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Valence (chemistry)

About: Valence (chemistry) is a research topic. Over the lifetime, 24937 publications have been published within this topic receiving 645252 citations. The topic is also known as: valency.


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TL;DR: In this paper, the first gas phase electronic spectrum of V2 was reported, which was generated in an expansion cooled molecular beam by laser vaporization of vanadium metal, and the transition is of the type 3Πu(a)←3Σ−g(a), and the ground state electronic configuration was assigned the 3 ǫ−g state as the ground electronic state.
Abstract: We report of the first gas‐phase electronic spectrum of V2. The dimer was generated in an expansion cooled molecular beam by laser vaporization of vanadium metal. Using the technique of resonant two photon ionization spectroscopy a strong band system with origin near 7000 A was observed. Rotationally resolved spectra of this band system conclusively demonstrate that the transition is of the type 3Πu(a)←3Σ−g(a), and we assign the 3Σ−g state as the ground electronic state of V2. The short ground state bond length re″=1.77 A and high vibrational frequency ωe″=535 cm−1 are indicative of extensive 3d‐orbital participation in the bonding of this molecule. The unusual case (a) coupling and large second‐order spin‐orbit splitting observed in the 3Σ−g state implies that the ground state electronic configuration contains a half‐filled π(3d) or δ (3d) orbital. The most plausible valence configuration consistent with the data is σg(3d)2πu(3d)+σg(4s)2δg(3d)2. In the excited state there is strong evidence of predissoci...

113 citations

Journal ArticleDOI
Martin Jansen1
TL;DR: This tutorial review focuses on the chemistry of gold as an anion, displaying the integral ionic charge number of 1-.
Abstract: Due to relativistic and classical shell structure effects, the 6s orbital of gold is significantly contracted and energetically stabilized. This is reflected by a strikingly high electron affinity, and a distinct tendency to adopt negatively polarized valence states. This tutorial review focuses on the chemistry of gold as an anion, displaying the integral ionic charge number of 1−. Two synthetic approaches to compounds containing monoatomic gold anions have become available: (1) reacting elemental gold with molten caesium and an oxide, e.g.Cs2O; (2) metathesis reactions involving Au− dissolved in liquid ammonia. Both procedures have proven to be rather versatile. Aurides synthesized along these routes are surveyed, in particular with respect to their structures and bonding properties.

113 citations

Journal ArticleDOI
TL;DR: Three new mixed valence trinuclear Co(II/III) compounds synthesized by reacting a di-Schiff base ligand with cobalt perchlorate hexahydrate and sodium azide show catecholase-like activities in the aerial oxidation of 3,5-di-tert-butylcatechol to the corresponding o-quinone.
Abstract: Three new mixed valence trinuclear Co(II/III) compounds cis-[Co3L2(MeOH)2(N3)2(μ1,1-N3)2] (1), trans-[Co3L2(H2O)2(N3)2(μ1,1-N3)2]·(H2O)2 (2) and [Co3LR2(N3)3(μ1,3-N3)] (3) have been synthesized by reacting a di-Schiff base ligand (H2L) or its reduced form [H2LR] (where H2L = N,N′-bis(salicylidene)-1,3-propanediamine and H2LR = N,N′-bis(2-hydroxybenzyl)-1,3-propanediamine) with cobalt perchlorate hexahydrate and sodium azide. All three products have been characterized by IR, UV-Vis and EPR spectroscopies, ESI-MS, elemental, powder and single crystal X-ray diffraction analyses. Complex 1 is an angular trinuclear species in which two terminal octahedral Co(III)N2O4 centers coordinate to the central octahedral cobalt(II) ion through μ2-phenoxido oxygen and μ1,1-azido nitrogen atoms along with two mutually cis-oxygen atoms of methanol molecules. On the other hand, in linear trinuclear complex 2, in addition to the μ2-phenoxido and μ1,1-azido bridges with terminal octahedral Co(III) centres, the central Co(II) is bonded with two mutually trans-oxygen atoms of water molecules. Thus the cis–trans configuration of the central Co(II) is solvent dependent. In complex 3, the two terminal octahedral Co(III)N2O4 centers coordinate to the central penta-coordinated Co(II) ion through double phenoxido bridges along with the nitrogen atom of a terminal azido ligand. In addition, the two terminal Co(III) are connected through a μ1,3-azido bridge that participates in pnicogen bonding interactions (intermolecular N–N interaction) as an acceptor. Both the cis and trans isomeric forms of 1 and 2 have been optimized using density functional theory (DFT) calculations and it is found that the cis configuration is energetically more favorable than the trans one. However, the trans configuration of 2 is stabilized by the hydrogen bonding network involving a water dimer. The pnicogen bonding interactions have been demonstrated using MEP surfaces and CSD search which support the counter intuitive electron acceptor ability of the μ1,3-azido ligand. Complexes 1–3 exhibit catecholase-like activities in the aerial oxidation of 3,5-di-tert-butylcatechol to the corresponding o-quinone. Kinetic data analyses of this oxidation reaction in acetonitrile reveal that the catecholase-like activity follows the order: 1 (kcat = 142 h−1) > 3 (kcat = 99 h−1) > 2 (kcat = 85 h−1). Mechanistic investigations of the catalytic behaviors by X-band EPR spectroscopy and estimation of hydrogen peroxide formation indicate that the oxidation reaction proceeds through the reduction of Co(III) to Co(II).

113 citations

Journal ArticleDOI
TL;DR: Rotational spectra of KrCuF and KrCuCl have been measured, using a pulsed jet cavity Fourier transform microwave spectrometer, and produced good evidence for weak noble gas-noble metal chemical bonding.
Abstract: Rotational spectra of KrCuF and KrCuCl have been measured in the frequency range 8-18 GHz, using a pulsed jet cavity Fourier transform microwave spectrometer. The molecules were prepared by ablating Cu metal with a pulsed Nd:YAG laser (1064 nm) and allowing the plasma to react with appropriate precursors (Kr plus SF(6) or Cl(2)) contained in the backing gas of the jet (Ar or Kr). Rotational constants, internuclear distances, vibration frequencies, and (83)Kr, Cu, and Cl nuclear quadrupole coupling constants have all been evaluated. The Kr-Cu bonds are short and the complexes are rigid. The (83)Kr coupling constant of KrCuF is large (128.8 MHz). The Cu nuclear quadrupole coupling constants differ radically from those of uncomplexed CuF and CuCl molecules. The results are supported by those of ab initio calculations, which have also yielded Mulliken populations, MOLDEN plots of valence molecular orbitals and Laplace concentrations, and electron localization functions. The results are consistent with those reported earlier for other noble gas-noble metal halide complexes. The results have been used to assess the nature of the bonding in the complexes and have produced good evidence for weak noble gas-noble metal chemical bonding.

113 citations

Journal ArticleDOI
TL;DR: In this paper, the effects of metal doping in nanostructured (M-TiO2) with the objectives to define the location of metal ions in the host matrices, identifying their stable valence states and environments as well as the incidence on the structural, electronic and optical properties of M- TiO2 were investigated.

112 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20231,521
20222,997
2021616
2020611
2019584
2018577