Relevant bibliographies by topics / Binaphtyle

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Binaphtyle'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Binaphtyle"

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Fadouach, M., B. Benali, A. Kadiri, C. Cazeau-Dubroca, and G. Nouchi. "Etude comparative en luminescence UV-visible du 1,1′-binaphtyle et du 2,2′-binaphtyle." Spectrochimica Acta Part A: Molecular Spectroscopy 48, no. 10 (October 1992): 1491–500. http://dx.doi.org/10.1016/0584-8539(92)80156-q.

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Assongo, C. Kenfack, B. Kabouchi, and B. Benali. "Etude des spectres d’absorption UV du 1,1′-binaphtyle et 2,2′-binaphtyle et de leurs auto-associations par le modèle d’interaction monopôle–dipôle atomique (AMDI)." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 56, no. 5 (April 2000): 941–46. http://dx.doi.org/10.1016/s1386-1425(99)00184-5.

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Sumi, Kenzo, Takao Ikariya, and Ryoji Noyori. "Efficient synthesis of optically active 2-amino-2'-diphenylphosphino-1,1'-binaphthyl and its derivatives." Canadian Journal of Chemistry 78, no. 6 (June 1, 2000): 697–703. http://dx.doi.org/10.1139/v99-248.

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Optically active 2-amino-2'-diphenylphosphino-1,1'-binaphthyls having various functional groups, such as amino, alkoxycarbonylamino, acylamino, mono- and dialkylamino, and sulfonylamino at C2 position were prepared. The key intermediate of the above aminophosphines was 2-carbamoyl-2'-diphenylphosphinyl-1,1'-binaphthyl synthesized from optically active 2-cyano-2'-diphenylphosphinyl-1,1'-binaphthyl. The transformation of the carbamoyl group to an amino group was effected by the Hofmann reaction.Key words: aminophosphine ligand, Hofmann reaction, optically active phosphine ligand.
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Benali, B., M. Fadouach, B. Kabouchi, A. Kadiri, and G. Nouchi. "Effet de la polarité du solvant sur les propriétés des états électroniques excités du 1,1′-binaphtyle: étude par spectroscopie UV-visible." Spectrochimica Acta Part A: Molecular Spectroscopy 49, no. 8 (July 1993): 1163–69. http://dx.doi.org/10.1016/0584-8539(93)80075-l.

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Jackson, S. David, Geoffrey Webb, and Nicola C. Young. "Adsorption of Chiral 2,2‘-Substituted-1,1’-Binaphthalenes onto Silica-Supported Palladium and Nickel." Adsorption Science & Technology 24, no. 3 (April 2006): 257–68. http://dx.doi.org/10.1260/026361706778812853.

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The nature of the adsorption of a series of 2,2‘-substituted-1,1’-binaphthalenes over supported palladium and nickel catalysts has been studied. Adsorption has been shown to occur through the 2,2‘-substituted functional groups. Where this is not possible, no adsorption of the binaphthyl is observed. Adsorption of 2,2’-diamino-1,1’-binaphthalene occurred solely on the metal components of the catalysts. However, total coverage of the metal surface was not obtained, with only specific sites being available for adsorption. Adsorption of 2,2‘-dihydroxy-1,1’-binaphthalene occurred on the metal components but also spilled over onto the support. Adsorption was detected for 2-hydroxy-2‘-methoxy-1,1’-binaphthalene but no spill-over was observed, indicating that both hydroxy groups are involved in the spill-over process. Co-adsorption and sequential adsorption studies revealed that there are a variety of adsorption sites that favour different binaphthyls.
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Hoshi, Takashi, Hiroshi Shionoiri, Masayoshi Katano, Toshio Suzuki, Masayoshi Ando, and Hisahiro Hagiwara. "(R)-2,2′-Bis(stannyl)-1,1′-binaphthyls as a New Chiral Bis-Metallic Binaphthyl Catalyst." Chemistry Letters 31, no. 6 (June 2002): 600–601. http://dx.doi.org/10.1246/cl.2002.600.

