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dc.contributor.authorYuriy V. Zatsikhaen_US
dc.contributor.authorCole D. Holstromen_US
dc.contributor.authorKullapa Chanawannoen_US
dc.contributor.authorAllen J. Osinskien_US
dc.contributor.authorChristopher J. Ziegleren_US
dc.contributor.authorVictor N. Nemykinen_US
dc.date.accessioned2018-09-05T03:33:50Z-
dc.date.available2018-09-05T03:33:50Z-
dc.date.issued2017-01-01en_US
dc.identifier.issn1520510Xen_US
dc.identifier.issn00201669en_US
dc.identifier.other2-s2.0-85018509543en_US
dc.identifier.other10.1021/acs.inorgchem.6b02806en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018509543&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/57009-
dc.description.abstract© 2017 American Chemical Society. The 1,3,7,9-tetraferrocenylazadipyrromethene (3) and the corresponding 1,3,5,7-tetraferrocene aza-BODIPY (4) were prepared via three and four synthetic steps, respectively, starting from ferrocenecarbaldehyde using the chalcone-type synthetic methodology. The novel tetra-iron compounds have ferrocene groups directly attached to both the α- and the β-pyrrolic positions, and the shortest Fe-Fe distance determined by X-ray crystallography for 3 was found to be ∼6.98 Å. These new compounds were characterized by UV-vis, nuclear magnetic resonance, and high-resolution electrospray ionization mass spectrometry methods, while metal-metal couplings in these systems were probed by electro- and spectroelectrochemistry, chemical oxidations, and Mossbauer spectroscopy. Electrochemical data are suggestive of the well-separated stepwise oxidations of all four ferrocene groups in 3 and 4, while spectroelectrochemical and chemical oxidation experiments allowed for characterization of the mixed-valence forms in the target compounds., while spectroelectrochemical and chemical oxidation experiments allowed for characterization of the mixed-valence forms in the target compounds.. Intervalence charge-transfer band analyses indicate that the mixed-valence [3]+and [4]+complexes belong to the weakly coupled class II systems in the Robin-Day classification. This interpretation was further supported by Mossbauer spectroscopy in which two individual doublets for Fe(II) and Fe(III) centers were observed in room-temperature experiments for the mixed-valence [3]n+and [4]n+species (n = 1-3). The electronic structure, redox properties, and UV-vis spectra of new systems were correlated with Density Functional Theory (DFT) and time-dependent DFT calculations (TDDFT), which are suggestive of a ferrocene-centered highest occupied molecular orbital and chromophore-centered lowest unoccupied molecular orbital in 3 and 4 as well as predominant spin localization at the ferrocene fragment attached to the α-pyrrolic positions in [3]+and [4]+.en_US
dc.subjectChemistryen_US
dc.titleObservation of the strong electronic coupling in near-infrared-absorbing tetraferrocene aza-dipyrromethene and aza-BODIPY with direct ferrocene-α- and ferrocene-β-pyrrole bonds: Toward molecular machinery with four-bit information storage capacityen_US
dc.typeJournalen_US
article.title.sourcetitleInorganic Chemistryen_US
article.volume56en_US
article.stream.affiliationsUniversity of Minnesota Duluthen_US
article.stream.affiliationsUniversity of Manitobaen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Akronen_US
Appears in Collections:CMUL: Journal Articles

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