Nazario Martin

Summary

Affiliation: Universidad Complutense
Country: Spain

Publications

  1. ncbi request reprint New challenges in fullerene chemistry
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040, Madrid, Spain
    Chem Commun (Camb) . 2006
  2. ncbi request reprint Highly efficient retro-cycloaddition reaction of isoxazolino[4,5:1,2][60]- and -[70]fullerenes
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, E 28040 Madrid, Spain
    J Org Chem 72:3840-6. 2007
  3. doi request reprint Electron-deficient fullerenes in triple-channel photosystems
    Javier López-Andarias
    Departamento de Quimica Organica, Universidad Complutense, IMDEA Nanoscience, Madrid, Spain
    Chem Commun (Camb) 51:7543-5. 2015
  4. doi request reprint Organocatalysis for new chiral fullerene-based materials
    Rosa M Girón
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    Faraday Discuss 173:311-22. 2014
  5. doi request reprint Catalytic stereodivergent functionalization of H2@C60
    Enrique E Maroto
    Departamento de Quimica Organica I, Facultad de Ciencias Quimicas, Ciudad Universitaria, s n 28040 Madrid, Spain
    Chem Commun (Camb) 50:740-2. 2014
  6. doi request reprint Tetrathiafulvalene: the advent of organic metals
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040 Madrid, Spain
    Chem Commun (Camb) 49:7025-7. 2013
  7. doi request reprint Two experiments that impacted the fate of fullerenes
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040, Madrid, Spain
    Chem Commun (Camb) 49:1039-41. 2013
  8. ncbi request reprint Regioselective intramolecular Pauson-Khand reactions of C60: an electrochemical study and theoretical underpinning
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, 28040 Madrid, Spain
    Chemistry 11:2716-29. 2005
  9. ncbi request reprint Electronic communication in tetrathiafulvalene (TTF)/C60 systems: toward molecular solar energy conversion materials?
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, E 28040 Madrid, Spain
    Acc Chem Res 40:1015-24. 2007
  10. doi request reprint Electron donor-acceptor interactions in regioselectively synthesized exTTF(2)-C(70)(CF(3))(10) dyads
    Yuta Takano
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain
    Chemistry 16:5343-53. 2010

Collaborators

  • Dirk M Guldi
  • Francesco Giacalone
  • Edmund Leary
  • Yang Wang
  • Roberto Otero
  • Timothy Clark
  • Takeshi Akasaka
  • Yao Ting Wu
  • Israel Fernández
  • Naomi Sakai
  • Stefan Matile
  • Lawrence T Scott
  • Julius Rebek
  • Maurizio Prato
  • Albert Poater
  • Shunichi Fukuzumi
  • Sheng Zhang
  • M Teresa Gonzalez
  • Salvatore Filippone
  • Enrique E Maroto
  • Juan Marco-Martínez
  • Carmen Atienza
  • Emilio M Pérez
  • Javier López-Andarias
  • Laura Rodríguez-Pérez
  • Juan Luis Lopez
  • M Angeles Herranz
  • Enrique Ortí
  • Beatriz M Illescas
  • Luis Sanchez
  • Silvia Reboredo
  • Sara Vidal
  • Marta Izquierdo
  • Alberto Insuasty
  • Raul Garcia
  • Agustín Molina-Ontoria
  • Jose Santos
  • María Gallego
  • Margarita Suarez
  • Joaquín Calbo
  • Fulvio G Brunetti
  • Gustavo Fernandez
  • Yuta Takano
  • Rosa M Girón
  • Maria Angeles Herranz
  • Ma Ángeles Herranz
  • Carlos Romero-Nieto
  • Helena Isla
  • Juan Luis Delgado
  • Pierre Antoine Bouit
  • Antonio Muñoz
  • Ángel Martín-Domenech
  • Rafael Viruela
  • Roberto Martinez-Alvarez
  • Sonia Vela
  • Javier Ramos-Soriano
  • Shu Seki
  • Tsubasa Mikie
  • Carmen Villegas
  • Jaime Mateos-Gil
  • Santiago Casado
  • Yasujiro Murata
  • Maria Sierra
  • Andrea La Rosa
  • Rodolfo Miranda
  • Manuel Alcamí
  • Daniele Stradi
  • Fernando Martin
  • Christian Urban
  • Juan L Delgado
  • Juan Aragó
  • Javier Rojo
  • Vanesa Marcos
  • José L Segura
  • David Canevet
  • Enrique Maroto
  • Bruno Grimm
  • Andreas Gouloumis
  • Mateusz Wielopolski
  • Miquel Solà
  • Takahiro Tsuchiya
  • Roberto J Brea
  • Wolfgang Seitz
  • Marta C Díaz
  • Dolores Molero
  • Emilio Manuel Pérez
  • Ya Chu Hsieh
  • Paula Pla
  • Rafael M Krick-Calderon
  • Alfonso Pérez-Sánchez

Detail Information

Publications68

  1. ncbi request reprint New challenges in fullerene chemistry
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040, Madrid, Spain
    Chem Commun (Camb) . 2006
    ....
