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dc.contributor.authorMuñoz-Castro A.
dc.date.accessioned2020-09-02T22:24:09Z
dc.date.available2020-09-02T22:24:09Z
dc.date.issued2020
dc.identifier10.1039/c9cp05790k
dc.identifier.citation22, 3, 1422-1426
dc.identifier.issn14639076
dc.identifier.urihttps://hdl.handle.net/20.500.12728/5518
dc.descriptionδ-Bonds have been intimately related to metal-metal bonds of d-elements since the archetypal d4-d4 [Re2Cl8]2- ion with a σ2π4δ2 bond. Currently, the notion of multiple superatom arrangements as initial steps toward molecular materials within the building-up approach is dominated by P-shell characteristics, as given in the well-described Au25(SR)18 ligand protected cluster. In this work we rationalize the Au22(dppo)6 cluster as a triple-bonded 22-valence electron (ve) supermolecule, featuring a bonding scheme based on 1D + 1D shell combinations, which largely contrasts with the 14-ve Au38(SR)24 with mainly 1P + 1P patterns mimicking a F2 molecule. The resulting Π4Δ2-bonding pattern shows an unprecedented superatomic counterpart of a d-shell based bond inherently related to transition-metal dimers, adding useful key aspects to the understanding of species based on cluster-assembly. © 2020 the Owner Societies.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.titleTriple 1D1D superatomic bonding. Au22(dppo)6 as a Π4- And Δ2-triply bonded cluster based on Au11 assembled units
dc.typeArticle


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