Relevant bibliographies by topics / Carbazoli

Contents

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

Academic literature on the topic 'Carbazoli'

Author: Grafiati
Published: 10 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "Carbazoli"

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Manu, Tripathi* Shweta Shukla Meera Kumari Amresh Gupta. "Recent advancement of carbazole hybrid: a privileged scaffold in new drug discovery." International Journal of Advances in Pharmacy Medicine and Bioallied Sciences 10, no. 3 (2022): 123–34. https://doi.org/10.5281/zenodo.7709108.

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Carbazole comprises an important class of heterocycles. Carbazole is a tricyclic molecule having a coal tar carbon backbone, and also it has the structural properties of numerous compounds used in electronics for the manufacturing of polymers or dyes and electroluminescent materials, owing to its luminous quality. It has been reported that diverse biological activities include anti-cytotoxicity, bacteria-related problems, neurological problems, etc. Some carbazole derivatives were created such carbazoles with N-substitution, benzocarbazoles, furocarbazoles, pyrrolo-carbazoles, imidazo-carbazol
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Hsiao, Sheng-Huei, and Shu-Wei Lin. "Electrochemical synthesis of electrochromic polycarbazole films from N-phenyl-3,6-bis(N-carbazolyl)carbazoles." Polymer Chemistry 7, no. 1 (2016): 198–211. http://dx.doi.org/10.1039/c5py01407g.

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Sweta, Shukla, and Gupta Sujeet. "Carbazole derivatives: an attractive scaffold in anticancer lead discovery." International Journal of Advances in Pharmacy Medicine and Bioallied Sciences 10, no. 2 (2022): 88–93. https://doi.org/10.5281/zenodo.7066183.

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Cancer is one of the leading chronic diseases with a high mortality rate worldwide.  Current statistical studies on cancer estimates from the World Health Organization (WHO) in 2020, cancer is the first or second leading cause of death. Although cancer remains a devastating diagnosis, several decades of preclinical progress in cancer biology and biotechnology have recently led to the successful development of several biological agents that substantially improve survival and quality of life for some patients. For over half a century, the carbazole skeleton has been the key structural motif
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Liebau, Verena, Mathias Noltemeyer, Jörg Magull, and Uwe Klingebiel. "Carbazolylsilane: Synthese und Kristallstrukturen / Carbazolylsilanes: Synthesis and Crystal Structures." Zeitschrift für Naturforschung B 59, no. 9 (2004): 1045–50. http://dx.doi.org/10.1515/znb-2004-0916.

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Carbazole reacts with n-BuLi and fluorosilanes to give the lithium carbazolide (1) which crystallizes as a dimer from THF. In the reactions of 1 and difluorosilanes, F2SiR2, the carbazolylsilanes C12H8N-SiFR2 (2 - 4 R = Me (2), i Pr (3), t-Bu (4)), are obtained. Bis(carbazolyl)silanes, (C12H8N)2SiFR, are formed in the reaction of 1 with trifluorosilanes, F3SiR, in a molar ratio of 2:1, R = t-Bu (5), Ph (6), Me (7). Using F3SiMe and 1 in a molar ratio of 1:3 the tris(carbazolyl)silane (C12H8N)3SiMe (8) is isolated. The carbazolylfluorosilane 3 reacts with n-BuLi to give 1 and n-butyldiisopropyl
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Karaaslan, Cigdem, Hande Gurer-Orhan, Sibel Suzen, et al. "Behaviour of 9-Ethyl-9H-carbazole Hydrazone Derivatives Against Oxidant Systems." Croatica chemica acta 92, no. 1 (2019): 87–94. http://dx.doi.org/10.5562/cca3481.

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Antioxidants are helpful in prevention of several diseases related with oxidative stress including neurodegenerative disorders. In recent studies, carbazoles were given proof of promising antioxidant activities. In this article, 9-ethyl-9H-carbazole hydrazone derivatives were synthesized, characterized and their in vitro antioxidant activity and possible cytotoxic effects were investigated. Furthermore, protective effect of the synthesized derivatives against amyloid β-induced damage in PC12 neuronal cells was examined by using MTT assay. The newly synthesized carbazoles were found to have rad
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Luparello, Claudio, Ilenia Cruciata, Andreas C. Joerger, et al. "Genotoxicity and Epigenotoxicity of Carbazole-Derived Molecules on MCF-7 Breast Cancer Cells." International Journal of Molecular Sciences 22, no. 7 (2021): 3410. http://dx.doi.org/10.3390/ijms22073410.

