File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/0010-8545(90)80082-5
- Scopus: eid_2-s2.0-0003127134
- WOS: WOS:A1990CM32600008
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Photochemistry and photophysics of Trans-d2-dioxo complexes of osmium(VI)
Title | Photochemistry and photophysics of Trans-d2-dioxo complexes of osmium(VI) |
---|---|
Authors | |
Issue Date | 1990 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ccr |
Citation | Coordination Chemistry Reviews, 1990, v. 97, p. 93-104 How to Cite? |
Abstract | Trans-[OsVI(L)(O)2](ClO4)2 (where L= I4TMC, ISTMC, 1GTMC, CRMe3) and trans-[OsVI(CN)4(O)2](Ph4AS) 2 complexes display vibronic structured pin-allowed and spin-forbidden transitions at 300-320 and 345-370nm. The 3[(dxy)1(dπ)1] excited states of trarts-dioxoosmium(VI) are emissive and long-lived [lifetimes 0.4 to 1.6μs] both in solid state and in fluid solutions. For trans-[OsVI(l4TMC)(O)2]2+, the Os=O bond in the 3[(dxy)1(dπ)1) state is Ca. O,063Å longer than in the ground state. Trans-dioxoosmium(VI) complexes function as a powerful one-electron oxidant with E(OsVI/OsV) ranging from 1.1 to 2.3V vs. N.H.E. Photo-induced oxygen atom transfer reactions have been observed with trialkyiphosphines, dialkylsuiphides, and alkenes. |
Persistent Identifier | http://hdl.handle.net/10722/167374 |
ISSN | 2021 Impact Factor: 24.833 2020 SCImago Journal Rankings: 5.166 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yam, VWW | en_US |
dc.contributor.author | Che, CM | en_US |
dc.date.accessioned | 2012-10-08T03:06:11Z | - |
dc.date.available | 2012-10-08T03:06:11Z | - |
dc.date.issued | 1990 | en_US |
dc.identifier.citation | Coordination Chemistry Reviews, 1990, v. 97, p. 93-104 | en_US |
dc.identifier.issn | 0010-8545 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/167374 | - |
dc.description.abstract | Trans-[OsVI(L)(O)2](ClO4)2 (where L= I4TMC, ISTMC, 1GTMC, CRMe3) and trans-[OsVI(CN)4(O)2](Ph4AS) 2 complexes display vibronic structured pin-allowed and spin-forbidden transitions at 300-320 and 345-370nm. The 3[(dxy)1(dπ)1] excited states of trarts-dioxoosmium(VI) are emissive and long-lived [lifetimes 0.4 to 1.6μs] both in solid state and in fluid solutions. For trans-[OsVI(l4TMC)(O)2]2+, the Os=O bond in the 3[(dxy)1(dπ)1) state is Ca. O,063Å longer than in the ground state. Trans-dioxoosmium(VI) complexes function as a powerful one-electron oxidant with E(OsVI/OsV) ranging from 1.1 to 2.3V vs. N.H.E. Photo-induced oxygen atom transfer reactions have been observed with trialkyiphosphines, dialkylsuiphides, and alkenes. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ccr | en_US |
dc.relation.ispartof | Coordination Chemistry Reviews | en_US |
dc.title | Photochemistry and photophysics of Trans-d2-dioxo complexes of osmium(VI) | en_US |
dc.type | Article | en_US |
dc.identifier.email | Yam, VWW:wwyam@hku.hk | en_US |
dc.identifier.email | Che, CM:cmche@hku.hk | en_US |
dc.identifier.authority | Yam, VWW=rp00822 | en_US |
dc.identifier.authority | Che, CM=rp00670 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/0010-8545(90)80082-5 | - |
dc.identifier.scopus | eid_2-s2.0-0003127134 | en_US |
dc.identifier.volume | 97 | en_US |
dc.identifier.spage | 93 | en_US |
dc.identifier.epage | 104 | en_US |
dc.identifier.isi | WOS:A1990CM32600008 | - |
dc.publisher.place | Netherlands | en_US |
dc.identifier.scopusauthorid | Yam, VWW=18539304700 | en_US |
dc.identifier.scopusauthorid | Che, CM=7102442791 | en_US |
dc.identifier.issnl | 0010-8545 | - |