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Hatano, Bunpei, Kazuyuki Hashimoto, Hiroshi Katagiri, Tatsuro Kijima, Satoshi Murakami, Shigeru Matsuba, and Miho Kusakari. "Enantioresolution of 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl Oxide Using Inclusion Complex with Chiral 2,2′-Dihydroxy-1,1′-binaphtyl." Journal of Organic Chemistry 77, no. 7 (March 19, 2012): 3595–97. http://dx.doi.org/10.1021/jo202630p.

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Kitamura, Sayaka, Kazuki Nakabayashi, Takashi Wakabayashi, Nobuo Tajima, Michiya Fujiki, and Yoshitane Imai. "Photoexcited state chirality transfer. Hidden tunability of circularly polarized luminescent binaphthyl–anthracene tandem molecular systems." RSC Advances 5, no. 83 (2015): 67449–53. http://dx.doi.org/10.1039/c5ra10716d.

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Circularly polarized luminescent properties of binaphthyl with two achiral anthracenes were tuned by exploiting photoexcited-state chirality transfer from the binaphthyl to anthracenes when open- or closed-type binaphthyl structure was chosen.
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Ogunlaja, Adeniyi S., Eric Hosten, Richard Betz, and Zenixole R. Tshentu. "Selective removal of isoquinoline and quinoline from simulated fuel using 1,1′-binaphthyl-2,2′-diol (BINOL): crystal structure and evaluation of the adduct electronic properties." RSC Advances 6, no. 45 (2016): 39024–38. http://dx.doi.org/10.1039/c6ra03854a.

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1,1′-Binaphthyl-2,2′-diol/quinoline (BINOL/QUN) and 1,1′-binaphthyl-2,2′-diol/isoquinoline (BINOL/ISOQUN) adducts were successfully synthesized. Isothermal titration calorimetry (ITC) involving 1,1′-binaphthyl-2,2′-diol (BINOL) and isoquinoline confirming interaction.
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Hoshi, Takashi, Hiroshi Shionoiri, Masayoshi Katano, Toshio Suzuki, Masayoshi Ando, and Hisahiro Hagiwara. "ChemInform Abstract: (R)-2,2′-Bis(stannyl)-1,1′-binaphthyls as a New Chiral Bis-metallic Binaphthyl Catalyst." ChemInform 33, no. 43 (May 19, 2010): no. http://dx.doi.org/10.1002/chin.200243040.

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Dissertations / Theses on the topic "Binaphtyle"

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Pieters, Grégory. "Synthèse et propriétés de nouvelles architectures moléculaires hélicoïdales." Versailles-St Quentin en Yvelines, 2010. http://www.theses.fr/2010VERS0059.

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Ces travaux de recherches s'articulent autour de la synthèse et de l'étude des propriétés de nouvelles architectures moléculaires hélicoïdales. La première partie concerne la synthèse d'une nouvelle plateforme moléculaire à motif diarylnaphtalene et son utilisation pour la synthèse de plusieurs molécules hélicoïdales polysubstituées. Ainsi a partir de ces briques moléculaires, des 6,11-diamino-[6]-hélicènes et des cyclooctahélicènes ont été prépares, selon une séquence réactionnelle simple et courte. Une seconde partie est dédiée à l’évolution de cette sequence réactionnelle dont l’étape clé est une substitution électrophile aromatique. En effet, a partir d’un motif binaphtyle ou ortho-terphényles, il a été possible d’orienter sélectivement l’accès a des molécules planes ou hélicoïdales. Ce chapitre est conclu par leur utilisation dans la construction de nouveaux clusters de bores dérives de l’ortho-carborane. En plus de la synthèse et de la caractérisation, les propriétés de ces nouvelles molécules ont été étudiées (arrangement a l'état solide, conformation en solution) et de nombreux calculs théoriques ont été entrepris afin d'expliquer certaines sélectivités observes ou de déterminer les barrières de racémisation des édifices synthétises
This work is dealing with the synthesis and properties of new helical molecular architectures. The first part is dedicated to the synthesis of a new molecular platform based on diarylnaphthalene compounds and their use as key starting material new polysubstituted molecules such as 6,11-diamino-[6]-helicenes and cyclooctahelicenes have been elaborated using a short and facile reaction sequence;. In the second part the study aims to control the aromatic electrohpilic subtitution key step. In this context, starting from binaphthyl or terphenyl patterns, we were able to selectively control the outcome of the reaction and obtain planar or helical architectures. Finally, novel architectures have been obtain by mixing some of these molecules with valuable boron cluster derivatives. In addition to the synthesis, physical properties of these new architectures have been studied (crystal packing, conformation in solution…) and theorical calculations investigated in order to explain some of the observed selectivities and to determine racemization barriers
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Hadidi, Rim. "Dichroïsme circulaire de photoélectrons (PECD) en couche de valence : systèmes à base d’acides aminés et dérivés de binaphtyles." Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASS135.

