Дисертації з теми "Heteroacenes"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-28 дисертацій для дослідження на тему "Heteroacenes".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте дисертації для різних дисциплін та оформлюйте правильно вашу бібліографію.
Kulisic, Niksa. "Heteroacenes as potential materials for molecular electronics." Doctoral thesis, Università degli studi di Trieste, 2010. http://hdl.handle.net/10077/3609.
Повний текст джерелаIn this thesis, different strategies for obtaining azaacenes suitable for solution-based processing techniques have been investigated and developed. The first synthetic approach involved the condensation of commercially available compounds which include the diamines 2,3-diaminobenzene, 2,3-diaminonaphtalene and 2,3-diaminophenazine and the bromoanilic acid and embelin. This synthetic route yielded a series of dihydroazaacenes with 5 and 7 fused aromatic rings. The low overall solubility of this azaacenes did not permit an extensive characterization of the compounds. A second synthetic approach was developed to investigate both C-N exchange and lateral expansion of the π-conjugation. Through this approach a tetraazaoctacene derivative was obtained and characterized. However it lacked of solubility necessary for being compatible with solution-processing techniques. A third strategy was based on the introduction of solubilizing groups on such extended tetraazaoctacene core. While the di-substitution did not render the azaoctacene soluble in neutral media, tetra-substitution yielded a derivative with enhanced solubility in neutral solvent.
1981
Purushothaman, Balaji. "PARTIALLY HALOGENATED ACENES AND HETEROACENES FOR ORGANIC ELECTRONICS." UKnowledge, 2011. http://uknowledge.uky.edu/gradschool_diss/124.
Повний текст джерелаGrimminger, Marsha Loth. "PERIODIC TRENDS IN STRUCTURE FUNCTION RELATIONSHIP OF ORGANIC HETEROACENES." UKnowledge, 2011. http://uknowledge.uky.edu/gradschool_diss/850.
Повний текст джерелаAppleton, Anthony Lucas. "Synthesis and characterization of large linear heteroacenes and their derivatives." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37225.
Повний текст джерелаPaulus, Fabian [Verfasser], and Uwe H. F. [Akademischer Betreuer] Bunz. "N-Heteroacenes in Organic Field-Effect Transistors / Fabian Paulus ; Betreuer: Uwe Bunz." Heidelberg : Universitätsbibliothek Heidelberg, 2016. http://d-nb.info/1180615247/34.
Повний текст джерелаGranger, Devin B. "ACENES, HETEROACENES AND ANALOGOUS MOLECULES FOR ORGANIC PHOTOVOLTAIC AND FIELD EFFECT TRANSISTOR APPLICATIONS." UKnowledge, 2017. http://uknowledge.uky.edu/chemistry_etds/76.
Повний текст джерелаDoan, Thu Hong. "Synthesis, self-assembly and photophysical evaluation of fluorophores derived from acenes, heteroacenes and quinazolines." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMC205.
Повний текст джерелаOrganic semiconductors (OSCs) are a highly attractive research field due to their potentials as active layers in optoelectronic devices such as organic field-effect transistors (OFETs), organic photovoltaic (OPVs) and organic light emitting diodes (OLEDs). Polycyclic aromatic compounds as well as heteroaromatics are considered as promising materials for OSCs due to their semi conductivity properties, optical properties and geometric structures. The mentioned systems and their photophysical properties were investigated in three chapters of my thesis. In the first chapter, a study on a set of linear, angular and condensed acenes consisting of heteroatom linkages with unique aggregations was described and analyzed. The angular and π-extended N-fused heteroacenes are the main class studied in the second chapter. Their synthesis is based on the Suzuki-Miyaura coupling and the Cadogan reactions. Besides acenes and N-fused heteroacenes, N-heteroaromatics have gained attention in material area. One of them is the quinazoline class that is known as an electron withdrawing unit in push-pull structures for intramolecular charge transfer (ICT). The investigation of the relationships between the electron donor-acceptor-donor (D-A-D) quinazoline-based structures and their photoluminescence properties is the main work mentioned in the third chapter
Wong, Hok-lai, and 黃學禮. "Design, synthesis, photochromic and photophysical studies of dithienylethene-containing heteroacenes, alkynyls, diimines and theirmetal complexes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B45874748.
