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Relevant bibliographies by topics / Triptycen

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Academic literature on the topic 'Triptycen'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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Journal articles on the topic "Triptycen"

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Chakraborty, Sourav, Snehasish Mondal, Rina Kumari, Sourav Bhowmick, Prolay Das, and Neeladri Das. "Synthesis, characterization and DNA interaction studies of new triptycene derivatives." Beilstein Journal of Organic Chemistry 10 (June 5, 2014): 1290–98. http://dx.doi.org/10.3762/bjoc.10.130.

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A facile and efficient synthesis of a new series of triptycene-based tripods is being reported. Using 2,6,14- or 2,7,14-triaminotriptycenes as synthons, the corresponding triazidotriptycenes were prepared in high yield. Additionally, we report the transformation of 2,6,14- or 2,7,14-triaminotriptycenes to the corresponding ethynyl-substituted triptycenes via their tribromo derivatives. Subsequently, derivatization of ethynyl-substituted triptycenes was studied to yield the respective propiolic acid and ethynylphosphine derivatives. Characterization of the newly functionalized triptycene derivatives and their regioisomers were carried out using FTIR and multinuclear NMR spectroscopy, mass spectrometry, and elemental analyses techniques. The study of the interaction of these trisubstituted triptycenes with various forms of DNA revealed interesting dependency on the functional groups of the triptycene core to initiate damage or conformational changes in DNA.

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Daub, Jörg, Lothar Jakob, and Josef Salbeck. "Chirale Elektronentransfer-aktive Chinone mit Triptycen-Teilstrukturen: Synthesekonzeption und Eigenschaften." Chemische Berichte 121, no. 12 (December 1988): 2187–94. http://dx.doi.org/10.1002/cber.19881211218.

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Pei, Bao-Jian, Wing-Hong Chan, and Albert W. M. Lee. "Oxadisilole Fused Triptycene and Extended Triptycene: Precursors of Triptycyne and Extended Triptycyne." Journal of Organic Chemistry 75, no. 21 (November 5, 2010): 7332–37. http://dx.doi.org/10.1021/jo1016025.

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McGlinchey, Michael J., and Kirill Nikitin. "Palladium-Catalysed Coupling Reactions En Route to Molecular Machines: Sterically Hindered Indenyl and Ferrocenyl Anthracenes and Triptycenes, and Biindenyls." Molecules 25, no. 8 (April 22, 2020): 1950. http://dx.doi.org/10.3390/molecules25081950.

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Pd-catalysed Stille and Suzuki cross-couplings were used to prepare 9-(3-indenyl)-, 6, and 9-(2-indenyl)-anthracene, 7; addition of benzyne led to the 9-Indenyl-triptycenes, 8 and 9. In 6, [4 + 2] addition also occurred to the indenyl substituent. Reaction of 6 through 9 with Cr(CO)6 or Re2(CO)10 gave their M(CO)3 derivatives, where the Cr or Re was complexed to a six- or five-membered ring, respectively. In the 9-(2-indenyl)triptycene complexes, slowed rotation of the paddlewheel on the NMR time-scale was apparent in the η5-Re(CO)3 case and, when the η6-Cr(CO)3 was deprotonated, the resulting haptotropic shift of the metal tripod onto the five-membered ring also blocked paddlewheel rotation, thus functioning as an organometallic molecular brake. Suzuki coupling of ferrocenylboronic acid to mono- or dibromoanthracene yielded the ferrocenyl anthracenes en route to the corresponding triptycenes in which stepwise hindered rotations of the ferrocenyl groups behaved like molecular dials. CuCl2-mediated coupling of methyl- and phenyl-indenes yielded their rac and meso 2,2′-biindenyls; surprisingly, however, the apparently sterically crowded rac 2,2′-Bis(9-triptycyl)biindenyl functioned as a freely rotating set of molecular gears. The predicted high rotation barrier in 9-phenylanthracene was experimentally validated via the Pd-catalysed syntheses of di(3-fluorophenyl)anthracene and 9-(1-naphthyl)-10-phenylanthracene.

