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Université de Bordeaux
LabEx AMADEusCluster of Excellence
Cluster of excellence

AMADEus Seminar - Dr. David Curiel - Thursday 23 march 2017 - 11:00 am ENSCBP (Amphi 1)

le jeudi 23 mars 2017 de 11h à 12h

Dr. David Curiel

Department of Organic Chemistry
Faculty of Chemistry, University of Murcia, 30100-Murcia (Spain)

“Study of cabazolocarbazole isomers as organic semiconductors”

Dernière mise à jour jeudi 16 mars 2017
AMADEus Seminar - Dr. David Curiel - Thursday 23 march 2017 - 11:00 am ENSCBP (Amphi 1)


Conjugated systems based on fused aromatic and heteroaromatic rings constitute the family of heteroacenes. The infinite variety of possible structures represents an endless source or novel organic semiconductors. In this regard, carbazolocarbazoles, resulting from the fusion of two carbazole units, belong to the subgroup of pyrrole-based azaacenes. These hexacyclic molecules admit several structural geometries. Accordingly, due to the critical influence of the molecular structure on the solid state packing and the subsequent charge transport, a series of carbazolocarbazoles have been synthesized with the aim of studying the effect of isomerism on the electronic properties of these polyheteroaromatic molecules. 


Dr. David Curiel received his degree in chemistry from the University of Alicante in 1996. Then he moved to the University of Murcia where he obtained his PhD in 2002 working in the synthesis of ferrocenyl-substituted heterocycles. Since 2002 to 2004 he worked as a Marie Curie Postdoctoral Fellow at the University of Oxford (UK) focusing his research in the preparation of interlocked structures via anion-directed self-assembly. In 2005 he moved to the University of Sydney (Australia) to work as a Postdoctoral Researcher in the synthesis of metalloporphyrin-based dyads and triads for the study of charge separation processes used in the exploration of artificial photosynthesis. Back in Spain, during the period 2006-2010 he was contracted as a research fellow of the “Ramón y Cajal” Program at the University of Murcia, where he continued working in the area of anion recognition and sensing. Currently, he holds a position as a Contracted Lecturer and Researcher at that institution. His research interests are included in the areas of supramolecular chemistry and, more recently, in the synthesis of molecular materials for its application to organic electronics.

Relevant publications:

-“Homotrimetallic oxazolo-ferrocene complexes displaying tunable cooperative interactions between metal centers and redox-switchable character” A. Tárraga, P. Molina, D. Curiel, M.D. Velasco, Organometallics, 2001, 20, 2145-2152.

-“Indolocarbazoles: a new family of anion sensors” D. Curiel, A. Cowley, P.D. Beer, Chem. Commun. 2005, 236.

-“Anion-templated assembly of interpenetrated and interlocked structures” Beer, Paul D.; Sambrook, Mark R.; Curiel, David, Chem. Commun., 2006, 2105-2117.

- “Photoinduced electron transfer in a β,β'-pyrrolic fused ferrocene-(zinc porphyrin)-fullerene.” David Curiel, Kei Ohkubo, Jeffrey R.Reimers, Shunichi Fukuzumi, Maxwell J Crossley, Phys. Chem. Chem. Phys., 2007, 9(38) 5260-5266.

- “A new open benzodipyrrole-based chemosensor for hydrogenpyrophosphate anion in aqueous environment” David Curiel, Arturo Espinosa, Miriam Más-Montoya, Guzmán Sánchez, Alberto Tárraga, Pedro Molina, Chem. Commun., 2009, 15, 7539-7541.

-“Isomeric carbazolocarbazoles: synthesis, characterization and comparative study in Organic Field Effect Transistors Miriam Más-Montoya, Rocío Ponce Ortiz, David Curiel, Arturo Espinosa , Magali Allain, Antonio Facchetti, Tobin J. Marks,  Journal of Materials Chemistry C, 2013, 1, 1959-1969.

-“Complexation and sensing of dicarboxylate anions and dicarboxylic acidsDavid Curiel, Miriam Más-Montoya, Guzmán Sánchez, Coordination Chemistry Reviews, 2015, 284, 19-66.

-“Doped-carbazolocarbazoles as hole transporting materials in small molecule solar cells with different architectures” David Curiel, Miriam Más-Montoya, Markus Hummert, Moritz Riede, Karl Leo, Organic Electronics, 2015, 17, 28-32.

Figure dans les rubriques