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The carbazole compounds PK9320 (1-(9-ethyl-7-(furan-2-yl)-9H-carbazol-3-yl)-N-methylmethanamine) and PK9323 (1-(9-ethyl-7-(thiazol-4-yl)-9H-carbazol-3-yl)-N-methylmethanamine), second-generation analogues of PK083 (1-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamine), restore p53 signaling in Y220C p53-mutated cancer cells by binding to a mutation-induced surface crevice and acting as molecular chaperones. In the present paper, these three molecules have been tested for mutant p53-independent genotoxic and epigenomic effects on wild-type p53 MCF-7 breast adenocarcinoma cells, employing a combinat
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Beresneviciute, Raminta, Anil Kumar, Dovydas Blazevicius, et al. "Carbazolyl Electron Donor and Pyridinyl Electron Acceptor Containing Derivatives as Potential Host Materials for Green Organic Light-Emitting Diodes." Molecules 30, no. 9 (2025): 1911. https://doi.org/10.3390/molecules30091911.

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Here, we present two series of new electroactive compounds containing electron donors (carbazolyl) and electron acceptor (pyridinyl) fragments as potential host materials. The objective compounds 9-(2-ethylhexyl)-3,6-di [3-(methoxypyridin-3-yl)carbazol-9-yl]carbazoles RB71 and RB74 were synthesized by an Ullmann coupling reaction between the intermediate derivatives: 9-(2-ethylhexyl)-3,6-diiodocarbazole and corresponding 3-(methoxypyridin-3-yl)-9H-carbazole. Other target derivatives, 9-alkyl-3-[N-(9-alkylcarbazol-3-yl)-N-(4-methylpyridin-2-yl)amino]carbazoles RB70 and RB75, were also prepared,
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Nitin Kumar, Neetika lal, Vishal Nemaysh, and Pratibha Mehta Luthra. "Synthesis and in vitro anticancer activity of novel 1,4-dimethyl-9-H-carbazol-3-yl) methanamine derivatives against human glioma U87 MG cell line." World Journal of Advanced Research and Reviews 19, no. 1 (2023): 1099–108. http://dx.doi.org/10.30574/wjarr.2023.19.1.1446.

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Glioblastoma Multiforme (GBM) is most aggressive type of brain tumor in adults. 1,4-dimethyl carbazoles exhibits significant anticancer activities in literature. In this research article, we synthesized a series of novel 1,4-dimethyl-9-H-carbazol-3-yl)methanamine and its derivatives (13-24) and evaluated their in vitro cytotoxicity activities against human glioma U87 MG cell line using MTT assay for 24 h phase time period. All final carbazole derivatives were well confirmed by NMR and HRMS spectroscopy techniques. In series, few compound (15-17) found excellent in vitro anticancer activity (IC
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Krucaite, Gintare, and Saulius Grigalevicius. "Low Molar Mass Carbazole-Based Host Materials for Phosphorescent Organic Light-Emitting Diodes: A Review." Coatings 15, no. 4 (2025): 398. https://doi.org/10.3390/coatings15040398.

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The second-generation phosphorescent organic light-emitting diodes are formed using phosphorescent emitters, which can theoretically achieve 100% internal quantum efficiency. However, these emitting materials usually suffer from triplet–triplet annihilation (TTA) and/or concentration-quenching effects. To address the disadvantages, host–guest systems are used in the emitting layer, where the guest is dispersed into a host matrix. Carbazole is one of the most commonly used electron-donating fragments, which is widely applied as a building block for the synthesis of the mentioned host materials.
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Lifshits, Liubov M., Varun Singh, Matthias Zeller, and Jeremy K. Klosterman. "Ethyl 4-(9H-carbazol-9-yl)benzoate: fivefold superstructure with ten crystallographically independent molecules refined from a twinned crystal." Acta Crystallographica Section C Structural Chemistry 72, no. 11 (2016): 901–9. http://dx.doi.org/10.1107/s2053229616015825.

