Abstract
The new very-intense vertical-axis Laue diffractometer (VIVALDI) at the Institut Laue-Langevin has been used to probe the single-crystal structure of [(t-Bu2AlMe2)(2)Li](-)[{Ph(2-C5H4N)N}(6)HLi8](+), with data proving that the molecular main-group-metal cluster cation component incorporates interstitial hydride. Variations in nitrogen coordination mode and distortion of the metal core are in accord with octahedral hydride coordination (H-Li = 1.92(2), 2.04(2), 2.07(2) Angstrom), two metal centers being nonbonding with respect to hydride ((HLi)-Li-... = 2.86(2) Angstrom).
| Original language | English |
|---|---|
| Pages (from-to) | 4527-4530 |
| Number of pages | 4 |
| Journal | Organometallics |
| Volume | 23 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 2004 |
Bibliographical note
ID number: ISI:000223991700001Fingerprint
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