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Publication List (PDF, 311 KB)

50. C. M. Cruz, J. C. Walsh, M. Juríček
    Bending pyrenacenes to fill gaps in singlet-fission-based solar cells
    Org. Mater. 2022, 4, 163–169. Special Issue on Supramolecular Chemistry.
     
51. L. Valenta, M. Juríček
    The taming of Clar’s hydrocarbon
    Chem. Commun. 2022, 58, 10896–10906. Invited Feature Article.
     
52. D. Čavlović, D. Häussinger, O. Blacque, P. Ravat, M. Juríček
    Nonacethrene unchained: A cascade to chiral contorted conjugated hydrocarbon with two sp³-defects
    JACS Au 2022, 2, 1616–1626. ACS Editors’ Choice Article.
     
53. M. G. Rasmussen, M. F. Jespersen, O. Blacque, K. V. Mikkelsen, M. Juríček, M. B. Nielsen
    Subphthalocyanine–triangulene dyads: Property tuning for light-harvesting device applications
    Energy Sci. Eng. 2022, 10, 1752–1762. Special Issue Journal’s 10^th Anniversary
     
54. D. Göbel, S. Míguez-Lago, M. J. Ruedas-Rama, A. Orte, A. G. Campaña, M. Juríček
    Circularly polarized luminescence of [6]helicenes through excited-state intramolecular proton transfer
    Helv. Chim. Acta 2022, 105, e202100221.
     
55. L. Valenta, M. Mayländer, P. Kappeler, O. Blacque, T. Šolomek, S. Richert, M. Juríček
    Trimesityltriangulene: A persistent derivative of Clar's hydrocarbon
    Chem. Commun. 2022, 58, 3019–3022.
    Highlighted in Chemistry Views (06.02.2022).
     
56. Y. Wang, M. Rickhaus, O. Blacque, K. K. Baldridge, M. Juríček, J. S. Siegel
    Cooperative weak dispersive interactions actuate catalysis in a shape-selective abiological racemase
    J. Am. Chem. Soc. 2022, 144, 2679–2684.
    Highlighted in Chimia 2022, 76, 594
     
57. Y. Yang, M. Juríček
    Fullerene wires assembled inside carbon nanohoops
    ChemPlusChem 2022, 87, e202100468. Invited Review Article.
     

42. Y. Yang, S. Huangfu, S. Sato, M. Juríček
    Cycloparaphenylene double nanohoop: Structure, lamellar packing, and encapsulation of C₆₀ in the solid state
    Org. Lett. 2021, 23, 7943–7948.
     
43. Y. Yang, O. Blacque, S. Sato, M. Juríček
    Cycloparaphenylene-phenalenyl radical and its dimeric double nanohoop
    Angew. Chem. Int. Ed . 2021, 60,13529–13535.
    Hot & Frontispiece Article.
    Highlighted in Chimia, 2021, 75, 436.
     
44. P. Ribar, L. Valenta, T. Šolomek, M. Juríček
    Rules of nucleophilic additions to zigzag nanographene diones
    Angew. Chem. Int. Ed. 2021, 60, 13521–13528.
    Highlighted in Chimia, 2021, 75, 887.
     
45. P. Ravat, O. Blacque, M. Juríček
    Benzo[cd]triangulene: A spin 1/2 graphene fragment
    J. Org. Chem. 2020, 85, 92–100.
     
46. T. Šolomek, P. Ravat, M. Juríček
    ‘Forbidden’ electrocyclizations of diradicaloids
    Trends Chem. 2019, 1, 705–706. Invited “Mechanism of the Month” Article.
     
47. P. Ribar, T. Šolomek, M. Juríček
    Gram-scale synthesis and supramolecular complex of precursors of Clar’s hydrocarbon triangulene
    Org. Lett. 2019, 21, 7124–7128. Top 5 Most Read Article (15.09.2019).
     
48. D. Čavlović, M. Juríček
    Molecular magnetic switches
    Chimia 2019, 73, 313–316.
     
49. P. Ravat, T. Šolomek, M. Juríček
    Helicenes as chiroptical photoswitches
    ChemPhotoChem 2019, 3, 180–186. Invited Concept Article.
     

Postdoctoral, Graduate, and Undergraduate Research
 

24. 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.
     
23. 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.
     
22. 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.
     
21. 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.
     
20. 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. 
     
19. 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.
     
18. 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. 
     
17. 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. 
     
16. 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.  
     
15. 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. 
     
14. 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. 
     
13. 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. 
     
12. 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. 
     
11. 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. 
     
10. 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. 
     
9. 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. 
    
8. 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.
     
7. 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. 
    
6. 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. 
    
5. 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. 
    
4. 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. 
    
3. 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. 
    
2. 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. 
    
1. 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.