Abstract
The triallylphosphine-substituted clusters [Ru-3(CO)(10){P(CH2CH=CH2)(3)}], [Ru-3(CO)(10){P(CH2CH=CH2)(3)}(2)] and [Ru-3(CO)(10) {sigma;pi-CH2=CHCH2P(CH2CH=CH2)(2)}] have been prepared; reaction of [Ru-3(CO)(10){sigma;pi-CH2=CHCH2P(CH2CH=CH2)(2)}] with phosphines/phosphites leads to cleavage of the Ru-allyl pi-bond and formation of [Ru-3(CO)(11){P(CH2CH=CH2)(3)}(PR3)]. (C) 2004 Elsevier B.V. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 443-446 |
| Number of pages | 4 |
| Journal | Inorganic Chemistry Communications |
| Volume | 7 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2004 |
Bibliographical note
ID number: ISI:000189229800037Fingerprint
Dive into the research topics of 'Reversible pi-coordination of triallylphosphine in a trinuclear ruthenium carbonyl cluster'. Together they form a unique fingerprint.Cite this
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