  2. ncbi request reprint Highly efficient retro-cycloaddition reaction of isoxazolino[4,5:1,2][60]- and -[70]fullerenes
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, E 28040 Madrid, Spain
    J Org Chem 72:3840-6. 2007
    ..In contrast to previous electrochemical retro-cycloaddition processes observed in fulleropyrrolidines, isoxazolinofullerenes were stable under oxidative conditions...
  3. doi request reprint Electron-deficient fullerenes in triple-channel photosystems
    Javier López-Andarias
    Departamento de Quimica Organica, Universidad Complutense, IMDEA Nanoscience, Madrid, Spain
    Chem Commun (Camb) 51:7543-5. 2015
    ..Fullerenes of increasing electron deficiency are designed, synthesized and evaluated in multicomponent surface architectures to ultimately build gradients in LUMO levels with nine components over 350 meV down to -4.22 eV. ..
  4. doi request reprint Organocatalysis for new chiral fullerene-based materials
    Rosa M Girón
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    Faraday Discuss 173:311-22. 2014
    ..The versatility of this reaction allows chiral fullerenes to be obtained at will, thus opening up a new avenue in the use of enantiomerically pure carbon nanostructures in materials science. ..
  5. doi request reprint Catalytic stereodivergent functionalization of H2@C60
    Enrique E Maroto
    Departamento de Quimica Organica I, Facultad de Ciencias Quimicas, Ciudad Universitaria, s n 28040 Madrid, Spain
    Chem Commun (Camb) 50:740-2. 2014
    ..The stereodivergent synthesis of either the cis or the trans endohedral cycloadduct is achieved with excellent diastereo- and enantioselectivities. ..
  6. doi request reprint Tetrathiafulvalene: the advent of organic metals
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040 Madrid, Spain
    Chem Commun (Camb) 49:7025-7. 2013
    ....
  7. doi request reprint Two experiments that impacted the fate of fullerenes
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040, Madrid, Spain
    Chem Commun (Camb) 49:1039-41. 2013
    ....
  8. ncbi request reprint Regioselective intramolecular Pauson-Khand reactions of C60: an electrochemical study and theoretical underpinning
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, 28040 Madrid, Spain
    Chemistry 11:2716-29. 2005
    ..Cyclic voltammetry reveals that the presence of the cyclopentenone's carbonyl group connected directly to the C60 core results in PK compounds with remarkable electron-accepting ability...
  9. ncbi request reprint Electronic communication in tetrathiafulvalene (TTF)/C60 systems: toward molecular solar energy conversion materials?
    Nazario Martin
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, E 28040 Madrid, Spain
    Acc Chem Res 40:1015-24. 2007
    ..These long-lived radical pairs are called to play an important role for the conversion of sunlight into chemical or electrical power...
  10. doi request reprint Electron donor-acceptor interactions in regioselectively synthesized exTTF(2)-C(70)(CF(3))(10) dyads
    Yuta Takano
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain
    Chemistry 16:5343-53. 2010
    ....
  11. ncbi request reprint Anefficient approach to chiral fullerene derivatives by catalytic enantioselective 1,3-dipolar cycloadditions
    Salvatore Filippone
    Departamento de Quimica Organica I, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Spain
    Nat Chem 1:578-82. 2009
    ..Furthermore, well-defined chiral carbon atoms linked to the fullerene sphere are able to perturb the inherent symmetry of the fullerene π-system as revealed by circular dichroism measurements...
  12. ncbi request reprint Self-assembly of C(60) pi-extended tetrathiafulvalene (exTTF) dyads on gold surfaces
    Maria Sierra
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, E 28040 Madrid, Spain
    Langmuir 22:10619-24. 2006
    ....
