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ACS Omega|August 29, 2019
Large Synthetic Molecule that either Folds or Aggregates through Weak Supramolecular Interactions Determined by SolventCristina Oliveras-González, Mathieu Linares, David B Amabilino, et al.
Journal of the American Chemical Society|April 21, 2005
Chiral molecular metals: syntheses, structures, and properties of the AsF(6)(-) salts of racemic (+/-)-, (R)-, and (S)-tetrathiafulvalene-oxazoline derivativesCéline Réthoré, Narcis Avarvari, Enric Canadell, et al.
Angewandte Chemie (International Ed. in English)|November 11, 1999
Gold(I) and Gold(0) Complexes of Phosphinine-Based MacrocyclesMézailles, Avarvari, Maigrot, et al.
Chirality|May 19, 2023
Tuning the photophysical and chiroptical properties of [4]helicene-diketopyrrolopyrrolesMaurizio Mastropasqua Talamo, Thomas Cauchy, Francesco Zinna, et al.
Chemical Communications (Cambridge, England)|June 30, 2018
Spontaneous separation of on-surface synthesized tris-helicenes into two-dimensional homochiral domainsJingyi Li, Kévin Martin, Narcis Avarvari, et al.
Molecules (Basel, Switzerland)|April 30, 2021
Mono- and Binuclear Copper(II) and Nickel(II) Complexes with the 3,6-Bis(picolylamino)-1,2,4,5-Tetrazine LigandOleh Stetsiuk, Abdelkrim El-Ghayoury, Francesc Lloret, et al.
Organic & Biomolecular Chemistry|September 30, 2014
Thiophene-benzoquinones: synthesis, crystal structures and preliminary coordination chemistry of derived anilate ligandsMatteo Atzori, Flavia Pop, Thomas Cauchy, et al.
The Journal of Organic Chemistry|October 25, 2001
The CH by N Replacement Effects on the Aromaticity and Reactivity of PhosphininesGilles Frison, Alain Sevin, Narcis Avarvari, et al.
Dalton Transactions (Cambridge, England : 2003)|September 4, 2008
Synthesis and reactivity of silylated tetrathiafulvalenesAurélien Hameau, Fabrice Guyon, Michael Knorr, et al.
Inorganic Chemistry|July 18, 2012
Tetrathiafulvalene-triazine-dipyridylamines as multifunctional ligands for electroactive complexes: synthesis, structures, and theoretical studyDiana G Branzea, Arnaud Fihey, Thomas Cauchy, et al.
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