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Collect. Czech. Chem. Commun. 2009, 74, 323-333
https://doi.org/10.1135/cccc2008184
Published online 2009-02-16 15:45:21

Preferential formation of homochiral silver(I) complexes upon coordination of two aza[6]helicene ligands to Ag+ ions

Jiří Míšek, Miloš Tichý, Irena G. Stará, Ivo Starý* and Detlef Schröder*

Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, v.v.i., Flemingovo nám. 2, 166 10 Prague 6, Czech Republic

Crossref Cited-by Linking

  • Oschwald Johannes, Reger David, Frühwald Stefan, Warmbrunn Vera, Görling Andreas, Jux Norbert, Drewello Thomas: Experimental and Theoretical Structure Elucidation of the [2 : 1] Complex Ion of Carbo[n]helicene with n=6, 7 and 8 and Ag+. ChemPhysChem 2023, 24. <https://doi.org/10.1002/cphc.202300496>
  • Hoyer Matthias, Gross Jürgen H.: Molecular ion formation on activated field emitters in atmospheric pressure field desorption mass spectrometry. Anal Bioanal Chem 2023, 415, 2307. <https://doi.org/10.1007/s00216-023-04652-4>
  • Gauthier Etienne S., Rodríguez Rafael, Crassous Jeanne: Metal‐Based Multihelicenic Architectures. Angewandte Chemie 2020, 132, 23036. <https://doi.org/10.1002/ange.202004361>
  • Gauthier Etienne S., Rodríguez Rafael, Crassous Jeanne: Metal‐Based Multihelicenic Architectures. Angew Chem Int Ed 2020, 59, 22840. <https://doi.org/10.1002/anie.202004361>
  • Dhbaibi Kais, Favereau Ludovic, Crassous Jeanne: Enantioenriched Helicenes and Helicenoids Containing Main-Group Elements (B, Si, N, P). Chem. Rev. 2019, 119, 8846. <https://doi.org/10.1021/acs.chemrev.9b00033>
  • Rebrov Oleksii, Kulyk Kostiantyn, Ryding Mauritz, Thomas Richard D., Uggerud Einar, Larsson Mats: Chirally sensitive collision induced dissociation of proton‐bound diastereomeric complexes of tryptophan and 2‐butanol. Chirality 2017, 29, 115. <https://doi.org/10.1002/chir.22679>
  • Saleh Nidal, Shen Chengshuo, Crassous Jeanne: Helicene-based transition metal complexes: synthesis, properties and applications. Chem. Sci. 2014, 5, 3680. <https://doi.org/10.1039/C4SC01404A>
  • Sen Ananya, Le Barbu‐Debus Katia, Scuderi Debora, Zehnacker‐Rentien Anne: Mass Spectrometry Study and Infrared Spectroscopy of the Complex Between Camphor and the Two Enantiomers of Protonated Alanine: The Role of Higher‐Energy Conformers in the Enantioselectivity of the Dissociation Rate Constants. Chirality 2013, 25, 436. <https://doi.org/10.1002/chir.22164>
  • Mahjoub Ahmed, Le Barbu-Debus Katia, Zehnacker Anne: Structural Rearrangement in the Formation of Jet-Cooled Complexes of Chiral (S)-1,2,3,4-Tetrahydro-3-isoquinolinemethanol with Methyl Lactate: Chirality Effect in Conformer Selection. J. Phys. Chem. A 2013, 117, 2952. <https://doi.org/10.1021/jp400998e>
  • Weimar Marko, Correa da Costa Rosenildo, Lee Fu-Howe, Fuchter Matthew J.: A Scalable and Expedient Route to 1-Aza[6]helicene Derivatives and Its Subsequent Application to a Chiral-Relay Asymmetric Strategy. Org. Lett. 2013, 15, 1706. <https://doi.org/10.1021/ol400493x>