  13. ncbi request reprint Electronic interactions in a new pi-extended tetrathiafulvalene dimer
    Marta C Díaz
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, 28040 Madrid, Spain
    Chemistry 12:2709-21. 2006
    ..Oxidation of 14(2+) forms the tetracation 14(4+) which is constituted by two aromatic anthracene units bearing four aromatic, almost orthogonal 1,3-dithiolium cations...
  14. doi request reprint Charge transfer-assisted self-limited decyanation reaction of TCNQ-type electron acceptors on Cu(100)
    Christian Urban
    Dep de Física de la Materia Condensada, Universidad Autonoma de Madrid, Madrid, Spain
    Chem Commun (Camb) 50:833-5. 2014
    ..Combined Scanning Tunneling Microscopy/X-ray Photoelectron Spectroscopy experiments and Density Functional Theory calculations relate the self-limiting behavior to the transfer of electrons from the metal to the molecule. ..
  15. doi request reprint [2,2']paracyclophane-based π-conjugated molecular wires reveal molecular-junction behavior
    Agustín Molina-Ontoria
    Departamento de Química Orgánica, Facultad de Química, Universidad Complutense, Madrid, Spain
    J Am Chem Soc 133:2370-3. 2011
    ..If hole transfer is assumed to be the dominant charge transfer (CT) mechanism, CT is facilitated in one direction (from C(60) to ZnP via pCp) but disfavored in the other direction (from ZnP to C(60) via pCp)...
  16. ncbi request reprint Exceptionally strong electronic communication through hydrogen bonds in porphyrin-C60 pairs
    Luis Sanchez
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense de Madrid, 28040 Madrid, Spain
    Angew Chem Int Ed Engl 45:4637-41. 2006
  17. doi request reprint Donor-acceptor conjugates of lanthanum endohedral metallofullerene and pi-extended tetrathiafulvalene
    Yuta Takano
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 132:8048-55. 2010
    ..0 x 10(8) s(-1)) in toluene. Transient absorption spectroscopy experiments confirmed these observations...
  18. doi request reprint Supramolecular One-Dimensional n/p-Nanofibers
    Alberto Insuasty
    Departamento de Quimica Organica I, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, E 28040 Madrid, Spain
    Sci Rep 5:14154. 2015
    ..Furthermore, photogenerated radical ion pairs, formed upon visible light irradiation of the n/p-nanohybrids, feature lifetimes on the range of 0.9-1.2 ns. ..
  19. doi request reprint Controlling the crystalline three-dimensional order in bulk materials by single-wall carbon nanotubes
    Javier López-Andarias
    Departamento de Quimica Organica, Facultad de C C Químicas, Universidad Complutense de Madrid, 28040 Madrid and IMDEA Nanociencia, 28049 Madrid, Spain
    Nat Commun 5:3763. 2014
    ....
  20. pmc Enantioselective cycloaddition of münchnones onto [60]fullerene: organocatalysis versus metal catalysis
    Juan Marco-Martínez
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 136:2897-904. 2014
    ..Further functionalization of the pyrrolinofullerene carboxylic acid derivatives has been carried out by esterification and amidation reactions. ..
  21. doi request reprint Large exTTF-based dendrimers. Self-assembly and peripheral cooperative multiencapsulation of C60
    Gustavo Fernandez
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 130:10674-83. 2008
    ..The calculated values for D demonstrate the decrease of this magnitude with increasing dendrimer size...
  22. doi request reprint Cyclobuteno[60]fullerenes as Efficient n-Type Organic Semiconductors
    Silvia Reboredo
    Universidad Complutense de Madrid, Av Complutense S N, 28040, Madrid, Spain
    Chemistry 22:13627-31. 2016
    ....
  23. doi request reprint Enantiospecific cis-trans isomerization in chiral fulleropyrrolidines: hydrogen-bonding assistance in the carbanion stabilization in H2O@C60
    Enrique E Maroto
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 137:1190-7. 2015
    ..On the basis of the experimental results and computational calculations, a plausible reaction mechanism involving the hydrogen-bonding assistance of the inner water molecule in the carbanion stabilization of endofullerene is proposed. ..