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Nous avons étudié en détail la photodynamique VUV et le PECD (un effet chiroptique intense) de l'acide aminé Proline (Pro) en phase gaz, seul acide aminé naturel contenant un cycle pyrrolidine. Plusieurs températures ont été utilisées pour faire varier la population de conformères de Pro native, afin d'effectuer une analyse complète des conformères à l'aide des calculs PECD CMS Xα, et ce faisant de raffiner le paysage conformationnel. Le signe des asymétries, similaire au cas de l’alanine, renforce le scenario astrophysique en lien avec l’homochiralité, sans contraintes de température. De plus, nous avons étudié, le PECD sur des acides aminés aromatiques (tryptophane & tyrosine), des chromophores importants des protéines. Nous avons également étendu la portée de nos études de PECD vers de grands édifices moléculaires tels que des dipeptides à base d’acides aminés (c-Pro-Pro, Gly-Pro et Pro-Gly), jusqu’à des systèmes beaucoup plus complexes comme des nanoparticules homochirales (Pro, Trp et Tyr), pour tester, phénoménologiquement, les limites de sensibilité du PECD par rapport à la complexité moléculaire. Enfin, nous présentons pour la première fois l'étude d'une famille de 3 molécules à chiralité axiale (dérivées de binaphtyles), dont nous avons notamment étudié l'influence de l'angle diédral sur le PECD
We studied in great details, the VUV photodynamics and PECD (an intense chiroptical effect) of the gas phase amino acid Proline (Pro), the only naturally occurring amino acid containing a pyrrolidine ring. Several temperatures were used to vary the conformer population of the nascent Pro in order to perform a comprehensive conformer analysis of the PECD with the help of CMS-Xα PECD calculations allowing to refine the conformational landscape. The sign of the chiral asymmetry, similar to the one of alanine, strengthen the astrophysical scenario in link to the origin of homochirality, without any temperature constraints. We studied also, the PECD of two aromatic amino-acids (tryptophan & tyrosine), which are important chromophores of proteins. We extended the scope of our PECD studies to larger amino-acids-based systems, such as dipeptides (c-Pro-Pro, Gly-Pro and Pro-Gly), up to much more complex systems like homochiral nanoparticles (Pro, Trp and Tyr), to test, phenomenologically, the limits of sensitivity of PECD with respect to molecular complexity. Finally, we present for the first time the study of a family of 3 molecules with axial chirality (binaphthyls derivatives), of which we studied in particular the influence of the dihedral angle on the PECD
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Lockhart, Stephen Crawford. "Carbenes and binaphthyls in asymmetric catalysis." Thesis, University of Glasgow, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.440333.

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Kabwit, Rodriguez Yav. "Structure and reactivity of selected binaphthyl derivatives." Thesis, Cape Peninsula University of Technology, 2013. http://hdl.handle.net/20.500.11838/729.

