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dc.contributor.authorGuajardo Maturana R.
dc.contributor.authorMuñoz-Castro A.
dc.date.accessioned2020-09-02T22:19:29Z
dc.date.available2020-09-02T22:19:29Z
dc.date.issued2016
dc.identifier10.1016/j.cplett.2016.03.013
dc.identifier.citation651, , 34-38
dc.identifier.issn00092614
dc.identifier.urihttps://hdl.handle.net/20.500.12728/4756
dc.descriptionThe successive addition of one, two and three equivalents of iodide to [Au3(CH3N=COCH3)3], gives rise to the [Au3In(CH3N=COCH3)3] (n = 2, 4, 6) oxidized systems. Such structures have been studied by using scalar relativistic DFT calculations and TD-DFT. Our results demonstrate a stronger ligand-to-metal charge donation, which increases in covalency. The long metal-metal contacts observed through the series result from the similarly population of bonding, non-bonding and slightly anti-bonding combinations of the 6s-Au atomic shells in the [Au3]n+ core, leading to distances in the range of the sum of their van der Waals radii for all the systems. © 2016 Elsevier B.V. All rights reserved.
dc.language.isoen
dc.publisherElsevier B.V.
dc.titleInsights into metal-ligand and metal-metal interaction in coinage metal triangles. Insights of d10-d10, d10-d8 and d8-d8 contacts from [Au3In(CH3N=COCH3)3] (n = 2, 4, 6) via relativistic DFT calculations
dc.typeArticle


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