Henri-Pierre J. de Rouville

Chargé de Recherche

Laboratoire LSAMM
Université  de Strasbourg
Institut Le Bel
4, rue Blaise Pascal
67000 Strasbourg-France

email: Henri-Pierre J. de Rouville

 : 0000-0002-9508-6446



Henri-Pierre Jacquot de Rouville graduated from the University Paul Sabatier of Toulouse. In 2007, he joined C. Joachim’s Group and obtained a PhD degree for his synthesis of technomimetic molecules for nanomechanical applications under the supervision of Professor G. Rapenne (CEMES-CNRS, Toulouse). From 2010 to 2012, he joined Professor J. F. Stoddart’s Group as a postdoctoral fellow where he investigated the chemistry of mechanically interlocked molecules. Then, he moved back to France where he worked as a postdoctoral fellow with N. McClenaghan (ISM, Bordeaux). In 2013, he was appointed as Chargé de Recherche (Full Time Researcher at the CNRS) at the laboratory ITODYS, Paris. In November 2017, he moved at the Institut de Chemistry of Strasbourg where he joined the LSAMM research group.

  • Professional Experience

2017 – Present: Chargé de Recherche Classe Normale (CRCN) au CNRS
Université de Strasbourg, Institut de Chimie, UMR – CNRS 7177 (Strasbourg, France)

2013 – 2017: Chargé de Recherche de 2ème Classe (CR2) of the CNRS
Laboratory ITODYS, UMR – CNRS 7086 (Paris, France)

2012 – 2013: Post-doctoral Research Fellow
Institut des Sciences Moléculaires (Bordeaux, France)
Advisor: Dr. Nathan McClenaghan

2010 – 2012: Postdoctoral Research Fellow
Northwestern University (Evanston, IL, USA)
Advisor: Prof. Fraser Stoddart

2007 – 2010: Doctor of Philosophy in Chemistry
University Paul Sabatier (Toulouse, France)
Advisor: Prof. Gwénaël Rapenne
Title: Synthesis of Technomimetic Molecules for Applications in Nanomechanics

  • Research Interests

Molecular Mechanics | Molecular Switches and Machines | Organic Synthesis | Supramolecular Chemistry | Electro- and Photo-Active Molecules

  • Publications

26. Synthesis, electronic and photophysical properties of a bisacridinium-Zn(II) porphyrin conjugate
A. Edo-Osagie, D. Sánchez-Resa, D. Serillon, E. Bandini, C. Gourlaouen, H.-P. Jacquot de Rouville,* B. Ventura,* V. Heitz* C. R. Chimie, 2021, 24, 1–9 (Link).

25. Molecular Recognition by Chalcogen Bond: Selective Charge-transfer Crystal Formation of Dimethylnaphthalene with Selenadiazolotetracyano naphthoquinodimethane
Y. Ishigaki, K. Asai, H.-P. Jacquot de Rouville, T. Shimajiri, V. Heitz, H. Fujii-Shinomiya, T. Suzuki,* Eur. J. Org. Chem., 2021, 6, 990–997 (Link).

24. N-substituted Acridinium as a Multi-Responsive Recognition Unit in Supramolecular Chemistry
H.-P. Jacquot de Rouville,* J. Hu, V. Heitz,* ChemPlusChem, 2021, 86, 110–129 (Link).

23. A Bis-Acridinium Macrocycle as Multi-Responsive Receptor and Selective Phase Transfer Agent of Perylene
J. Hu, J. S. Ward, A. Chaumont, K. Rissanen, J.-M. Vincent,* V. Heitz,* H.-P. Jacquot de Rouville,* Angew. Chem. Int. Ed.2020, 59, 2320623212 (Link).

22. Electron Storage System Based on a Two-Way Inversion of Redox Potentials
A. GossetL. WilbrahamŠ. Nováková LachmanováR. SokolováG. DupeyreF. TuyèrasP. OchsenbeinC. PerruchotH.-P. Jacquot de RouvilleH. Randriamahazaka,* L. Pospíšil,* I. Ciofini,* M. Hromadová,* Philippe P. Lainé* J. Am. Chem. Soc. 2020, 142, 5162–5176 (Link).

21. Self-Complementary and Narcissistic Self-Sorting of bis-Acridinium Tweezers
H.-P. Jacquot de Rouville,* C. Gourlaouen, V. Heitz* Dalton Trans., 2019, 48 87258730 (Link).

20. Surface manipulation of a curved polycyclic aromatic hydrocarbon-based nanovehicle molecule equipped with triptycene wheels
W.-H. Soe, C. Duranda, O. Guillermet, S. Gauthier, H.-P. Jacquot de Rouville, S. Srivastava, C. Kammerer, G. Rapenne, C. Joachim Nanotechnology 201829, 495401 (Link).

19. Entwined Dimers Formation from Self-Complementary bis-Acridiniums
H.-P. Jacquot de Rouville,* N. Zorn, E. Leize-Wagner, V. Heitz* Chem. Commun. 2018, 54, 10966–10969 (Link).

18. From the Synthesis of Nanovehicles to Participation in the First Nanocar Race—View from the French Team
H.-P. Jacquot de Rouville, C. Kammerer and G. Rapenne Molecules 201823(3), 612 (Link).

17. A Chemically-Responsive bis-Acridinium Receptor
A. Gosset, Z. Xu, F. Maurel, L.-M. Chamoreau, S. Nowak, G. Vives, C. Perruchot, V. Heitz, H.-P. Jacquot de Rouville New J. Chem. 2018, 42, 4728–4734 (Link).

