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dc.contributor.authorPal, Amlan K.
dc.contributor.authorAdusumalli, Venkata Nanda Kishor Babu
dc.date.accessioned2020-09-02T23:34:27Z
dc.date.available2020-09-02T23:34:27Z
dc.date.issued2019-09-03
dc.identifier261011857
dc.identifier27378438-093f-4dcd-bb1b-11ed6d3ca481
dc.identifier85072596645
dc.identifier000487373300001
dc.identifier.citationPal , A K & Adusumalli , V N K B 2019 , ' Panchromatic Ru(II)-polypyridyl complexes as NIR emitters ' , New Journal of Chemistry , vol. In press . https://doi.org/10.1039/C9NJ03644Jen
dc.identifier.issn1144-0546
dc.identifier.otherORCID: /0000-0002-5677-5070/work/61370159
dc.identifier.urihttps://hdl.handle.net/10023/20538
dc.descriptionAKP thanks the Leverhulme Trust for an early career fellowship (ECF-2017-326), ScotCHEM for a short-term Postgraduate and Early Career Researcher Exchange (PECRE) fellowship and University of St Andrews for financial support. VNKBA thanks the UGC for a fellowship.en
dc.description.abstractTwo novel mer-Ru(II) heteroleptic complexes containing stongly donating tridendate ligands (dgpy and dgpz) were synthesised and optoelectronically characterised. These complexes exhibited quasi-reversible ligand- and metal-based redox events and panchromatic absorption with the lowest energy absorption maxima trailing up to 750 nm. These panchromatic dyes were found to be NIR emissive at λPL ~ 835 nm with associated excited-state lifetimes (τPL) of ~ 10 ns. The enhanced photophysical properties of these complexes compared to those of [Ru(tpy)2]2+ (tpy = 2,2′:6′,2′′-terpyridine; λabs < 575 nm, λPL ~ 629 nm and τPL ~ 0.25 ns) are due to the larger 3MLCT-3MC energy-gap as a combined effect of larger bite angle and strong σ-donation offered by the dgpy and dgpz ligands.
dc.format.extent4
dc.format.extent1250129
dc.language.isoeng
dc.relation.ispartofNew Journal of Chemistryen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titlePanchromatic Ru(II)-polypyridyl complexes as NIR emittersen
dc.typeJournal articleen
dc.contributor.sponsorThe Leverhulme Trusten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.1039/C9NJ03644J
dc.description.statusPeer revieweden
dc.date.embargoedUntil2020-09-03
dc.identifier.grantnumberECF-2017-326en


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