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Dissertations / Theses on the topic 'Carbazol'

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1

Gehring, André Philipe. "Biologisch aktive Carbazol-Derivate." Diss., lmu, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-155544.

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Kutz, Sebastian K. "Regioselektive Synthese substituierter Carbazol-1,4-chinone." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-200963.

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Die Ziele dieser Arbeit waren die Darstellung der Naturstoffe Murrayachinon-B–E und Pyrayachinon-A–C, sowie die Synthese einiger nicht natürlicher, potentiell anti-Tuberkulose-aktiver Carbazole und Carbazolchinone. Für die Darstellung der aus der Pflanze Murraya euchrestifolia Hayata isolierten Naturstoffe wurden verschiedene synthetische Herangehensweisen untersucht: Die Transformation eines 7 Hydroxycarbazolchinons in die Zielverbindungen gelang nicht, ebenso wie die Syntheseroute über eine trioxygenierte Vorstufe. 7-Methoxy-3-methyl-1-tosyloxycarbazol (A) ließ sich jedoch in einer Ausbeut
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3

Gehring, André Philipe [Verfasser]. "Biologisch aktive Carbazol-Derivate / André Philipe Gehring." München : Verlag Dr. Hut, 2013. http://d-nb.info/1033041726/34.

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4

Clavijo, Allancán Graciela Andrea. "Síntesis de carbazol-tio- y aminoquinonas antitumorales." Tesis, Universidad de Chile, 2013. http://repositorio.uchile.cl/handle/2250/138265.

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Magíster en Química área de Especialización en Química Medicinal y Memoria para optar al Título de Químico<br>Los derivados quinónicos poseen interesantes aplicaciones en áreas de la química de materiales y medicinal. Estos compuestos pueden ser encontrados tanto en la naturaleza como obtenerse sintéticamente, su síntesis ha despertado interés, debido a la posibilidad de funcionalizarlas, con el objetivo de mejorar sus propiedades, y también obtener nuevas estructuras. En este trabajo se informa la síntesis y caracterización de una serie de amino-, tio- y carbazolquinonas estructuralment
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5

Asche, Christian. "Strukturoptimierung von Benzo(b)carbazol-Derivaten als Zytostatika." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=966453743.

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6

Strödke, Benjamin. "Carbazol- und ß-Carbolin-Derivate als neuartige Kinase-Inhibitoren." Diss., lmu, 2008. http://nbn-resolving.de/urn:nbn:de:bvb:19-86055.

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Strödke, Benjamin. "Carbazol- und b-Carbolin-Derivate als neuartige Kinase-Inhibitoren." München Verl. Dr. Hut, 2008. http://d-nb.info/989216705/04.

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8

Gehring, André Philipe [Verfasser], and Franz [Akademischer Betreuer] Bracher. "Biologisch aktive Carbazol-Derivate / André Philipe Gehring. Betreuer: Franz Bracher." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2013. http://d-nb.info/1033270881/34.

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9

Strödke, Benjamin. "Carbazol- und [beta]-Carbolinderivate [beta-Carbolinderivate] als neuartige Kinase-Inhibitoren." München Verl. Dr. Hut, 2008. http://d-nb.info/989216705/04.

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10

Marques, Paulo Wilmar Barbosa. "Propriedades fotofísicas do copolímero polifluoreno-carbazol e aplicações eletro-ópticas." Universidade Federal do Amazonas, 2009. http://tede.ufam.edu.br/handle/tede/4361.

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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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12

Cuadrado, Santolaria Alba. "Semiconductores orgánicos derivados del carbazol y su aplicación en dispositivos electrónicos." Doctoral thesis, Universitat de Barcelona, 2019. http://hdl.handle.net/10803/667874.

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En los últimos años se han llevado a cabo intensas investigaciones dentro del campo de los materiales orgánicos semiconductores, principalmente enfocados a su aplicación en dispositivos electrónicos y optoelectrónicos como son los OTFTs, los OLEDs y las celdas solares orgánicas. Los materiales orgánicos aún no han adquirido el protagonismo de los materiales inorgánicos en estas áreas, ya que estos últimos presentan mejores eficiencias y mayores valores de movilidades de carga. No obstante, su fácil procesamiento, la posibilidad de recubrir grandes superficies flexibles, su ligereza y su bajo c
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13

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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14

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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Rettenmaier, Jürgen. "Synthese von TiO2-Nanopartikeln und Carbazol-Farbstoffderivaten für optische Anwendungen in anorganisch-organischen Hybridpolymeren." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=966042549.