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Elbert, Sven M., Tobias Kirschbaum, Frank Rominger, and Michael Mastalerz. "Proving Triptycene Homoconjugation with the Same Chromophore but Different Connectivity to the Core." Organic Materials 03, no. 02 (April 2021): 097–102. http://dx.doi.org/10.1055/s-0041-1726304.

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Homoconjugation is a phenomenon discussed for various π-systems where classical conjugation is broken by e.g. methylene units but still a stabilization by electronic communication exists. In this respect, triptycene with its rigid C3 symmetric geometry is an ideal scaffold to study this phenomenon. Although several studies based on triptycene strengthen the hypothesis of homoconjugation, in all described cases the electronic communication through space relies on different π-blades. Here, two triptycenes are presented having the exact same π-extended chromophore, but differently annulated to the bicyclic core. Both compounds were investigated by spectroscopic as well as computational means and compared with the corresponding model compound, elucidating the influence of the attachment site to the triptycene core on potential homoconjugation.

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Ebersberger, Sabine. "Das Triptychon in der Kunsttherapie." Musik-, Tanz- und Kunsttherapie 24, no. 3 (July 2013): 128–34. http://dx.doi.org/10.1026/0933-6885/a000123.

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Der vorliegende Beitrag widmet sich dem Triptychon als therapeutische Methode in der Kunsttherapie. Triptychen sind dreiteilige Gemälde, die als sogenannte Flügelaltäre im 15. und 16. Jahrhundert Bekanntheit erlangten. In der Auseinandersetzung mit den therapeutischen Wirkfaktoren (vgl. Grawe, 2000 ; 2004 ) diskutiert der Beitrag die methodischen Stärken des Triptychons als Bildformat und zeigt auf, wie diese in der kunsttherapeutischen Arbeit praktisch nutzbar gemacht werden können. Exemplarische Bildbeispiele verdeutlichen diese Methode.

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Tomioka, Hideo, and Junichi Nakajima. "Thermolysis and photolysis of 1-substituted triptycenes. Divergent fragmentation pathways of the triptycyl skeleton." Journal of the Chemical Society, Perkin Transactions 1, no. 6 (1996): 563. http://dx.doi.org/10.1039/p19960000563.

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Martens, Didier. "Un disciple tardif de Rogier de la Pasture: Maître Johannes (alias Johannes Hoesacker?)." Oud Holland - Quarterly for Dutch Art History 114, no. 2-4 (2001): 79–106. http://dx.doi.org/10.1163/187501701x00406.

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AbstractThe triptych which has hung above the main altar of Our Lady of the Immaculate Conception at Maria-ter-Heide (Brasschaat, near Antwerp) since the nineteenth century unfolds a highly unusual iconographical programme. The representation on the central panel is a 'Holy Kinship' with Saint Anne; the left and right shutters show a 'Tree of Jesse', and the 'Kinship of Effra and Ismeria' respectively. This unusual combination of themes, and the coat of arms of the abbey at Tongerlo on the staff of the kneeling donor on the left shutter, enable us to identify the triptych from an old description, predating 1615, of the art treasures in the abbey at Tongerlo. As early as 1888 canon Van Spilbeek was able to demonstrate on the basis of two entries in the abbey's ledgers that the retable was made around 1513-1515. It was commissioned by the then abbot of Tongerlo, Antonius Tsgrooten. The painter's name appears on both bills of payment of 1513-1515. He was called Johannes, and he was married to Marie Hoesacker. His apparent lack of a surname might intimate that he was a foundling. Hitherto, the triptych in Maria-ter-Heide was the only known work by 'Johannes'. The author suggests that he also painted the monumental triptych with scenes from the lives of Christ and Mary which has been on loan to the museum at Àvila since 1971 from the Provincial Council. In 1968 Karel G. Boon attributed this work to an anonymous North-Netherlandish painter. According to Boon the same artist painted two wings with John the Baptist and Saint Agnes (Paris, private collection) and a 'Baptism of Christ' (Madrid, private collection). 'Johannes' could be the maker of these three works. What is more, the painter of the triptych in Maria-ter-Heide could be credited with two retable wings which have been in the Museo de Santa Cruz in Toledo since the 19608. Their subjects are 'Saint Andrew with Saint Francis' and 'Saint James with Saint Antony of Padua'; on the back of these panels is a 'Visitation'. Judging by the numerous figures he borrowed from Rogier van der Weyden, 'Johannes' seems to have been fascinated by the great Brussels master. His interest in Van der Weyden's art and the fact that he worked for the abbot of Tongerlo suggest that he was active in Brabant. The Dutch elements which Boon claimed to recognise on the Àvila triptych are quite inconspicuous, proving how dangerous it is to determine an artist's provenance solely on the basis of aesthetic impressions. The iconographic programme on the triptychs in Maria-ter-Heide and Avila and the retable wings in Toledo is highly unusual. This indicates that they were not made for the open market on the painter's own initiative, but were ordered specially. Perhaps 'Johannes' ability to convert such iconographic programmes into pictures was one of the reasons for his success a success which, in view of the presence of two of his works in Castile, assumes an international dimension.

