scholarly journals Characterization of a transient +2 sulfur oxidation state intermediate from the oxidation of aqueous sulfide

10.2172/97033 ◽  
1995 ◽  
Author(s):  
M.A. Vairavmurthy ◽  
Weiqing Zhou
Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4139
Author(s):  
Barbora Vénosová ◽  
Ingrid Jelemenská ◽  
Jozef Kožíšek ◽  
Peter Rapta ◽  
Michal Zalibera ◽  
...  

Two 15-membered octaazamacrocyclic nickel(II) complexes are investigated by theoretical methods to shed light on their affinity forwards binding and reducing CO2. In the first complex 1[NiIIL]0, the octaazamacrocyclic ligand is grossly unsaturated (π-conjugated), while in the second 1[NiIILH]2+ one, the macrocycle is saturated with hydrogens. One and two-electron reductions are described using Mulliken population analysis, quantum theory of atoms in molecules, localized orbitals, and domain averaged fermi holes, including the characterization of the Ni-CCO2 bond and the oxidation state of the central Ni atom. It was found that in the [NiLH] complex, the central atom is reduced to Ni0 and/or NiI and is thus able to bind CO2 via a single σ bond. In addition, the two-electron reduced 3[NiL]2− species also shows an affinity forwards CO2.


2021 ◽  
Author(s):  
Ruth Weller ◽  
Lutz Ruppach ◽  
Alena Shlyaykher ◽  
Frank Tambornino ◽  
Gunnar Werncke

Herein we describe the synthesis and characterization of a variety of new quasilinear metal(I/II) silylamides of the type [M(N(Dipp)SiR3)2]0,− (M = Cr − Co) with different silyl substituents (SiR3 =...


2011 ◽  
Vol 418-420 ◽  
pp. 617-620
Author(s):  
Ying Sun ◽  
Lan Ying Ge

Aluminophosphate molecular sieve and Ni(II)-containing APO-5 materials were synthesized hydrothermally and characterized by various analytical and spectroscopic techniques. It indicates that the nickel ions with a divalent oxidation state can incorporate into the tetrahedral coordination in mesoporous aluminophosphate very well. The better crystallizing temperature is explored. A stronger crystalline form is obtained with the addition of HF. Further, microporous aluminophosphate molecular sieves and Ni(II) ions remain in a tetrahedral geometry even after calcination at 550 °C.


Inorganics ◽  
2021 ◽  
Vol 9 (9) ◽  
pp. 72
Author(s):  
Dafydd D. L. Jones ◽  
Samuel Watts ◽  
Cameron Jones

Sterically bulky β-diketiminate (or Nacnac) ligand systems have recently shown the ability to kinetically stabilize highly reactive low-oxidation state main group complexes. Metal halide precursors to such systems can be formed via salt metathesis reactions involving alkali metal complexes of these large ligand frameworks. Herein, we report the synthesis and characterization of lithium and potassium complexes of the super bulky anionic β-diketiminate ligands, known [TCHPNacnac]− and new [TCHP/DipNacnac]− (ArNacnac = [(ArNCMe)2CH]−) (Ar = 2,4,6-tricyclohexylphenyl (TCHP) or 2,6-diisopropylphenyl (Dip)). The reaction of the proteo-ligands, ArNacnacH, with nBuLi give the lithium etherate compounds, [(TCHPNacnac)Li(OEt2)] and [(TCHP/DipNacnac)Li(OEt2)], which were isolated and characterized by multinuclear NMR spectroscopy and X-ray crystallography. The unsolvated potassium salts, [{K(TCHPNacnac)}2] and [{K(TCHP/DipNacnac)}∞], were also synthesized and characterized in solution by NMR spectroscopy. In the solid state, these highly reactive potassium complexes exhibit differing alkali metal coordination modes, depending on the ligand involved. These group 1 complexes have potential as reagents for the transfer of the bulky ligand fragments to metal halides, and for the subsequent stabilization of low-oxidation state metal complexes.


2018 ◽  
Vol 47 (10) ◽  
pp. 3223-3226 ◽  
Author(s):  
Sabine Frischhut ◽  
Thomas F. Fässler

The first alkenyl-functionalized, uncharged deltahedral germanium clusters [{Si(SiMe3)3}3Ge9(CH2)nCHCH2] (n = 1 or 3) comprising five Ge0 atoms are presented.


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