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Probing elementary steps of nickel-mediated bond activation in gas-phase reactions: Ligand- and cluster-size effects
Ist Teil von
Journal of catalysis, 2011-12, Vol.284 (2), p.126-137
Ort / Verlag
San Diego: Elsevier Inc
Erscheinungsjahr
2011
Link zum Volltext
Quelle
Elsevier ScienceDirect Journals Complete
Beschreibungen/Notizen
With a little help from my friends: While “naked” Ni
+ is reluctant to bring about bond activation of small inert molecules, ligated species as well as nickel-containing dimeric clusters NiM
+ can activate methane and ethane, respectively. A summary of nickel chemistry in the gas phase is presented which is not only characterized by a remarkable reactivity that can be tuned by ligands over a broad scope, but also by a large diversity with respect to the reaction mechanisms observed for the individual gaseous nickel species.
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► Generation and reactivity of nickel species in the gas phase. ► Reactivity of gaseous nickel complexes tuned by ligands over a broad scope. ► A plethora of different reaction mechanisms observed for gaseous nickel species.
Mass-spectrometry-based experiments, complemented by computational studies, are presented which demonstrate the richness of nickel-containing reagents when employed in various bond-activation processes and conducted under single-collision conditions. We will address the chemistry of “naked” atomic Ni
+, the dramatic effects of ligands L or of the size of clusters, which they exhibit in thermal reactions of NiL
+ or
Ni
n
+
(
n
=
2–30). Special emphasis will be paid to identify elementary steps and to uncover mechanistic principles; as an example, various aspects of the face-selective dehydrogenation of cyclohexane by homo- and heteronuclear cluster-ion dimers are discussed in some detail for the first time.