Synthesis of [POCOP]-pincer iron and cobalt complexes via Csp3–H activation and catalytic application of iron hydride in hydrosilylation reactions

RSC Advances ◽  
2015 ◽  
Vol 5 (20) ◽  
pp. 15660-15667 ◽  
Author(s):  
Shaofeng Huang ◽  
Hua Zhao ◽  
Xiaoyan Li ◽  
Lin Wang ◽  
Hongjian Sun

Csp3–H bond activation in pincer ligand (Ph2PO(o-C6H2-(4,6-tBu2)))2CH2 (1) (POCH2OP) was achieved by Fe(PMe3)4 and CoMe(PMe3)4 to afford (POCHOP)Fe(H) (PMe3)2 (2) and (POCHOP)Co(PMe3)2 (4).

2018 ◽  
Vol 42 (6) ◽  
pp. 4646-4652 ◽  
Author(s):  
Hua Zhang ◽  
Junyang Xing ◽  
Yanhong Dong ◽  
Shangqing Xie ◽  
Shishuai Ren ◽  
...  

The sp2 C–H bond activation of the HCN moiety in diphenylphosphino benzalimines was realized using CoMe(PMe3)4 with the elimination of methane.


2018 ◽  
Vol 42 (19) ◽  
pp. 15578-15586 ◽  
Author(s):  
Fei Yang ◽  
Yangyang Wang ◽  
Faguan Lu ◽  
Shangqing Xie ◽  
Xinghao Qi ◽  
...  

[CNC]-pincer Co hydrides were synthesized via selective C–H/C–F activation and catalyzed hydrosilylation of carbonyl compounds.


2020 ◽  
Vol 44 (35) ◽  
pp. 15109-15121
Author(s):  
Adelew Estifanos Filkale ◽  
Chandni Pathak

Biaryl scaffolding ligands form dicobalt clusters, which serve as efficient catalysts in enaminone synthesis under ambient conditions.


2019 ◽  
Vol 38 (21) ◽  
pp. 4093-4104 ◽  
Author(s):  
Lennart T. Scharf ◽  
Alexander Kowsari ◽  
Thorsten Scherpf ◽  
Kai-Stephan Feichtner ◽  
Viktoria H. Gessner

RSC Advances ◽  
2015 ◽  
Vol 5 (25) ◽  
pp. 19402-19408 ◽  
Author(s):  
Gengyu Zhu ◽  
Lin Wang ◽  
Hongjian Sun ◽  
Xiaoyan Li

The introduction and changes of the substituents at the middle carbon atom of the preligand dipyrrolmethane have a significant impact on the reaction results.


2021 ◽  
Author(s):  
alexander Reckziegel ◽  
Manjinder Kour ◽  
Beatrice Battistella ◽  
Stefan Mebs ◽  
Katrin Beuthert ◽  
...  

We report on the synthesis of a variety of trigonal imido cobalt complexes [Co(NAryl)L<sub>2</sub>)<sup>–</sup>, (L = N(Dipp)SiMe<sub>3</sub>), Dipp = 2,6-diisopropylphenyl) bearing very long Co–NAryl bonds of around 1.75 Å. The electronic structure was interrogated using a variety of physical and spectroscopic methods indicating the first authenticated examples of cobalt bound imidyl species. Computational studies corroborate these findings and reveal that the high-spin state of these complexes gives rise to unpaired spin-density on the imide nitrogen and leads to its imidyl character. Obtained complexes are capable of intermolecular H atom abstraction from C–H bonds that yields the corresponding cobalt amides. Exchange of the Dipp-substituent on the imide by the smaller mesityl function (2,4,6-trimethylphenyl) effectuates the unexpected Me<sub>3</sub>Si shift from the ancillary ligand set to the imide nitrogen, followed by intramolecular C–H bond activation.<br>


2020 ◽  
Vol 26 (53) ◽  
pp. 12194-12205 ◽  
Author(s):  
Daniel Werner ◽  
Uwe Bayer ◽  
Dorothea Schädle ◽  
Reiner Anwander

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