Procedimiento para la obtención de micro- o nanopartículas sólidas

Procedimiento para la obtencion de micro- o nanoparticulas solidas. La invencion proporciona un nuevo procedimiento para la obtencion de micro- o nanoparticulas solidas con estructura homogenea. Se proporciona un procedimiento que permite obtener micro- o nanoparticulas solidas de estructura homogenea, con un tamano de particula inferior a 10 ƒÊm donde el compuesto solido procesado revela la naturaleza, cristalina, amorfa, polimorfica, etc..., propia del compuesto de partida. De acuerdo con la invencion se proporciona un procedimiento que ademas permite obtener micro- o nanoparticulas solidas con una morfologia sustancialmente esferoidal.Peer reviewedConsejo Superior de Investigaciones Científicas (Esspaña), Centro de Investigación Biomédica en Red en Bioingeniería Biomateriales y Nanomedicina (CIBER-BBN)A1 Solicitud de patente con informe sobre el estado de la técnic

A surface confined yttrium(III) bis-phthalocyaninato complex: a colourful switch controlled by electrons

AMs of a Y(III) double-decker complex on ITO have been prepared and their electrical and optical properties explored, exhibiting three accessible stable redox states with characteristic absorption bands in the visible spectra, corresponding to three complementary colors (i.e., green, blue and red). These absorption bands are exploited as output signals of this robust ternary electrochemical switch, behaving hence as an electrochromic molecular-based device.This work was funded by ERC StG 2012-306826 e-GAMES, the EU project ITN iSwitch (GA no. 642196), the Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), DGI (Spain) BE-WELL CTQ2013-40480-R, and Generalitat de Catalunya 2014-SGR-17. I. A. acknowledges CIBER-BBN for a grant.Peer reviewe

Three Redox States of a Diradical Acceptor−Donor−Acceptor Triad: Gating the Magnetic Coupling and the Electron Delocalization

The diradical acceptor–donor–acceptor triad 1••, based on two polychlorotriphenylmethyl (PTM) radicals connected through a tetrathiafulvalene(TTF)–vinylene bridge, has been synthesized. The generation of the mixed-valence radical anion, 1•–, and triradical cation species, 1•••+, obtained upon electrochemical reduction and oxidation, respectively, was monitored by optical and ESR spectroscopy. Interestingly, the modification of electron delocalization and magnetic coupling was observed when the charged species were generated and the changes have been rationalized by theoretical calculations.This work was supported by the DGI grant (CTQ2013-40480- R), the Networking Research Center on Bioengineering, Biomaterials, and Nanomedicine (CIBER-BBN), and the Generalitat de Catalunya (grant 2014-SGR-17). ICMAB acknowledges support from the Spanish Ministry of Economy and Competitiveness, through the “Severo Ochoa” Programme for Centres of Excellence in R&D (SEV-2015-0496). M.S. is enrolled in the Material Science Ph.D. program of UAB and is grateful to MEC for a FPU predoctoral grant. S.V. and M.F. are thankful to the LabEx-Chemistry of Complex Systems for postdoctoral grants (ANR-10-LABX-0026CSC) and to the regional High-Performance Computing (HPC) center in Strasbourg for computational resources. We thank Amable Bernabé for the MALDI spectroscopy.Peer reviewe

Two-dimensional self-assembly and electrical properties of the donor-acceptor tetrathiafulvalene-polychlorotriphenylmethyl radical on graphite substrates

The electron donor-acceptor tetrathiafulvalene-polychlorotriphenylmethyl (PTM) radical dyad, which shows a strong interplay between intra- and intermolecular charge transfer processes in solution, has been deposited by drop-casting on highly oriented pyrolytic graphite substrates, and its self-assembled structure has been investigated. Conducting atomic force microscopy revealed that the presence of a PTM radical in the molecules enhances the electrical conduction by almost two orders of magnitude and that this enhancement occurs in spite of the poor molecular orientation control achieved with drop-casting. Moreover, the study also reveals that the presence of a tetrathiafulvalene subunit in the deposited molecules can result in slightly asymmetric I-V curves

