspunkte der vorliegenden Arbeit waren stereoselektive Synthesen von Reissert-Verbindungen über chirale N-Acylisochinoliniumsalze. Es galt die Konfiguration der erhaltenen Produkte zu beweisen und deren Synthesepotential zu erforschen. Ein Ziel dieser Arbeit war es, weiterführende Reaktionen für die Synthese von alkaloidanalogen Substanzen zu entwickeln. Es gelang, die Reissert-Reaktion mit Chlorameisensäurementhylester erfolgreich auf andere Heterocyclen als Isochinolin auszudehnen. Die Annahme eine stereoselektiven Verlaufes mußte korrigiert werden. Das Reissert-Produkt konnte mit eine
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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 f
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Thireau, Jérémy. "Conception et synthèse de ligands fluorescents des récepteurs de la mélatonine." Thesis, Orléans, 2013. http://www.theses.fr/2013ORLE2003.

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La mélatonine est une neurohormone synthétisée au niveau de la glande pinéale durant la période nocturne chez l'ensemble des mammifères. Les sécrétions de cette hormone circulante par voie sanguine permette à tout système doté de récepteurs mélatoninergiques (MT1, MT2) de transmettre l'information de photopériode entrainant ainsi une adaptation aux périodes jour/nuit. La mélatonine est impliquée dans de nombreuses fonctions biologiques mais aussi dans diverses pathologies du système nerveux central tel que les troubles du rythmes circadien, l'anxiété, la dépression… A l'heure actuelle, il exis
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CHEHIMI, MOHAMED-MEHDI. "Applications de l'esca a l'analyse de materiaux organiques : etude de quelques merocyanines." Paris 7, 1988. http://www.theses.fr/1988PA077218.

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Examen des possibilites offertes par l'esca pour l'etude des polarites des liaisons, la distribution des cgarges et les transferts de charge intramoleculaires dans les composes organiques. Etude des correlations energie de liaison - charge atomique afin d'estimer les charges portees par les heteroatomes des merocyanines etudiees. Etude des problemes poses par l'analyse esca des composes organiques et des effets de la polarisation electrique du porte-echantillon
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Souffrin, Agathe. "Conception, synthèse et évaluation pharmacologique de maléimides, inhibiteurs potentiels de l'intégrase du VIH-1." Thesis, Tours, 2012. http://www.theses.fr/2012TOUR3801/document.

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Notre équipe de recherche a récemment développé les premiers inhibiteurs d’une enzyme à DDE, la transposase MOS1, une enzyme analogue à l’intégrase du VIH-1. Ces molécules, de type bisfurylmaléimides, ont également montré une efficacité contre les activités enzymatiques de l’intégrase du VIH. En se basant sur ces résultats, nous avons entrepris la synthèse de nouveaux bisfurylmaléimides dans le but d’identifier de nouveaux inhibiteurs de l’intégrase et de proposer de nouvelles molécules dans la lutte contre le virus responsable du SIDA. L’originalité de notre démarche est l’utilisation de la t
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Books on the topic "Heterocyclic Dye"

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

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Krohn, Karsten, and Ulrich Wolf. Kurze Einführung in die Chemie der Heterocyclen. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-99650-3.

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Sharma, Upendra K., and Erik V. Van der Eycken, eds. Flow-Chemie für die Synthese von Heterocyclen. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-51912-3.

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1944-, Wolf Ulrich, ed. Kurze Einführung in die Chemie der Heterocyclen. Teubner, 1994.

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Hofmann, F. B. Nicotine Psychopharmacology. Springer Berlin Heidelberg, 2009.

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Strekowski, Lucjan. Heterocyclic Polymethine Dyes: Synthesis, Properties and Applications. Springer, 2010.

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Flow-Chemie Für Die Synthese Von Heterocyclen. Spektrum Akademischer Verlag GmbH, 2024.

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Kurze Einführung in die Chemie der Heterocyclen. Vieweg+Teubner Verlag, 1994.

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Selected Non-heterocyclic Polycyclic Aromatic Heterocyclines (Environmental Health Criteria). World Health Organization, 1998.

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Kotschy, András, and Géza Timári. Heterocycles from Transition Metal Catalysis: Formation and Functionalization. Kotschy Andras Timari Geza, 2011.

