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Crystal structure of carbonyl(2-oxopyridin-1(2H)-olato-k2 O,O′)(triphenylarsine-κAs)rhodium(I), C24H19AsNO3Rh

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This article is published in Zeitschrift Fur Kristallographie-new Crystal Structures.The article was published on 2021-01-26 and is currently open access. It has received 4 citations till now. The article focuses on the topics: Triphenylarsine & Rhodium.

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Journal ArticleDOI

The crystal structure of (carbonato κ2 O,O′)(2-oxopyridin-1(2H)-olato-κN)tris(trimethylphosphine)rhodium(III) water solvate, C15H33NO5P3Rh

TL;DR: In this paper , the orthorhombic Pnma (no. 62), a = 19.8694(11) Å, b = 12.5765(7) À, c = 8.6990(5) Ð, V = 2173.8(2) Á3, Z = 1, Rgt (F) = 0.0394, wRref (F 2) =0.0941, T = 100 K, α = β = γ = 90°.
Journal ArticleDOI

The crystal structure of dicarbonyl-(N-nitroso-N-oxido-phenylamine-κ 2 O,O)-rhodium(I), C8H5N2O4Rh

TL;DR: In this paper , the authors proposed a monoclinear monoclonality approach to monocline monophotonicity and showed that it is possible to achieve monoclanic monophonic monophony with the use of monocular microscopy.
References
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Journal ArticleDOI

A short history of SHELX

TL;DR: This paper could serve as a general literature citation when one or more of the open-source SH ELX programs (and the Bruker AXS version SHELXTL) are employed in the course of a crystal-structure determination.
Journal ArticleDOI

OLEX2: a complete structure solution, refinement and analysis program

TL;DR: OLEX2 seamlessly links all aspects of the structure solution, refinement and publication process and presents them in a single workflow-driven package, with the ultimate goal of producing an application which will be useful to both chemists and crystallographers.
Book

Catalysis of organic reactions

TL;DR: A collection of 33 papers and posters from a conference in Boca Raton, Florida, May 1990, in which chemists from the chemical and pharmaceutical industries, and from academia, discuss their work on the use of catalysis in organic synthesis is presented in this article.
Journal ArticleDOI

Structure and solution behaviour of rhodium(I) Vaska-type complexes for correlation of steric and electronic properties of tertiary phosphine ligands

TL;DR: In this article, the synthesis of rhodium(I) Vaska-type complexes of the general form trans-[Rh(CO)X(PX3)] (X=halide, X aryl or alkyl substituent) when incorporating tertiary phosphine ligands was discussed.
Journal ArticleDOI

Steric vs. electronic anomaly observed from iodomethane oxidative addition to tertiary phosphine modified rhodium(I) acetylacetonato complexes following progressive phenyl replacement by cyclohexyl [PR3 = PPh3, PPh2Cy, PPhCy2 and PCy3]

TL;DR: Spectroscopic and low temperature X-ray crystallographic data of the rhodium complexes (1-4) indicate a systematic increase in both steric and electronic parameters of the phosphine ligands as phenyl groups on the tertiary phosphine are progressively replaced by cyclohexyl groups in the series.
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