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Graduate School of Chemical and Molecular Sciences Zurich

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Publication List (PDF, 311 KB)

  1. P. Ravat, T. Šolomek, D. Häussinger, O. Blacque, M. Juríček
    Dimethylcethrene: A chiroptical diradicaloid photoswitch
    J. Am. Chem. Soc. 2018, 140, 10839–10847.
    Highlighted in Chimia, 2018, 72, 725.
     
  2.  M. Juríček
    The three C's of cethrene
    Chimia 2018, 72, 322–327.
     
  3. T. Šolomek, P. Ravat, Z. Mou, M. Kertesz, M. Juríček
    Cethrene: The chameleon of Woodward–Hoffmann rules
    J. Org. Chem. 2018, 83, 4769–4774.
     
  4. P. Ravat, R. Hinkelmann, D. Steinebrunner, A. Prescimone, I. Bodoky, M. Juríček
    Configurational stability of [5]helicenes
    Org. Lett. 2017, 19, 3707–3710.
     
  5. M. Rickhaus, M. Mayor, M. Juríček
    Chirality in curved polyaromatic systems
    Chem. Soc. Rev. 2017, 46, 1643–1660. Cover Article.
     
  6. P. Ribar, T. Šolomek, L. Le Pleux, D. Häussinger, A. Prescimone,
    M. Neuburger, M. Juríček
    Donor–acceptor molecular triangles
    Synthesis 2017, 49, 899–909.
    Highlighted in Synfacts 2017, 13, 0363.
     
  7. P. Ravat, P. Ribar, M. Rickhaus, D. Häussinger, M. Neuburger, M. Juríček
    Spin-delocalization in a helical open-shell hydrocarbon
    J. Org. Chem. 2016, 81, 12303–12317. ACS Editors’ Choice Article.
     
  8. P. Ravat, T. Šolomek, P. Ribar, M. Juríček
    Biradicaloid with a twist: Lowering the singlet–triplet gap
    Synlett 2016, 27, 1613–1617. Cover Article.
     
  9. M. Rickhaus, M. Mayor, M. Juríček
    Strain-induced helical chirality in polyaromatic systems
    Chem. Soc. Rev. 2016, 45, 1542–1556.
     
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  1. P. Ravat, T. Šolomek, M. Rickhaus, D. Häussinger, M. Neuburger, M. Baumgarten, M. Juríček
    Cethrene: A helically chiral biradicaloid isomer of heptazethrene
    Angew. Chem. Int. Ed. 2016, 55, 1183–1186.
    Highlighted in Chimia 2016, 70, 207. 

Postdoctoral, Graduate, and Undergraduate Research
 

  1. E. J. Dale, D. P. Ferris, N. A. Vermeulen, J. J. Henkelis, I. Popovs, M. Juríček, J. C. Barnes, S. T. Schneebeli, J. F. Stoddart
    Cooperative reactivity in an extended-viologen-based cyclophane
    J. Am. Chem. Soc. 2016, 138, 3667–3670.
     
  2. Y. Yan,† M. Juríček,† F.-X. Coudert, N. A. Vermeulen, S. Grunder, A. Dailly, W. Lewis, A. J. Blake, J. F. Stoddart, M. Schröder
    Non-interpenetrated metal–organic frameworks based on copper(II) paddlewheel and oligoparaxylene-isophthalate linkers: Synthesis, structure, and gas adsorption
    J. Am. Chem. Soc. 2016, 138, 3371–3381. † Equal contributions.
     
  3. E. J. Dale, N. A. Vermeulen, M. Juríček, J. C. Barnes, R. M. Young, M. R. Wasielewski, J. F. Stoddart
    Supramolecular explorations: Exhibiting the extent of extended cationic cyclophanes
    Acc. Chem. Res. 2016, 49, 262–273.
     
  4. J. C. Barnes, E. J. Dale, A. Prokofjevs, A. Narayanan, I. C. Gibbs-Hall, M. Juríček, C. L. Stern, A. A. Sarjeant, Y. Y. Botros, S. I. Stupp, J. F. Stoddart
    Semiconducting single crystals comprising segregated arrays of complexes of C60
    J. Am. Chem. Soc. 2015, 137, 2392–2399.
     
  5. E. J. Dale, N. A. Vermeulen, A. A. Thomas, J. C. Barnes, M. Juríček, A. K. Blackburn, N. L. Strutt, A. A. Sarjeant, C. L. Stern, S. E. Denmark, J. F. Stoddart
    ExCage
    J. Am. Chem. Soc. 2014, 136, 10669–10682. 
     
  6. M. Juríček,† J. C. Barnes,† N. L. Strutt,† N. A. Vermeulen, K. C. Ghooray, E. J. Dale, P. R. McGonigal, A. K. Blackburn, A.-J. Avestro, J. F. Stoddart
    An ExBox [2]catenane
    Chem. Sci. 2014, 5, 2724–2731. † Equal contributions.
     
  7. S. M. Dyar, J. C. Barnes, M. Juríček, J. F. Stoddart, D. T. Co, R. M. Young, M. R. Wasielewski
    Electron transfer and multi-electron accumulation in ExBox4+
    Angew. Chem. Int. Ed. 2014, 53, 5371–5385. 
     
  8. M. Juríček, N. L. Strutt, J. C. Barnes, A. M. Butterfield, E. J. Dale, K. K. Baldridge, J. F. Stoddart, J. S. Siegel
    Induced-fit catalysis of corannulene bowl-to-bowl inversion
    Nat. Chem. 2014, 6, 222–228. Featured in C&E News 2014, 92, 25, Nature Chemistry News and Views 2014, 6, 177–178, Chemistry World: February 25, 2014. 
     
