Sebastien GoebUMR CNRS - MOLTECH-ANJOU - Chercheur CNRS

• UFR SCIENCES
• DEP ENS SCIENCES Chimie - Recherche Dép Chimie - SCIENCES
  0241735064
• 2 Boulevard de Lavoisier - 49045 - ANGERS CEDEX 01
• UMR CNRS - MOLTECH-Anjou - CNRS Researcher
• K112

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Discipline

Supramolecular chemistry - Coordination driven Self-Assembly - Molecular Hosts - Redox Systems

Publications

[61] Comparing the self-assembly processes of two redox-active exTTF-based regioisomer Ligands

Dekhtiarenko M., Allain M., Carré V., Aubriet F., Voitenko Z., Sallé M.,* Goeb S.*

New J. Chem., 2021, 45, 21015-21019. IF = 3.591

[60] Exciton Coupling in Redox-Active Salen based Self-Assembled Metallacycles

Herasymchuk K., Allain M., MacNeil G. A., Carré V., Aubriet F., Leznoff D. B., Sallé M.,* Goeb S.,* Storr T.*

Chem. Eur. J., 2021, 27, 16161 – 16172. IF = 5.236

[59] Reversible pH-Controlled Catenation of a Benzobisimidazole-based Tetranuclear Rectangle

Dekhtiarenko M., Pascal S.,* Elhabiri M., Mazan V., Canevet D., Allain M., Carré V., Aubriet F., Voitenko Z., Sallé M.,* Siri O.,* Goeb S.*

Chem. Eur. J. (Hot Paper), 2021, 27, 15922 - 15927. IF = 5.236

[58] Electron-Rich Coordination Receptors based on Tetrathiafulvalene derivatives: Controlling the Host-Guest binding

Goeb S.,* Sallé M.*

Acc. Chem. Res., 2021, 54, 4, 1043–1055. IF = 20.832

[57] A self-assembled tetrathiafulvalene box

Krykun S., Croué V., Alévêque O., Levillain E., Allain M., Mézière C., Carré V., Aubriet F., Voitenko Z., Goeb S.,* Sallé M.*

Org. Chem. Front., 2021, 2021,8, 883-890. IF = 5.076

 

[56] Tuning the structure and the properties of dithiafulvene metalla-assembled tweezers

Dekhtiarenko M., Krykun S., Carré V., Aubriet F., Canevet D., Allain M., Voitenko Z., Sallé M.,* Goeb S.*

Org. Chem. Front., 2020, 7, 2040-2046. IF = 5.076

[55] Chiral Self-Sorting in Truxene-based Metallacages

Séjourné S., Labrunie A., Dalinot C., Benchohra A., Carré V., Aubriet F., Allain M., Sallé M.,* Goeb S.*

Inorganics, 2020, 6, 44-54. IF = 2.93

[54] Metalla-Assembled Electron-Rich Tweezers: Redox-Controlled Guest Release through Supramolecular Dimerization

Krykun S., Dekhtiarenko M., Canevet D., Carré V., Aubriet F., Levillain E., Allain M., Voitenko Z., Sallé M.,* Goeb S.*

Angew. Chem. Int. Ed. (Hot Paper), 2020, 59, 716-720. IF = 12.257

[53] Coordination-driven assembly of a supramolecular square and oxidation to a tetra-ligand radical species

Herasymchuk K., Miller J. J, MacNeil G., Sergeenko A., McKearney D., Goeb S., Sallé M., Kaake L., Leznoffa D. B., Storr T.*

Chem. Commun., 2019, 55, 6082-6085. IF = 6.290

[52] Redox-controlled hybridization of helical foldamers

Faour L., Gautier C., Goeb S., Allain M., Levillain E., Canevet D.,* Sallé M.*

Chem. Commun., 2019, 55, 5743-5746. IF = 6.290

[51] Tuning the electronic properties and the planarity degree in the π-extended TTF series: The prominent role of heteroatoms

