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- Publisher Website: 10.1002/chem.201000880
- Scopus: eid_2-s2.0-78249232005
- PMID: 20859961
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Article: Syntheses and photophysical properties of N-pyridylimidazol-2-ylidene tetracyanoruthenates(II) and photochromic studies of their dithienylethene- containing derivatives
Title | Syntheses and photophysical properties of N-pyridylimidazol-2-ylidene tetracyanoruthenates(II) and photochromic studies of their dithienylethene- containing derivatives |
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Authors | |
Keywords | carbenes heterocycles photochromism ruthenium triplet sensitization |
Issue Date | 2010 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/chemistry |
Citation | Chemistry - A European Journal, 2010, v. 16 n. 42, p. 12642-12649 How to Cite? |
Abstract | A series of tetracyanoruthenate(II) with chelating pyridyl N-heterocyclic carbene ligands (NHC-py) was synthesized and characterized. Their photophysical and electrochemical properties as well as the photochromic behavior of their dithienylethene-containing complexes were studied. Photocyclization was found to take place upon irradiation into the metal-to-ligand charge transfer (MLCT) absorption bands of these complexes, and evidence is provided to support the triplet-sensitizing reaction pathway. Enlightening chemistry: Luminescent tetracyanoruthenates(II) with chelating pyridyl N-heterocyclic carbene ligands have been synthesized and their dithienylethene-containing complexes have been shown to display interesting photochromic properties (see figure). © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Persistent Identifier | http://hdl.handle.net/10722/133594 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.058 |
References |
DC Field | Value | Language |
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dc.contributor.author | Duan, G | en_HK |
dc.contributor.author | Yam, VWW | en_HK |
dc.date.accessioned | 2011-05-24T02:11:33Z | - |
dc.date.available | 2011-05-24T02:11:33Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Chemistry - A European Journal, 2010, v. 16 n. 42, p. 12642-12649 | en_HK |
dc.identifier.issn | 0947-6539 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/133594 | - |
dc.description.abstract | A series of tetracyanoruthenate(II) with chelating pyridyl N-heterocyclic carbene ligands (NHC-py) was synthesized and characterized. Their photophysical and electrochemical properties as well as the photochromic behavior of their dithienylethene-containing complexes were studied. Photocyclization was found to take place upon irradiation into the metal-to-ligand charge transfer (MLCT) absorption bands of these complexes, and evidence is provided to support the triplet-sensitizing reaction pathway. Enlightening chemistry: Luminescent tetracyanoruthenates(II) with chelating pyridyl N-heterocyclic carbene ligands have been synthesized and their dithienylethene-containing complexes have been shown to display interesting photochromic properties (see figure). © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_HK |
dc.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/chemistry | en_HK |
dc.relation.ispartof | Chemistry - A European Journal | en_HK |
dc.subject | carbenes | en_HK |
dc.subject | heterocycles | en_HK |
dc.subject | photochromism | en_HK |
dc.subject | ruthenium | en_HK |
dc.subject | triplet sensitization | en_HK |
dc.title | Syntheses and photophysical properties of N-pyridylimidazol-2-ylidene tetracyanoruthenates(II) and photochromic studies of their dithienylethene- containing derivatives | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0947-6539&volume=16&issue=42&spage=12642&epage=12649&date=2010&atitle=Syntheses+and+photophysical+properties+of+N-pyridylimidazol-2-ylidene+tetracyanoruthenates(II)+and+photochromic+studies+of+their+dithienylethene-containing+derivatives | - |
dc.identifier.email | Yam, VWW:wwyam@hku.hk | en_HK |
dc.identifier.authority | Yam, VWW=rp00822 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/chem.201000880 | en_HK |
dc.identifier.pmid | 20859961 | - |
dc.identifier.scopus | eid_2-s2.0-78249232005 | en_HK |
dc.identifier.hkuros | 185269 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78249232005&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 16 | en_HK |
dc.identifier.issue | 42 | en_HK |
dc.identifier.spage | 12642 | en_HK |
dc.identifier.epage | 12649 | en_HK |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Duan, G=36623500000 | en_HK |
dc.identifier.scopusauthorid | Yam, VWW=18539304700 | en_HK |
dc.identifier.issnl | 0947-6539 | - |