1981
DOI: 10.1002/9780470166291.ch2
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Chlorotris(Triphenylphosphine)Rhodium(I): Its Chemical and Catalytic Reactions

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Cited by 118 publications
(11 citation statements)
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“…The interaction of hydrogen with transition metals is a key process in organometallic chemistry. Furthermore, reversible oxidative addition and reductive elimination reactions of H 2 with transition metal complexes constitute fundamental steps in many catalytic cycles. , Such processes have been widely studied not only in organometallic chemistry but also in surface chemistry and hydrogenase enzymes , and in connection with their relevance to chemical hydrogen storage. , In effect, the binding, storage, and release of H 2 under mild conditions are of major importance, but despite the investigations of several H 2 carrier species, e.g., amine borane, Mg, , or Al , systems, there have been relatively few instances where reversible absorption and release of hydrogen has been effected under mild conditions for main-group compounds. Two examples involve the use of metal-free frustrated Lewis pair systems and antiaromatic boron-containing organic rings . In addition, several main-group compounds have been shown to react with H 2 under ambient conditions to yield hydrides. These include low-valent group 13 and 14 element compounds, which feature frontier orbitals with small energy separations and suitable symmetry to react with H 2 and whose reactivity can mimic that of transition metal complexes .…”
mentioning
confidence: 99%
“…The interaction of hydrogen with transition metals is a key process in organometallic chemistry. Furthermore, reversible oxidative addition and reductive elimination reactions of H 2 with transition metal complexes constitute fundamental steps in many catalytic cycles. , Such processes have been widely studied not only in organometallic chemistry but also in surface chemistry and hydrogenase enzymes , and in connection with their relevance to chemical hydrogen storage. , In effect, the binding, storage, and release of H 2 under mild conditions are of major importance, but despite the investigations of several H 2 carrier species, e.g., amine borane, Mg, , or Al , systems, there have been relatively few instances where reversible absorption and release of hydrogen has been effected under mild conditions for main-group compounds. Two examples involve the use of metal-free frustrated Lewis pair systems and antiaromatic boron-containing organic rings . In addition, several main-group compounds have been shown to react with H 2 under ambient conditions to yield hydrides. These include low-valent group 13 and 14 element compounds, which feature frontier orbitals with small energy separations and suitable symmetry to react with H 2 and whose reactivity can mimic that of transition metal complexes .…”
mentioning
confidence: 99%
“…[1] Late transition metals employed to catalyze this transformation have exhibited impressive performances. In its homogeneous incarnation, transition-metal catalyzed hydrogenation is best mediated by rhodium (notably Wilkinsons catalyst) [2] or iridium [3] complexes. Other metals have fared better in heterogeneous systems, as is the case for palladium whose use in its supported form, Pd/C, is ubiquitous.…”
mentioning
confidence: 99%
“…Transition metal complexes are widely used as homogeneous catalysts in the synthesis of fine chemicals, natural products, and pharmaceuticals. One of the most prominent homogeneous catalysts is Wilkinson’s catalyst [RhCl­(PPh 3 ) 3 ]. It was first utilized as efficient catalyst in various chemical conversions such as hydrogenation of alkenes and alkynes, hydrosilylation, oxidation, and isomerization. Importantly, the catalytic activity of Wilkinson’s catalyst in hydrogenation has been successfully employed in the synthesis of pharmaceuticals such as the antiparasitic agent ivermectin, , whose antiviral property is currently discussed in the context of COVID-19 treatment . Moreover, Wilkinson’s catalyst has been applied efficiently in parahydrogen induced polarization (PHIP) to boost sensitivity in liquid NMR and to study reaction intermediates in the catalytic cycle …”
Section: Introductionmentioning
confidence: 99%