Organic free radicals as circularly polarized luminescence

Chiroptical properties of two chiral atropisomers of propeller‐like trityl‐based radical derivatives have been analyzed. A new absolute configuration (AC) assignment has been made, according to the combination of experimental and theoretical data. In this sense, their ACs have been determined through the comparison of the Cotton effects recorded by electronic circular dichroism (ECD) with the theoretical ECD of the open shell structures obtained by TD‐DFT calculations. Finally, their circularly polarized luminescence (CPL) responses have been addressed. Remarkably, this is the first description of organic free radicals as intrinsic CPL emitters. Opposite signed CPL has been detected for each pair of conformers, with acceptable luminescent dissymmetry factors (|glum|≈0.5–0.8×10−3) considering their pure organic nature. In fact, highly efficient chiral emissions have been demonstrated, according to the comparison of |glum| with their respective absorption anisotropy factors (|gabs|). This pioneering study lays the foundations for the optimization of new magnetically active organic chiral emitters.The authors are grateful for the financial support received from: MOTHER (MAT2016-80826-R) granted by the DGI (Spain), GenCat (2017-SGR-918) financed by DGR (Catalunya) and the Spanish Ministry of Economy and Competitiveness, through the “Severo Ochoa” Programme for Centres of Excellence in R&D (SEV-2015-0496) and through the “Proyecto interdisciplinar de frontera“, FIP-2018 HECTIC-PTM. We acknowledge the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (ERC-2015-STG-677023). This study has been also supported by the Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), an initiative funded by the VI National R&D&I Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions and financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund. P. M. B. gratefully acknowledges financial support from the Juan de la Cierva-Formación 2015 programme (FJCI-2015-23577) supported by MINECO. A. G. C. also thanks RyC-2013-12943 contract from MINECO. We also acknowledge Prof. O. Trapp for kindly suppling the DCxplorer software

Optimized polarization build-up times in dissolution DNP-NMR using a benzyl amino derivative of BDPA

The synthesis of two novel BDPA-like radicals, a benzyl amino (BAm-BDPA, 7) and a cyano (CN-BDPA, 5) derivative, is reported and their behaviour as polarizing agents for fast dissolution Dynamic Nuclear Polarization (DNP) is evaluated. The radical 7 is a promising candidate for DNP studies since it is soluble in neat [1-13C]pyruvic acid (PA), and therefore the use of an additional glassing agent for sample homogeneity is avoided. In addition, a 60 mM sample of 7 offers optimum 13C NMR signal enhancements using fairly short polarization times (about 1800 s). It is shown that DNP-NMR measurements using 7 can be performed much more efficiently in terms of the signal enhancement per polarization build-up time unit than when using the reference OX63 or BDPA radicals. These enhanced features are translated to a substantial reduction of polarization times that represents an optimum temporary use of the DNP polarizer and allow economized liquid helium consumption.This research was supported by the DGI Grants “POMAs” (CTQ2010-19501) and “Be-Well” (CTQ2013-40480 R), MINECO (CTQ2012-32436), AGAUR Grant (2014SGR-0017) and MINECO Grant (PTA 2011-5037-I) for the subprogram Personal T´ecnico de Apoyo. We also thank the Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), the Consejo Superior de Investigaciones Cient´ıcas for the JAE Grant, and Amable Bernab´e for his work in MALDI spectrometry. NMR studies were carried out at the joint NMR facility of the Universitat Aut`onoma de Barcelona and CIBER-BBN (Cerdanyola del Vall`es).Peer reviewe

Controlled crystallization of Mn12 single-molecule magnets by compressed CO2 and its influence on the magnetization relaxation

6 pages, 6 figures, 2 tables.Micro- and sub-micro particles of complex [Mn12O12(O2CC6H5)16(H2O)4] ( 1) with controlled size and polymorphism have been prepared by dense-gas crystallization techniques, showing a remarkable particle size influence on the magnetization relaxation rates.This work was supported by DGI (Spain) under projects MAT2002-0043 and MAT2003-04699 and by the European Commission under the NoE MAGMANET (Contract NMP3- CT-2005-515767) and QUEMOLNA Marie Curie RTN (Contract MRTN-CT-2003-5044880). Javier Campo and Nora Ventosa thank the Ramon y Cajal Program of Ministerio de Educación y Tecnología (Spain) for their contracts. Maria Muntó thanks the Consejo Superior de Investigaciones Científicas (CSIC) for her PhD bursary and Jordi Gómez- Segura thanks the European Community for his PhD grant.Peer reviewe