Повний текст джерелаLevick, Matthew Thomas. "Connective-Pummerer cyclisations and SmI2-mediated cascade reactions for the synthesis of nitrogen-containing heteroacenes." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/connectivepummerer-cyclisations-and-smi2mediated-cascade-reactions-for-the-synthesis-of-nitrogencontaining-heteroacenes(762eea6e-0dc0-4397-8af0-07413517db63).html.
Повний текст джерелаKast, Hannelore [Verfasser]. "Fused S,N-heteroacenes and thiophene-substituted Ruthenium(II) complexes for organic solar cells / Hannelore Kast." Ulm : Universität Ulm, 2016. http://d-nb.info/1105590380/34.
Повний текст джерелаBrombosz, Scott M. "Alkynylated acenothiadiazoles and N-heteroacenes: synthesis, functionalization, and study of the optical properties for optoelectronic and sensory materials." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37102.
Повний текст джерелаSchaffroth, Manuel Verfasser], and Uwe H. F. [Akademischer Betreuer] [Bunz. "N-Heteroacene: Theoretische Betrachtungen und neue Motive / Manuel Schaffroth ; Betreuer: Uwe Bunz." Heidelberg : Universitätsbibliothek Heidelberg, 2015. http://d-nb.info/1180396871/34.
Повний текст джерелаSchaffroth, Manuel [Verfasser], and Uwe H. F. [Akademischer Betreuer] Bunz. "N-Heteroacene: Theoretische Betrachtungen und neue Motive / Manuel Schaffroth ; Betreuer: Uwe Bunz." Heidelberg : Universitätsbibliothek Heidelberg, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:16-heidok-188726.
Повний текст джерелаHenne, Florian [Verfasser]. "Synthese und Charakterisierung von S,N-Heteroacenen zur Anwendung in organischen Solarzellen / Florian Henne." Ulm : Universität Ulm, 2020. http://d-nb.info/1223546284/34.
Повний текст джерелаLindner, Benjamin Daniel Verfasser], and Uwe H. F. [Akademischer Betreuer] [Bunz. "Elektronenarme N-Heteroacene: Ein Weg zu neuen Elektronentransportmaterialien / Benjamin Daniel Lindner ; Betreuer: Uwe Bunz." Heidelberg : Universitätsbibliothek Heidelberg, 2014. http://d-nb.info/1177810735/34.
Повний текст джерелаLindner, Benjamin [Verfasser], and Uwe H. F. [Akademischer Betreuer] Bunz. "Elektronenarme N-Heteroacene: Ein Weg zu neuen Elektronentransportmaterialien / Benjamin Daniel Lindner ; Betreuer: Uwe Bunz." Heidelberg : Universitätsbibliothek Heidelberg, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:16-heidok-160517.
Повний текст джерелаKolmer-Anderl, Nicole Patrizia Desiree [Verfasser], and Matthias [Akademischer Betreuer] Rehahn. "N-Heteroacene als funktionale Halbleiter in anorganisch-organischen Feldeffekttransistoren / Nicole Patrizia Desiree Kolmer-Anderl. Betreuer: Matthias Rehahn." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2014. http://d-nb.info/1110980353/34.
Повний текст джерелаKolmer-Anderl, Nicole [Verfasser], and Matthias [Akademischer Betreuer] Rehahn. "N-Heteroacene als funktionale Halbleiter in anorganisch-organischen Feldeffekttransistoren / Nicole Patrizia Desiree Kolmer-Anderl. Betreuer: Matthias Rehahn." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2014. http://nbn-resolving.de/urn:nbn:de:tuda-tuprints-43113.
Повний текст джерелаSchönberger, Astrid [Verfasser], Matthias [Akademischer Betreuer] Rehahn, and Michael [Akademischer Betreuer] Reggelin. "Synthese von N-Heteroacen-funktionalisierten Polymeren als organische Halbleiter / Astrid Schönberger ; Matthias Rehahn, Michael Reggelin." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2018. http://d-nb.info/1163394238/34.