16. Photodriven [2]Rotaxane-[2]Catenane Interconversion
A. Tron, H.-P. Jacquot de Rouville, A. Ducrot, J. H. R. Tucker, M. Baroncini, A. Credi, N. D. McClenaghan Chem. Commun. 201551, 2810–2813. (Link)

15. Formation of a Hydrogen-bonded Barbiturate [2]-Rotaxane
A. Tron, P. Thornton, M. Rocher, H.-P. Jacquot de Rouville, J.-P. Desvergne, B. Kauffmann, T. Buffeteau, D. Cavagnat, J. Tucker, N. McClenaghan Org. Lett. 201416, 1358–1361. (Link)

14. An Electrochemically and Thermally Switchable Donor-Acceptor [c2]Daisy Chain Rotaxane
C. J. Bruns, J. Li, M. Frasconi, S. T. Schneebeli, J. Iehl, H.-P. Jacquot de Rouville, S. I. Stupp, G. A. Voth, J. F. Stoddart Angew. Chem. Int. Ed. 2014, 53, 1953–1958. (Link)

13. π–Dimerization of viologen subunits around the core of C60 from twelve to six directions
J. Iehl, M. Frasconi, H.-P. Jacquot de Rouville, N. Renaud, S. M. Dyar, N. L. Strutt, R. Carmieli, M. R. Wasielewski, M. A. Ratner, J.-F. Nierengarten, J. F. Stoddart Chem. Sci. 20134, 1462–1469. (Link)

12. Chameleonic Binding of the Dimethyldiazaperopyrenium Dication by Cucurbit[8]uril
K. J. Hartlieb, A. N. Basuray, C. Ke, A. A. Sarjeant, H.-P. Jacquot de Rouville, T. Kikuchi, R. S. Forgan, J. W. Kurutz, J. F. Stoddart Asian J. Org. Chem. 20132, 225–229. (Link)

11. Beyond Perylene Diimides – Diazaperopyrenium as Chameleonic Nanoscale Building Blocks
A. N. Basuray, H.-P. Jacquot de Rouville, K. J. Hartlieb, A. C. Fahrenbach, J. F. Stoddart Chem. Asian. J. 2013, 8, 524–532. (Link)

10. The Chameleonic Nature of Diazaperopyrenium Recognition Processes
A. N. Basuray, H.-P. Jacquot de Rouville, K. J. Hartlieb, T. Kikuchi, N. L. Strutt, C. J. Bruns, M. W. Ambrogio, A.-J. Avestro, S. T. Schneebeli, A. C. Fahrenbach, J. F. Stoddart Angew. Chem. Int. Ed. 2012, 51, 11872–11877. (Link)

9. A Naphthalene Diimide [2]Rotaxane
H.-P. Jacquot de Rouville, J. Iehl, C. J. Bruns, P. L. McGrier, M. Frasconi, A. A. Sarjeant, J. F. Stoddart Org. Lett. 2012, 14, 5188–5191. (Link)

8. STM Manipulation of Boron-Subphthalocyanine Nano-Wheel Dimers on Au(111)
A. Nickel, J. Meyer, R. Ohmann, H.-P. Jacquot de Rouville, G. Rapenne, C. Joachim, G. Cuniberti, F. Moresco J. Phys.: Condens. Matter. 2012, 24, 404001. (Link)

7. Synthesis and STM Imaging of Symmetric and Dissymmetric Ethynyl-Bridged Dimers of Boron-Subphthalocyanine Bowl-Shaped Nano-Wheels
H.-P. Jacquot de Rouville
, R. Garbage, F. Ample, A. Wadewitz, J. Meyer, F. Moresco, C. Joachim, G. Rapenne Chem. Eur. J. 2012, 18, 8925–8928. (Link)

6. Synthesis of Polycyclic Aromatic Hydrocarbon-Based Nanovehicles Equipped with Triptycene Wheels
H.-P. Jacquot de Rouville, R. Garbage, R. E. Cook, A. R. Pujol, A. M. Sirven, G. Rapenne Chem. Eur. J. 2012, 18, 3023–3031. (Link)

5. A Neutral Redox-Switchable [2]Rotaxane
J.-C. Olsen, A. C. Fahrenbach, A. Trabolsi, D. C. Friedman, S. K. Dey, C. M. Gothard, A. K. Shveyd, T. B. Gasa, J. M. Spruell, M. A. Olson, C. Wang, H.-P. Jacquot de Rouville, Y. Y. Botros, J. F. Stoddart Org. Biomol. Chem. 2011, 9, 7126–7133. (Link)

4. Synthesis of a Photoswitchable Azobenzene-Functionalized Tris(indazol-1-yl)borate Ligand and its Ruthenium(II) Cyclopentadienide Complex
H.-P. Jacquot de Rouville
, D. Villenave, G. Rapenne Tetrahedron 2010, 66, 1885–1891. (Link)

3. Prototypes of Molecular Motors Based on Star-Shaped Organometallic Ruthenium Complexes
G. Vives, H.-P. Jacquot de Rouville, A. Carella, J.-P. Launay, G. Rapenne Chem. Soc. Rev. 2009, 6, 1551–1561. (Link)

2. Synthesis and Analytical Resolution of Chiral Pyrazoles from Dihydrocarvone
H.-P. Jacquot de Rouville, G. Vives, E. Tur, J. Crassous, G. Rapenne New J. Chem. 2009, 2, 293–299. (Link)

1. A Family of Electron-Triggered Molecular Motors Based on Aromatic Building Blocks
H.-P. Jacquot de Rouville, G. Vives, G. Rapenne, Pure Appl. Chem. 2008, 80, 659–667. (Link)