Publications

P24: “Probing halogen–halogen interactions in solution.”                        Virgile Ayzac, Matthieu Raynal, Benjamin Isare, Julien Idé, Patrick Brocorens, Roberto Lazzaroni, Thibaut Etienne, Antonio Monari, Xavier Assfeld and Laurent Bouteiller *                                                                Phys. Chem. Chem. Phys.2017, 29, 32443-32450.              http://pubs.rsc.org/en/content/articlepdf/2017/cp/c7cp06996k

P23: “Real-Time Control of the Enantioselectivity of a SupramolecularCatalyst Allows Selecting the Configuration of Consecutively Formed  Stereogenic Centers.”                                                                              Jeremy M. Zimbron, Xavier Caumes, Yan Li, Christophe M. Thomas, Matthieu Raynal* and Laurent Bouteiller                                                              Angew. Chem. Int. Ed., 2017, 56, 14016-14019                                                   Hal Id: hal-01611679                                                                                           http://onlinelibrary.wiley.com/doi/10.1002/anie.201706757/abstract     Highlight in Chemistry World: https://www.chemistryworld.com/news/chiral-catalyst-switches-selectivity-in-seconds/3008016.article               

P22: “Unexpected Solvent Influence on the Rheology of Supramolecular Polymers.”                                                                                                         Bruno G. Alvarenga, Matthieu Raynal, Laurent Bouteiller,* and Edvaldo Sabadini*                                                                                                                       Macromolecules, 2017, 50, 6631-6636                                                            http://pubs.acs.org/doi/abs/10.1021/acs.macromol.7b00786                                                                             

P21: “Tuning the structure of 1,3,5-benzenetricarboxamide self-assemblies through stereochemistry.”                                                                    Xavier Caumes, Arianna Baldi, Geoffrey Gontard, Patrick Brocorens, Roberto Lazzaroni, Nicolas Vanthuyne, Claire Troufflard, Matthieu Raynal* and Laurent Bouteiller                                                                       Chem. Commun., 2016, 52, 13369-13372                                                               Hal Id: hal-01394304                                                                                     http://dx.doi.org/10.1039/c6cc07325e                                                              Part of the Themed issue: Chirality at the Nanoscale                 http://pubs.rsc.org/en/journals/articlecollectionlanding?sercode=cc&themeid=09509a32-e033-4c3a-87f6-33c3e1733873

P20: “Tuning the nature and stability of self-assemblies formed by ester benzene 1,3,5-tricarboxamides: the crucial role played by the substituents.”                                                                                                                          Alaric Desmarchelier, Bruno Giordano Alvarenga, Xavier Caumes, Ludovic Dubreucq,  Claire Troufflard,  Martine Tessier, Nicolas Vanthuyne, Julien Idé, Thomas Maistriaux, David Beljonne, Patrick Brocorens, Roberto Lazzaroni, Matthieu Raynal* and Laurent Bouteiller                                                                                                                                    Soft Matter, 2016, 12, 7824-7838                                                                           Hal Id: hal-01362222                                                                                   http://dx.doi.org/10.1039/c6sm01601d

P19: “Correlation between the selectivity and the structure of an asymmetric catalyst built on a chirally amplified supramolecular helical scaffold.
Alaric Desmarchelier, Xavier Caumes, Matthieu Raynal,* Anton Vidal-Ferran, Piet W. N. M. van Leeuwen, and Laurent Bouteiller
J. Am. Chem. Soc., 2016, 138, 4908-4916                                               http://dx.doi/10.1021/jacs.6b01306                                                                 Highlight in Nature Nanotechnologyhttp://www.nature.com/nnano/reshigh/2016/0516/full/nnano.2016.76.html

P18: “Induced circular dichroism in phosphine gold(I) arylacetylide urea complexes through hydrogen-bonded chiral co-assemblies.”
Julien Dubarle-Offner, Jamal Moussa, Hani Amouri,* Benjamin Jouvelet, Laurent Bouteiller, and Matthieu Raynal*
Chem. Eur. J., 2016, 22, 3985-3990                                                                             Hal Id: hal-01318173
http://dx.doi.org/10.1002/chem.201504441

P17: “Bisurea-based supramolecular polymers.”
Benjamin Isare, Sandrine Pensec, Matthieu Raynal and Laurent Bouteiller*
C. R. Chimie, 2016, 19, 148-156                                                                                Hal Id: hal-01390906
http://dx.doi.org/10.1016/j.crci.2015.06.013

P16:Structural control of bisurea-based supramolecular polymers: influence of an ester moiety.”
Mohammed Dirany, Virgile Ayzac, Benjamin Isare, Matthieu Raynal,* and Laurent Bouteiller*
Langmuir, 2015, 31, 11443-11451
http://dx.doi.org/10.1021/acs.langmuir.5b02974

P15:Revisiting the assembly of amino ester-based benzene-1,3,5-tricarboxamides: chiral rods in solution.”
Alaric Desmarchelier, Matthieu Raynal,* Patrick Brocorens, Nicolas Vanthuyne and Laurent Bouteiller,*
Chem. Commun., 2015, 51, 7397-7400.                                                            Hal Id: hal-01141988
http://dx.doi.org/10.1039/c5cc01513h