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Book chapters on the topic "Heterocyclic Dye"

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Armitage, Bruce A. "Cyanine Dye–Nucleic Acid Interactions." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/7081_2007_109.

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Signorini, R., C. Ferrante, D. Pedron, et al. "Highly Efficient Multiphoton Absorption in a New Quadrupolar Heterocyclic Dye." In Organic Nanophotonics. Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0103-8_21.

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Bartsch, Herbert. "Heterocyclen." In Die systematische Nomenklatur organischer Arzneistoffe. Springer Vienna, 1998. http://dx.doi.org/10.1007/978-3-7091-7512-5_6.

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Krohn, Karsten, and Ulrich Wolf. "Benzokondensierte Fünfring-Heterocyclen." In Kurze Einführung in die Chemie der Heterocyclen. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-99650-3_4.

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Krohn, Karsten, and Ulrich Wolf. "Benzokondensierte Sechsring-Heterocyclen." In Kurze Einführung in die Chemie der Heterocyclen. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-99650-3_6.

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Krohn, Karsten, and Ulrich Wolf. "Fünfring-Heterocyclen mit einem Heteroatom." In Kurze Einführung in die Chemie der Heterocyclen. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-99650-3_3.

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Van Mileghem, Seger, Cedrick Veryser, and Wim M. De Borggraeve. "Durchflussunterstützte Synthese von Heterocyclen über Mehrkomponentenreaktionen." In Flow-Chemie für die Synthese von Heterocyclen. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-51912-3_3.

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Krohn, Karsten, and Ulrich Wolf. "Sechsring-Heterocyclen mit einem Heteroatom (Pyrane, Pyrone)." In Kurze Einführung in die Chemie der Heterocyclen. Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-99650-3_5.

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Sullivan, Ryan J., and Stephen G. Newman. "Durchflussunterstützte Synthese von Heterocyclen bei hohen Temperaturen." In Flow-Chemie für die Synthese von Heterocyclen. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-51912-3_4.

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Baumann, Marcus, and Ian R. Baxendale. "Durchflusschemieansätze angewendet auf die Synthese von gesättigten Heterocyclen." In Flow-Chemie für die Synthese von Heterocyclen. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-51912-3_5.

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Conference papers on the topic "Heterocyclic Dye"

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Pavlopoulos, Theodore G., and Joseph H. Boyer. "Quasi-Aromatic Heterocyclics As Laser Dyes." In OE/LASE '89, edited by E. R. Menzel. SPIE, 1989. http://dx.doi.org/10.1117/12.951562.

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Devine, Robert L. S., William H. Steier, Malcolm R. Mclean, Mamoun Badr, and L. R. Dalton. "Second-order nonlinear optical organic molecules with conjugated heterocyclic backbones." In OSA Annual Meeting. Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.mc2.

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Second-order nonlinear optical organic molecules are currently under intense investigation due to the very large nonlinearities which are possible. The role of conjugation in facilitating through-bond interactions in such optically nonlinear molecules is well known.
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Reinhardt, Bruce A., Lawrence L. Brott, Stephen J. Clarson, Ramamurthi Kannan, and Ann G. Dombroskie. "Optical power limiting in solution via two-photon absorption: new aromatic heterocyclic dyes with greatly improved performance." In Optical Science, Engineering and Instrumentation '97, edited by Christopher M. Lawson. SPIE, 1997. http://dx.doi.org/10.1117/12.279298.

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Guimarães, Willian, Andre Formiga, Renan Guerra, and Luis Huamaní. "Study of the water oxidation mechanism by ruthenium(ii) complexes containing N-heterocyclic ligands." In Congresso de Iniciação Científica UNICAMP. Universidade Estadual de Campinas, 2019. http://dx.doi.org/10.20396/revpibic2720192314.

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HENRIQUE GONCALVES DEFANTE, LUIS, and Ronaldo Aloise Pilli. "Adition of Nitro Compounds to N-Acyliminium Íons and Coupling with Aldehaydes Performed by N-Heterocyclic Carbenes." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-51083.