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Bonaccorsi, Paola, Maria Luisa Di Gioia, Antonella Leggio, Lucio Minuti, Teresa Papalia, Carlo Siciliano, Andrea Temperini, and Anna Barattucci. "Synthesis of enantiopure sugar-decorated six-armed triptycene derivatives." Beilstein Journal of Organic Chemistry 9 (November 8, 2013): 2410–16. http://dx.doi.org/10.3762/bjoc.9.278.

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A new class of molecules with a triptycene rigid core surrounded by six monosaccharide residues was synthesized. Hexakis(bromomethyl) substituted triptycene was converted into a six-armed triptycene azide (2,3,6,7,14,15-hexakis(azidomethyl)-9,10-dihydro-9,10-[1’,2’]benzenoanthracene). The key step of the synthesis was the cycloaddition of the azide to 2-propyn-1-yl β-D-gluco- or galactopyranosides. All products were isolated in good yields and were fully characterized.

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Locke, Gemma M., Keith J. Flanagan, and Mathias O. Senge. "Towards triptycene functionalization and triptycene-linked porphyrin arrays." Beilstein Journal of Organic Chemistry 16 (April 17, 2020): 763–77. http://dx.doi.org/10.3762/bjoc.16.70.

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Herein, 9,10-diethynyltriptycene is investigated for its use as a rigid isolating unit in the synthesis of multichromophoric arrays. Sonogashira cross-coupling conditions are utilized to attach various porphyrins and boron dipyrromethenes (BODIPYs) to the triptycene scaffold. While there are previous examples of triptycene porphyrin complexes, this work reports the first example of a linearly connected porphyrin dimer, linked through the bridgehead carbons of triptycene. Symmetric and unsymmetric examples of these complexes are demonstrated and single crystal X-ray analysis of an unsymmetrically substituted porphyrin dimer highlights the evident linearity in these systems. Moreover, initial UV–vis and fluorescence studies show the promise of triptycene as a linker for electron transfer studies, showcasing its isolating nature.

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Dissertations / Theses on the topic "Triptycen"

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Baumgärtner, Kevin [Verfasser], and Michael [Akademischer Betreuer] Mastalerz. "Triptycen- und Pyren-basierte polycyclische aromatische Kohlenwasserstoffe / Kevin Baumgärtner ; Betreuer: Michael Mastalerz." Heidelberg : Universitätsbibliothek Heidelberg, 2018. http://d-nb.info/1177044234/34.

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Ueberricke, Lucas [Verfasser], and Michael [Akademischer Betreuer] Mastalerz. "Die Kristallstrukturen aromatischer π-Systeme sowie deren Modifikation durch endständige Triptycen-Einheiten / Lucas Ueberricke ; Betreuer: Michael Mastalerz." Heidelberg : Universitätsbibliothek Heidelberg, 2021. http://d-nb.info/1232324108/34.

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Kohl, Bernd [Verfasser], and Michael [Akademischer Betreuer] Mastalerz. "Auf Triptycen basierende Pyren-fusionierte Pyrazaacene - Eine Kombination aus Porosität und optoelektronischen Eigenschaften / Bernd Kohl ; Betreuer: Michael Mastalerz." Heidelberg : Universitätsbibliothek Heidelberg, 2017. http://d-nb.info/1180738683/34.