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Cordeiro, Diéricon Sousa. "Efeitos das interações inter e intramoleculares na fotofísica e morfologia de filmes finos de derivados de carbazol." Universidade Federal de Goiás, 2018. http://repositorio.bc.ufg.br/tede/handle/tede/8221.

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Kutz, Sebastian K. Verfasser], Hans-Joachim [Akademischer Betreuer] [Knölker, and Peter [Akademischer Betreuer] Metz. "Regioselektive Synthese substituierter Carbazol-1,4-chinone / Sebastian K. Kutz. Betreuer: Hans-Joachim Knölker. Gutachter: Hans-Joachim Knölker ; Peter Metz." Dresden : Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2016. http://d-nb.info/109704890X/34.

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18

Marotto, Annalisa. "Etablierung und Anwendung von biophysikalischen und molekularbiologischen Methoden zur Untersuchung von Wirkmechanismen neuer Indol-, Carbazol- und Oligopyrrolcarboxamid-Derivate als potentielle antitumoraktive Stoffe." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=963928287.

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19

Fumagalli, Fernando. "Química de alcaloides carbazólicos: síntese de Claurailas e de biblioteca de análogos estruturais." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-01072015-095954/.

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Compostos heterociclos estão muito presentes em nossas vidas, desde processos biológicos até em fármacos. Dentre esses compostos, os carbazóis, vem ultimamente se mostrando promissores como alternativa terapêutica para diversas doenças, principalmente para o câncer. Muitos carbazóis são produtos naturais, como é o caso das Claurailas A-D. Baseando-se na estrutura da Clauraila A, esse trabalho propôs o desenvolvimento de uma biblioteca de análogos desse alcaloide a fim de prospecção biológica. Para a síntese da Clauraila A foram estudadas condições ideais da ciclodeidrogenação da diarilamina pr
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20

Montoia, Andreia, and 92-98243-2460. "Síntese de derivados carbazólicos e beta-carbolínicos e avaliação da atividade antimalárica in vitro." Universidade Federal do Amazonas, 2017. http://tede.ufam.edu.br/handle/tede/6198.

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Submitted by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br) on 2018-03-02T15:45:37Z No. of bitstreams: 2 Reprodução Não Autorizada.pdf: 47716 bytes, checksum: 0353d988c60b584cfc9978721c498a11 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)<br>Approved for entry into archive by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br) on 2018-03-02T15:45:50Z (GMT) No. of bitstreams: 2 Reprodução Não Autorizada.pdf: 47716 bytes, checksum: 0353d988c60b584cfc9978721c498a11 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf84
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Li, Junming. "The performance characterization of carbazole/dibenzothiophene derivatives in modern OLEDs." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät, 2017. http://dx.doi.org/10.18452/17678.

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Ein vielversprechendes Design für organische lichtemittierende Dioden (OLEDs) verwendet eine Wirt-Gast-Strategie durch Dispergieren einer kleinen Menge eines hocheffizienten Emitters (der Gast) in eine passende Transportmatrix (der Wirt). Die Aufgabe des Wirts ist den Exzitonentranport zum Emitter sicherzustellen und den Zerfall von Triplet-Exzitonen zu verhindern, und damit eine hohe Bauteilperformance zu erreichen. Die vorliegende Arbeit konzentriert sich auf die Beziehung zwischen Molekülstruktur und optoelektrischer Eigenschaften von Carbazol/Dibenzothiophen-Derivaten. Die Untersuchung um
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Camargo, João Pedro Corrêa [UNESP]. "Preparação e caracterização de biossensores baseado na eletrocodeposição de grafeno/polipirrol/acetilcolinesterase para determinação de pesticidas em amostras de frutas e vegetais." Universidade Estadual Paulista (UNESP), 2017. http://hdl.handle.net/11449/149943.

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Submitted by JOAO PEDRO CORREA DE CAMARGO null (joaoquimica1991@hotmail.com) on 2017-03-08T13:32:00Z No. of bitstreams: 1 Autoarquivamento da dissertação.pdf: 2161327 bytes, checksum: 64d6d1f91de22d90ab86fa2387b3aca1 (MD5)<br>Rejected by LUIZA DE MENEZES ROMANETTO (luizamenezes@reitoria.unesp.br), reason: Solicitamos que realize uma nova submissão seguindo a orientação abaixo: Incluir o número do processo de financiamento nos agradecimentos da dissertação/tese. Corrija esta informação e realize uma nova submissão com o arquivo correto. Agradecemos a compreensão. on 2017-03-13T13:22:
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Camargo, João Pedro Corrêa. "Preparação e caracterização de biossensores baseado na eletrocodeposição de grafeno/polipirrol/acetilcolinesterase para determinação de pesticidas em amostras de frutas e vegetais." Botucatu, 2017. http://hdl.handle.net/11449/149943.