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Thesis presented to the CAPE PENINSULA UNIVERSITY OF TECHNOLOGY for the degree of MASTER OF TECHNOLOGY Department of Chemistry, Cape Peninsula University of Technology, Cape Town Campus, Zonnebloem, October 2013
In this thesis, the complexation behaviour of the host compounds, 1,1’-binaphthyl- 2,2’-dicarboxylic acid (BNDA) and 1,1’-binaphthyl-2,2’-diol (BINOL) were investigated. These hosts are large, bulky and scissor shaped; they contain functionalities to selectively interact with other molecules. A series of small organic compounds, particularly amines, were used in the preparation of the complexes. BNDA formed three complexes with acyclic amines, two complexes with the cyclic amines and two complexes with a racemic amine in different solvents. All the complexes formed were salts. The amines used were diethylamine, di-nbutylamine, cyclohexylamine, dicyclohexylamine, and sec-butylamine. For the studies with the acyclic amines and cyclic amines, crystals were grown in methanol as a co-solvent. Similar experiments were conducted with BINOL. Successful complexation only occurred with cyclohexylamine and dicyclohexylamine respectively. An amine host, 1,1’-binaphthyl-2,2’- diamine (BINDIA) was also considered with acidic and amide guests to extend the study of the binaphthyl derivatives, but from the array of guests used, the host only formed an inclusion compound with dimethylacetamide (DMA). The structures of all the complexes were elucidated using single crystal X-ray diffraction. Thermal analysis was performed in order to determine the thermal stability of the complexes, including techniques such as thermogravimetry, differential scanning calorimetry and hot stage microscopy. The kinetics of desolvation was investigated for some of the complexes.
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Leung, King Sze. "SPECTROSCOPIC INVESTIGATION OF ENANTIOMERIC COMPOSITION AND PHOTOPHYSICAL STUDIES OF BINAPHTHYL DIAMINE." OpenSIUC, 2013. https://opensiuc.lib.siu.edu/theses/1204.

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Although the chemical and physical properties of enantiomers are identical, they exhibit different biological activities. Therefore, one enantiomer often shows maximum therapeutic activity, but the other enantiomer may have no effect, inhibit the ability of the therapeutic form, or can even be harmful. Since enantiomers can be found in different area, such as drugs, pesticides, waste compounds, etc, it is important and necessary to develop simple, fast, low cost, and accurate methods for determination of enantiomeric composition. Xu and McCarroll have developed a method to determine enantiomeric composition by steady-state fluorescence anisotropy based on guest and host theory, where the guest is the chiral analyte, and the host is the chiral selector. The first part of this thesis is an extension of this study investigating different chiral analytes. The chiral selectors that were chosen for this study are different sizes of cyclodextrins, and the chiral analytes that were selected to examine are binaphthyl derivatives, which are 1, 1'-bi-2-napththol (BOH), 1, 1'-binaphthyl-2, 2'-diyl hydrogen phosphate (BNP), and propanol hydrochloride. β-cyclodextrin (CD) was found to be a better chiral selector for determination of BNP enantiomeric composition in this system. Moreover, the chiral selector that was better for determination of BOH and propanol hydrochloride enantiomeric composition in the study was found to be α-CD and γ-CD, respectively. A temperature study was carried out to investigate the best temperature for the determination of BNP enantiomeric composition with β-CD as the chiral selector, and 10 °C was found to be the best temperature in the system. Following an unexpected observation of new species found to be produced after light exposure, a detailed study was applied in order to determine the possible mechanism of the reactions and the identity of the various chemical structures. This investigation is of relevance since BNA is used in various applications and was mentioned in the second part of this thesis. Beside fluorescence spectroscopy, other techniques were applied in this study, such as laser desorption/ionization mass spectrometry (LSI-MS), ultraviolet-visible spectroscopy (UV-Vis), nuclear magnetic resonance spectroscopy (NMR), and thin layer chromatography (TLC). There were 5 possible species that were determined when BNA in chloroform was exposed to 377 nm light, which are hypothesized as 7H-Dibenzo[c,g]carbazole (DBC), 7, 8-Diaza[5]helicene N.N'-Dioxide produced through oxidation and three additional compounds formed through excited state proton transfer (ESPT). Evidence supporting these hypotheses is discussed, as well as the need for further study to confirm the structures of the various species produced during light exposure.
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Nuruzzaman, Mohammad. "Use of 1,1'-Binaphthyl Derivatives in Asymmetric Synthesis and Enantiomeric Recognition." 京都大学 (Kyoto University), 2002. http://hdl.handle.net/2433/150090.