Krykun S., Croué V., Allain M., Voitenko Z., Aragó J., Ortí O.,* Goeb S.,* Sallé M.*

J. Mater. Chem. C, 2018, 6, 13190-13196. IF = 5.976

[50] Functionalised tetrathiafulvalene- (TTF-) macrocycles: Recent trends in applied Supramolecular chemistry

Jana A., Bähring S., Ishida M., Goeb S., Canevet D., Sallé M.,*Jeppesen J. O.,* Sessler J. L.*

Chem. Soc. Rev., 2018, 47, 5616-5645. IF = 38.62

[49] Redox-driven transformation of a discrete molecular cage into an infinite 3D coordination polymer

Szalóki G., Krykun S., Croué V., Allain M., Morille Y., Aubriet F., Carré V., Voitenko Z., Goeb S.,* Sallé M.*

Chem. Eur. J., 2018, 24, 11273-11277. IF = 5.32

[48] A M2L2 Redox-active Metalla-Macrocycle Based on Electron-rich 9-(1,3-dithiol-2-ylidene)Fluorene

Krykun S., Allain M., Carré V., Aubriet F., Voitenko Z., Goeb S.,* Sallé M.*

Inorganics, 2018, 6, 44-54. IF = 2.93

[47] Self-assembled Cofacial Zinc Porphyrin Supramolecular Nanocapsules as tuneable 1O2 Photosensitizers

Colomban C., Fuertes-Espinosa C., Goeb S., Salle M., Costas M., Blancafort L.,* Ribas X.*

Chem. Eur. J., 2018, 24, 4371-4381. IF = 5.32

[46] Design of Zn-, Cu-, and Fe-Coordination Complexes Confined in a Self-Assembled Nanocage

Colomban C., Martin-Diaconescu V., Parella T., Goeb S., García-Simón C., Lloret-Fillol J., Costas M.,* Ribas X.*

Inorg. Chem. 2018, 57, 3529-3539. IF = 4.86

[45] Controlling the Host-Guest Interaction Mode through a Redox Stimulus

Szaloki G., Croue V., Carre V., Aubriet F., Aleveque O., Levillain E., E Allain M., Arago J., Orti., Goeb S.,* Salle M.*

Angew. Chem. Int. Ed., 2017, 56, 16272-16276. IF = 11.99

[44] A self-assembled M2L4 cage incorporating electron-rich 9-(1,3-dithiol-2-ylidene)fluorene units

Croué V., Krykun S., Allain M., Morille Y., Aubriet F., Carré V., Voitenko Z., Goeb S.,* Sallé M.*

New J. Chem., 2017, 41, 3238-3241. IF = 3.26

[43] Reversible C60 Ejection from a Metallocage through the Redox‐Dependent Binding of a Competitive Guest

Colomban C., Szalóki G., Allain M., Gómez L., Goeb S.,* Sallé M.*, Costas M.*, Ribas X.*

Chem. Eur. J., 2017, 23, 3016-3022. IF = 5.32

[42] C60 Recognition from Extended Tetrathiafulvalene Bis-acetylide Platinum(II) Complexes

Bastien G., Dron P. I., Vincent M., Canevet D., Allain M., Goeb S.,* Sallé M.*

Org. Lett., 2016, 18, 5856–5859. IF = 6.58

[41] Neutral versus Polycationic Coordination Cages: A Comparison Regarding Neutral Guest Inclusion

Szalóki G., Croué V., Allain M., Goeb S.,* Sallé M.*

Chem. Commun., 2016, 52, 10012-10015. IF = 6.32

[40] Reversible Guest Uptake/Release by a Redox-Controlled Assembling/Disassembling of a Coordination Cage

Croué V., Goeb S.,* Szalóki G., Allain M., Sallé M.*

Angew. Chem. Int. Ed., 2016, 55, 1746-50. IF = 11.99

[39] Tuning the size of a redox-active tetrathiafulvalene-based self-assembled ring by adjusting the metal coligand

