Abstract
A survey of the use of Os-187 satellite subspectra in H-1 and P-31{H-1} spectra of triosmium carbonyl clusters is reported. By varying evolution delays in HMQC spectra of [Os-3(mu-H)(2)(CO)(10)] we have selectively extracted the values for (1)J(Os,H) and (2)J(Os,H), respectively. An analysis of the principal modes of phosphine coordination in triosmium clusters demonstrates that P-31{H-1} Os-187 satellite subspectra are diagnostic for equatorial coordination [(1)J(Os, P) = 211-223 Hz] or for axial coordination (perpendicular to the plane of the cluster) [(1)J(Os, P) approximate to 147 Hz]. Chelating and bridging diphosphines yield Os-187 satellite subspectra which are the sum of A(2)X and AA'X spin systems. If significant P-P coupling is present, the AA'X component requires simulation. All observed (2)J(Os,P) trans-equatorial couplings fall in the range 38-65 Hz. Copyright (C) 2001 John Wiley Sons, Ltd.
| Original language | English |
|---|---|
| Pages (from-to) | 107-113 |
| Journal | Magnetic Resonance in Chemistry |
| Volume | 40 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 2002 |
Subject classification (UKÄ)
- Inorganic Chemistry
Free keywords
- constants
- coupling
- satellite analysis
- H-1 NMR
- P-31 NMR
- NMR
- Os-187 NMR
- triosmium carbonyl clusters