Повний текст джерела"Organic chemistry and semiconductor physics of N-heteroacenes." Thesis, 2011. http://library.cuhk.edu.hk/record=b6075366.
Повний текст джерелаThesis (Ph.D.)--Chinese University of Hong Kong, 2011.
Includes bibliographical references.
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstract also in Chinese.
Gao, Peng [Verfasser]. "Thiophene-containing organic semiconducting heteroacenes for electronic applications / Peng Gao." 2009. http://d-nb.info/1005635897/34.
Повний текст джерела"Molecular engineering of N-heteroacenes and macrocyclic arenes: design, synthesis and properties." 2013. http://library.cuhk.edu.hk/record=b5884306.
Повний текст джерелаThesis (Ph.D.)--Chinese University of Hong Kong, 2013.
Includes bibliographical references.
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstract also in Chinese.
"Solution-processed thin film transistors of N-heteroacenes: synthesis, assembly and semiconductor physics." 2015. http://repository.lib.cuhk.edu.hk/en/item/cuhk-1291973.
Повний текст джерелаCiou, Guan-Ting, and 邱冠婷. "Roles of electron-withdrawing end caps in the solid-state packing and OFET performance of penta-fused heteroacenes." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/p73s78.
Повний текст джерела國立交通大學
應用化學系碩博士班
107
Solid-state structures of conjugated molecules play an important role in the field-effect transistor (FET) performances of the molecules. Penta-fused heteroacenes are useful building blocks for molecules used in optoelectronic devices. Here, a series of 5 heteroacene derivatives (Penta-fused heteroacenes: 4,5-Bis(2-ethylhexyl)-dithieno[2,3-d:2',3'-d']thieno[3,2-b:4,5-b']dipyrrole) were studied. The molecules were divided into three groups based on the chemical structures of their substituents. Crystal arrays of these derivatives were prepared by the PDMS-assisted crystallization (PAC) procedure. By analyzing the optical microscopy (OM) images, grazing incidence X-ray diffraction (GIXRD) patterns, Electron diffraction patterns (ED) and OFET performances of these derivatives, it was found that the different molecular symmetry and intermolecular interaction based on substituents can significantly affect the solid-state morphology and the OFET performances of the molecules.
Kolmer-Anderl, Nicole Patrizia Desiree. "N-Heteroacene als funktionale Halbleiter in anorganisch-organischen Feldeffekttransistoren." Phd thesis, 2014. https://tuprints.ulb.tu-darmstadt.de/4311/1/Dissertation_NicoleKolmerAnderl.pdf.
Повний текст джерелаSchönberger, Astrid. "Synthese von N-Heteroacen-funktionalisierten Polymeren als organische Halbleiter." Phd thesis, 2018. https://tuprints.ulb.tu-darmstadt.de/7563/7/Dissertation-Astrid-Sch%C3%B6nberger.pdf.
Повний текст джерелаSaalfrank, Christian. "Lewis-Basen stabilisierte, aromatische Verbindungen des Bors : Darstellung und Reaktivität." Doctoral thesis, 2020. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-210578.