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The photophysical properties of organic fluorophores are sensitive to the local sterics of the surrounding environment. Restriction of torsional motion in aggregates and crystals can give rise to enhanced emissive behavior.N-Aryl-substituted carbazoles serve an essential role as ubiquitous host matrices for organic light-emitting diodes, due to their large band gaps and high triplet energies, and so studies connecting photophysical behaviors with detailed crystallographic structural information are important. To elucidate the structural changes involved in the excited-state charge-transfer pro
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Dissertations / Theses on the topic "Carbazoli"

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Marrelli, Mariangela. "Progettazione, sintesi e valutazione dell'attivita biologica di nuovi carbazoli." Paris 5, 2011. http://www.theses.fr/2011PA05P605.

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Ce travail de thèse a été réalisé au Laboratoire de Pharmacognosie de l’Université Paris Descartes et au Laboratoire de Phytopharmacie du Département des Sciences Pharmaceutiques de l’Université de Calabre. L’objectif du travail était de synthétiser de nouveaux carbazoles conçus comme analogues d’un cis stilbène naturel, la combrétastatine A4 (CA-4) et d’évaluer les activités biologiques des composés réalisés. Des travaux antérieurs réalisés au laboratoire de l’Université Paris Descartes ont conduit à la synthèse de composés à potentialité antivasculaire, analogues de la combrétastatine A-4. D
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Marrelli, Mariangela. "Progettazione, sintesi e valutazione dell'attività biologica di nuovi carbazoli." Doctoral thesis, Universita degli studi di Salerno, 2011. http://hdl.handle.net/10556/243.

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2008 - 2009<br>Il presente lavoro di tesi è stato svolto presso il laboratorio di Fitofarmacia del Dipartimento di Scienze Farmaceutiche dell’Università della Calabria e presso il Laboratorio di Farmacognosia dell’Università Paris Descartes di Parigi. L’attività di ricerca è stata dedicata alla sintesi di nuovi carbazoli concepiti come analoghi dello stilbene naturale combretastatina A-4 (CA-4) ed alla successiva valutazione dell’attività biologica in vitro dei composti ottenuti. Presso il Laboratorio di Farmacognosia dell’Università Paris Descartes erano stati già sintetizzati degli analogh
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Knott, Kerstin. "Iron-mediated Synthesis of the Antiostatins." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1237582907592-42405.

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Within this thesis the first total syntheses of eight biologically active natural products from the family of carbazole alkaloids, antiostatins A1 to A4 and B2 to B5, were established. Spectroscopic data of the synthesised natural products are in good agreement with the isolated antiostatins from Streptomyces cyaneus 2007-SV1, which confirms the molecular structures assigned to the natural products. The total synthesis of the antiostatins A1 to A4 and B2 to B5 were achieved employing the iron-mediated synthesis to form the carbazole nucleus from a cyclohexadienylium iron salt and appropriate a
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Knott, Kerstin. "Iron-mediated Synthesis of the Antiostatins." Doctoral thesis, Technische Universität Dresden, 2008. https://tud.qucosa.de/id/qucosa%3A24053.

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Within this thesis the first total syntheses of eight biologically active natural products from the family of carbazole alkaloids, antiostatins A1 to A4 and B2 to B5, were established. Spectroscopic data of the synthesised natural products are in good agreement with the isolated antiostatins from Streptomyces cyaneus 2007-SV1, which confirms the molecular structures assigned to the natural products. The total synthesis of the antiostatins A1 to A4 and B2 to B5 were achieved employing the iron-mediated synthesis to form the carbazole nucleus from a cyclohexadienylium iron salt and appropriate a
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Ottone, Chiara. "Nouveaux copolymères donneur-accepteur : préparation, caractérisation physico-chimique et application des cellules photovoltaïques organiques." Phd thesis, Université de Grenoble, 2012. http://tel.archives-ouvertes.fr/tel-00864002.

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Ce travail de thèse concerne l'élaboration de nouveaux copolymères à faible bande interdite de type " push-pull ", constitués par une unité donneuse d'électrons (push) et une unité acceptrice d'électrons (pull) en modulant les relations structures-propriétés par stratégie de synthèse. Des copolymères constitués par des unités acceptrices d'électrons (dérivées du benzothiadiazole ou du thienopyrrolodione) et donneuses d'électrons (3,6-carbazole, 2,7-carbazole, dialkoxybezodithiophène) ont été obtenus par différentes méthodes de couplage carbone carbone (C-C). Des études physico-chimiques par de
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Dufour, Fabien. "Synthèse en série carbazolique, analogues d'ellipticine, et dihydrocarbazolocarbazoles." Thesis, Metz, 2007. http://www.theses.fr/2007METZ031S/document.