  24. doi request reprint Buckyballs
    Juan L Delgado
    IMDEA Nanoscience, Campus de Cantoblanco, 28049, Madrid, Spain
    Top Curr Chem 350:1-64. 2014
    ..The number of possible non-IPR carbon cages is almost infinite and the near future will show us whether they will become a reality. ..
  25. doi request reprint Chiral fullerenes from asymmetric catalysis
    Enrique E Maroto
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense de Madrid UCM, Avda Complutense s n, E 28040 Madrid, Spain
    Acc Chem Res 47:2660-70. 2014
    ....
  26. ncbi request reprint Hydrogen-bonding motifs in fullerene chemistry
    Luis Sanchez
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain
    Angew Chem Int Ed Engl 44:5374-82. 2005
    ....
  27. ncbi request reprint Diastereoselective synthesis of fulleropyrrolidines from suitably functionalized chiral cyclobutanes
    Beatriz M Illescas
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Org Chem 70:6929-32. 2005
    ..The new C(60)-based cyclobutane derivatives 7a,b and 9 are suitably functionalized for further incorporation into peptide surrogates...
  28. doi request reprint Efficient light harvesters based on the 10-(1,3-dithiol-2-ylidene)anthracene core
    Pierre Antoine Bouit
    IMDEA Nanociencia, Ciudad Universitaria de Cantoblanco, 28049 Madrid, Spain
    Org Lett 15:4166-9. 2013
    ..Electrochemistry and theoretical calculations allowed the understanding of these singular electronic properties. The molecular structures were unambiguously confirmed by X-ray diffraction. ..
  29. ncbi request reprint Spectroscopic characterization of photolytically generated radical ion pairs in single-wall carbon nanotubes bearing surface-immobilized tetrathiafulvalenes
    M Angeles Herranz
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense de Madrid, E 28040 Madrid, Spain
    J Am Chem Soc 130:66-73. 2008
    ..New conduction band electrons, injected from photoexcited exTTF, shift the transitions that are associated with the van Hove singularities to lower energies...
  30. doi request reprint Complexation and Electronic Communication between Corannulene-Based Buckybowls and a Curved Truxene-TTF Donor
    María Gallego
    IMDEA Nanoscience, Faraday 9, Ciudad Universitaria de Cantoblanco, 28049, Madrid, Spain
    Chemistry . 2017
    ..In the case of truxTTF*C38H14, photoexcitation yielded the charge-separated state truxTTF*+*C38H14*- with a lifetime of ~160 ps...
  31. doi request reprint Effect of substituents and protonation on the mechanism of 1,3-dipolar retro-cycloaddition reaction of pyrrolidino[60]- and [70]fullerenes
    Enrique Maroto
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, Madrid, Spain
    J Mass Spectrom 46:1016-29. 2011
    ..The protonation of the NH group inhibits the cycloreversion process, and therefore different fragmentations take place. The detailed mechanisms of the formation and evolution of the intermediate fragments are described...
  32. doi request reprint Tetrafullerene conjugates for all-organic photovoltaics
    Gustavo Fernandez
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040 Madrid, Spain
    J Org Chem 73:3189-96. 2008
    ....
  33. doi request reprint Electroactive carbon nanoforms: a comparative study via sequential arylation and click chemistry reactions
    Jaime Mateos-Gil
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    Nanoscale 7:1193-200. 2015
    ....
  34. pmc Stereodivergent synthesis of chiral fullerenes by [3 + 2] cycloadditions to C₆₀
    Enrique E Maroto
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 136:705-12. 2014
    ..Theoretical DFT calculations are in very good agreement with the experimental data. On the basis of this agreement, a plausible reaction mechanism is proposed. ..
  35. doi request reprint Does a cyclopropane ring enhance the electronic communication in dumbbell-type C₆₀ dimers?
    Andrea La Rosa
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Org Chem 79:4871-7. 2014
    ..This strengthens the idea that cyclopropane behaves as a quasi-double bond. ..
  36. doi request reprint Switching the stereoselectivity: (fullero)pyrrolidines "a la carte"
    Enrique E Maroto
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 134:12936-8. 2012
    ..Fullerenes are revealed as a useful benchmark to develop suitable catalysts to control the stereochemical outcome and to shed light on the mechanism involved in the related 1,3-dipolar cycloaddition. ..