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Orientador: Ivana Cesarino<br>Abstract: A new biosensor was developed by a simple electrocodeposition of reduced graphene oxide (rGO), polypyrrole (PPy) and the enzyme acetylcholinesterase (AChE) on surface of platinum (Pt) electrode. In potential range of -0.2 to +0.5 V vs. Ag/AgCl/KCl (3.0 mol L-1), using differential pulse voltammetry (DPV), it was observed a process in + 0.1 V and this corresponds to the dimerization of electrochemical oxidation products of thiocholine, resulting in ditio-bis-choline. The biosensor developed was evaluated using DPV in the analysis of carbaryl, which inhibi
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Teixeira, Milena Elias. "Aplicação do eletrodo de diamante dopado com boro modificado pelo método Sol-Gel para determinação e degradação de carbaril." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/75/75135/tde-19032013-164142/.

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São apresentados os resultados do estudo das propriedades eletroquímicas do eletrodo de diamante dopado com boro (DDB) e do eletrodo de DDB modificado diretamente pelo método Sol-Gel com PbOx, para a determinação de carbaril. Mostrou-se que uma polarização anódica (3,0 V vs Ag/AgCl, 30 min) seguida de uma catódica (-3,0 V vs Ag/AgCl, 30 min), em meio ácido, são apropriadas para otimizar o desempenho catalítico da superfície. As imagens de AFM mostraram alterações topológicas significativas no eletrodo de PbOx/DDB, assim como as imagens digitais apresentaram uma provável mistura de óxidos de ch
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Börger, Carsten, Micha P. Krahl, Margit Gruner, Olga Kataeva, and Hans-Joachim Knölker. "First total synthesis of the biscarbazole alkaloid oxydimurrayafoline." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-139201.

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We report the first total synthesis of oxydimurrayafoline via nucleophilic substitution at the benzylic position at C-3 of the carbazole framework<br>Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
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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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Börger, Carsten, Micha P. Krahl, Margit Gruner, Olga Kataeva, and Hans-Joachim Knölker. "First total synthesis of the biscarbazole alkaloid oxydimurrayafoline." Royal Society of Chemistry, 2012. https://tud.qucosa.de/id/qucosa%3A27812.

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We report the first total synthesis of oxydimurrayafoline via nucleophilic substitution at the benzylic position at C-3 of the carbazole framework.<br>Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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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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Ferrucio, Bianca. "Avaliação de melanócitos humanos expostos ao inseticida carbaril e à radiação solar em cultura." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/9/9141/tde-28052015-085252/.

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O carbaril (metilcarbamato de naftila), um inseticida de amplo espectro, foi recentemente associado ao desenvolvimento de melanoma cutâneo em estudo epidemiológico de coorte com trabalhadores agrícolas norte-americanos, expostos também à radiação solar, o principal fator etiológico para o desenvolvimento de tumores cutâneos. Apesar de abrangente e bem planejado, aquele estudo epidemiológico não é suficiente para caracterizar a contribuição direta do inseticida e da radiação solar na melanomagênese. Diversos estudos têm explorado o efeito sinérgico de determinadas substâncias químicas à radiaçã
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García, Palominos Cecilia Loreto. "Evaluación del efecto raleador de cianamida hidrogenada en manzanos var. red king oregon, braeburn y red chief." Tesis, Universidad de Chile, 2005. http://www.repositorio.uchile.cl/handle/2250/101766.

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Foschi, Simone. "Synthesis, Characterization and Conformational Studies of Modified Carbazole-bis-aryl-boranes." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020. http://amslaurea.unibo.it/20686/.

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During this project we have synthetized different compounds belonging to the class of amino-boranes for the study of bis-aryl-B=N system. We have decided to keep unchanged the aryl components and change only the amine to observe the effect of that on the B=N bond. The used amines are modified carbazoles with functional groups chosen to amplify or disempower the steric and the conjugation effect. We have found that the evaluation of steric barrier was possible studying the gearing aryls rotation around the C-B bonds, while the conjugation barrier is instead given by the energy needed to break t
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Börger, Carsten, Olga Kataeva, and Hans-Joachim Knölker. "Novel approach to biscarbazole alkaloids via Ullmann coupling – synthesis of murrastifoline-A and bismurrayafoline-A." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-139195.