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L’ellipticine, alcaloïde tétracyclique naturel au squelette 6H-pyrido[4,3-b]carbazole, et certains de ses dérivés possèdent des propriétés antitumorales. L’objectif de ce travail a été, d’une part de trouver une méthode de synthèse de deux types d’intermédiaires précis non décrits à notre connaissance (dérivés du carbazole et de la pyridine), puis de synthétiser des analogues d’ellipticine possédant un cycle saturé supplémentaire, ces modifications structurales pouvant être intéressantes du point de vue de l’activité biologique. Initialement envisagée à partir de dérivés du furane par ouvertur
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Leontyev, Alexey E. "Carbazole-Fluorenone Dyes." Bowling Green State University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1245273099.

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Kirst, Juliane. "Synthese halogenierter Carbazole und Totalsynthese der Amaryllisalkaloide Pratosin und Hippadin." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-21142.

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Während meiner Dissertation beschäftigte ich mich mit der Synthese von polyhalogenierten Carbazolderivaten. Das Carbazolgerüst wurde über den Palladiumvermittelten, bestehend aus Buchwald-Hartwig-Aminierung und oxidativer Cyclisierung, aufgebaut. Die Halogensubstituenten wurden entweder am Carbazol eingeführt oder bereits über die Startmoleküle in die Synthese eingebracht. Somit konnten verschiedene halogenierte halogenierte Derivate synthetisiert werden. Diese Verbindungen konnten in einer Kooperation mit Herrn Prof. Gutzeit aus der Fachrichtung Biologie der TU Dresden auf ihre Aktivität in d
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Krahl, Micha P. "Regioselektive Synthese oxygenierter Carbazole." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2007. http://nbn-resolving.de/urn:nbn:de:swb:14-1168004377329-87485.

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In der heutigen Wirkstoffforschung stellen vor allem multiresistente Krankheitserreger eine große Herausforderung an die Wissenschaft dar. Noch sterben z.B. an der Tuberkulose jährlich etwa 1.7 Millionen Menschen, davon 69000 allein in Europa (WHO-Angaben, 2004). Die Tuberkulose verursacht neben AIDS die meisten Todesfälle unter den Infektionskrankheiten. Ein großes Problem sind die zahlreichen Neuerkrankungen, die mit herkömmlichen Mitteln nicht mehr behandelt werden können, sowie zunehmende Medikamentenallergien. Somit ist ein wichtiges Gebiet der Wirkstoff-forschung, neben der Weiterentwick
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Krahl, Micha P. "Regioselektive Synthese oxygenierter Carbazole." Doctoral thesis, Technische Universität Dresden, 2006. https://tud.qucosa.de/id/qucosa%3A24953.

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In der heutigen Wirkstoffforschung stellen vor allem multiresistente Krankheitserreger eine große Herausforderung an die Wissenschaft dar. Noch sterben z.B. an der Tuberkulose jährlich etwa 1.7 Millionen Menschen, davon 69000 allein in Europa (WHO-Angaben, 2004). Die Tuberkulose verursacht neben AIDS die meisten Todesfälle unter den Infektionskrankheiten. Ein großes Problem sind die zahlreichen Neuerkrankungen, die mit herkömmlichen Mitteln nicht mehr behandelt werden können, sowie zunehmende Medikamentenallergien. Somit ist ein wichtiges Gebiet der Wirkstoff-forschung, neben der Weiterentwick
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Books on the topic "Carbazoli"

1

Ryszard, Chrząszcz, ed. Barwniki karbazolowe. Politechnika Krakowska, 1986.

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2

E, Sirotkina E., Lopatinskiĭ V. P, and Institut khimii nefti (Rossiĭskai͡a akademii͡a nauk), eds. Khimii͡a monomerov na osnove karbazola. "Nauka," Sibirskai͡a izdatelʹskai͡a firma RAN, 1995.

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Sattler, Kristin S. Theoretische und experimentelle Studien zur DNA-Interkalation von Carbazol-Derivaten. [s.n.], 1994.

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Rehn, Carsten. Theoretische Studien zur DNA-Interkalation von Anthrachinon-, 9-Aminoacridin-, Isochinolin- und Pyrrolo-carbazol-1,3-dion-Derivaten sowie Synthese von Pyrrolo-carbazol-1,3-dionen. [s.n.], 1995.

