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dc.contributor.authorMuñoz Gómez, José Les_ES
dc.contributor.authorMonteagudo, Evaes_ES
dc.contributor.authorLloveras, Vegaes_ES
dc.contributor.authorParella, Teodores_ES
dc.contributor.authorVeciana, Jaumees_ES
dc.contributor.authorVidal Gancedo, Josées_ES
dc.date.accessioned2017-04-27T13:50:28Z-
dc.date.available2017-04-27T13:50:28Z-
dc.date.issued2016-02-22-
dc.identifier.citationRSC Advances 6(32): 27077-27082 (2016)es_ES
dc.identifier.issn2046-2069-
dc.identifier.urihttp://hdl.handle.net/10261/148936-
dc.description.abstractThe 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.es_ES
dc.description.sponsorshipThis 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´ıcas 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).es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2013-40480 Res_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccesses_ES
dc.subjectDynamic nuclear-polarizationes_ES
dc.subjectMagnetic-resonancees_ES
dc.subjectEnhanced NMRes_ES
dc.subjectSpectroscopyes_ES
dc.titleOptimized polarization build-up times in dissolution DNP-NMR using a benzyl amino derivative of BDPAes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1039/C6RA00635C-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1039/C6RA00635Ces_ES
dc.contributor.funderDirección General de Investigación Científica y Técnica, DGICT (España)es_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España)es_ES
dc.contributor.funderGeneralitat de Catalunyaes_ES
dc.contributor.funderCentro de Investigación Biomédica en Red Bioingeniería, Biomateriales y Nanomedicina (España)es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002809es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100005053es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100008737es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
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item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeartículo-
item.cerifentitytypePublications-
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