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Andrejević, Tina P., Darko P. Ašanin, Nada D. Savić, Nevena Lj Stevanović, Miloš I. Djuran, and Biljana Đ. Glišić. "DNA/BSA BINDING STUDY OF DINUCLEAR GOLD(III) COMPLEXES WITH AROMATIC NITROGEN-CONTAINING HETEROCYCLES AS BRIDGING LIGANDS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.312a.

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In recent decades, a special attention has been devoted to gold(III) complexes as potential antitumor agents due to their structural similarity to platinum(II) complexes. One of the possible mechanisms of the mode of antitumor activity of gold(III) complexes could include their interaction with DNA. However, the effectiveness of the therapeutic agents also depends on the degree of its binding to proteins present in the blood plasma, because, in this way, it is transported to the cell. Considering this, we investigated the interactions of three dinuclear gold(III) complexes of the general formu
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Yang, Zhen, Yefei Wang, Matjaž Finšgar, Jiajia Wu, and Wengang Ding. "Novel High-Efficient Key Component of Steel Corrosion Inhibitors Formulation for Acidification: Indolizine Derivatives of the Conventional N-Heterocyclic Quaternary Ammonium Salts." In SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213814-ms.

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Abstract Acidizing, the widely used technique for well stimulation, requires a great consumption of effective Corrosion Inhibitors (CIs), due to the severe and fast corrosion of metallic equipment caused by strong hot acid as soon as the acidizing fluids are pumping down to reservoir. This paper presents a new concept of indolizine derivative inhibitors with remarkable inhibition effectiveness for steel under acidizing condition, which will reduce the cost and environmental burden of acidizing CIs significantly. Indolizine derivatives of several quinolinium salts (serves as main component of c
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Lazić, Anita, Ivana Đorđević, Kristina Gak Simić та ін. "Correlation of structure and potential pharmacological activity of spirohidantoins derived from α-Tetralone". У 37th International Congress on Process Industry. SMEITS, 2024. http://dx.doi.org/10.24094/ptk.024.279.

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Hydantoin is a nonaromatic five-membered heterocycle, which is considered a valuable, privileged scaffold in medicinal chemistry. The importance of the hydantoin scaffold in drug dis-covery has been reinforced by several medicines in clinical use, such as anticonvulsants (phenyto-in), antibiotics (nitrofurantoin), anticancer drugs (enzalutamide) and keratolytics (allantoin). To design new potentially pharmacologically active compounds, six spirohydantoin derivatives were synthetized and fully characterized by determination of the melting points, elemental analysis, FT-IR, 1H and 13C NMR spectr
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Ungur, Nicon, Aurelian Gulea, and Tatiana Erhan. "Synthesis and study of the same hydrazincarbothioamides as privilege pharmacophores in pharmacology." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab05.

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Hydrazinecarbothioamides represent a privileged class of pharmacophores in pharmacology, thanks to an impressive number of derivatives that exhibit outstanding antimicrobial, anticancer and antifungal properties [1]. The presence of electron donor atoms such as N(nitrogen) and S(sulfur) substantially widen the spectrum of use. In the framework of theoretical studies on the structure of biologically active compounds with valuable properties were highlighted following common structural elements such as substitution of a hydrogen atom from the nitrogen atom (N) with the benzene ring, the introduc
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Reports on the topic "Heterocyclic Dye"

1

Boyer, Joseph H. Heterocycles as Laser Dyes. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada251574.

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2

Pavlopoulos, Theodore G., and Joseph H. Boyer. Quasi-Aromatic Heterocyclics as Laser Dyes. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada207134.

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3

Altstein, Miriam, and Ronald J. Nachman. Rational Design of Insect Control Agent Prototypes Based on Pyrokinin/PBAN Neuropeptide Antagonists. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7593398.bard.

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Abstract:
The general objective of this study was to develop rationally designed mimetic antagonists (and agonists) of the PK/PBAN Np class with enhanced bio-stability and bioavailability as prototypes for effective and environmentally friendly pest insect management agents. The PK/PBAN family is a multifunctional group of Nps that mediates key functions in insects (sex pheromone biosynthesis, cuticular melanization, myotropic activity, diapause and pupal development) and is, therefore, of high scientific and applied interest. The objectives of the current study were: (i) to identify an antagonist bioph
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