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Rogge, Martina. Synthese und Reaktivität O-funktionalisierter (Indol-3-yl)-ethene als Präcursoren neuer funktionalisierter [b]-annelierter Indole und Carbazole. [s.n.], 1994.

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Caruso, Anna, ed. Carbazole Derivatives: Latest Advances and Prospects. MDPI, 2023. http://dx.doi.org/10.3390/books978-3-0365-7289-5.

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Carbazole Dendrimers for Solar Cells Putting. Ormond, Jennifer, 2023.

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Bauermeister, Michael. Eisen-vermittelter Aufbau von Carbazol-Alkaloiden. 1991.

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Sumpter, W. C., and F. M. Miller. Heterocyclic Compounds with Indole and Carbazole Systems. Wiley & Sons, Incorporated, John, 2009.

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Sumpter, W. C., and F. M. Miller. Chemistry of Heterocyclic Compounds, Indole and Carbazole Systems. Wiley & Sons, Incorporated, John, 2008.

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Book chapters on the topic "Carbazoli"

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Gooch, Jan W. "Carbazole." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1913.

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Bhattacharyya, P., and D. P. Chakraborty. "Carbazole Alkaloids." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1987. http://dx.doi.org/10.1007/978-3-7091-8906-1_4.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_44.

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Chakraborty, D. P., and Shyamali Roy. "Carbazole Alkaloids III." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1991. http://dx.doi.org/10.1007/978-3-7091-9119-4_2.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_41.

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Chakraborty, D. P., and Shyamali Roy. "Carbazole Alkaloids IV." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6051-0_3.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_42.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_36.

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Schomburg, Dietmar, and Ida Schomburg. "carbazole 1,9a-dioxygenase 1.14.12.22." In Class 1 Oxidoreductases. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36265-1_76.

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Nojiri, Hideaki, and Toshio Omori. "Carbazole Metabolism by Pseudomonads." In Pseudomonas. Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6097-7_5.

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Conference papers on the topic "Carbazoli"

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Chen, Li-Yin, and Yu-Hsiang Cheng. "Highly sensitive ammonia gas sensing up to ppb-region based on a carbazole-triazine derivative." In Organic and Hybrid Sensors and Bioelectronics XVII, edited by Ioannis Kymissis, Emil J. List-Kratochvil, and Sahika Inal. SPIE, 2024. http://dx.doi.org/10.1117/12.3027652.

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Darracq, Bruno, Didier Riehl, michael Canva, et al. "Photorefractive Sol-Gel Films." In The European Conference on Lasers and Electro-Optics. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/cleo_europe.1996.cwk4.

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We shall report about photorefractive hybrid xerogel film that were, for the first time to the best of our knowledge, synthesised by the sol-gel process. The silica backbone possesses covalently anchored non-linear optical chromophores (disperse red one) and charge transporting groups (carbazole units). The starling solutions were obtained from copolymerization of carbazole- and DRl-attached silane monomers with tetraethoxysilane (TEOS). A small amount of 2,4,7-trinitrofluorenone was also added to increase the photosensitivity in the visible. Thin films of thicknesses ranging from 0.5 to 5 mic
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Wada, Tatsuo, Yadong Zhang, Hiromi Kimura-Suda, Tetsuya Aoyama, Su-An Choi, and Hiroyuki Sasabe. "Multifunctional Photoresponses in Carbazole Main-Chain Polymers." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.thc.2.

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Electronic and optical properties of organic charge-transfer (CT) compounds have attracted a lot of attention from both fundamental science and practical applications. Remarkable progress have been made in development of electroactive CT materials such as organic metals, conducting polymers, and organic photoconductors (OPCs). Among them, OPCs are widely used for electrophotographic applications. Besides photoconductive properties, it has been elucidated experimentally and theoretically that organic inter- and intracharge transfer compounds exhibit large nonlinear optical (NLO) responses. We h
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Sun, Run G., Yunzhang Wang, Xiaoming Zou, et al. "Electroluminescence of carbazole-substituted polyacetylenes." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Zakya H. Kafafi. SPIE, 1998. http://dx.doi.org/10.1117/12.332631.