Correlation of the EPR properties of perchlorotriphenylmethyl radical and their efficiency as DNP polarizers

Water soluble perchlorinated trityl (PTM) radicals were found to be effective 95 GHz DNP (dynamic nuclear polarization) polarizers in ex situ (dissolution) 13C DNP (Gabellieri et al., Angew Chem., Int. Ed. 2010, 49, 3360). The degree of the nuclear polarization obtained was reported to be dependent on the position of the chlorine substituents on the trityl skeleton. In addition, on the basis of the DNP frequency sweeps it was suggested that the 13C NMR signal enhancement is mediated by the Cl nuclei. To understand the DNP mechanism of the PTM radicals we have explored the 95 GHz EPR characteristics of these radicals that are relevant to their performance as DNP polarizers. The EPR spectra of the radicals revealed axially symmetric g-tensors. A comparison of the spectra with the 13C DNP frequency sweeps showed that although the solid effect mechanism is operational the DNP frequency sweeps reveal some extra width suggesting that contributions from EPR forbidden transitions involving 35,37Cl nuclear flips are likely. This was substantiated experimentally by ELDOR (electron-electron double resonance) detected NMR measurements, which map the EPR forbidden transitions, and ELDOR experiments that follow the depolarization of the electron spin upon irradiation of the forbidden EPR transitions. DFT (density functional theory) calculations helped to assign the observed transitions and provided the relevant spin Hamiltonian parameters. These results show that the 35,37Cl hyperfine and nuclear quadrupolar interactions cause a considerable nuclear state mixing at 95 GHz thus facilitating the polarization of the Cl nuclei upon microwave irradiation. Overlap of Cl nuclear frequencies and the 13C Larmor frequency further facilitates the polarization of the 13C nuclei by spin diffusion. Calculation of the 13C DNP frequency sweep based on the Cl nuclear polarization showed that it does lead to an increase in the width of the spectra, improving the agreement with the experimental sweeps, thus supporting the existence of a new heteronuclear assisted DNP mechanism

An Enantiopure Propeller‐Like Trityl‐Brominated Radical: Bringing Together a High Racemization Barrier and an Efficient Circularly Polarized Luminescent Magnetic Emitter

A new persistent organic free radical has been synthetized with Br atoms occupying the ortho‐ and para‐positions of a trityl core. After the isolation of its two propeller‐like atropisomers, Plus (P) and minus (M), their absolute configurations were assigned by a combination of theoretical and experimental data. Remarkably, no hints of racemization were observed up to 60 °C for more than two hours, due to the higher steric hindrance imposed by the bulky Br atoms. Therefore, when compared to its chlorinated homologue (t1/2=18 s at 60 °C), an outstanding stability against racemization was achieved. A circularly polarized luminescence (CPL) response of both enantiomers was detected. This free radical shows a satisfactory luminescent dissymmetry factor (|glum(592 nm)|≈0.7×10−3) despite its pure organic nature and low luminescence quantum yield (LQY). Improved organic magnetic CPL emitters derived from the reported structure can be envisaged thanks to the wide possibilities that Br atoms at para‐positions offer for further functionalization.The authors are grateful for the financial support received from: MOTHER project (MAT2016-80826-R) granted by the DGI (Spain), GenCat (2017-SGR-918) financed by DGR (Catalunya) and the Spanish Ministry of Economy and Competitiveness (PGC2018-095808-B-I00 and PGC2018-101181-B-I00 projects) and through the “Severo Ochoa” Programme for Centres of Excellence in R&D (SEV-2015-0496) and through the “Proyecto Interdisciplinar de Frontera“, FIP-2018 HECTIC-PTM. We acknowledge the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (ERC-2015-STG-677023). This study has been also supported by the Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), an initiative funded by the VI National R&D&I Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions and financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund. P. M. B. gratefully acknowledges financial support from the Juan de la Cierva-Formación 2015 programme (FJCI-2015-23577) supported by MINECO and, together with J.V, A. G. C. also thanks RyC-2013-12943 contract from MINECO. We also thankthe Servei de Ressonància Magnètica Nuclear, Universitat Autònoma de Barcelona, for allocating instrument time to this project