  37. doi request reprint A new exTTF-crown ether platform to associate fullerenes: cooperative n-π and π-π effects
    Bruno Grimm
    Institute of Physical and Theoretical Chemistry and Interdisciplinary Center for Molecular Materials, University of Erlangen, 91058 Erlangen, Germany
    J Am Chem Soc 132:17387-9. 2010
    ....
  38. ncbi request reprint Self-association and electron transfer in donor-acceptor dyads connected by meta-substituted oligomers
    Agustín Molina-Ontoria
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 131:12218-29. 2009
    ..0 micros...
  39. doi request reprint Determining the Attenuation Factor in Molecular Wires Featuring Covalent and Noncovalent Tectons
    Sonia Vela
    Departamento de Quimica Organica I, Facultad de Quimicas, Universidad Complutense de Madrid, 28040, Madrid, Spain
    Angew Chem Int Ed Engl 55:15076-15080. 2016
    ..07±0.01 Å-1 ). Hydrogen-bonding interactions and p-phenylene oligomers of different lengths are responsible for efficient electron transfer in the molecular wires...
  40. doi request reprint Stereodivergent-at-Metal Synthesis of [60]Fullerene Hybrids
    Juan Marco-Martínez
    Departamento de Quimica Organica I, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040, Madrid, Spain
    Angew Chem Int Ed Engl . 2017
    ..DFT calculations underpin the observed configurational stability at the metal center, which does not undergo an epimerization process...
  41. ncbi request reprint Photochemical site-selective synthesis of [70]methanofullerenes
    Sara Vidal
    Organic Chemistry Department, Complutense University of Madrid, Avda Complutense s n, 28040 Madrid, Spain
    Chem Commun (Camb) 52:12733-12736. 2016
    ..Photovoltaic preliminary results revealed a slightly beneficial performance for α-pure [70]PCBM site-isomer devices...
  42. doi request reprint Supramolecular pentapeptide-based fullerene nanofibers: effect of molecular chirality
    Alberto Insuasty
    Departamento de Quimica Organica, Facultad de C C Químicas, Universidad Complutense de Madrid, 28040 Madrid, Spain
    Chem Commun (Camb) 51:10506-9. 2015
    ..The supramolecular organization of new fullerene derivatives endowed with peptides as biomolecular templates affords ordered nanofibers of several micrometres length based on hydrogen bonds and π-π interactions. ..
  43. doi request reprint Reaction of diazocompounds with C70: unprecedented synthesis and characterization of isomeric [5,6]-fulleroids
    Sara Vidal
    Departamento de Quimica Organica I, Facultad de Quimica, Universidad Complutense de Madrid, Avda Complutense s n, 28040 Madrid, Spain
    Chem Commun (Camb) 51:16774-7. 2015
    ..Interestingly, the chemical reactivity of [5,6]-fulleroids reveals the same trend (a > b > c > d) to that observed for pristine C70 (α > β > γ > δ). ..
  44. ncbi request reprint Concave versus planar geometries for the hierarchical organization of mesoscopic 3D helical fibers
    Juan Luis Lopez
    Departamento de Quimica Organica, Facultad de C C Químicas, Universidad Complutense de Madrid, Spain
    Angew Chem Int Ed Engl 51:3857-61. 2012
    ..Control over the hierarchical growth by H bonding, π-π, and solvophobic interactions made possible the efficient generation of electroactive 3D helical fibers...
  45. ncbi request reprint Electron transfer in a supramolecular associate of a fullerene fragment
    María Gallego
    Departamento de Quimica Organica, Fac C C Químicas, Universidad Complutense de Madrid, Av Complutense S N, 28040 Madrid Spain http www ucm es info fullerene
    Angew Chem Int Ed Engl 53:2170-5. 2014
    ....
  46. doi request reprint Asymmetric Organocatalysis in Fullerenes Chemistry: Enantioselective Phosphine-catalyzed Cycloaddition of Allenoates onto C60
    Juan Marco-Martínez
    Departamento de Quimica Organica I, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040 Madrid Spain http www ucm es info fullerene
    Angew Chem Int Ed Engl 52:5115-9. 2013
    ..Furthermore, the sector rule previously used to assign the chirality in [60]fullerenes has been corrected in the light of these new experimental findings...
  47. doi request reprint Controlling the spatial arrangement of organic magnetic anions adsorbed on epitaxial graphene on Ru(0001)
    Daniele Stradi
    Departamento de Quimica, Universidad Autonoma de Madrid, Cantoblanco 28049, Madrid, Spain
    Nanoscale 6:15271-9. 2014
    ....
