Synthesis and Characterization of Bi- and Trinuclear Molybdenum Carbonyl Compounds Obtained by Ligand Exchange Reactions of [Et4N]3[Mo3(CO)9(OMe)3]

2004 ◽  
Vol 23 (6) ◽  
pp. 1352-1358 ◽  
Author(s):  
Rafael A. Adrian ◽  
Marsha M. Yaklin ◽  
Kevin K. Klausmeyer
2013 ◽  
Vol 68 (5-6) ◽  
pp. 518-532 ◽  
Author(s):  
Claas Loh ◽  
Carsten Glock ◽  
Steffen Ziemann ◽  
Helmar Görls ◽  
Sven Krieck ◽  
...  

The metathesis reaction of strontium diiodide [(thf)5SrI2] with K[N(Ph)iPr] in THF yields [(thf)4Sr{N(Ph)iPr}2] (1). Ligand exchange reactions with 1,2-dimethoxyethane (DME), tetramethylethylenediamine (TMEDA), and pentamethyldiethylenetriamine (PMDETA) allow the isolation of the corresponding adducts [(dme)2Sr{N(Ph)iPr}2] (2), [(tmeda)(thf)Sr{N(Ph)iPr}2] (3) and [(pmdeta)Sr{N(Ph)iPr}2] (4), respectively. Magnesiation of N-isopropylaniline with dibutylmagnesium in THF leads to the formation of [(thf)2Mg{N(Ph)iPr}2] (5). A similar reaction in TMEDA gives nearly insoluble crystalline [(tmeda)Mg{N(Ph)iPr}2] (7), whereas the mother liquor contains heteroleptic [(tmeda)(nBu)Mg{N(Ph)iPr}] (6). Magnesiation of N-isopropylaniline in 2,2,5,5-tetramethyltetrahydrofuran (Me4thf) yields [(Me4thf)Mg{N(Ph)iPr}2] (8) with a threecoordinate metal center. In hydrocarbons this complex loses the bulky ether base, and the solvent-free dimer [Mg{N(Ph)iPr}2]2 (9) can be isolated. Reaction of this complex with 1,2- dimethoxyethane or metalation of N-isopropylaniline with dibutylmagnesium in DME yield the dme adduct, [(dme)Mg{N(Ph)iPr}2] (10). The crystal structures show that the nitrogen atoms of the magnesium-bound N-isopropylanilide ions are in planar environments whereas strontium-bound N-isopropylanilide ions show rather short contacts between the alkaline earth metal and the ipsocarbon atoms of the phenyl groups leading to a pyramidalization of the coordination of the nitrogen atoms


Synthesis ◽  
2018 ◽  
Vol 50 (09) ◽  
pp. 1737-1749 ◽  
Author(s):  
Tetsuaki Fujihara ◽  
Yasushi Tsuji

Herein, copper-catalyzed borylative and silylative transformations of allenes using borylcopper or silylcopper as the active catalytic species are described. First, the synthesis and characterization of borylcopper and silylcopper complexes are briefly introduced. Next, the borylative transformations of allenes are summarized including hydro­boration, carboboration, and borylative allylation of carbonyl compounds. We next deal with the silylative transformations of allenes such as hydrosilylation, carbosilylation, and silylative allylation of carbonyl compounds.1 Introduction2 Synthesis of Borylcopper and Silylcopper Complexes3 Borylative Transformations4 Silylative Transformations5 Conclusions and Future Outlook


2020 ◽  
Vol 4 (1) ◽  
pp. 46-58
Author(s):  
Saema Salim ◽  
Qamar Ali

Hydrazones are a unique division of compounds found in various syntheses. They have an important role in synthetic chemistrydue to their different biological properties, such as antifungal, anticonvulsant, antibacterial, antimalarial, anti-inflammatory and anti-TB properties. This paper reports the syntheses of a series of 3 hydrazones based on the condensation of 2,4-dimethylphenyl hydrazine HCl with different aromatic carbonyl compounds. The structures of the synthesized compounds were confirmed by EIMS. These compounds can act as ideal candidates in chemosensor chemistry.


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