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Reinhard, Dennis [Verfasser], and Michael [Akademischer Betreuer] Mastalerz. "Von Triptycen-basierten polycyclischen Kohlenwasserstoffen und porösen Metall-assistierten Salphen-organischen Komplexen und Materialien / Dennis Reinhard ; Betreuer: Michael Mastalerz." Heidelberg : Universitätsbibliothek Heidelberg, 2021. http://nbn-resolving.de/urn:nbn:de:bsz:16-heidok-288268.

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Schumann, Patrick Reiner. "Diastereomere Makrocyclen auf Basis von Bistriazol-Dienophilen und Sorbyl- und Sorboyl-Derivaten." Doctoral thesis, Universitätsbibliothek Chemnitz, 2008. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-200800489.

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Gegenstand der vorliegenden Arbeit ist die Untersuchung makrocyclischer Strukturen, welche über eine Sequenz von zwei Diels-Alder-Reaktionen synthetisiert wurden. Dabei wurden leichtzugängliche Sorbinsäure- und Sorbyl-Abkömmlinge mit aliphatisch-verknüpften Bis-(1,2,4-triazolin-3,5-dionen) kombiniert. Infolge der Prochiralität der eingesetzten Bisdiene können stereochemisch-differenzierte Reaktionsprodukte auftreten. Besonderes Augenmerk lag auf der stereochemischen Zuordnung, welche in vielen Fällen mittels NMR-Spektroskopie oder Einkristall-Röntgenstrukturanalyse gelang.

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Sirven, Agnès. "Nano-machines : vers la synthèse d'un treuil moléculaire." Thesis, Toulouse 3, 2015. http://www.theses.fr/2015TOU30200.

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Dans le domaine des nanomachines, des progrès considérables ont été réalisés. Il est désormais possible de synthétiser une machine moléculaire et de contrôler son mouvement grâce à une source d'énergie chimique, lumineuse ou électrique, de façon à ce qu'il soit unidirectionnel. Un nouveau défi a surgi : comment rendre ce mouvement utile ? Comment utiliser le travail d'une machine moléculaire au niveau nanoscopique, mésoscopique ou macroscopique ? Cette thèse s'inscrit à la suite de la démonstration du contrôle de la rotation d'un moteur moléculaire. Ce moteur est un complexe de ruthénium(II) dont la rotation de la partie mobile, le rotor, est contrôlée par la pointe d'un microscope à effet tunnel. Afin de déterminer le travail limite fournit par ce moteur, nous avons synthétisé un nanotreuil intégrant le moteur moléculaire déjà étudié dans l'équipe avec une chaîne latérale permettant d'accrocher par chimie clic différents types de fragments moléculaires. Ces fragments ayant des natures chimiques différentes (fullerènes, triptycènes, porphyrines), ils interagiront de manière plus ou moins importante avec la surface. De ce fait, la rotation du moteur pourra ou ne pourra pas entraîner leur déplacement sur la surface, ce qui nous permettra d'estimer le travail du moteur. Cette thèse décrit la synthèse des différentes sous-unités de ce nanotreuil : le moteur dissymétrique, la chaîne et les différentes charges. Après avoir développé différentes stratégies visant à intégrer la chaîne sur le rotor, la synthèse de chacun des fragments moléculaires fera l'objet des chapitres suivants. Enfin, un chapitre mettra en perspective l'intégration possible du moteur dans des systèmes d'engrenages en vue de la récupération du travail dans un réseau supramoléculaire
In the field of molecular machines, considerable developments have been achieved. Nowadays, it is possible to synthesize a molecular machine with a directional control on its motion thanks to chemical, light or electrical energy source. A new challenge has arised: how make that movement useful ? How use the work of a molecular machine at a nano-, meso- or macro-level ? This thesis is in line with the demonstration and control of the molecular motor rotation. This motor consists in a ruthenium(II) complexe whom rotation of the movable part, i.e. the rotor, is controlled by the scanning tunnelling microscope tip. In order to estimate its motive power, we have synthesized a nanowinch incorporating the molecular motor synthesized in the team. This motor has been desymmetrized to be able to incorporate a chain allowing to connect by click chemistry several kind of molecular fragments. These fragments (fullerenes, triptycenes, porphyrines) will interact more or less with the surface of deposition. Therefore, the motor rotation will or will not make them move on the surface, giving us the possibility to estimate the motor torque. In this thesis, the synthesis of the different parts of the nanowinch is described : the dissymmetric molecular motor, the linker and the loads. After developping the synthetic strategies allowing us to incorporate the linker on the rotor, the synthesis of each fragment will be detailled in the following chapters. A concluding chapter will deal with the possible integration of that type of complexes into molecular gears in order to exploit the torque in a supramolecular network