  48. doi request reprint Highly ordered n/p-co-assembled materials with remarkable charge mobilities
    Javier López-Andarias
    Departamento de Quimica Organica I, Facultad de Ciencias Química, Universidad Complutense, E 28040 Madrid, Spain
    J Am Chem Soc 137:893-7. 2015
    ..This easy methodology offers great possibilities to achieve highly ordered n/p-materials for potential applications in different areas such as optoelectonics and photovoltaics. ..
  49. doi request reprint Modified SWCNTs with amphoteric redox and solubilizing properties
    Laura Rodríguez-Pérez
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, 28040 Madrid Spain, Fax 34 91 394 4103
    Chemistry 20:7278-86. 2014
    ....
  50. ncbi request reprint Modified SWCNTs with Amphoteric Redox and Solubilizing Properties
    Laura Rodríguez-Pérez
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, 28040 Madrid Spain, Fax 34 91 394 4103
    Chemistry 20:7177. 2014
    ..Read the full text of the article at 10.1002/chem.201400183. ..
  51. ncbi request reprint 1H and 13C spectral assignment of 2(1H)-pyridone derivatives
    Dolores Molero
    CAI RMN, Universidad Complutense, E 28040 Madrid, Spain
    Magn Reson Chem 42:704-8. 2004
    ..1H and 13C NMR spectroscopic data for 4-aryl-3,4-dihydro-6-methyl-2(1H)pyridone derivatives were fully assigned by a combination of one- and two- dimensional experiments (DEPT, HMBC, HMQC, COSY, NOE)...
  52. doi request reprint Nanorods versus nanovesicles from amphiphilic dendrofullerenes
    Antonio Muñoz
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, 28040 Madrid, Spain
    J Am Chem Soc 133:16758-61. 2011
    ..These amphiphilic fullerene derivatives aggregate forming micelles, nanorods, or hollow vesicles depending on the concentration and on the solid substrate...
  53. doi request reprint Unambiguous one-molecule conductance measurements under ambient conditions
    Edmund Leary
    Instituto Madrileño de Estudios Avanzados, Facultad de Ciencias Módulo 9, 3a planta Avda Fco Tomás y Valiente, 7 Ciudad Universitaria de Cantoblanco, 28049, Madrid, Spain
    Nano Lett 11:2236-41. 2011
    ..By characterizing and controlling the junction, we can draw stronger conclusions about the observed variation in molecular conductance than was previously possible...
  54. doi request reprint Linear and hyperbranched electron-acceptor supramolecular oligomers
    Jose Santos
    Departamento de Quimica Organica, Facultad de C C Químicas, Universidad Complutense de Madrid, Av Complutense S N, 28040, Madrid, Spain
    Chem Asian J 6:1848-53. 2011
    ..These polymers constitute two of the first examples of n-type supramolecular polymers reported to date...
  55. pmc Electron transfer in Me-blocked heterodimeric alpha,gamma-peptide nanotubular donor-acceptor hybrids
    Roberto J Brea
    Departamento de Quimica Organica, Facultad de Quimica, Universidad de Santiago, E 15782 Santiago de Compostela, Spain
    Proc Natl Acad Sci U S A 104:5291-4. 2007
    ....
  56. ncbi request reprint Materials for organic solar cells: the C60/pi-conjugated oligomer approach
    José L Segura
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, E 28040, Madrid, Spain
    Chem Soc Rev 34:31-47. 2005
    ..In the final section, the applicability of selected materials for the fabrication of photovoltaic devices is analyzed...
  57. doi request reprint Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
    Javier Ramos-Soriano
    Departamento de Quimica Organica, Fac CC Quimicas, Universidad Complutense de Madrid, Av Complutense S N, 28040 Madrid, Spain and Glycosystems Laboratory, Instituto de Investigaciones Químicas IIQ, CSIC Universidad de Sevilla, Av Americo Vespucio 49, 41092 Seville, Spain
    Chem Commun (Camb) 52:10544-6. 2016
    ..This strategy for the obtention of clicked adducts of [60]fullerene is of special interest for biological applications. ..
