Carbon-hydrogen bond activation by transition metal complexes. Oxidative addition of alkyl methacrylate to ruthenium. The structure of hydrido(2-n-butoxycarbonylpropenyl-C1,O)tris(triphenylphosphine)ruthenium(II)

1976 ◽  
Vol 98 (13) ◽  
pp. 3874-3884 ◽  
Author(s):  
Sanshiro Komiya ◽  
Takashi Ito ◽  
Martin Cowie ◽  
Akio Yamamoto ◽  
James A. Ibers
Keyword(s):  
Hydrogen Bond ◽  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Bond Activation ◽  
Oxidative Addition ◽  
Alkyl Methacrylate ◽  
Carbon Hydrogen Bond Activation

Aerobic oxygenation catalyzed by first row transition metal complexes coordinated by tetradentate mono-carbon bridged bis-phenanthroline ligands: intra- versus intermolecular carbon–hydrogen bond activation

2019 ◽  
Vol 48 (19) ◽  
pp. 6396-6407 ◽  
Author(s):  
Kaiji Shen ◽  
Yael Diskin-Posner ◽  
Linda J. W. Shimon ◽  
Gregory Leitus ◽  
Raanan Carmieli ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Transition Metal ◽  
Hydrogen Bonds ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Bond Activation ◽  
Carbon Hydrogen Bond Activation ◽  
Carbon Hydrogen Bonds ◽  
Phenanthroline Ligands

Intra- and intermolecular aerobic oxygenation is initiated by activation of carbon–hydrogen bonds and/or O2 and propagated by an autoxidation pathway.

Recent Advances in Transition Metal Catalyzed C-H Functionalization Reactions Involving Aza/Oxabicyclic Alkenes

Synthesis ◽  
2021 ◽  
Author(s):  
Masilamani Jeganmohan ◽  
Pinki Sihag
Keyword(s):  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Ring Opening ◽  
Bond Activation ◽  
Considerable Progress ◽  
Double Bonds ◽  
Facial Selectivity ◽  
Ring Opening Reactions ◽  
Metal Catalyzed

Bicyclic alkenes, including Oxa- and azabicyclic alkenes can be readily activated by using transition-metal complexes with facial selectivity, because of the intrinsic angle strain on carbon-carbon double bonds of these unsymmetrical bicyclic systems. During last decades considerable progress has been done in the area of ring-opening of bicyclic strained ring by employing the concept of C-H activation. This Review comprehensively compiles the various C-H bond activation assisted reactions of oxa- and azabicyclic alkenes, viz., ring-opening reactions, hydroarylation as well as annulation reactions.

scholarly journals The Exchange of Cyclometalated Ligands

Molecules ◽  
2021 ◽  
Vol 26 (1) ◽  
pp. 210
Author(s):  
Alexander D. Ryabov
Keyword(s):  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Bond Activation ◽  
Bond Cleavage ◽  
Cyclopalladated Complexes ◽  
Derivatives Of ◽  
Cyclometalated Ligand ◽  
Incoming Ligand

Reactions of cyclometalated compounds are numerous. This account is focused on one of such reactions, the exchange of cyclometalated ligands, a reaction between a cyclometalated compound and an incoming ligand that replaces a previously cyclometalated ligand to form a new metalacycle: + H-C*~Z ⇄ + H-C~Y. Originally discovered for PdII complexes with Y/Z = N, P, S, the exchange appeared to be a mechanistically challenging, simple, and convenient routine for the synthesis of cyclopalladated complexes. Over four decades it was expanded to cyclometalated derivatives of platinum, ruthenium, manganese, rhodium, and iridium. The exchange, which is also questionably referred to as transcyclometalation, offers attractive synthetic possibilities and assists in disclosing key mechanistic pathways associated with the C–H bond activation by transition metal complexes and C–M bond cleavage. Both synthetic and mechanistic aspects of the exchange are reviewed and discussed.

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