			Home About us Contact

Anionic Complexes (anionic + complex)

Distribution by Scientific Domains

Chemistry	83%

Selected Abstracts

ChemInform Abstract: Theoretical Study of Binding Interactions and Vibrational Raman Spectra of Water in Hydrogen-Bonded Anionic Complexes: (H2O)n - (n = 2 and 3), H2O×××X - (X: F, Cl, Br, and I), and H2O×××M - (M: Cu, Ag, and Au).

CHEMINFORM, Issue 18 2008
De-Yin Wu
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Synthesis, structure and reactivity of cationic base-stabilized gallyleneiron complexes,

APPLIED ORGANOMETALLIC CHEMISTRY, Issue 6-7 2003
Keiji Ueno
Abstract Addition of 2,2,-bipyridine (bpy) to an acetonitrile solution of dichlorogallyliron complex FpGaCl2 (1: Fp = (,-C5H5)Fe(CO)2) afforded almost quantitatively a salt consisting of a cationic base-stabilized gallylene complex [FpGaCl·bpy]+ ([3a]+) and an anionic complex [FpGaCl3], ([4],). Reaction of Fp,GaCl2 (Fp, = Fp (1), Fp* (2); Fp* = (,-C5Me5)Fe(CO)2) with NaBPh4 in the presence of a bidentate donor (Do2) gave [Fp,GaCl·Do2]BPh4 where Do2 was bpy or 1,10-phenanthroline (phen). These cationic complexes may be useful precursors for the synthesis of gallyleneiron complexes with various substituents on the gallium atom. Indeed, reaction of [Fp*GaCl·phen]BPh4 ([5b]BPh4) with NaSpTol or Me3SiSpTol afforded the gallyleneiron complex [Fp*GaSpTol·phen]BPh4 ([6]BPh4), the first example of a gallium,transition metal complex having a thiolate group on the gallium atom. The molecular structures of [5b]BPh4 and [6]BPh4 were determined by single crystal X-ray diffraction. Copyright © 2003 John Wiley & Sons, Ltd. [source]

Mono- and Binuclear Arylnickel Complexes of the ,-Diimine Bridging Ligand 2,2,-Bipyrimidine (bpym)

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 6 2010
Axel Klein
Abstract The mono- and binuclear organometallic NiII complexes [(,-bpym){Ni(Mes)Br}n] (bpym = 2,2,-bipyrimidine; n = 1 or 2; Mes = mesityl = 2,4,6-trimethylphenyl) were prepared and characterised electrochemically and spectroscopically (NMR, UV/Vis/NIR) in detail. The long-wavelength absorptions for the binuclear complex reveal a marked electronic coupling of the two metal centres over the ligand bridge via their low-lying ,*-orbitals. While the mononuclear complex undergoes rapid dissociation of the bromido ligand after one-electron reduction the binuclear derivative exhibits reversible reductive electrochemistry and both of them yield stable radical anionic complexes with mainly bpym ligand centred spin density as shown by EPR spectroscopy of the free ligand bpym and the nickel complexes. The molecular structure of the binuclear bpym complex [(,-bpym){Ni(Mes)Br}2] was studied by EXAFS in comparison to the mononuclear analogue [(bpym)Ni(Mes)Br] revealing markedly increased Ni,C/N distance of the first coordination shell for the binuclear derivative suggesting an optimum overlap for the mononuclear complex, while two nickel complex fragments {Ni(Mes)Br} are seemingly too large to fit into the bis-chelate coordination site. [source]

The Role of Axial Ligation in Nitrate Reductase: A Model Study by DFT Calculations on the Mechanism of Nitrate Reduction

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 34 2008
Kuntal Pal
Abstract The reactivity differences of the model anionic complexes [Mo(mnt)2(X)(PPh3)], [mnt2, = 1,2-dicyanoethylenedithiolate; X = SPh (1a), SEt (1b), Cl (1c), Br (1b)] towards oxygen atom transfer from nitrate, which is a key step performed by nitrate reductase, has been investigated by density functional theory calculations. Unlike complexes 1a and 1b, complexes 1c and 1d do not react with nitrate. Thermodynamically, all these complexes have a similar ability to generate the pentacoordinate active state [Mo(mnt)2(X)], by dissociation of PPh3, although the inaccessibility of the dxy orbital in 1c,d and the instability of the corresponding nitrate-bound enzyme substrate (ES) type complex contributes to their failure to reduce nitrate. The nature of the ES complex for 1a,b is described. The variation in the experimental data due to the change of axial ligation from SPh to SEt on the catalytic pathway has also been addressed. The gas-phase and solvent-corrected potential energy surface for the reaction of 1a,b with nitrate are established with fully optimized minima and transition states.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]

Anionic Bridged Bis(amidinate) Lithium Lanthanide Complexes: Efficient Bimetallic Catalysts for Mild Amidation of Aldehydes with Amines

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 9 2009
Junfeng Wang
Abstract Anionic bridged bis(amidinate) lithium lanthanide complexes have been found to be efficient catalysts for the amidation of aldehydes with amines under mild conditions. The activity follows the order: yttriumanionic complexes show higher activity and a wider range of scope for the amines. A cooperation of the lanthanide and lithium metals in this process is proposed to contribute to the high activity of the present catalyst. [source]

Synthetic Diether-linked Cationic Lipids for Gene Delivery

CHEMICAL BIOLOGY & DRUG DESIGN, Issue 3 2006
Dongliang Liu
Quaternary ammonium lipids 2a,p, with diether linkages between hydrocarbon chains and their ammonium headgroups, were synthesized as potential vectors for cationic liposome-mediated gene delivery. Varying the length of carbon chains and quaternary ammonium heads as well as different anionic complexes will enable the study of the structure,function relationships of these cationic lipids in terms of gene delivery properties. [source]