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Bermudez, Veronica, Francois Kajzar, S. Niziol, et al. "Linear and nonlinear optical properties of polyvinyl carbazole and polyvinyl-carbazole-substituted thin films." In International Symposium on Optical Science and Technology. SPIE, 2000. http://dx.doi.org/10.1117/12.408503.

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Andreev, Vladimir A., Anatoly L. Ivanov, Sergey M. Kazakov, Alexander V. Kukhta, Dennis V. Murtazaliev, and Gennadii M. Sorokin. "Electron impact excitation of carbazole vapor." In SPIE Proceedings, edited by Victor F. Tarasenko. SPIE, 2004. http://dx.doi.org/10.1117/12.562980.

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Aoyama, Tetsuya, Takafumi Sassa, Nicolai Mooren, et al. "Photorefractive properties of conjugated carbazole polymers." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Klaus Meerholz. SPIE, 2003. http://dx.doi.org/10.1117/12.510805.

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Wada, Tatsuo, and Hiroyuki Sasabe. "Multifunctional Carbazole Polymers for Nonlinear Optics." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.thc.5.

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Electric and optical properties of organic charge-transfer (CT) compounds have been attracted a lot of attention from both fundamental science and practical applications. Remarkable progress have been made in development of electroactive CT materials such as organic metals, conducting polymers, and organic photoconductor. Recently organic intracharge transfer compounds have been experimentally and theoretically elucidated to exhibit anomalously large nonlinear optical responses.1 Nonlinear optical properties of several CT complex systems have been studied and recently photorefractive effects h
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9

Bivol, Valeriu V., Stephan V. Robu, Galina Dragalina, L. Bostan, A. M. Prisacari, and A. Coban. "New photoresists from carbazol-containing photopolymers." In 2000 International Conference on Application of Photonic Technology (ICAPT 2000), edited by Roger A. Lessard and George A. Lampropoulos. SPIE, 2000. http://dx.doi.org/10.1117/12.406305.

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10

Lin, Jiann T., K. R. J. Thomas, Yu-Tai Tao, and Chung-Wen Ko. "Light-emitting carbazole derivatives for electroluminescent materials." In International Symposium on Optical Science and Technology, edited by Zakya H. Kafafi. SPIE, 2002. http://dx.doi.org/10.1117/12.457490.

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Reports on the topic "Carbazoli"

1

Steele, W. V., and R. D. Chirico. Thermodynamics of the hydrodenitrogenation of carbazole. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5089483.

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2

Barrett, Christopher J., Biswajit Choudhury, Almeria L. Natansohn, and Paul L. Rochon. Azo-Carbazole Polymethacrylates as Single-Component Electro-Optic Materials. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada348946.

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3

Steele, W. V., R. D. Chirico, S. E. Knipmeyer, and A. Nguyen. The thermodynamic properties of 2-aminobiphenyl (an intermediate in the carbazole/hydrogen reaction network). Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6307021.

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4

พงษ์สามารถ, สุนันท์, สุชาดา สุขหร่อง та ดวงเดือน เมฆสุริเยนทร์. ความปลอดภัยของการบริโภคสารสกัดเปลือกทุเรียน และการทำสารให้บริสุทธิ์ : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 1998. https://doi.org/10.58837/chula.res.1998.20.

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การศึกษาทำให้หนูถีบจักรและหนูขาวเพศผู้ป้อนให้กินสารสกัดคาร์โบไฮเดรตจากเปลือกทุเรียนขนาดสูงมาก DF[subscript I] และ DF[subscript II] เป็นสารโพลี่แซคคาไรด์มีกลูโคสเป็นน้ำตาลหลักและมีน้ำตาลพวกแรมโนสและอราบิโนส ฟรุกโตสพบเฉพาะใน DF[subscript I] ทำการทดลองตรวจสอบการเกิดพิษเฉียบพลันในสัตว์ทดลองเมื่อให้กินขนาด 2 ก/กก. น้ำหนักตัว/1 วัน ของสาร DF[subscript I] หรือ DF[subscript II] ไม่พบมีการตายหรือมีความเป็นพิษที่รุนแรงกับหนูถีบจักรและหนูขาวที่ให้กินสารทดลอง อย่างไรก็ดีในกลุ่มหนูถีบจักรพบว่าค่าเฉลี่ยของน้ำหนักตัวเพิ่มมีค่าต่ำมาก (p is less than or equal to 0.05) เป็นเวลา 3-4 วัน หลังวันให้กิน DF[subscrip
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