Publications

Post-doctoral research: 

  1. Dydio, P.;# Key, H. M.;# Nazarenko, A.; Rha, J. Y-E.; Seyedkazemi, V.; Clark, D. S.; Hartwig, J. H. Science, 2016, 354, 102-106: An artificial metalloenzyme with the kinetics of native enzymes.

# -equal contribution  

http://science.sciencemag.org/content/354/6308/102

– Highlighted in Chemical & Engineering News 2016, 94, 8

  1. Key, H. M.;# Dydio, P.;# Clark, D. S.; Hartwig, J. H. Nature, 2016, 534, 534-537: Artificial Catalysis by Heme Proteins Containing Noble Metal Porphyrins.

# -equal contribution

http://www.nature.com/nature/journal/vaop/ncurrent/abs/nature17968.html

– Highlighted in Chemical & Engineering News 2016, 25, 6

– Highlighted in Nature 2016, 537, 156

– Highlighted in Angew. Chem. In. Ed. 2016 (10.1002/anie.201607222)

– Highlighted in Chemistry World RSC, 6/14/2016: Metal ion swap improves artificial enzymes

– Highlighted in Nature Podcast on 06/16/2016

– Highlighted in The Daily Californian, 7/04/2016: Berkeley Lab researchers combine synthetic, natural catalysts to create new reactions

Doctoral research 

  1. Dydio, P.; Detz, R. J.; de Bruin, B.; Reek, J. N. H., in preparation: Binding-Induced Substrate Distortion as the Origin of Exceptional Activity of Supramolecular Catalyst
  1. Théveau, L.; Bellini, R.; Dydio, P.; Szabo, Z.; van der Werf, A.; Sander, R. A.; Reek, J. N. H.; Moberg, C. Organometallics, 2016, 1956–1963: Cofactor-Controlled Chirality of Tropoisomeric Ligand.

http://pubs.acs.org/doi/abs/10.1021/acs.organomet.6b00265

  1. Dydio, P.; Reek, J. N. H. Chem. Sci. 2014, 5, 2135−2145: Supramolecular control of selectivity in transition metal catalysis through substrate preorganization. REVIEW

http://pubs.rsc.org/en/Content/ArticleLanding/2014/SC/c3sc53505c#!divAbstract

  1. Dydio, P.; Detz, R. J.; de Bruin, B.; Reek, J. N. H. J. Am. Chem. Soc. 2014, 136, 8418–8429: Beyond Classical Reactivity Patterns: Hydroformylation of Vinyl and Allyl Arenes to Valuable b-and g-Aldehyde Intermediates using Supramolecular Catalysis.

http://pubs.acs.org/doi/abs/10.1021/ja503033

  1. Dydio, P.; Reek, J. N. H. Nat. Protoc. 2014, 9, 1183−1191: Scalable and chromatography-free synthesis of 2-(2-formylalkyl)arenecarboxylic acid derivatives through the supramolecularly controlled hydroformylation of vinylarene-2-carboxylic acids.

http://www.nature.com/nprot/journal/v9/n5/full/nprot.2014.077.html

  1. Dydio, P.; Breuil, P.-A. R.; Reek, J. N. H. Isr. J. Chem. 2013, 53, 61-74: Dynamic Combinatorial Chemistry in Chemical Catalysis. REVIEW

http://onlinelibrary.wiley.com/doi/10.1002/ijch.201200083/abstract                          

  1. Dydio, P.; Ploeger, M.; Reek, J. N. H. ACS Catal. 2013, 3, 2939–2942: Selective Isomerization-Hydroformylation Sequence: a Strategy to Valuable α-Methyl-Branched Aldehydes from Terminal Olefins.

http://pubs.acs.org/doi/abs/10.1021/cs400872a

  1. Dydio, P.; Detz, R. J.; Reek, J. N. H. J. Am. Chem. Soc. 2013, 135, 10817-10828: Precise Supramolecular Control of Selectivity in the Rh-catalyzed Hydroformylation of Terminal and Internal Alkenes.

http://pubs.acs.org/doi/abs/10.1021/ja4046235

  1. Dydio, P.; Reek, J. N. H. Angew. Chem., Int. Ed. 2013, 52, 3878-3882: Supramolecular control of selectivity in hydroformylation of vinyl arenes: easy access to valuable b-aldehyde intermediates.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201209582/abstract