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Vaton-Chanvrier, Laurence. "Synthèse et greffage sur silice de dérivés de l'acide cholique. Evaluation de l'énantiosélectivité par chromatographie liquide haute performance." Rouen, 1999. http://www.theses.fr/1999ROUES078.

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La synthèse de plusieurs dérivés de l'acide cholique, mettant à profit les diverses possibilités de transformations régio-sélectives de ce composé, a permis de préparer différentes phases stationnaires chirales, afin d'évaluer, par chromatographie liquide haute performance, le potentiel énantiosélectif de ce stéroïde greffé sur silice. Le choix des différentes structures tient compte de l'introduction d'une oléfine terminale, nécessaire au greffage sur silice. Trois phases stationnaires, préparées à partir de sélecteurs représentatifs de l'ensemble des précurseurs retenus, se sont montré énantiosélectives, à des degrés divers. La phase stationnaire la plus apte à la discrimination chirale a permis l'optimisation des conditions de phase mobile et le choix de différentes séries de solutés appartenant à plusieurs classes de composés (aminoalcools, amines, hydantoïnes, composés à motif 1,1'-binaphthyle), utilisés pour l'étude des mécanismes de séparation chirale. Le sélecteur le plus énantiosélectif est également employé pour une étude comparative de trois modes de greffage. La méthode de greffage la mieux adaptée est appliquée à la préparation de l'ensemble des phases stationnaires, dont l'énantiosélectivité est évaluée par chromatographie en phase liquide, dans les conditions de phase mobile définies, avec les séries de solutés sélectionnés. L'étude des mécanismes de reconnaissance met en évidence le rôle prépondérant des interactions par liaisons hydrogène. Des études complémentaires, centrées sur un couple soluté/phase stationnaire choisi, ont permis la détermination de la stoechiométrie 1 : 1 du complexe, et des grandeurs thermodynamiques liées à sa formation au sein de la colonne chromatographique. Une approche des mécanismes de reconnaissance chirale par modélisation moléculaire confirme le rôle prépondérant des liaisons hydrogène dans le processus de discrimination énantiomérique.
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Matthes, Burkhard. "Isolierung und Synthese von chinoiden Naturstoffen und Strukturberechnungen an verbrückten 1,1-́Binaphthylen." [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=971357285.

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Wang, Hao. "Artifical Light-Driven Chiral Molecular Switches Based on Halogenated and Cyclic Azo-Binaphthyl Derivatives." Kent State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1586518390107867.

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Okucu, Şakir. "Beiträge zur Chemie von 2,2'-bis(methylphosphino)-substituierten 1,1'-Binaphthyl- und 1,8-bisphosphinosubstituierten Naphthalin-Derivaten." kostenfrei, 2006. http://www.digibib.tu-bs.de/?docid=00013530.

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Books on the topic "Binaphtyle"

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1,1'-binaphthyl-based chiral materials: Our journey. London: Imperial College Press, 2010.

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Juskowiak, Bernard. Związki amfifilowe zawierające ugrupowanie fluoryzujące i ich zastosowanie w analizie chemicznej. Poznań: Wydawn. Nauk. UAM, 1995.

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Book chapters on the topic "Binaphtyle"

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Imai, Yoshitane. "Circularly Polarized Luminescence of Axially Chiral Binaphthyl Fluorophores." In Circularly Polarized Luminescence of Isolated Small Organic Molecules, 11–30. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2309-0_2.

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Liu, Na, Xing Wang, Hui Cao, Chun Hai Chen, and Wan Jin Zhang. "Synthesis of a Novel Hollow Sphere Having Rigid Binaphthyl Macrocycle as Shell." In Solid State Phenomena, 219–22. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-30-2.219.