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Unprecedented Ullmann couplings of murrayafoline-A with either 6-bromo- or 4-bromocarbazole derivatives provide highly efficient synthetic routes to the biscarbazole alkaloids murrastifoline-A (6 steps, 66% overall yield) and bismurrayafoline-A (6 steps, 28% overall yield)<br>Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
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FLAMBEAU, JEAN-PIERRE BLOCK J. C. "ESSAIS DE BIOTRANSFORMATION DU CARBAZOLE /." [S.l.] : [s.n.], 1990. ftp://ftp.scd.univ-metz.fr/pub/Theses/1990/Flambeau.Jean_Pierre_1.SMZ9016.pdf.

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Flambeau, Jean-Pierre. "Essai de biotransformation du carbazole." Metz, 1990. http://docnum.univ-lorraine.fr/public/UPV-M/Theses/1990/Flambeau.Jean_Pierre_1.SMZ9016.pdf.

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Ce travail consiste en une étude sur la biodégradation d'un sous-produit de cokéfaction polycyclique, très peu soluble dans l'eau et ayant un noyau structural indolique : le carbazole. Le but de cette étude est de produire par voie bactérienne de l'indole en utilisant le carbazole comme substrat. Pour cela, il a été nécessaire de sélectionner les genres bactériens capables d'utiliser le carbazole comme source de carbone et de rendre cette molécule soluble dans l'eau pour favoriser sa biodégradation. La dynamique des cultures bactériennes ayant comme substrat le carbazole ou le carbazole dissou
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Scott, Tricia L. "Palladium-catalyzed synthesis of carbazole derivatives and formal total syntheses of several naturally occurring carbazole alkaloids." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2075.

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Thesis (Ph. D.)--West Virginia University, 2001.<br>Title from document title page. Document formatted into pages; contains x, 83 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 75-78).
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Börger, Carsten, Olga Kataeva, and Hans-Joachim Knölker. "Novel approach to biscarbazole alkaloids via Ullmann coupling – synthesis of murrastifoline-A and bismurrayafoline-A." Royal Society of Chemistry, 2012. https://tud.qucosa.de/id/qucosa%3A27811.

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Unprecedented Ullmann couplings of murrayafoline-A with either 6-bromo- or 4-bromocarbazole derivatives provide highly efficient synthetic routes to the biscarbazole alkaloids murrastifoline-A (6 steps, 66% overall yield) and bismurrayafoline-A (6 steps, 28% overall yield).<br>Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
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Lav, Thanh-Xuan Chevrot Claude. "Réseaux et réseaux interpénétrés carbazole / pérylène à hétérojonctions volumiques." [S.l.] : [s.n.], 2009. http://biblioweb.u-cergy.fr/theses/08CERG0370.pdf.

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41

Degbia, Wangata Saint-Martial. "Semi-conducteurs organiques [pi]-conjugués pour l'élaboration de dispositifs photovoltaïques hybrides solides à colorant." Thesis, Tours, 2014. http://www.theses.fr/2014TOUR4044/document.

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Ce travail a consisté à élaborer de nouveaux verres moléculaires transporteurs de trou dérivés du carbazole pour remplacer le spiro-OMeTAD (matériau de référence) dans les cellules solaires hybrides à colorant tout solide. Nous avons synthétisé différents dérivés du carbazole 3, 6, 9 substitués, établi leurs principales propriétés physico-chimiques et les avons utilisés en DSSC solide. Nous avons mis en évidence l'intérêt de greffer des groupements bis(4-méthoxyphényl)amines en positions 3, 6 et des aryles en position 9 du carbazole pour obtenir des matériaux performants. Finalement, cette str
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42

Boudreault, Pierre-Luc. "SYNTHÈSE ET CARACTÉRISATION DE NOUVEAUX SEMI-CONDUCTEURS ORGANIQUES À BASE DE CARBAZOLE ET D’INDOLO[3,2-b]CARBAZOLE." Thesis, Université Laval, 2010. http://www.theses.ulaval.ca/2010/27896/27896.pdf.

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43

Boudreault, Pierre-Luc. "Synthèse et caractérisation de nouveaux semi-conducteurs organiques à base de carbazole et d'indolo[3,2-b]carbazole." Doctoral thesis, Université Laval, 2010. http://hdl.handle.net/20.500.11794/22285.