– Very Important Paper and Back Cover Art Article

– Highlighted in Nat. Chem. 2013, 5, 250                                                                                                                 

  1. Dydio, P.; Rubay, C.; Gadzikwa, T.; Lutz, M.; Reek, J. N. H. J. Am. Chem. Soc. 2011, 133, 17176-17179: “Cofactor”-Controlled Enantioselective Catalysis.

http://pubs.acs.org/doi/abs/10.1021/ja208589c

– Highlighted in Chemical & Engineering News 2011, 89, 13

– Highlighted in Chemistry World RSC, 10/18/2011: Cofactor control of catalysis enantioselectivity

  1. Dydio, P.; Dzik, W. I.; Lutz, M.; de Bruin, B.; Reek, J. N. H. Angew. Chem., Int. Ed. 2011, 50, 396-400: Remote Supramolecular Control of Catalyst Selectivity in the Hydroformylation of Alkenes.

http://onlinelibrary.wiley.com/doi/10.1002/anie.201005173/abstract

– HOT paper and Back Cover Art Article

– Highlighted in ChemCatChem 2011, 3, 619-621

– Highlighted in Wiley ChemistryViews, 01/24/2011: Control of Selectivity in Hydroformylation

Pre-doctoral research:

  1. Lichosyt, D.; Dydio, P.; Jurczak, J. Chem. Eur. J. 2016, DOI: 10.1002/chem.201603555: Phosphate Anion Sensing by Azulene-Based Macrocyclic Receptors.
  1. Jurczak, J.; Dydio, P.; Stepniak, P.; Zieliński, T. Sensor Actuat B Chem. 2016, 237, 621–627: Diamidonaphthalenodipyrrole-derived Fluorescent Sensors for Anions.

http://www.sciencedirect.com/science/article/pii/S0925400516310048

  1. Jurczak, J.; Dydio, P.; Stepniak, P.; Zieliński, T. RSC Adv. 2016, 6, 41568-41571: A hybrid macrocyclic anion receptor exploiting the pyrrole-2,5-diacetamide unit.


http://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra05804c#!divAbstract

 

  1. Dydio, P.; Lichosyt, D.; Jurczak, J. Chem. Soc. Rev. 2011, 40, 2971-2985: Amide- and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors.

http://pubs.rsc.org/en/content/articlelanding/2011/cs/c1cs15006e#!divAbstract

  1. Dydio, P.; Lichosyt, D.; Zieliński, T.; Jurczak, J. Chem. Eur. J. 2012, 18, 13686-13701: 7,7’-Diamino-2,2’-diindolylmethane: a Building Block for Highly Efficient and Selective Anion Receptors Studies in Solution and in the Solid State.

http://onlinelibrary.wiley.com/doi/10.1002/chem.201201909/abstract

  1. Jurczak, J.; Chmielewski, M. J.; Dydio, P.; Lichosyt, D.; Ulatowski, F.; Zieliński, T. Pure Appl. Chem. 2011, 83, 1543-1554: Benzopyrrole derivatives as effective anion receptors in highly competitive solvents.

https://www.degruyter.com/view/j/pac.2011.83.issue-8/pac-con-10-11-11/pac-con-10-11-11.xml

  1. Dydio, P.; Zieliński, T.; Jurczak, J. Org. Lett. 2010, 12, 1076-1078: 7,7′-Diureido-2,2′-diindolylmethanes: Anion Receptors Effective in a Highly Competitive Solvent, Methanol.

http://pubs.acs.org/doi/abs/10.1021/ol1000395

  1. Dydio, P.; Zieliński, T.; Jurczak, J. Chem. Commun. 2009, 4560-4562:
    Anion receptors based on 7,7’-diamido-2,2’-diindolylmethane.

http://pubs.rsc.org/en/Content/ArticleLanding/2009/CC/b907164d#!divAbstract

  1. Dydio P.; Zieliński T.; Jurczak, J. J. Org. Chem. 2009, 74, 1525-1530:
    Bishydrazide Derivatives of Isoindoline as Simple Anion Receptors.

http://pubs.acs.org/doi/abs/10.1021/jo802288u?journalCode=joceah

  1. Zieliński T.; Dydio P.; Jurczak, J. Tetrahedron 2008, 64, 568-574: Synthesis, structure and the binding properties of the amide-based anion receptors derived from 1H-indole-7-amine.

http://www.sciencedirect.com/science/article/pii/S0040402007018947