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Metal-to-metal electron-transfer emission in cyanide-bridged chromium : ruthenium complexes : effects of configurational mixing between ligand field and charge transfer excited states

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Metal-to-metal electron-transfer emission in cyanide-bridged chromium : ruthenium complexes : effects of configurational mixing between ligand field and charge transfer excited states

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dc.contributor.author Chen, Yuan-Jang pl
dc.contributor.author Odongo, Onduru S. pl
dc.contributor.author McNamara, Patrick G. pl
dc.contributor.author Szaciłowski, Konrad [SAP11115985] pl
dc.contributor.author Endicott, John F. pl
dc.date.accessioned 2015-08-21T12:17:31Z
dc.date.available 2015-08-21T12:17:31Z
dc.date.issued 2008 pl
dc.identifier.issn 0020-1669 pl
dc.identifier.uri http://ruj.uj.edu.pl/xmlui/handle/item/14830
dc.language eng pl
dc.title Metal-to-metal electron-transfer emission in cyanide-bridged chromium : ruthenium complexes : effects of configurational mixing between ligand field and charge transfer excited states pl
dc.type JournalArticle pl
dc.description.physical 10921-10934 pl
dc.abstract.en Irradiations of the transition metal-to-transition metal charge transfer (MMCT) absorption bands of a series of cyanide-bridged chromium(III)-ruthenium(II) complexes at 77 K leads to near-infrared emission spectra of the corresponding chromium(II)-ruthenium(III) electron transfer excited states. The lifetimes of most of the MMCT excited states increase more than 10-fold when their am(m)ine ligands are perdueterated. These unique emissions have weak, low frequency vibronic sidebands that correspond to the small excited-state distortions in metal-ligand bonds that are characteristic of transition metal electron transfer involving only the non-bonding metal centered d-orbitals suggesting that the excited-state Cr(II) center has a triplet spin configuration. However, most of the electronically excited complexes probably have overall doublet spin multiplicity and exhibit an excitation energy dependent dual emission with the near in energy Cr(III)-centered and MMCT doublet excited states forming an unusual mixed valence pair. pl
dc.description.volume 47 pl
dc.description.number 23 pl
dc.identifier.doi 10.1021/ic8011266 pl
dc.identifier.eissn 1520-510X pl
dc.title.journal Inorganic Chemistry pl
dc.language.container eng pl
dc.subtype Article pl


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