  58. ncbi request reprint Synthesis and photoluminescent properties of 1,1'-binaphthyl-based chiral phenylenevinylene dendrimers
    Enrique Díez-Barra
    Facultad de Ciencias Quimicas, Universidad de Castilla La Mancha, 13071 Ciudad Real, Spain
    J Org Chem 68:3178-83. 2003
    ..Finally, the redox properties of the dendrimers were determined by cyclic voltammetry, showing the influence of the functional groups at the peripheral positions of the dendrimer on the redox behavior of these systems...
  59. doi request reprint Coordinating Electron Transport Chains to an Electron Donor
    Carmen Villegas
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, 28040, Madrid, Spain
    Org Lett 17:5056-9. 2015
    ..Electrochemical assays corroborate the redox gradients along the designed electron transport chains, and complementary absorption and fluorescence titrations prove the assembly of ZnP-2 and ZnP-3 hybrids. ..
  60. doi request reprint High degree of polymerization in a fullerene-containing supramolecular polymer
    Helena Isla
    Departamento de Quimica Organica, Fac C C Químicas, Universidad Complutense de Madrid, Av Complutense S N, 28040 Madrid Spain http www ucm es info fullerene
    Angew Chem Int Ed Engl 53:5629-33. 2014
    ..A MW above 150 kDa has been found experimentally in solution, while in the solid state the monomer forms extraordinarily long, straight, and uniform fibers with lengths reaching several microns...
  61. doi request reprint Exploiting multivalent nanoparticles for the supramolecular functionalization of graphene with a nonplanar recognition motif
    Fulvio G Brunetti
    IMDEA Nanoscience, C Faraday, 9 Ciudad Universitaria de Cantoblanco, 28049 Madrid, Spain
    Chemistry 19:9843-8. 2013
    ..We amplified these weak forces through multivalent gold nanoparticles. Our results show that planarity is not a prerequisite for recognition motifs for graphene. ..
  62. doi request reprint Formation of self-assembled chains of tetrathiafulvalene on a Cu(100) surface
    Yang Wang
    Departamento de Química C 13, Universidad Autonoma de Madrid, Cantoblanco, Madrid, Spain
    J Phys Chem A 115:13080-7. 2011
    ....
  63. ncbi request reprint Synthesis of soluble donor-acceptor double-cable polymers based on polythiophene and tetracyanoanthraquinodimethane (TCAQ)
    Francesco Giacalone
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense, 28040, Madrid, Spain
    Org Lett 5:1669-72. 2003
    ..The absorption and emission data reveal that the optical properties can be finely tuned by modifying the ratio of monomers in the copolymerization process...
  64. doi request reprint The chemistry of pristine graphene
    Laura Rodríguez-Pérez
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria s n, 28040, Madrid, Spain
    Chem Commun (Camb) 49:3721-35. 2013
    ..Current approaches for the preparation of modified pristine graphene are the aim of this review...
  65. doi request reprint A fully conjugated TTF-π-TCAQ system: synthesis, structure, and electronic properties
    Jose Santos
    Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Complutense, Ciudad Universitaria, 28040 Madrid, Spain
    Chemistry 17:2957-64. 2011
    ..0±0.2) ps) charge recombination to reconstitute the electronic ground state. Such ultrafast charge separation and recombination processes come as a consequence of the very short vinyl linkage between the two electroactive units...
  66. doi request reprint Tuning the electronic properties of nonplanar exTTF-based push-pull chromophores by aryl substitution
    Raul Garcia
    Departamento de Quimica Organica, Facultad de Quimica, Universidad Complutense de Madrid, 28040 Madrid, Spain
    J Org Chem 77:10707-17. 2012
    ..The electronic absorption spectra are characterized by low- to medium-intense charge-transfer bands that extend to the near-infrared...
  67. doi request reprint Chiral recognition of carbon nanoforms
    Emilio M Pérez
    Facultad de Ciencias Módulo C IX, 3ª planta, Ciudad Universitaria de Cantoblanco, Madrid, Spain
    Org Biomol Chem 10:3577-83. 2012
    ....
  68. doi request reprint Wraparound hosts for fullerenes: tailored macrocycles and cages
    David Canevet
    IMDEA Nanociencia, Facultad de Ciencias, Ciudad Universitaria de Cantoblanco, Madrid, Spain
    Angew Chem Int Ed Engl 50:9248-59. 2011
    ..In this Minireview, we highlight some of the important breakthroughs that this class of fullerene hosts has already produced...