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Torkelsson, Sara. "Triptych." Thesis, Högskolan i Borås, Institutionen Textilhögskolan, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-20726.

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Movement in relation to clothing has been conceptualized in many collections before mine. Mostly in terms of garments that move when the body moves. The aim for this project is to have another approach to movement. The attempt is to create a movement that is like a rhythm flowing through the collection. This approach allows me to work with static garments which together creates a rhythm. Movement is an abstract event and impossible to capture in a concrete way. To start my investigation about how I could picture movement I divided movement into three different categories. First, “the speedfull movement” which stands for “the actual” true movement, the one no one can ever capture except from the eye. “Trace of movement”, which represent that slight second where two cinematic pictures meets and creates an illusion of movement. “Static movement”, is the lines that in painting or sculpture can create an illusion of movement. The only movement that I therefore can create in a garment is always static. But, by butting them together in three I create a movement in between the garments. The movement is static but at the same time I could capture some of those “traces of movement” where two cinematic pictures meet. The movement in my collection is an interpretation of how static pictures create motion as seen in cinematographic images. The tools I use to accomplish this movement are perspectives, rhythm and pleating.
Program: Master Programme in Fashion and Textile Design

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Hartman, Lee Chen Yi. "Beowulf triptych." Diss., UMK access, 2005.

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Thesis (M.M.)--Conservatory of Music. University of Missouri--Kansas City, 2005.
"A thesis in music composition." Advisor: Chen Yi. Typescript. Vita. Title from "catalog record" of the print edition Description based on contents viewed June 23, 2006. Online version of the print edition.

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Cannon, Susan. "Anubis : an orchestral triptych." Thesis, Birmingham City University, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680196.

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The aim of my research is to develop a compositional style of orchestral writing that is rich in polarities. This will be achieved through practice-based research using a range of compositional techniques as springboards to create a highly-charged symphonic language, contextualised by a discussion of the influence of stimuli on the compositional process. This thesis comprises a portfolio of seven musical works with supporting commentary documenting the research process and providing contextual and analytical detail. Using a range of influences such as myth and nature as springboards, my research consists of the development of an individual compositional language in which texture plays an important part. Central to this approach is the role of dialogue between polarities such as rhythmical versus timeless, calm and ethereal versus agitated and aggressive, polyphonic density and textural mass versus clarity of line. The research culminates in a triptych of orchestral pieces collectively entitled Anubis (entitled ‘Anubis’, ‘Isis’ and ‘Ammit’ respectively). Each piece forms a movement of Anubis yet can be performed in a stand-alone form. Also included in the portfolio are a number of supporting works that serve as experiments in the use of texture, structure and narrative, as well as exploring how stimuli can be a powerful tool in the creation of striking sonic textures, which then function within complex compositional structures in the main work. The commentary documents the research journey, charting the evolution of my musical language from piece to piece whilst explaining the relationship between source stimuli and resulting compositional response. The completed work, Anubis, comprises three movements exploring a range of textural polarities within a cohesive and consistent sound-world.

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Amro, Kassem. "Conception, synthèse et caractérisation de systèmes π-conjugués organosiliciés pour l'élaboration des dispositifs optoélectroniques." Thesis, Montpellier 2, 2010. http://www.theses.fr/2010MON20207/document.

