Synthesis and characterization of the hypoelectronic ruthenaborane {(eta(5)-C5Me5)Ru}(2){eta(6)-C6H6)Ru}B7H7}

Citation
Xj. Lei et al., Synthesis and characterization of the hypoelectronic ruthenaborane {(eta(5)-C5Me5)Ru}(2){eta(6)-C6H6)Ru}B7H7}, ORGANOMETAL, 20(7), 2001, pp. 1479-1481
Citations number
18
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
20
Issue
7
Year of publication
2001
Pages
1479 - 1481
Database
ISI
SICI code
0276-7333(20010402)20:7<1479:SACOTH>2.0.ZU;2-7
Abstract
The thermal conversion ofcommo-{1-(Cp*Ru)(mu -H)B4H9}(2)Ru, 1, into {(eta ( 5)-C5Me5)Ru}(2){eta (6)-C6H6)Ru}B7H7}, 2, is described. Compound 2 is a sin gle cage, hypoelectronic triruthenaborane in which the C6H6 ligand is deriv ed from the reaction solvent. As an (n -1) skeletal electron pair (sep) clo sed, deltahedral cluster, 2 constitutes a structural link between 10 fragme nt metallaboranes with (n + 1) and (n) sep as well as with one with (n - 2) sep. This series establishes a connection between decreasing average coord ination number of the cluster boron atoms with decreasing sep thereby provi ding a useful B-11 NMR chemical shift correlation.