Publication:
Synthesis and photochemical response of Ru(II)-coordinated double-decker silsesquioxane

dc.contributor.authorsKucuk, Asuman Celik; Matsui, Jun; Miyashita, Tokuji
dc.date.accessioned2022-03-14T08:43:42Z
dc.date.accessioned2026-01-11T13:40:29Z
dc.date.available2022-03-14T08:43:42Z
dc.date.issued2018
dc.description.abstractA double-decker silsesquioxane based bis(terpyridine) ruthenium(II) complex (2Tpy/Ru-DDSQ), a member of the polyhedral oligomeric silsesquioxane (POSS) class, has been synthesized. Its structure has been characterized using comprehensive techniques such as nuclear magnetic resonance (H-1 NMR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and UV-visible spectroscopy. This work not only deals with the synthesis of 2Tpy/Ru-DDSQ but also provides the first comprehensive investigation based on the photoluminescence and electrochemical features of a POSS member. With this structure, an efficient anodic photocurrent response has been obtained. This result has been attributed to the perfect arrangement of ruthenium(II)-bis(terpyridine) (tpy) ([Ru(Tpy)(2)](2+)) moieties in the DDSQ nano building blocks. Therefore, 2Tpy/Ru-DDSQ can be considered as a promising candidate for the development of new generation photosensitizers.
dc.identifier.doi10.1039/C7RA12290J
dc.identifier.issn2046-2069
dc.identifier.urihttps://hdl.handle.net/11424/242181
dc.identifier.wosWOS:000422863900055
dc.language.isoeng
dc.publisherROYAL SOC CHEMISTRY
dc.relation.ispartofRSC ADVANCES
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMETALLO-SUPRAMOLECULAR POLYMERS
dc.subjectSURFACE-PLASMON RESONANCE
dc.subjectSULFATE MICELLAR-SOLUTION
dc.subjectRUTHENIUM(II) COMPLEXES
dc.subjectBUILDING-BLOCKS
dc.subjectNETWORKS
dc.subjectCORE
dc.subjectLUMINESCENCE
dc.subjectNANOPARTICLE
dc.subjectENHANCEMENT
dc.titleSynthesis and photochemical response of Ru(II)-coordinated double-decker silsesquioxane
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage2156
oaire.citation.issue4
oaire.citation.startPage2148
oaire.citation.titleRSC ADVANCES
oaire.citation.volume8

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