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Cette thèse porte sur la synthèse et la caractérisation de nouveaux semi-conducteurs organiques à base de carbazole et d'indolo[3,2-b]carbazole. La synthèse de petites molécules et de polymères a été accomplie dans le but de fabriquer des transistors organiques à effet de champ (TOECs). Plusieurs techniques de mise en oeuvre ont été utilisées pour déposer les films et obtenir les meilleures performances possibles. Tout d'abord, l'évaporation sous vide des petites molécules a permis d'obtenir des films avec un haut degré de cristallinité, qui furent analysés par diffraction des rayons-X (DRX) e
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44

Hesse, Ronny, Anne Jäger, Arndt W. Schmidt, and Hans-Joachim Knölker. "Palladium(II)-catalysed total synthesis of naturally occurring pyrano[3,2-a]carbazole and pyrano[2,3-b]carbazole alkaloids." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-149135.

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Seven naturally occurring pyranocarbazole alkaloids (pyrayafoline A–E, O-methylmurrayamine A and O-methylmahanine) have been obtained by total synthesis using a palladium(II)-catalysed oxidative cyclisation of a diarylamine to an orthogonally diprotected 2,7-dihydroxycarbazole as key step.
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Chapman, Madelaine A. "The electropolymerisation of indolo{3,2,1-jk}carbazole and pyrrolo{3,2,1-jk}carbazole : an electrochemical computational and spectroscopic study." Thesis, University of Edinburgh, 2004. http://hdl.handle.net/1842/13360.

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The electropolymerisation of a range of 5-substituted indoles has been shown previously to result in the formation of redox-active films. The oxidation potentials of both the indole monomers and their polymers can be altered by substitution of the monomer with different electron-withdrawing groups. Both the indole monomers and polymers also have high fluorescence quantum yields. However the fluorescence wavelengths of the indole polymers are not tuneable by substitution. In this thesis the work on the electropolymerisation of indole(s) is extended to two monomers which have larger conjugated s
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Sonntag, Martin. "New carbazole based materials for optoelectronic applications." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=982072864.

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47

Simmance, Timothy Graham. "New Carbazole-Based Materials for LED Applications." Thesis, University of Sheffield, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489740.

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48

Blair, Emily. "Characterisation of poly (2,7-carbazole) photovoltaic cells." Thesis, Université Laval, 2011. http://www.theses.ulaval.ca/2011/28384/28384.pdf.

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49

Capeto, Fabíola Araújo. "Estudo da contratilidade de segmentos isolados de esôfago e estômago de fetos de ratas sujeitos a modelo experimental de atresia de esôfago induzida por doxorrubicina." reponame:Repositório Institucional da UFC, 2014. http://www.repositorio.ufc.br/handle/riufc/8339.

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CAPETO, Fabíola Araújo. Estudo da contratilidade de segmentos isolados de esôfago e estômago de fetos de ratas sujeitos a modelo experimental de atresia de esôfago induzida por doxorrubicina. 2014. 91 f. Dissertação (Mestrado em Cirurgia) - Universidade Federal do Ceará. Faculdade de Medicina, Fortaleza, 2014.<br>Submitted by denise santos (denise.santos@ufc.br) on 2014-06-26T11:35:24Z No. of bitstreams: 1 2014_dis_facapeto.pdf: 11528744 bytes, checksum: eb5878a9baf49d702a691373552becd7 (MD5)<br>Approved for entry into archive by denise santos(denise.santos@ufc.br) on 2014-06-26T11:35:44Z (GMT
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Barcelos-Drzewinski, Isabel de. "Nouveaux polyesters à groupe carbazolique dans la chaîne, relations synthèse-structure-propriétés." Paris 13, 1995. http://www.theses.fr/1995PA132015.

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Le travail porte sur la synthèse, la caractérisation et l'étude des propriétés des polyesters à groupes carbazoliques n-substitues dans la chaîne. La première étape du travail à consisté à mettre au point la synthèse des monomères: les acides n-alkylcarbazole-3,6-dicarboxyliques (alkyl = butyl et octyl). Dans un deuxième temps, la synthèse en masse des polyesters a été réalisée, selon deux procédés: continu (a partir des diacides correspondants et de l'éthylène glycol) et discontinu (a partir du diester isole). La solubilité de certains des polyesters préparés a permis d'étudier la cinétique d
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