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Ce travail porte sur la conception de nouveaux composés π-conjugués, potentiellement utilisable en électronique organique en tant que matériaux actifs dans des dispositifs tels que les OLEDs, les cellules photovoltaïques et les capteurs optiques. Dans ce but, nous avons exploité le motif silacyclopentadiène appelé également silole, possédant un bon rendement quantique de fluorescence à l'état solide et une excellente conduction des électrons. Dans un premier temps, l'introduction de groupements structurants (triptycène, stilbènes..) sur le silacyclopentadiène a permis de moduler l'arrangement moléculaire dans la couche active et par conséquent, les propriétés d'électroluminescence. Des diodes possédant des performances très encourageantes furent ainsi obtenues. Dans un deuxième temps, des dérivés siloles présentant une structure tridimensionnelle et une architecture spirosilole (accepteur)-bithiophène (donneur) furent synthétisées. Une cellule photovoltaïque basée sur ces édifices présentant des performances encourageantes fut ensuite mis au point. Enfin, l'étude des mécanismes de transfert d'énergie entre un film de polymère fonctionnalisé par un groupement sensible silole et des composés nitroaromatiques nous a permis de réaliser un nouveau type de capteur optique hautement sensible pour la détection d'explosifs
This work concerns the design of new π-conjugated compounds, potentially useful in organic electronics as active materials in devices such as OLEDs, photovoltaic cells and optical sensors. To this end, silacyclopentadiene, alias silole, groups were used exhibiting high fluorescence quantum yields in the solid state and excellent electron conductivities. Firstly, the introduction of structurizing groups (triptycene, stilbenes etc.) at the silacyclopentadiene allowed tuning of the molecular arrangement in the active layer and, consequently, the electroluminescence properties. Diodes showing very encouraging activities were thus obtained. Secondly, silole derivatives possessing a three-dimensional structure and a spirosilole (acceptor) - bithiophene (donor) architecture were synthesized. A photovoltaic cell based on these molecules was then developed exhibiting encouraging activity. Finally, a study of the mechanisms of energy transfer between a polymer film functionalized by a sensitive silole group and nitroaromatic compounds enabled the development of a new type of highly sensitive optical sensor for the detection of explosives

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Books on the topic "Triptycen"

1

(Firm), EnBW, ed. Emil Wachter: Triptychen. [Karlsruhe]: EnBW Energie Baden Württemberg AG, 2010.

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Xaxulis Karedi: Khakhulʹskiĭ triptikh = The Khakhuli triptych = Le triptyque de Chachouli = Das Triptychon von Chachuli. Tʻbilisi: "Xelovneba", 1988.

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Cary, Joyce. Triptych. Harmondsworth, Middlesex: Penguin Books, 1985.

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Triptych. Victoria, B.C: Ekstasis Editions, 2010.

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Slaughter, Karin. Triptych. London: Random House Publishing Group, 2008.

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Rothenberg, Jerome. Triptych. New York, NY: New Directions, 2007.

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Cary, Joyce. Triptych. London: Joseph, 1986.

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Triptych. [Alberta, Canada]: Dragon Moon Press, 2010.

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Vokolek, Václav. Triptych. Brno: Petrov & Host, 1995.

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Drvota, Mojmir. Triptych. Praha: Český spisovatel, 1995.

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Book chapters on the topic "Triptycen"

1

Nikolaev, Igor, and Evgeny Zhuzhoma. "Triptych." In Flows on 2-dimensional Manifolds, 257–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/bfb0093611.

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Han, Ying, and Chuan-Feng Chen. "Triptycene-Derived Macrocyclic Arenes." In Handbook of Macrocyclic Supramolecular Assembly, 1–43. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1744-6_7-1.

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Han, Ying, and Chuan-Feng Chen. "Triptycene-Derived Macrocyclic Arenes." In Handbook of Macrocyclic Supramolecular Assembly, 139–80. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2686-2_7.

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Acevedo-Muñoz, Ernesto R. "Transitional Triptych." In A Companion to Luis Buñuel, 340–61. Oxford, UK: Blackwell Publishing Ltd, 2013. http://dx.doi.org/10.1002/9781118324882.ch16.

