scholarly journals Recent Methodologies That Exploit C–C Single-Bond Cleavage of Strained Ring Systems by Transition Metal Complexes

2017 ◽  
Vol 117 (13) ◽  
pp. 9404-9432 ◽  
Author(s):  
Gabriele Fumagalli ◽  
Steven Stanton ◽  
John F. Bower

Molecules ◽  
2021 ◽  
Vol 26 (1) ◽  
pp. 210
Author(s):  
Alexander D. Ryabov

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.



1980 ◽  
Vol 11 (16) ◽  
Author(s):  
J. C. T. R. BURCKETT ST LAURENT ◽  
H. E. HOSSEINI ◽  
J. SINCLAIR ◽  
J. F. NIXON




2017 ◽  
Vol 117 (13) ◽  
pp. 8908-8976 ◽  
Author(s):  
Christopher G. Newton ◽  
Shou-Guo Wang ◽  
Caio C. Oliveira ◽  
Nicolai Cramer


2002 ◽  
Vol 74 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Akio Yamamoto

On the basis of fundamental studies on the carbon­oxygen bond cleavage of various carboxylic acid derivatives, novel, atom-efficient, and environmentally benign catalytic processes to convert them into acids, aldehydes, and ketones have been developed.



1980 ◽  
Vol 44 ◽  
pp. L17-L20 ◽  
Author(s):  
J.C.T.R. Burckett St Laurent ◽  
H.E. Hosseini ◽  
J. Sinclair ◽  
J.F. Nixon


1992 ◽  
Vol 47 (1) ◽  
pp. 74-78 ◽  
Author(s):  
Dieter Sellmann ◽  
Michael Geck ◽  
Matthias Moll

In order to investigate the potential conversion of coordinated NO into N2 ligands at Ru sulfur centers, the cationic Ru nitrosyl complex meso-[Ru(NO)('S5')]Br (1)** was synthesized by template alkylation of [NBu4][Ru(NO)('S2')2]** with (BrC2H4)2S. 1 is reactive towards nucleophiles. Reaction with azide yields N2O, N2 and [Ru('S5')]2 (2), reaction with LiNH2, NH3 and NEt3 leads to C-S bond cleavage in the 'S5' ligand of 1 and to the formation of a Ru nitrosyl vinylthioetherthiolate complex.



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