P14: Organogel formation rationalized by Hansen solubility parameters: influence of gelator structure.”
Julien Bonnet, Gad Suissa, Matthieu Raynal and Laurent Bouteiller*,
Soft Matter, 2015, 11, 2308-2312.                                                                       Hal Id: hal-01671934
http://dx.doi.org/10.1039/c5sm00017c

P13: Organogel formation rationalized by Hansen solubility parameters: dos and don’ts.”
Julien Bonnet, Gad Suissa, Matthieu Raynal and Laurent Bouteiller*,
Soft Matter, 2014, 10, 3154-3160.                                                                         Hal Id: hal-01122532
http://dx.doi.org/10.1039/c4sm00244j

P12 : “Supramolecular catalysis. Part 1: non-covalent interactions as a tool for building and modifying homogeneous catalysts.”
Matthieu. Raynal*, Pablo Ballester, Anton Vidal-Ferran and Piet W. N. M. van Leeuwen,
Chem. Soc. Rev., 2014, 43, 1660-1733.                                                             HAL Id : hal-01637204
http://dx.doi.org/10.1039/c3cs60027k

P11 : “Supramolecular catalysis. Part 2: artificial enzyme mimics.”
Matthieu. Raynal*, Pablo Ballester, Anton Vidal-Ferran and Piet W. N. M. van Leeuwen,
Chem. Soc. Rev., 2014, 43, 1734-1787.                                                                    HAL Id : hal-01637213
http://dx.doi.org/10.1039/c3cs60037h

P10 : “Tunable asymmetric catalysis through ligand stacking in chiral rigid rods.”
Matthieu. Raynal*, François Portier, Piet W. N. M. van Leeuwen and Laurent Bouteiller,
J. Am. Chem. Soc., 2013, 135, 17687-17690.
http://dx.doi.org/10.1021/ja408860s

P9 : “Efficient near-UV emitters based on cationic bis-pincer Ir(III) carbene complexes.”
Noviyan Darmawan, Pierre Braunstein, Herwig Buchholz, Susanne Heun, Matteo Mauro, Junyou Pan, Matthieu Raynal, Cheng-Han Yand and Luisa de Cola,
Inorg. Chem., 2013, 52 10756-10765.
http://dx.doi.org/10.1021/ic302695q

P8 : Enantioselective supramolecular catalysis induced by remote chiral diols.”
Piet W. N. M. van Leeuwen*, David Rivillo, Matthieu Raynal and Zoraida Freixa,
J. Am. Chem. Soc., 2011, 133, 18562-18565.
http://dx.doi.org/10.1021/ja207912d

P7 : “Organogel formation rationalized by Hansen solubility parameters.”
Matthieu Raynal and Laurent Bouteiller*
Chem. Commun. 2011, 47, 8271-8273.
http://dx.doi.org/10.1039/c1cc13244j

P6 : “Hydrogen bonded supramolecular polymers in moderately polar solvents.”
Farid Ouhib, Matthieu Raynal, Benjamin Jouvelet, Benjamin Isare and Laurent Bouteiller*,
Chem. Commun., 2011, 47, 10683-10685.
http://dx.doi.org/10.1039/c1cc14590h

P5: “Reaction intermediates in the synthesis of new hydrido, N-Heterocyclic dicarbene Ir(III) pincer complexes.”
Matthieu Raynal, Roberto Pattacini, Catherine S. J. Cazin, Christophe Vallée, Hélène Olivier-Bourbigou and Pierre Braunstein*
Organometallics, 2009, 28, 4028-4047.
http://dx.doi.org/10.1021/om900226c

P4: “Remarkable base effect in the synthesis of mono- and dinuclear iridium(I) NHC complexes.”
Matthieu Raynal, Catherine S. J. Cazin, Christophe Vallée, Hélène Olivier-Bourbigou and Pierre Braunstein*,
Organometallics, 2009, 28, 2460-2470.
http://dx.doi.org/10.1021/om900125j

P3: “A new stable CNHC^CH^CNHC N-heterocyclic dicarbene ligand: its mono- and dinuclear Ir(I) and Ir(I)-Rh(I) complexes.”
Matthieu Raynal, Catherine S. J. Cazin, Christophe Vallée, Hélène Olivier-Bourbigou and Pierre Braunstein*
Dalton Trans. 2009, 3824-3832.
http://dx.doi.org/10.1039/b902733e
 
P2: “Unprecedented cubane-type silver cluster with a novel phosphinite functionalized
N-heterocyclic carbene ligand.”
Matthieu Raynal, Xianghao Liu, Roberto Pattacini, Christophe Vallée, Hélène Olivier-Bourbigou and Pierre Braunstein*
Dalton Trans. 2009, 7288-7293.
http://dx.doi.org/10.1039/b911439d

P1: “An unprecedented, figure-of-eight, dinuclear iridium(I) dicarbene and new iridium(III) ‘pincer’ complexes.”
Matthieu Raynal, Catherine S. J. Cazin, Christophe Vallée, Hélène Olivier-Bourbigou and Pierre Braunstein*
Chem. Commun. 2008, 34, 3983-3985.
http://dx.doi.org/10.1039/b808806c