Bivaud S., Goeb S.,* Croué V., Allain M., Pop F., Sallé M.*

Beilstein J. Org. Chem., 2015, 11, 966-971. IF = 2.34

[38] Metal-driven Self-Assembly: the Case of Redox-Active Discrete Architectures (Cover Page)

Croué V., Goeb S.,* Sallé M.*

Chem. Commun., 2015, 51(34), 7275-89. IF = 6.32

[37] Self-Assembled Cages from the Electroactive Bis(pyrrolo)-tetrathiafulvalene (BPTTF) Building Block

Bivaud S., Goeb S., Balandier J-Y., Chas M., Allain M., Sallé M.*

Eur. J. Inorg. Chem., 2014, 14, 2440-2448. IF = 2.69

[36] Electron-Rich Arene−Ruthenium Metalla-architectures Incorporating Tetrapyridyl− Tetrathiafulvene Donor Moieties

Vajpayee V., Bivaud S., Goeb S., Croué V., Allain M., Popp B. V., Garci A., Therrien B.,* Sallé M.*

Organometallics, 2014, 33(7), 1651-1658. IF = 3.86

[35] A Self-Assembled Electro-active M8L4 Cage Based on Tetrathiafulvalene Ligands

Goeb S.,* Bivaud S., Croué V., Vajpayee V., Allain M., Sallé M.*

Materials, 2014, 7(1), 611-622. IF = 3.23

[34] Self-assembled Containers Based on Extended Tetrathiafulvalene

Bivaud S., Goeb S.,* Croué V., Allain M., Sallé M.*

J. Am. Chem. Soc., 2013, 134, 10018-10021. IF = 12.11

[33] A Metal-Directed Self-Assembled Electroactive Cage with Bis(pyrrolo)tetrathiafulvalene (BPTTF) Side Walls

Bivaud S., Balandier J-Y., Chas M., Allain M., Goeb S., Sallé M.*

J. Am. Chem. Soc., 2012, 134, 11968-11970. IF = 12.11

[32] A BPTTF-based self-assembled electron-donating triangle capable of C60 binding

Goeb S., Bivaud S., Dron P. I., Balandier J-Y., Chas M., Sallé M.*

Chem. Commun., 2012, 48, 3106-3108. IF = 6.32

[31] Chemistry at Boron: Synthesis and Properties of Red to Near-IR Fluorescent Dyes Based on Boron-Substituted Diisoindolomethene Frameworks

Ulrich G., Goeb S., De Nicola A., Retailleau P., Ziessel R.*

J. Org. Chem., 2011, 76, 4489-4505. IF = 4.85

[30] Tetrathiafulvalene-Based Architectures: From Guests Recognition to Self-Assembly

Canevet D., Balandier J-Y., Lyskawa J., Trippé G., Goeb S., Le Derf F., Sallé M.*

Phosphorus, Sulfur, and Silicon and the Related Elements, 2011, 186, 1153-1168. IF = 0.81

[29] Phosphorescent Self-Assembled PtII Tetranuclear Metallocycles

Goeb S.,* Prusakova V., Wang X., Vézinat A., Sallé M.,* Castellano F. N.*

Chem. Comm., 2011, 47, 4397-4399. IF = 6.32

[28] Homogeneous Photocatalytic Hydrogen Production using -conjugated Pt(II) Arylacetylide Sensitizers

Wang X., Goeb S., Ji Z., Pogulaichenko N. A., Castellano F. N.*

Inorg. Chem., 2011, 50, 705-707. IF = 4.86

 

[27] A Self-assembled Bis(pyrrolo)Tetrathiafulvalene-Based Redox Active Square

Balandier J-Y, Chas M., Goeb S., Dron P. I., Rondeau D., Belyasmine A., Gallego N., Sallé M.*

New J. Chem., 2011, 35, 165-168. IF = 3.26

 

