Achiral and chiral NNN-pincer nickel complexes with oxazolinyl backbone: application in transfer hydrogenation of ketones

2021 ◽  
Author(s):  
Rahul A Jagtap ◽  
Shidheshwar B Ankade ◽  
Rajesh G. Gonnade ◽  
Benudhar Punji

We describe the synthesis of new NNN-oxazolinyl pincer nickel complexes and their application in the transfer hydrogenation of ketones. The achiral NNN-ligands, R’2-oxazolinyl-2-C6H4-NH-C(O)CH2NEt2 [(R’2-OxNNNEt2)–H; R’ = H (3a), R’ =...

2019 ◽  
Vol 33 (6) ◽  
pp. e4932 ◽  
Author(s):  
Zijing Wang ◽  
Xiaoyan Li ◽  
Shangqing Xie ◽  
Tingting Zheng ◽  
Hongjian Sun

Author(s):  
Samaila Abubakar ◽  
Musa Muktari ◽  
Rifkatu Kambel Dogara

We reported the antimicrobial activities of cobalt and nickel complexes containing imino-NHC ligands. Complex 2 was synthesized by direct reaction of the insitu generated free carbene from 2-[2-(3-benzylimidazol-1-yl)ethyliminomethyl]phenol ligand with NiCl2 diglyme while complexes 3-5 were previously reported as catalysts in the transfer hydrogenation reaction of ketones. The compounds 1-5 were screened for antimicrobial sensitivity test against four gram-negative bacteria Escherichia Coli (E-coli), Shigella, Klebsiella Pneumoniae (K. Pneumoniae) and Salmonella Typhi (S.Typhi) and a gram positive bacteria Staphylocossus aureus (S.aureus). At a varying concentrations of 100, 200, 300, 400 and 500 µg/mL, significant activities were recorded using disc diffusion methods. The cobalt complex 3 was found to have higher activities compared with the corresponding nickel complexes and among the three nickel complexes, nickel complex with pyridine as wingtip was found to be more active than the one with a benzyl group. Similarly, the nickel centre with mononuclear was found to be more active than the tri-nuclear nickel complex.  Except for the cobalt complex 3 no activity was recorded against S. typhi for all the nickel compounds. 


2016 ◽  
Vol 45 (25) ◽  
pp. 10389-10401 ◽  
Author(s):  
Daniel A. Zurita ◽  
Marcos Flores-Alamo ◽  
Juventino J. García

The one-pot synthesis of 1,2-disubstituted benzimidazoles by the transfer hydrogenation of azobenzene, using benzylamine as a hydrogen donor is reported, catalyzed by 2 mol% of [Ni(COD)2] : dippe.


2018 ◽  
Vol 873 ◽  
pp. 8-14 ◽  
Author(s):  
Tiffany V. Roach ◽  
Michelle L. Schmitz ◽  
Valkyrie A. Leach ◽  
Marcus D. Miller ◽  
Benny C. Chan ◽  
...  

2020 ◽  
Author(s):  
Shogo Mori ◽  
Takahiro Aoki ◽  
Kaliyamoorthy Selvam ◽  
Shunichi Fukuzumi ◽  
Jieun Jung ◽  
...  

Despite the continuing popularity of radical reactions in organic synthesis, much remains to be explored in this area. Herein, we describe how spatiotemporal control can be exerted over the formation and reactivity of divergent exchangeable formamide radicals using nickel complexes with a semiconductor material (TiO<sub>2</sub>) under irradiation from near-UV–Vis light. Depending on the bipyridine ligand used and the quantity of the nickel complex that is hybridized on or nonhydridized over the TiO<sub>2</sub> surface, these radicals selectively undergo substitution reactions at the carbon center of carbon–bromine bonds that proceed via three different pathways. As the scalable production of formamides from CO<sub>2</sub> does not produce salt waste, these methods could add a new dimension to the search for carbon neutrality through the indirect incorporation of CO<sub>2</sub> into organic frameworks.


2021 ◽  
Vol 23 (5) ◽  
pp. 1910-1914
Author(s):  
Yuhan Wang ◽  
Zhiqian Chang ◽  
Yan Hu ◽  
Xiao Lin ◽  
Xiaowei Dou

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