Aviso: para depositar documentos, por favor, inicia sesión e identifícate con tu cuenta de correo institucional de la UCM con el botón MI CUENTA UCM. No emplees la opción AUTENTICACIÓN CON CONTRASEÑA
 

Improving the mesomorphism in bispyrazolate Pd(II) metallomesogens: an efficient platform for ionic conduction

dc.contributor.authorCuerva de Alaiz, Cristian
dc.contributor.authorCano Esquivel, María Mercedes
dc.contributor.authorSchmidt, Rainer
dc.date.accessioned2024-01-18T11:57:30Z
dc.date.available2024-01-18T11:57:30Z
dc.date.issued2023-02-07
dc.description.abstractThe introduction of structural asymmetry in metallomesogens is an established strategy to improve their mesomorphic behaviour in terms of lower melting temperatures and higher stability ranges of the mesophase, which is particularly important for metallomesogens that have potential application as electrolytes that require wide operational temperature ranges. Here in this work, a novel series of unsymmetrical bis(isoquinolinylpyrazolate)palladium(ii) compounds bearing four alkyl side-chains with different lengths are described. Rectangular and hexagonal columnar mesophases were formed with low melting temperatures of 42-45 degrees C in most cases, whereas the clearing temperatures reached values up to 412 degrees C. The charge transport properties have been studied by complex impedance spectroscopy, showing that the mesophase favours proton conduction in the absence of water or humidity. The exceptional thermal stability of these species makes them promising candidates to act as a platform for ionic conduction via the nanochannels originated in the columnar mesophases. The results presented confirm that introducing structural asymmetry in the Pd(ii) metallomesogens studied is a valid strategy to enhance the liquid crystalline properties, which opens new ways to develop water-free electrolytes based on unsymmetrical bis(isoquinolinylpyrazolate) Pd(ii) compounds for potential applications such as proton exchange membranes (PEMs).
dc.description.departmentDepto. de Física de Materiales
dc.description.facultyFac. de Ciencias Físicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipComunidad de Madrid
dc.description.sponsorshipUniversidad Complutense de Madrid
dc.description.statuspub
dc.identifier.citationCuerva, C., Cano, M., & Schmidt, R. (2023). Improving the mesomorphism in bispyrazolate Pd (II) metallomesogens: an efficient platform for ionic conduction. Dalton Transactions, 52(15), 4684-4691.
dc.identifier.doi10.1039/d2dt03754h
dc.identifier.essn1477-9234
dc.identifier.issn1477-9226
dc.identifier.officialurlhttps://pubs.rsc.org/en/content/articlelanding/2023/dt/d2dt03754h
dc.identifier.urihttps://hdl.handle.net/20.500.14352/93817
dc.issue.number15
dc.journal.titleDalton Transactions
dc.language.isoeng
dc.page.final4691
dc.page.initial4684
dc.publisherRoyal Society of Chemistry
dc.relation.projectIDCTQ2015-63858-P
dc.relation.projectIDPID2020-118078RB-100
dc.relation.projectIDY2020/NMT-6661
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu538.9
dc.subject.keywordColumnar mesophases
dc.subject.keywordPyrazolate ligands
dc.subject.keywordComplexes
dc.subject.ucmFísica del estado sólido
dc.subject.unesco2211 Física del Estado Sólido
dc.titleImproving the mesomorphism in bispyrazolate Pd(II) metallomesogens: an efficient platform for ionic conduction
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number52
dspace.entity.typePublication
relation.isAuthorOfPublication0376118d-4d5f-4c35-84ac-718b0178234c
relation.isAuthorOfPublication59784fb3-ebc6-4a19-82f7-a9ab1a3bd642
relation.isAuthorOfPublication4d468566-fa66-4e1c-8463-382517edca6e
relation.isAuthorOfPublication.latestForDiscovery0376118d-4d5f-4c35-84ac-718b0178234c

Download

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
C. Cuerva et al. Dalton Trans. 52 (2023) p4684_RG.pdf
Size:
3.44 MB
Format:
Adobe Portable Document Format

Collections