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Kirchentrojaner. "Das räumliche Triptychon." In kunst und kirche, 60–61. Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-99283-8_14.

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Carta, Mariolino. "Triptycene Polymer with Intrinsic Microporosity." In Encyclopedia of Membranes, 1936–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_1966.

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Carta, Mariolino. "Triptycene Polymer with Intrinsic Microporosity." In Encyclopedia of Membranes, 1–4. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_1966-1.

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Živsa, Irena. "Urzidil, Johannes: Prager Triptychon." In Kindlers Literatur Lexikon (KLL), 1–2. Stuttgart: J.B. Metzler, 2020. http://dx.doi.org/10.1007/978-3-476-05728-0_19456-1.

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Chen, Chuan-Feng, Han-Xiao Wang, Ying Han, and Ying-Xian Ma. "Triptycene-Derived Calixarenes, Heteracalixarenes and Analogues." In Calixarenes and Beyond, 467–84. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_18.

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Bernard, Mark. "A Triptych of Youth." In Halloween, 49–74. London ; New York : Routledge, 2020. | Series: Cinema and youth cultures: Routledge, 2019. http://dx.doi.org/10.4324/9781315185453-3.

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Conference papers on the topic "Triptycen"

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Paulos, Eric, Chris Myers, Rundong Tian, and Paxton Paulos. "Sensory triptych." In UIST '14: The 27th Annual ACM Symposium on User Interface Software and Technology. New York, NY, USA: ACM, 2014. http://dx.doi.org/10.1145/2642918.2647410.

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Verostko, Roman. "Gaia Triptych." In ACM SIGGRAPH 2004 Art gallery. New York, New York, USA: ACM Press, 2004. http://dx.doi.org/10.1145/1185884.1185968.

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Sanmartín-Matalobos, Jesús, Ana García-Deibe, Matilde Fondo, José Pérez-Lustres, Sourav Sourav Bhowmick, and Neeladri Das. "Synthesis and Characterization of a New Triptycene-Based Tripod." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a007.

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Liu, Lei, Zhou Li, and Jie Zhang. "Triptycene-Based Microporous Polymer Incorporating Thioamide Functionality: Preparation and Gas Storage Properties." In 1st International Electronic Conference on Materials. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecm-1-b012.

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Mallik, Samapika, and Mosim Ansari. "Effect of chain length on self-assembly of triptycene based polymer films." In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001506.

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Bernardini, M. G. "A New Astrophysical “Triptych”: GRB030329/SN2003dh/URCA-2." In GAMMA-RAY BURSTS: 30 YEARS OF DISCOVERY: Gamma-Ray Burst Symposium. AIP, 2004. http://dx.doi.org/10.1063/1.1810854.

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Sanmartín-Matalobos, Jesús, Ana García-Deibe, Martín Amoza, Matilde Fondo, Antonio Mota, Sourav Sourav Bhowmick, and Neeladri Das. "Computational and Experimental Studies Into the Conformations of a Triptycene-Based Ditopic Ligand." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-e007.

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Dultzin-Hacyan, Deborah. "NGC 7469. The perfect triptych: interaction, circumnuclear starbur stand black hole?" In Testing the AGN paradigm diagnostics. AIP, 1992. http://dx.doi.org/10.1063/1.42225.

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Chu, Mark, Donald Ruggiero Lo Sardo, and Douglas Guilbeault. "Millenia as Moment: A Triptych in 75 Colorgrams by Comp-syn." In C&C '21: Creativity and Cognition. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3450741.3466848.

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Claes, K., and I. Moorkens. "Using the Triptych model for future burden sharing—a case study for Flanders." In ENERGY 2007. Southampton, UK: WIT Press, 2007. http://dx.doi.org/10.2495/esus070391.

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Reports on the topic "Triptycen"

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Guo, Ruilan. Design, Synthesis and Characterization of Triptycene-Containing Macromolecules with Hierarchically Controlled Architectures as Functional Membrane Materials for Energy Applications. Office of Scientific and Technical Information (OSTI), March 2019. http://dx.doi.org/10.2172/1499993.

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