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Cd Garner

Bio: Cd Garner is an academic researcher. The author has contributed to research in topics: Crystal structure & X-ray crystallography. The author has an hindex of 1, co-authored 1 publications receiving 19 citations.


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Journal ArticleDOI
TL;DR: In order to study the reactivity pattern of Mo−Ot bonds associated with anionic sulfur ligands, precursor complexes MoO2L·D (H2L = S-methyl 3-(2-hydroxyphenyl)methylenedithiocarbazate; D = CH3OH (1), H2O (2)) were synthesized as discussed by the authors.
Abstract: In order to study the reactivity pattern of Mo−Ot bonds associated with anionic sulfur ligands, precursor complexes MoO2L·D (H2L = S-methyl 3-(2-hydroxyphenyl)methylenedithiocarbazate; D = CH3OH (1), H2O (2)) were synthesized. Complex 2 crystallizes in the orthorhombic space group P212121, with a = 6.079(1) A, b = 11.638(2) A, c = 17.325(2) A, V = 1225.7(4) A3, and Z = 4. In its reaction with PhNHOH, 1 forms a seven-coordinate oxaziridine compound [MoO(η2-ONPh)L·CH3OH] (3) by oxo-rearrangement (elimination−substitution) without a change in the molybdenum oxidation state. The crystal data for 3 are a = 9.573(3) A, b = 9.859(2) A, c = 10.604(3) A, α = 95.90(2)°, β = 95.81(2)°, γ = 112.12(2)°, V = 911.5(4) A3, Z = 2, and triclinic space group P1. In contrast to that of the precursor compound 1 (Mo−Ot = 1.700(4) A), the terminal Mo−Ot distance in 3 (1.668(2) A) is typical of Mo−O bonds of order 3, which drives the formation of an apparently unstable three-membered metallacycle via spectator oxo stabilization...

83 citations

Journal ArticleDOI
TL;DR: In this paper, the authors thank MICINN for "Juan de la Cierva" and "Ramon y Cajal" contracts and the Junta de Castilla y Leon (BU021 A09 and GR-172) for financial support.
Abstract: Ministerio de Ciencia e Innovacion (MICINN) and FEDER (CTQ2010-15358 and CTQ2009-09949/BQU) and Junta de Castilla y Leon (BU021 A09 and GR-172) for financial support. P.G.-G. and M.A.F.-R. thank MICINN for "Juan de la Cierva" and "Ramon y Cajal" contracts

72 citations

Journal ArticleDOI
TL;DR: In this paper, a micro-review gives an overview about advances in bioinorganic model chemistry for molybdenum-and tungsten-dependent oxidoreductases with respect to specific aspects of the evolution, structure or function of distinct active-site properties.
Abstract: This microreview gives an overview about advances in bioinorganic model chemistry for molybdenum- and tungsten-dependent oxidoreductases with respect to specific aspects of the evolution, structure or function of distinct active-site properties. The approaches to evaluate catalytic properties fine-tuned by the ligand sphere, interpret and assign enzyme spectra and to understand why two different metals are used for the same task but in distinct habitats and respective evolutionary aspects are discussed on the basis of exemplary case studies. This short review provides a personal perspective and appreciation of the complex problems associated with the respective foremost synthetic and analytical model chemistry and their solutions partly accompanied and supported by theoretical results.

54 citations

Journal ArticleDOI
TL;DR: The position of the LLCT band is largely dependent on the substituent type on the catechol frame and is qualitatively assigned as the 3b 1 (cat) → π*(aap) transition as mentioned in this paper.

52 citations