Повний текст джерелаThis thesis deals with the synthesis and examination of cyclic conjugated systems of boron. The central ring-moiety of the organic analogues were substituted with two boron centres in 1,4-position. 1 Synthesis and properties of a CAAC-stabilized 1,4 diborabenzene (87) The synthesis of an additional example of base-stabilized 1,4-diborabenzene follows preceding studies of the Braunschweig´s research group on this topic. The cyclohexyl-CAAC coordinated diboracumulene (84) was stirred under an atmosphere of purified acetylene with a pressure of approximately 1 bar. Quantum chemical calculations, conducted on 87 established a NICS(0) value of –2.6483 at the [B2C4]-ring (cf. NICS(0)benzene: –8.1723; B3LYP/Def2SVP-level of theory) confirming the existence of a ring current and thus aromaticity of this system. Reaction of the diborabenzene 87 with the alkali metals lithium and sodium were performed and the corresponding dianionic compounds (88) and (89) were generated. Instead, for the reduction with potassium, under similar reaction conditions, single crystals were obtained that provided the evidence for the connectivity of the monoanionic species (90) by X-ray diffraction. 2 Synthesis and reactivity of CAAC stabilised 9,10 diboraanthracenes The synthesis of 9,10‐(dibromo)diboraanthracene 63 was performed according to a published procedure that follows a series of salt‐metathesis reactions of o‐bis(trimethylsilyl)benzene (65) and borontribomide. After the coordination of the CAAC ligands to compound 90 the stepwise reductive abstraction of the bromides was performed (Scheme 3). A single electron reduction of 92 and 93 did not result in the expected neutral mixed valence systems but instead provided products that did not show an 11B NMR-spectroscopic signal. X Ray crystallographic examination of suitable single crystals of the compound 93 showed a salt-like structure. Both bromides of 93 had been abstracted, leaving the diboraanthracene fragment as a radical cation. The double reduction of 92 and 93 also yielded 11B-NMR silent products, again suggesting the presence of open-shell systems. X-Ray diffraction of suitable single crystals of the obtained compounds 103 und 104 indicate the formation of the desired neutral diboraanthracene species In the solid state. Low temperature EPR-experiments gave insights into the electronic ground state of the compounds 103 und 104. Singlet-triplet gaps were deduced to be ΔES→T = 0.43 kJ/mol (4.46 meV) for 103 and ΔES→T = 2.3 kJ/mol (23.8 meV) for 104. Both compounds are present in open shell singlet ground state. The reduction of 92 with an excess of elemental lithium permitted the synthesis of the dianionic diborataanthracene 110. Under photochemical conditions by insertion of a boron atom into the pyrrolidine moiety of the coordinated CAAC ligand 103 forms a zwitterionic spiro-compound 113. Furthermore, 103 und 104 were found to be suitable reagents for the activation of small molecules under mild conditions. The reaction of MeCAAC-species 103 with elemental sulfur yields compound 128 with an S3 bridge between the boron atoms. For the CyCAAC-stabilized diboraanthracene 104 the coordination of a CO molecule to the boron atoms was observed (140). Additionally, initial insights were obtained into the ability of the diboraanthracene 104 to act as a ligand in transition metal chemistry by the synthesis of the halfsandwich-compound 149. The half sandwich complex [η6-(9,10-(CyCAAC)2DBA)Cr(CO)3] (149) was prepared by the addition of 104 to [(MeCN)3Cr(CO)3] and the IR-spectrum of 149 indicated that compound 104 is a strongly electron donating ligand
Lai, Bo-Han, and 賴柏翰. "Roles of lateral and end-capping substituents in the solid-state packing and OFET performance of a multi-fused heteroacene." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/936dqb.
Повний текст джерела國立交通大學
應用化學系碩博士班
105
Solid-state structures of conjugated molecules play an important role in the field-effect transistor (FET) performances of the molecules. Multi-fused heteroacenes (HA) are useful building blocks for molecules used in optoelectronic devices. Although the influences of the constituent aromatic units on the chemical properties of HAs have been known, their influences on the physical structures of the HA derivatives have not been systematically studied. Here, a series of 8 heteroacene (HA) derivatives provided by Professor Ken-Tsung Wong’s laboratory at National Taiwan University were studied. The molecules were divided into three groups based on the chemical structures of their HA cores (HA1: 4,9-Bis(2-ethylhexyl)-thieno[3,2-b]thieno[2''',3''':4'',5'']pyrrolo[2'',3'':4',5']thieno[2',3':4,5]-thieno[2,3-d]pyrrole, HA2: 6,12-Bis(2-ethylhexyl)-Indolo[2'',3'':4',5']thieno[2',3':4,5]thieno[3,2-b]indole, HA3: 4,5-Bis(2-ethylhexyl)-dithieno[2,3-d:2',3'-d']thieno[3,2-b:4,5-b']dipyrrole). Crystal arrays of the HA derivatives were prepared by the PDMS-assisted crystallization (PAC) procedure. By analyzing the polarized optical microscopy (POM) images, grazing incidence X-ray diffraction (GIXRD) patterns, and OFET performances of the HA derivatives, it was found that the lateral alkyl substituents and the end-capping groups can significantly affect the solid-state morphology and the OFET performances of the molecules.