prof. dr. B.L. (Ben L.) Feringa


prof. dr. B.L. (Ben L.) Feringa


Postal address:
9747 AG
Phone: +31 50 363 4235Fax: +31 50 363 4296

Research interests

The research program of the Feringa group is focussed on synthetic organic chemistry. Over the years a unique expertise in stereochemistry has been acquired. Inspired by nature's principles of molecular assembly, recognition, transport, motion and catalysis, the goal is to exploit the full potential of synthetic chemistry to create new structures and functions. A major part of the research is directed towards nanotechnology and novel functional materials, such as molecular switches and motors. A second part of the program deals with the development (and application in chemical biology) of novel stereoselective synthesis methods and asymmetric catalysis. Control of chirality is the guiding principle in both programs.

Scientific program of the Feringa groupfrom molecules to molecular systems

The mission of the research programme in the Feringa group is to exploit the full potential of synthetic chemistry to create new structures, functions and chemical systems. Inspired by Nature's principles of molecular recognition, assembly, catalysis, transport and motion, the goal is to design novel functional (supra-) molecular materials as well as to develop new catalysts and synthetic methodology.

Three major areas of interest can be distinguished:
Molecular Nanoscience: with particular emphasis on the control of dynamics including switches, translational and rotary molecular motors, self-assembly and multifunctional nanosystems (read more).
Synthesis and catalysis: which a focus on the development of asymmetric catalysis, catalytic oxidation and coupling reactions and application of novel catalytic methods in synthesis (read more).
Biohybrid systems: the design of responsive biohybrid materials, artificial membranes, photopharmacology and methodology for biomolecular imaging (read more).

Chirality is a leading theme and over the years a broad expertise in fundamental aspects of chirality has been built including new asymmetric synthesis methodology, chiroptical phenomena, chiral amplification, and dynamic and supramolecular chirality. The research in the group has a strong multidisciplinary character.

Research programs

Subprogram 1: Molecular Nanoscience (Center for Systems Chemistry, Gravity program functional molecular systems and top research school Zernike Institute for Advanced Materials). The focus is currently on four major challenges e.g.:

  • Molecular switching: to trigger or address in a fully reversible manner a variety of functions. The projects range from the design of systems for molecular information storage and molecular electronics to responsive (smart) surfaces (read more).
  • Molecular organization: how to control and reversibly change assembly and organization at different hierarchical levels, in supramolecular materials and self-assembled monolayers on surfaces. Particular emphasis is on liquid crystal materials, low molecular weight gels and nanotube formation.
  • Molecular motors: how to control motion by exploring synthetic molecular motors. Light-driven rotary motors and catalytic motors are studied. The focus is on autonomous motion, the quest to make motors to perform work and the integration of molecular motors in nano-mechanical systems (read more).
  • Molecular systems: how to integrate various functions in dynamic complex molecular systems. A key challenge is the design of chemical systems out of thermodynamic equilibrium i.e. kinetically driven multifunctional systems.

Our systems approach to complex dynamic functions and materials in the past decade and the recent establishment of the Center for Systems Chemistry has greatly stimulated a strong multidisciplinary and cooperative effort at the interphase between chemistry, molecular biology, physics and surface sciences.

 Read more: Molecular Nanoscience


Subprogram 2: Synthesis and Catalysis (Center for Sustainable Catalysis, top Netherlands Research School for Catalysis NRSC-C). The following topics are addressed in this subprogram:

  • Asymmetric catalysis: we develop new chemo- regio- and stereoselective syntheses and focus on the so called "catalytic switch"; replacing stoichiometric by catalytic enantioselective methods in the synthesis of biological active compounds. In particular unique monodentate phosphoramidites, a privileged class of chiral ligands introduced by our group, are explored.
  • Novel catalytic methodology; current focus is on cross coupling with organolithium reagents and conversion of renewables.
  • Enzyme and DNA-based catalysis: asymmetric catalysis in water is studied i.e.the integration of enzyme and transition metal catalysis in multistep or cascade type transformations.
  • Catalytic oxidation: A significant expertise and effort in catalytic oxidation has been maintained over the years in view of the fundamental challenges associated with selective oxidation and the high relevance for our long-standing industrial cooperation.

 Read more: Asymmetric catalysis, synthesis and chirality


Subprogram 3: Biohybrid Systems (Center for Systems Chemistry, GBB and UMCG cooperation). Emphasis is on control and/or mimicking of biological function along the following lines:

  • Protein function: light-controlled switchable protein channels and enzyme activity
  • Photopharmacology: photoresponsive drugs and interference with biological pathways
  • Biohybrid assembly: the design of artificial membranes
  • Biomedical imaging: design of novel tracer methodology

In a small subprogram fundamental questions are addressed on chiral phenomena with a special emphasis or origin of homochirality (in the context of the European Biogenesis program), chiral amplification and autocatalysis (in the NWO-NSF astrochemistry program).

  1. A chiral self-sorting photoresponsive coordination cage based on overcrowded alkenes

    Stuckhardt, C., Roke, D., Danowski, W., Otten, E., Wezenberg, S. J. & Feringa, B. L., 15-Nov-2019, In : Beilstein Journal of Organic Chemistry. 15, p. 2767-2773 7 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Light-Modulated Self-Blockage of a Urea Binding Site in a Stiff-Stilbene Based Anion Receptor

    de Jong, J., Feringa, B. L. & Wezenberg, S. J., 16-Dec-2019, In : Chemphyschem. 20, 24, p. 3306-3310 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. Stereodivergent Anion Binding Catalysis with Molecular Motors

    Dorel, R. & Feringa, B. L., 7-Jan-2020, In : Angewandte Chemie-International Edition. 59, 2, p. 785-789 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  4. Ultrafast Excited State Dynamics in a First Generation Photomolecular Motor

    Sardjan, A. S., Roy, P., Danowski, W., Bressan, G., Nunes dos Santos Comprido, L., Browne, W. R., Feringa, B. L. & Meech, S. R., 23-Jan-2020, In : Chemphyschem. 21, p. 1-7 7 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  5. Unclicking of thioureas: Base catalyzed elimination of anilines and isothiocyanates from thioureas

    Vlatkovic, M. & Feringa, B. L., 5-Apr-2019, In : Tetrahedron. 75, 14, p. 2188-2192 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

View all (1,024) »

  1. Elected 2009 President of Bürgenstock Conference, Switzerland

    Bernard Feringa (Recipient), 17-May-2009

    Prize: Election to learned societyAcademic

  2. Chirality Medal 2009,

    Bernard Feringa (Recipient), 12-Jul-2009


  3. Tetrahedron Chair at BOSS symposium 2012

    Bernard Feringa (Recipient), 15-Jul-2012


View all (42) »

  1. W.S. Johnson Memorial Symposium Lecturer

    Bernard Feringa (Keynote speaker)

    Activity: Talk or presentationProfessional

  2. IOCF Yoshida Lectureship, Kyoto University, Osaka University

    Bernard Feringa (Invited speaker)

    Activity: Talk or presentationProfessional

  3. Siegfried Hunig Vorlesung, University of Wurzburg

    Bernard Feringa (Keynote speaker)

    Activity: Talk or presentationProfessional

View all (87) »

View graph of relations

ID: 71899