Synthesis and characterization of N-heterocyclic carbene–M⋯OEt2 complexes (M = Cu, Ag, Au). Analysis of solvated auxiliary-ligand free [(NHC)M]+ species

Author(s):  
Alvaro Muñoz-Castro ◽  
Guocang Wang ◽  
Tharun Teja Ponduru ◽  
H. V. Rasika Dias

We report the synthesis, characterization and computational analysis of coinage metal-ether and related –OH2 complexes supported by N-heterocyclic carbenes (NHC), SIPr and Et2CAAC.

RSC Advances ◽  
2015 ◽  
Vol 5 (101) ◽  
pp. 83149-83154 ◽  
Author(s):  
Di Kang ◽  
Xiaoyan Song ◽  
Jinfeng Xing

Rare-earth upconversion nanoparticles (UCNPs) with α and β phases were prepared. UCNPs with core–shell structure were prepared and modified to be hydrophilic by ligand-free hydrophilic modification.


Polyhedron ◽  
2018 ◽  
Vol 154 ◽  
pp. 382-389 ◽  
Author(s):  
T. Scattolin ◽  
L. Canovese ◽  
F. Visentin ◽  
C. Santo ◽  
N. Demitri

2011 ◽  
Vol 30 (10) ◽  
pp. 2755-2764 ◽  
Author(s):  
Christoph Topf ◽  
Christa Hirtenlehner ◽  
Manfred Zabel ◽  
Manuela List ◽  
Michel Fleck ◽  
...  

2013 ◽  
Vol 32 (11) ◽  
pp. 3135-3144 ◽  
Author(s):  
Animesh Das ◽  
Chandrakanta Dash ◽  
Mehmet Ali Celik ◽  
Muhammed Yousufuddin ◽  
Gernot Frenking ◽  
...  

2014 ◽  
Vol 137 (1) ◽  
pp. 162-164 ◽  
Author(s):  
Bin Li ◽  
Jiancheng Li ◽  
Herbert W. Roesky ◽  
Hongping Zhu

2006 ◽  
Vol 84 (2) ◽  
pp. 269-276 ◽  
Author(s):  
Floria Antolini ◽  
Peter B Hitchcock ◽  
Alexei V Khvostov ◽  
Michael F Lappert

The synthesis and characterization of complexes obtained from the reactions between Li[N-t-Bu(SiMe3)] (A) or the sodium analogue Na[N-t-Bu(SiMe3)] (B) and the cyanoarene RCN (R = Ph or 4-MeOC6H4) are discussed. These are the THF adduct [Li{µ-cis-N(t-Bu)C(Ph)N(SiMe3)}(THF)]2 (1), the TMEDA adduct Li[N(t-Bu)C(Ph)N(SiMe3)](TMEDA) (2), the neutral ligand-free lithium benzamidinate Li[N(t-Bu)C(C6H4OMe-4)N(SiMe3)] (3), and the THF adduct Li[N(t-Bu)C(C6H4OMe-4)N(SiMe3)](THF) (3a). The preparation and structure of the crystalline compound [Na{µ-cis-N(t-Bu)C(Ph)N(SiMe3)}(OEt2)]2 (4) is described. From the lithium benzamidinate 1 and Sn(II) chloride the tin(II) complex [Sn{N(t-Bu)C(Ph)N(SiMe3)}2] (5) was obtained. The molecular structures of the crystalline compounds 1, 4, and 5 were established by X-ray diffraction. In 1 and 4 the benzamidinato ligand is both chelating and bridging, with the Me3Si-substituted nitrogen atom as the bridging site. The central planar (MN)2 four-membered ring is a rhombus in 1, with almost equal Li—N bond lengths, whereas in 4 the bonds to Na(1) are significantly longer than those to Na(2). In 5, the ligand is N,N′-chelating. Key words: alkali metals, tin(II), benzamidinates, NMR spectra, X-ray structures.


2019 ◽  
Vol 31 (5) ◽  
pp. 1149-1152
Author(s):  
Mohammed Mujbel Hasson ◽  
Basim H. Al-Zaidi ◽  
Ahmad H. Ismail

Two new unsymmetrical imidazolium salts viz., [1-(4-ethylphenyl)-3-propyl-1H-imidazole-3-ium bromide] (3) and [1-(2,6-dimethylphenyl)-3-propyl-1H-imidazole-3-ium bromide] (4) have been synthesized via the reaction of propyl bromide with imidazole derivatives, [1-(4-ethylphenyl)-1Himidazole] (1) and [1-(2,6-dimethylphenyl)-1H-imidazole] (2) in absence of solvent. Then two new N-heterocyclic carbene silver complexes (5 and 6) were prepared through the reaction of imidazoluim salts (3 and 4) as a source of N-heterocyclic carbene with Ag2O by in situ method. These complexes can be used in the future as a transfer agent for preparing other transitional metal carbine complexes (NHCs) via transmetallation method. The formation of these compounds was confirmed by spectral analysis.


Sign in / Sign up

Export Citation Format

Share Document