Publications
- 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.
- L. Valenta, M. Juríček
The taming of Clar’s hydrocarbon
Chem. Commun. 2022, 58, 10896–10906. Invited Feature Article.
- 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.
- 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 10th Anniversary
- 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.
- 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).
- 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
- Y. Yang, M. Juríček
Fullerene wires assembled inside carbon nanohoops
ChemPlusChem 2022, 87, e202100468. Invited Review Article.
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- Frontispiece artwork picture to publication No: 41
- 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.
- 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.
- 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.
- P. Ravat, O. Blacque, M. Juríček
Benzo[cd]triangulene: A spin 1/2 graphene fragment
J. Org. Chem. 2020, 85, 92–100.
- T. Šolomek, P. Ravat, M. Juríček
‘Forbidden’ electrocyclizations of diradicaloids
Trends Chem. 2019, 1, 705–706. Invited “Mechanism of the Month” Article.
- 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).
- D. Čavlović, M. Juríček
Molecular magnetic switches
Chimia 2019, 73, 313–316.
- P. Ravat, T. Šolomek, M. Juríček
Helicenes as chiroptical photoswitches
ChemPhotoChem 2019, 3, 180–186. Invited Concept Article.
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Postdoctoral, Graduate, and Undergraduate Research
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.