[26] Supermolecular Chromophore Sensitized Near-Infrared to Visible Photon Upconversion

Singh-Rachford T. N., Nayak A., Muro-Small M. L., Goeb S., Therien M. J., Castellano F. N.*

J. Am. Chem. Soc, 2010, 132(40), 14203-14211. IF = 12.11

[25] Physical origin of the third order nonlinear optical response of orthogonal pyrrolo-tetrathiafulvalene derivatives

Iliopoulos K., Czaplicki R., El Ouazzani H., Balandier J-Y., Chas M., Goeb S., Sallé M., Gindre D., Sahraoui B.*

Appl. Phys. Lett., 2010, 97, 101104. IF = 3.14

[24] Excited State Absorption Properties of Pt(II) Terpyridyl Complexes Bearing π-Conjugated Arylacetylides

Wang X., Goeb S., Ji Z., Castellano F. N.*

J. Phys. Chem. B, 2010, 114(45), 14440-14449. IF = 3.17

[23] N-Aryl pyrrolo-tetrathiafulvalene based ligands: synthesis and metal coordination

Balandier J-Y., Chas M., Dron P. I., Goeb S., Canevet D., Belyasmine A., Allain M., Sallé M.*

J. Org. Chem., 2010, 75(5), 1589-1599. IF = 4.85

[22] Solvent-induced configuration mixing and triplet excited-state inversion: insights from transient absorption and transient dc photoconductivity measurements

She C., Rachford A. A., Wang X., Goeb S., El-Ballouli A. O., Castellano F. N.,* Hupp J. T.*

Phys. Chem. Chem. Phys., 2009, 11(38), 8586-8591. IF = 4.12

[21] Electronic energy transfer to the S2 level of the acceptor in functionalized boron dipyrromethene dyes

Harriman A., Mallon L. J., Goeb S., Ulrich G., Ziessel R.*

Chem. Eur. J., 2009, 15(18), 4553-4564. IF = 5.32

[20] Evolution of the Triplet Excited State in PtII Perylenediimides

Danilov E. O., Rachford A. A., Goeb S., Castellano F. N.*

J. Phys. Chem. A, 2009, 113(19), 5763-5768. IF = 2.84

[19] Ligand Localized Triplet Excited States in Platinum(II) Bipyridyl and Terpyridyl Peryleneacetylides

Rachford A. A., Goeb S., Ziessel R.,* Castellano F. N.*

Inorg. Chem., 2008, 47(10), 4348-4355. IF = 4.86

[18] Synthesis of novel tetrachromophoric cascade-type Bodipy dyes

Goeb S., Ziessel R.*

Tetrahedron Letters, 2008, 49(16), 2569-2574. IF = 2.19

[17] Accessing the triplet excited state in perylenediimides

Rachford A. A., Goeb S., Castellano, F. N.*

J. Am. Chem. Soc., 2008, 130(9), 2766-2767. IF = 12.11

[16] Solvent induced configuration mixing and triplet excited state inversion exemplified in a Pt(II) complex (Cover Page)

Goeb S., Rachford, A. A., Castellano F. N.*

Chem. Commun., 2008, 7, 814-816. IF = 6.32

[15] New Polypyridine Ligands Functionalized with Redox-Active Fr(II) Organometallic Fragmets

Paul F., Goeb S., Justaud F., Argouach G., Toupet L., Ziessel R., Lapinte C.*

Inorg. Chem., 2007, 46, 9036-9038. IF = 4.86

[14] Luminescent Charge-Transfer Platinum(II) Metallacycle

Hua F., Kinayyigit S., Rachford A. A., Shikhova E. A., Goeb S., Cable J. E., Adams C. J., Kirschbaum K., Pinkerton A., Castellano F. N.*

Inorg. Chem., 2007, 46, 8771-8783. IF = 4.86

[13] A near-IR emitting Bodipy-based dye fitted with ancillary light harvesting units

