Добірка наукової літератури з теми "Intramolecular π-dimer"
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Статті в журналах з теми "Intramolecular π-dimer"
Zhang, Mingzhen, Ryan Maloney, Hyunbum Jang, and Ruth Nussinov. "The mechanism of Raf activation through dimerization." Chemical Science 12, no. 47 (2021): 15609–19. http://dx.doi.org/10.1039/d1sc03444h.
Повний текст джерелаRivera, Augusto, Jicli José Rojas, Jaime Ríos-Motta, and Michael Bolte. "Crystal structure of 1-[(2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazin-2-yl)methyl]naphthalen-2-ol: a possible candidate for new polynaphthoxazine materials." Acta Crystallographica Section E Crystallographic Communications 71, no. 9 (August 26, 2015): 1089–92. http://dx.doi.org/10.1107/s2056989015015583.
Повний текст джерелаXu, Dong-Yan, Ying Liu, Ming-Li Liu, Jun-Fa Wei, and Jian-Min Dou. "[2-Oxido-1-naphthaldehyde (2-hydroxybenzoyl)hydrazonato]pyridinecopper(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 3, 2006): m671—m673. http://dx.doi.org/10.1107/s1600536806006696.
Повний текст джерелаKubono, Koji, Taisuke Matsumoto, and Masatsugu Taneda. "Crystal structure of 4-bromo-N-[(3,6-di-tert-butyl-9H-carbazol-1-yl)methylidene]aniline." Acta Crystallographica Section E Crystallographic Communications 75, no. 10 (September 10, 2019): 1429–31. http://dx.doi.org/10.1107/s2056989019012374.
Повний текст джерелаEl-Brollosy, Nasser R., Mohamed I. Attia, Hazem A. Ghabbour, Suchada Chantrapromma, and Hoong-Kun Fun. "6-(3,5-Dimethylbenzyl)-5-ethyl-1-[(2-phenylethoxy)methyl]pyrimidine-2,4(1H,3H)dione." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 10, 2012): o1031—o1032. http://dx.doi.org/10.1107/s1600536812009841.
Повний текст джерелаBorbulevych, Oleg Ya. "[1-(Benzylsulfonyl)-3-(4-nitrophenyl)-1,2,3,4-tetrahydroquinoxalin-2-yl](4-bromophenyl)methanone 2-methylpropanol hemisolvate." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (February 21, 2007): o1372—o1374. http://dx.doi.org/10.1107/s1600536807007143.
Повний текст джерелаOstrowska, Katarzyna, Davide Ceresoli, Katarzyna Stadnicka, Marlena Gryl, Marco Cazzaniga, Raffaella Soave, Bogdan Musielak та ін. "π–π-Induced aggregation and single-crystal fluorescence anisotropy of 5,6,10b-triazaacephenanthrylene". IUCrJ 5, № 3 (18 квітня 2018): 335–47. http://dx.doi.org/10.1107/s2052252518001987.
Повний текст джерелаAlcantara Emiliano, Sannyele, Sheyla Welma Duarte Silva, Mariano Alves Pereira, Valeria R.dos Santos Malta, and Tatiane Luciano Balliano. "Crystal structure and conformational analysis of 2-hydroxy-3-(2-methylprop-1-en-1-yl)naphthalene-1,4-dione." Acta Crystallographica Section E Crystallographic Communications 72, no. 2 (January 16, 2016): 188–90. http://dx.doi.org/10.1107/s2056989015024755.
Повний текст джерелаOkuda, Kensuke, Hiromi Watanabe, Takashi Hirota, Kazuma Gotoh, and Hiroyuki Ishida. "[(Z)-2-(3-Methyl-1,2,4-oxadiazol-5-yl)-2-(1-naphthyl)ethenylamino]formaldehyde oxime 1,4-dioxane hemisolvate." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (October 5, 2007): o4261—o4262. http://dx.doi.org/10.1107/s1600536807048301.
Повний текст джерелаBambi-Nyanguile, Sylvie-Mireille, Peter Mangwala Kimpende, Bernard Pirotte, and Luc Van Meervelt. "N-tert-Butyl-N′-[5-cyano-2-(4-methylphenoxy)phenylsulfonyl]urea, a new TXA2receptor antagonist." Acta Crystallographica Section C Crystal Structure Communications 69, no. 8 (July 13, 2013): 901–3. http://dx.doi.org/10.1107/s010827011301771x.
Повний текст джерелаДисертації з теми "Intramolecular π-dimer"
Iordache, Adriana. "Activation par transfert d'électron : applications aux systèmes commutables et à l'ingénierie moléculaire." Phd thesis, Grenoble, 2010. http://www.theses.fr/2010GRENV056.
Повний текст джерелаOne of the most important key to the development of nanosciences lies in our ability to monitor, modify or control nanometric materials. The addition or removal of electrons to or from given molecular objects can find useful applications in numerous arena of nanosciences: as signal transcription of interactions processes, as impulse to trigger conformational, configurational or directional mechanical changes at the molecular level or even as a way to control and activate the reactivity of molecular building blocks in organic synthesis. This work deals with two complementary processes associated to electron transfer: molecular movements in switchable architectures and activation of molecular building blocks to form conjugated macrocyclic structures The first part of this research work is devoted to the synthesis of porphyrin-based molecular tweezers and of ferrocene-based molecular pivots. The dynamic properties of these switchable molecular objects; relying on reversible π-dimerization processes, have been investigated by spectroscopic, electrochemical and spectroelectrochemical methods. In the second part of this manuscript we show few examples of electrochemically driven synthetic procedures for preparation of expanded porphyrins. Unlike chemical oxidants, which must often be tested empirically for a given transformation, under electrochemical conditions, one has the opportunity to tune the reactivity of the pyrrole-based reagent via the choice of anodic voltage. We especially established that the use of bipyrrole allows for the clean and high-yield production of cyclo[8]pyrrole; the requisite electrochemically-induced cyclization of four bipyrrole building blocks likely involving an electrolyte-based templating effect. The success of this approach leads us to propose that analogous electrochemical oxidation processes could be used to generate a range of new expanded porphyrin products