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Artykuły w czasopismach na temat "Intramolecular π-dimer"
Zhang, Mingzhen, Ryan Maloney, Hyunbum Jang i Ruth Nussinov. "The mechanism of Raf activation through dimerization". Chemical Science 12, nr 47 (2021): 15609–19. http://dx.doi.org/10.1039/d1sc03444h.
Pełny tekst źródłaRivera, Augusto, Jicli José Rojas, Jaime Ríos-Motta i 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, nr 9 (26.08.2015): 1089–92. http://dx.doi.org/10.1107/s2056989015015583.
Pełny tekst źródłaXu, Dong-Yan, Ying Liu, Ming-Li Liu, Jun-Fa Wei i Jian-Min Dou. "[2-Oxido-1-naphthaldehyde (2-hydroxybenzoyl)hydrazonato]pyridinecopper(II)". Acta Crystallographica Section E Structure Reports Online 62, nr 4 (3.03.2006): m671—m673. http://dx.doi.org/10.1107/s1600536806006696.
Pełny tekst źródłaKubono, Koji, Taisuke Matsumoto i 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, nr 10 (10.09.2019): 1429–31. http://dx.doi.org/10.1107/s2056989019012374.
Pełny tekst źródłaEl-Brollosy, Nasser R., Mohamed I. Attia, Hazem A. Ghabbour, Suchada Chantrapromma i 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, nr 4 (10.03.2012): o1031—o1032. http://dx.doi.org/10.1107/s1600536812009841.
Pełny tekst źródłaBorbulevych, 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, nr 3 (21.02.2007): o1372—o1374. http://dx.doi.org/10.1107/s1600536807007143.
Pełny tekst źródłaOstrowska, Katarzyna, Davide Ceresoli, Katarzyna Stadnicka, Marlena Gryl, Marco Cazzaniga, Raffaella Soave, Bogdan Musielak i in. "π–π-Induced aggregation and single-crystal fluorescence anisotropy of 5,6,10b-triazaacephenanthrylene". IUCrJ 5, nr 3 (18.04.2018): 335–47. http://dx.doi.org/10.1107/s2052252518001987.
Pełny tekst źródłaAlcantara Emiliano, Sannyele, Sheyla Welma Duarte Silva, Mariano Alves Pereira, Valeria R.dos Santos Malta i 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, nr 2 (16.01.2016): 188–90. http://dx.doi.org/10.1107/s2056989015024755.
Pełny tekst źródłaOkuda, Kensuke, Hiromi Watanabe, Takashi Hirota, Kazuma Gotoh i 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, nr 11 (5.10.2007): o4261—o4262. http://dx.doi.org/10.1107/s1600536807048301.
Pełny tekst źródłaBambi-Nyanguile, Sylvie-Mireille, Peter Mangwala Kimpende, Bernard Pirotte i 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, nr 8 (13.07.2013): 901–3. http://dx.doi.org/10.1107/s010827011301771x.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaOne 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