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Kano, Taichi, and Keiji Maruoka. "Chapter 17. Binaphthyl-derived Cyclic Amines and Their Salts as Asymmetric Organocatalysts." In Green Chemistry Series, 135–63. Cambridge: Royal Society of Chemistry, 2015. http://dx.doi.org/10.1039/9781782626435-00135.

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Takaya, Hidemasa, Tetsuo Ohta, and Kazushi Mashima. "New 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl—Ru(II) Complexes for Asymmetric Catalytic Hydrogenation." In Advances in Chemistry, 123–42. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/ba-1992-0230.ch008.

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Kano, Koji, Takashi Kitae, and Hiroshi Takashima. "Use of Electrostatic Interaction for Chiral Recognition. Enantioselective Complexation of Anionic Binaphthyls with Protonated Amino-β-Cyclodextrin." In Proceedings of the Eighth International Symposium on Cyclodextrins, 657–62. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-5448-2_142.

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Jin, Mingoo. "Luminescent Mechanochromism of a Chiral Complex: Distinct Crystal Structures and Color Changes of Racemic and Homochiral Gold(I) Isocyanide Complexes with a Binaphthyl Moiety." In Novel Luminescent Crystalline Materials of Gold(I) Complexes with Stimuli-Responsive Properties, 83–102. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-4063-9_3.

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"Introduction About 1,1'-Binaphthyls." In 1,1′-Binaphthyl-Based Chiral Materials, 1–12. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2009. http://dx.doi.org/10.1142/9781848164123_0001.

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Colonna, S., and D. Perdicchia. "Binaphthyl Phase-Transfer Catalysts." In Stereoselective Synthesis 1 Stereoselective Reactions of Carbon—Carbon Double Bonds, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-201-00065.

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"Main Chain Chiral-Conjugated Polymers." In 1,1′-Binaphthyl-Based Chiral Materials, 13–86. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2009. http://dx.doi.org/10.1142/9781848164123_0002.

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"Polybinaphthyls in Asymmetric Catalysis." In 1,1′-Binaphthyl-Based Chiral Materials, 87–150. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2009. http://dx.doi.org/10.1142/9781848164123_0003.

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Conference papers on the topic "Binaphtyle"

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Kim, Y., W. Cao, J. Goldhar, C. H. Lee, W. N. Herman, M. J. Lee, V. Jain, and M. M. Green. "Polarization properties of optical waveguides from chiral binaphthyl films." In Frontiers in Optics. Washington, D.C.: OSA, 2003. http://dx.doi.org/10.1364/fio.2003.thu3.

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Van Elshocht, Sven, Thierry Verbiest, Martti Kauranen, Andre Persoons, Liang Ma, Hua Cheng, Kwon Y. Musick, Lin Pu, and K. U. Leuven. "Nonlinear optical study of chiral 1,1-binaphthyl based helical polymers." In Organic Thin Films. Washington, D.C.: OSA, 1999. http://dx.doi.org/10.1364/otf.1999.fc5.

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Pozzi, Gianluca, Amedea Manfredi, Fernando Montanari, Marco Cavazzini, and Silvio Quici. "New Fluorous Chiral Phosphorous Ligands Based on the Binaphthyl Skeleton." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01819.

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Gladiali, Serafino, Serenella Medici, Giovanna Pirri, and Sonia Pulacchini. "Synthesis, Resolution and Use in Enantioselective Catalysis of an Axially Chiral Binaphthyl-templated P,S-heterodonor Ligand (binaps)." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01831.

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Kalinovskii, I. O., V. I. Mastshenko, R. A. Vinokur, Natalia I. Boiko, Peter V. Shibaev, and Valery P. Shibaev. "Atropenantiomers of novel 1,1'-binaphthyl derivatives: synthesis and use for cholesteric structure induction in low molecular mass and polymer nematics." In Liquid Crystals, edited by Marzena Tykarska, Roman S. Dabrowski, and Jerzy Zielinski. SPIE, 1998. http://dx.doi.org/10.1117/12.301265.

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