Article: Organoplatinum(II) complexes with chromophore-acceptor dyad studied by ultrafast time-resolved absorption spectroscopy

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TitleOrganoplatinum(II) complexes with chromophore-acceptor dyad studied by ultrafast time-resolved absorption spectroscopy
AuthorsLai, SW1 3
Chen, Y3
Kwok, WM1 2
Zhao, XJ3
To, WP1
Fu, WF3
Che, CM1
KeywordsChromophores
Electron transfer
Hydrogen
Platinum
Viologen
Issue Date2010
PublisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley-vch.de/publish/en/journals/alphabeticIndex/2451
CitationChemistry - An Asian Journal, 2010, v. 5 n. 1, p. 60-65 [How to Cite?]
DOI: http://dx.doi.org/10.1002/asia.200900304
AbstractThe photoinduced ET reaction from Pt IIchromophore to viologen acceptor in a new ultrafast time-resolved absorption spectroscopy has been reported. Photoinduced electron-transfer (ET) reactions are fundamental steps in photosynthesis, and which have led to extensive investigations into charge-separated species in artificial mimics. The development of the absorption maxima at 395 and 605 nm could be attributed to the formation of methyl viologen radical cation as a result of oxidative decomposition of TEOA. The back ET reaction rate constants of the two platinum (II) systems are slower than the forward electron-transfer reactions, despite the large driving force. Efforts to harness the slow back ET reactions of Pt II chromophore acceptor systems for light-induced multi-electron-transfer catalysis are in progress.
ISSN1861-4728
2011 Impact Factor: 4.5
2011 SCImago Journal Rankings: 0.391
DOIhttp://dx.doi.org/10.1002/asia.200900304
ISI Accession Number IDWOS:000273712600007
Funding AgencyGrant Number
State Key Project2007CB613304
National Natural Science Foundation of China/Research Grants Council Joint Research SchemeN_HKU 752/08
50418010
20671094
90610034
Research Grants Council of Hong KongHKU 7011/07P
HKU 7030/06P
The Chinese Academy of Sciences-Croucher Foundation Funding Scheme
Funding Information:

The authors are grateful to the State Key Project (2007CB613304), the National Natural Science Foundation of China/Research Grants Council Joint Research Scheme (N_HKU 752/08, 50418010), the National Natural Science Foundation of China (20671094, 90610034), Research Grants Council of Hong Kong (HKU 7011/07P, HKU 7030/06P), and The Chinese Academy of Sciences-Croucher Foundation Funding Scheme For Joint Laboratories for financial support.

ReferencesReferences in Scopus
GrantsPhosphorescent supramolecular metal-organic receptors for chemical recognition and biomolecular binding applications
Self-assembled metal coordination polymers and supramolecular systems containing π-conjugated organic ligands
DC Field
Value
dc.contributor.authorLai, SW
dc.contributor.authorChen, Y
dc.contributor.authorKwok, WM
dc.contributor.authorZhao, XJ
dc.contributor.authorTo, WP
dc.contributor.authorFu, WF
dc.contributor.authorChe, CM
dc.date.accessioned2010-09-06T06:21:12Z
dc.date.available2010-09-06T06:21:12Z
dc.date.issued2010
dc.description.abstractThe photoinduced ET reaction from Pt IIchromophore to viologen acceptor in a new ultrafast time-resolved absorption spectroscopy has been reported. Photoinduced electron-transfer (ET) reactions are fundamental steps in photosynthesis, and which have led to extensive investigations into charge-separated species in artificial mimics. The development of the absorption maxima at 395 and 605 nm could be attributed to the formation of methyl viologen radical cation as a result of oxidative decomposition of TEOA. The back ET reaction rate constants of the two platinum (II) systems are slower than the forward electron-transfer reactions, despite the large driving force. Efforts to harness the slow back ET reactions of Pt II chromophore acceptor systems for light-induced multi-electron-transfer catalysis are in progress.
dc.description.grantPhosphorescent supramolecular metal-organic receptors for chemical recognition and biomolecular binding applications
dc.description.grantSelf-assembled metal coordination polymers and supramolecular systems containing π-conjugated organic ligands
dc.description.grantcode82627
dc.description.grantcode99415
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationChemistry - An Asian Journal, 2010, v. 5 n. 1, p. 60-65 [How to Cite?]
DOI: http://dx.doi.org/10.1002/asia.200900304
dc.identifier.doihttp://dx.doi.org/10.1002/asia.200900304
dc.identifier.epage65
dc.identifier.hkuros170115
dc.identifier.isiWOS:000273712600007
Funding AgencyGrant Number
State Key Project2007CB613304
National Natural Science Foundation of China/Research Grants Council Joint Research SchemeN_HKU 752/08
50418010
20671094
90610034
Research Grants Council of Hong KongHKU 7011/07P
HKU 7030/06P
The Chinese Academy of Sciences-Croucher Foundation Funding Scheme
Funding Information:

The authors are grateful to the State Key Project (2007CB613304), the National Natural Science Foundation of China/Research Grants Council Joint Research Scheme (N_HKU 752/08, 50418010), the National Natural Science Foundation of China (20671094, 90610034), Research Grants Council of Hong Kong (HKU 7011/07P, HKU 7030/06P), and The Chinese Academy of Sciences-Croucher Foundation Funding Scheme For Joint Laboratories for financial support.

dc.identifier.issn1861-4728
2011 Impact Factor: 4.5
2011 SCImago Journal Rankings: 0.391
dc.identifier.issue1
dc.identifier.openurl
dc.identifier.pmid20014089
dc.identifier.scopuseid_2-s2.0-73949130804
dc.identifier.spage60
dc.identifier.urihttp://hdl.handle.net/10722/70258
dc.identifier.volume5
dc.languageeng
dc.publisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley-vch.de/publish/en/journals/alphabeticIndex/2451
dc.publisher.placeGermany
dc.relation.ispartofChemistry - An Asian Journal
dc.relation.referencesReferences in Scopus
dc.subjectChromophores
dc.subjectElectron transfer
dc.subjectHydrogen
dc.subjectPlatinum
dc.subjectViologen
dc.titleOrganoplatinum(II) complexes with chromophore-acceptor dyad studied by ultrafast time-resolved absorption spectroscopy
dc.typeArticle
Author Affiliations
  1. The University of Hong Kong
  2. Hong Kong Polytechnic University
  3. Technical Institute of Physics and Chemistry Chinese Academy of Sciences