  9. J. C. Barnes,† M. Juríček,† N. A. Vermeulen,† E. J. Dale, J. F. Stoddart
    Synthesis of ExnBox cyclophanes
    J. Org. Chem. 2013, 78, 11962–11969. † Equal contributions.  
     
  10. R. M. Young, S. M. Dyar, J. C. Barnes, M. Juríček, J. F. Stoddart, D. T. Co, M. R. Wasielewski
    Ultrafast conformational dynamics of electron accumulation in ExBox4+ cyclophane
    J. Phys. Chem. A 2013, 117, 12438–12448. 
     
  11. M. Juríček,† J. C. Barnes,† E. J. Dale, W.-G. Liu, N. L. Strutt, C. J. Bruns, N. A. Vermeulen, K. C. Ghooray, A. A. Sarjeant, C. L. Stern, Y. Y. Botros, W. A. Goddard, III, J. F. Stoddart
    Ex2Box: Interdependent modes of binding in a two-nanometer-long synthetic receptor
    J. Am. Chem. Soc. 2013, 135, 12736–12746. † Equal contributions. 
     
  12. D. Cao, M. Juríček, Z. J. Brown, A. C.-H. Sue, Z. Liu, J. Lei, A. K. Blackburn, S. Grunder, A. A. Sarjeant, A. Coskun, C. Wang, O. K. Farha, J. T. Hupp, J. F. Stoddart
    Three-dimensional architectures incorporating stereoregular donor–acceptor stacks
    Chem.–Eur. J. 2013, 19, 8457–8465. 
     
  13. J. C. Barnes,† M. Juríček,† N. L. Strutt, M. Frasconi, S. Sampath, M. A. Giesener, P. L. McGrier, J. C. Bruns, C. L. Stern, A. A. Sarjeant, J. F. Stoddart
    ExBox: A polycyclic aromatic hydrocarbon scavenger
    J. Am. Chem. Soc. 2013, 135, 183–192. † Equal contributions. Cover Article. Featured in JACS Spotlights: November 13, 2012, Chemistry World: October 15, 2012, C&E News: September 12, 2012. 
     
  14. F. J. van den Bruele, W. de Poel, H. W. M. Sturmans, S. Pintea, R. de Gelder, D. Wermeille, M. Juríček, A. E. Rowan, W. J. P. van Enckevort, E. Vlieg
    Monolayer and aggregate formation of a modified phthalocyanine on mica determined by a delicate balance of surface interactions
    Surf. Sci. 2012, 606, 830–835. 
     
  15. M. Juríček, K. Stout, P. H. J. Kouwer, A. E. Rowan
    The trisubstituted-triazole approach to extended functional naphthalocyanines
    J. Porphyrins Phthalocyanines 2011, 15, 898–907. 
     
  16. M. Juríček, K. Stout, P. H. J. Kouwer, A. E. Rowan
    Fusing triazoles: Toward extending aromaticity
    Org. Lett. 2011, 13, 3494–3497. Featured in Synfacts 2011, 9, 0958. 
     
  17. M. Juríček, P. H. J. Kouwer, A. E. Rowan
    Triazole: A unique building block for the construction of functional materials
    Chem. Commun. 2011, 47, 8740–8749. Feature Article.
      
  18. M. Juríček, M. Felici, P. Contreras-Carballada, J. Lauko, S. Rodríguez Bou, P. H. J. Kouwer, A. M. Brouwer, A. E. Rowan
    Triazole–pyridine ligands: A novel approach to chromophoric iridium arrays
    J. Mater. Chem. 2011, 21, 2104–2111. Hot Article: December 21, 2010. 
     
  19. S. Albert-Seifried, C. E. Finlayson, F. Laquai, R. H. Friend, T. M. Swager, P. H. J. Kouwer, M. Juríček, H. J. Kitto, S. Valster, R. J. M. Nolte, A. E. Rowan
    Multichromophoric phthalocyanine–perylenediimide “octads": A photophysical study
    Chem.–Eur. J. 2010, 16, 10021–10029. 
     
  20. M. Juríček, P. H. J. Kouwer, J. Rehák, J. Sly, A. E. Rowan
    A novel modular approach to triazole-functionalized phthalocyanines using click chemistry
    J. Org. Chem. 2009, 74, 21–25. The Journal of Organic Chemistry Featured Article. 
     
  21. M. Juríček, P. Kasák, M. Stach, M. Putala
    Potential 1,1'-binaphthyl NLO-phores with extended conjugation between positions 2 and 6, and 2' and 6'
    Tetrahedron Lett. 2007, 48, 8869–8873. 
     
  22. M. Juríček, H. Brath, P. Kasák, M. Putala
    Study on the electronic effects on stereoconservativity of Suzuki coupling in chiral groove of binaphthyl
    J. Organomet. Chem. 2007, 692, 5279–5284. 
     
  23. H. Brath, M. Dubovská, M. Juríček, P. Kasák, M. Putala
    Novel route to enantiopure 2,2'-diaryl-1,1'-binaphthalenes by stereoconservative Suzuki arylation at positions 2 and 2'
    Collect. Czech. Chem. Commun. 2004, 69, 1517–1536. 
     
  24. P. Kasák, H. Brath, M. Dubovská, M. Juríček, M. Putala
    Suzuki arylation at positions 2 and 2' of 1,1'-binaphthyls: Stereochemical result depending on the sense of polarity of substrates
    Tetrahedron Lett.     2004, 45, 791–794.