  • Révész Ágnes, Schröder Detlef, Rokob Tibor András, Havlík Martin, Dolenský Bohumil: Identification and interconversion of diastereomeric oligo-Tröger bases probed by ion mobility mass spectrometry. PCCP 2012, 14, 6987. <https://doi.org/10.1039/c2cp40585g>
  • Schröder Detlef: Ion clustering in electrospray mass spectrometry of brine and other electrolyte solutions. PCCP 2012, 14, 6382. <https://doi.org/10.1039/c2cp40586e>
  • Dytrtová Jana Jaklová, Jakl Michal, Schröder Detlef, Čadková Eva, Komárek Michael: Complexation between the fungicide tebuconazole and copper(II) probed by electrospray ionization mass spectrometry. Rapid Comm Mass Spectrometry 2011, 25, 1037. <https://doi.org/10.1002/rcm.4957>
  • Šádek Vojtěch, Schröder Detlef, Tsierkezos Nikos G.: Clustering of palladium(II) chloride in acetonitrile solution investigated by electrospray mass spectrometry. International Journal of Mass Spectrometry 2011, 304, 9. <https://doi.org/10.1016/j.ijms.2011.02.014>
  • Ducháčková Lucie, Roithová Jana, Milko Petr, Žabka Jan, Tsierkezos Nikos, Schröder Detlef: Comparative Study of Mono- and Dinuclear Complexes of Late 3d-Metal Chlorides with N,N-Dimethylformamide in the Gas phase. Inorg. Chem. 2011, 50, 771. <https://doi.org/10.1021/ic100759h>
  • Agrawal Divya, Schröder Detlef, Frech Christian M.: Observation of Binuclear Palladium Clusters upon ESI-MS Monitoring of the Suzuki–Miyaura Cross-Coupling Catalyzed by a Dichloro-bis(aminophosphine) Complex of Palladium. Organometallics 2011, 30, 3579. <https://doi.org/10.1021/om200274z>
  • Agrawal Divya, Zins Emilie‐Laure, Schröder Detlef: Intramolecular Scrambling of Aryl Groups in Organopalladium Complexes [ArPd(PPh3)2]+: From Solution to the Gas Phase, Back Again, and In‐Between. Chemistry — An Asian Journal 2010, 5, 1667. <https://doi.org/10.1002/asia.201000086>
  • Alkorta Ibon, Blanco Fernando, Elguero José, Schröder Detlef: Distinction between homochiral and heterochiral dimers of 1-aza[n]helicenes (n=1–7) with alkaline cations. Tet Asymm 2010, 21, 962. <https://doi.org/10.1016/j.tetasy.2010.05.032>
  • Roithová Jana, Schröder Detlef: Selective Activation of Alkanes by Gas-Phase Metal Ions. Chem. Rev. 2010, 110, 1170. <https://doi.org/10.1021/cr900183p>
  • Storch Jan, Čermák Jan, Karban Jindřich, Císařová Ivana, Sýkora Jan: Synthesis of 2-Aza[6]helicene and Attempts To Synthesize 2,14-Diaza[6]helicene Utilizing Metal-Catalyzed Cycloisomerization. J. Org. Chem. 2010, 75, 3137. <https://doi.org/10.1021/jo100252a>
  • Agrawal Divya, Schröder Detlef, Sale David A., Lloyd-Jones Guy C.: Electrospray Mass Spectrometric Studies of Two Palladium−Allyl Complexes of the Trost Standard Ligand. Organometallics 2010, 29, 3979. <https://doi.org/10.1021/om100591c>
  • Ganza Viktoria, Gross Jürgen H.: Gas-Phase Reactions of Laser-Desorbed Molecules with Ions from Electrospray. Eur J Mass Spectrom (Chichester) 2010, 16, 479. <https://doi.org/10.1255/ejms.1090>
  • Šámal Michal, Míšek Jiří, Stará Irena G., Starý Ivo: Organocatalysis with azahelicenes: the first use of helically chiral pyridine-based catalysts in the asymmetric acyl transfer reaction. Collect. Czech. Chem. Commun. 2009, 74, 1151. <https://doi.org/10.1135/cccc2009067>