Harriman A.,* Mallon L. J., Goeb S., Ziessel R.*

Phys. Chem. Chem. Phys., 2007, 9, 5199-5201. IF = 4.12

[12] Synthesis of Bisisoindolomethene Dyes Bearing Anisole or Ethylthiophene Residues for Red and Near-IR Fluorescence

Ulrich, G., Goeb S., De Nicola A., Retailleau P., Ziessel R.*

Synlett, 2007, 10, 1517-1520. IF = 2.15

[11] Convenient Synthesis of Green Diisoindolodithienylpyrromethene-Dialkynyl Borane Dyes

Goeb S., Ziessel R.*

Org. Lett., 2007, 9, 737-740. IF = 6.58

[10] Spectroscopic and Redox Properties of Novel d6-Complexes Engineered from All Z-Ethenylthiophene-bipyridine Ligands

Belbakra A., Goeb S., De Nicola A., Ziessel R.,* Sabatini C., Barbieri A., Barigelletti F.*

Inorg. Chem., 2007, 46, 839-847. IF = 4.86

[09] Photophysical Properties of Ruthenium(II) Tris(2,2'-bipyridine) Complexes Bearing conjugated Thiophene Appendages

Harriman A.,* Izzet, G., Goeb S., Nicola A. D., Ziessel R.*

Inorg. Chem., 2006, 45, 9729-9741. IF = 4.86

[08] New fluorescent aryl- or ethynylaryl-boron-substituted indacenes as promising dyes

Ulrich G., Goze C., Goeb S., Retailleau P., Ziessel R.*

New J. Chem., 2006, 30, 982–986. IF = 3.26

[07] Energy Transfer in Hybrids Based on a Thiophene-Substituted Ethynylbipyridine Dimer Decorated with Re(I), Ru(II), and Os(II) Units

Goeb S., De Nicola A., Ziessel R.,* Sabatini C., Barbieri A., Barigelletti F.*

Inorg. Chem., 2006, 45, 1173-1183. IF = 4.86

[06] Absorption Spectra, Photophysical Properties, and Redox Behavior of Ruthenium(II) Polypyridine Complexes Containing Accessory Dipyrromethene-BF2 Chromophores

Galletta M., Puntoriero F., Campagna S.,* Chiorboli C., Quesada M., Goeb S., Ziessel R.*

J. Phys. Chem. A., 2006, 110, 4348-4358. IF = 2.84

[05] Controlled Synthesis of Multinuclear Metal Complex Arrays by Cross Coupling of Coordinated Ligands

Goeb S., De Nicola A., Ziessel R.*

J. Org. Chem., 2005, 70, 6802-6808. IF = 4.85

[04] Binuclear Wirelike Dimers Based on Ruthenium(II)-Bipyridine Units Linked by Ethynylene-Oligothiophene-Ethynylene Bridges

Barbieri A., Ventura B., Flamigni L., Barigelletti F.,* Fuhrmann G., Bauerle P., Goeb S., Ziessel R.*

Inorg. Chem., 2005, 44, 8033-8043. IF = 4.86

[03] Stepwise Synthesis of Conjugatively Bridged Bipyridine Ligands from Thiophene and Alkyne Linkages

Goeb S., De Nicola A., Ziessel R.*

Synthesis, 2005, 7, 1169-1177. IF = 2.65

[02] Oligomeric Ligands Incorporating Multiple 5,5'-Diethynyl-2,2'-bipyridine Moieties Bridged and End-Capped by 3,4-Dibutylthiophene Units

Goeb S., De Nicola A., Ziessel R.*

J. Org. Chem., 2005, 70(5), 1518-1529. IF = 4.85

[01] A convenient method of producing thiophene linked bipyridine oligomers

De Nicola A., Goeb S., Ziessel R.*

Tetrahedron Letters, 2004, 45(42), 7963-7967. IF = 2.19

• Courriel : sebastien.goeb @ univ-angers.fr (sebastien.goeb @ univ-angers.fr)