Tailor-Made Luminescent Polymers through Unusual Metallophilic Interaction Arrays Au⋯Au⋯Ag⋯Ag
- Gil-Moles, M. 1
- Gimeno, M.C. 2
- López-De-Luzuriaga, J.M. 1
- Monge, M. 1
- Olmos, M.E. 1
- Pascual, D. 1
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1
Universidad de La Rioja
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2
Universidad de Zaragoza
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ISSN: 0020-1669
Year of publication: 2017
Volume: 56
Issue: 15
Pages: 9281-9290
Type: Article
More publications in: Inorganic Chemistry
Metrics
JCR (Journal Impact Factor)
- Year 2017
- Journal Impact Factor: 4.7
- Journal Impact Factor without self cites: 4.085
- Article influence score: 0.975
- Best Quartile: Q1
- Area: CHEMISTRY, INORGANIC & NUCLEAR Quartile: Q1 Rank in area: 5/45 (Ranking edition: SCIE)
SCImago Journal Rank
- Year 2017
- SJR Journal Impact: 1.892
- Best Quartile: Q1
- Area: Inorganic Chemistry Quartile: Q1 Rank in area: 6/73
- Area: Chemistry (miscellaneous) Quartile: Q1 Rank in area: 34/480
- Area: Physical and Theoretical Chemistry Quartile: Q1 Rank in area: 20/174
Scopus CiteScore
- Year 2017
- CiteScore of the Journal : 8.1
- Area: Inorganic Chemistry Percentile: 91
- Area: Physical and Theoretical Chemistry Percentile: 88
Journal Citation Indicator (JCI)
- Year 2017
- Journal Citation Indicator (JCI): 1.93
- Best Quartile: Q1
- Area: CHEMISTRY, INORGANIC & NUCLEAR Quartile: Q1 Rank in area: 1/46
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Abstract
A novel and efficient strategy for the synthesis of luminescent polymers bearing metallophilic interactions with unprecedented charge sequences has been designed. For this end suitable basic gold units such as [AuR2]-, bearing perhalophenyl derivatives, and dinuclear acid silver terpyridine species, [Ag2(terpy)2](CF3SO3)2, have been chosen. Their combination originates the polymeric derivatives [{AuR2}2Ag2(terpy)2]n (R = C6F5, C6Cl2F3) or [{Au(C6Cl5)2}Ag(terpy)]n. The change of the perhalophenyl group in the gold complex modulates the strength in the metallophilic contacts and, consequently, the polymer arrays and luminescent properties. The X-ray diffraction studies of these derivatives revealed that there are polymers with unusual + + - - + + - - charge sequences for the R = C6F5 and C6Cl2F3 species, whereas the more classical + - + - disposition was found for the bulkiest C6Cl5 derivative. Their luminescent properties also vary depending on the formation of these polymer arrays, and time-dependent density functional theory calculations were performed to determine the origin of the luminescence. © 2017 American Chemical Society.