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Book ChapterDOI

Transition Metal Complexes Containing Bidentate Phosphine Ligands

TLDR
In this paper, several transition metal complexes containing bidentate phosphine ligands are described, and a major complication in diphosphine complexes is the relative complexity of the ligands.
Abstract
Publisher Summary This chapter describes several transition metal complexes containing bidentate phosphine ligands. The bonding in metal–phosphine ligands due to the formation of π-type bonds between the metal and phosphorus atoms. Several techniques are used to study metal–phosphine complexes. These techniques include mass spectroscopy infrared spectroscopy, nuclear magnetic resonance, electronic spectroscopy, electron spin resonance, and Mossbauer spectroscopy. A major complication in diphosphine complexes is the relative complexity of the ligands. When a diphosphine complexes with a metal ion, the electron density on the phosphorus atom changes, and the ligand is restricted in the conformation it can assume. Thus the vibrational spectra of the free and coordinated ligands differ.

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Citations
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Journal ArticleDOI

Coordination chemistry of diphosphinoamine and cyclodiphosphazane ligands

TL;DR: The transition metal coordination and organometallic chemistry of acyclic diphosphazane ligands has grown rapidly in the last two decades and a stage has been reached that permits a delineation of similarities and contrasts with the chemistry of Diphosphinomethane type ligands.
Journal ArticleDOI

Gold-Komplexe von Diphosphinomethanen, I. Synthese und Kristallstruktur zweikerniger Gold(I)-Verbindungen

TL;DR: In this article, a 1:2-Komplexe with AuCl, Aul, and AuCH3 is described, and the results are of interest with respect to the short but nonbonding AuAu distance.
Journal ArticleDOI

Beiträge zur Strukturchemie von Silberhalogenid-Diphosphinomethan- und verwandten Komplexen†

TL;DR: The 1:1-komplex of AgBr with bis(diphenylphosphino)methane (dppm) was first reported in this article, where the structure consists of discrete bromide anions and trinuclear cations.
References
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Journal ArticleDOI

Structure and reactivity in complexes of iridium and rhodium. Part I. Crystal and molecular structure of bis-[1,2-bis(diphenylphosphino)ethane]rhodium(I) perchlorate

TL;DR: In this article, the exact conformation adopted in the cation by the bidentate diphosphine ligand, Ph2P·CH 2·CH2·PPh2, appears to be determined by non-bonded interactions between the phenyl substituents on the phosphorus atoms.
Journal ArticleDOI

Complex Compounds of Zero-valent Platinum

TL;DR: In this article, the existence of zero-valent platinum complexes was examined and it was shown that the triphenylphosphine complexes of platinum are hydrides [PtH2(PPh3)n] (n = 2, 3 or 4).
Journal ArticleDOI

Studies in the chemistry of technetium. Complexes of technetium-(II), -(III), and -(IV) with 1,2-bis(diphenylphosphino)ethane

TL;DR: In this article, the diphosphine 1,2-bis(diphenylphosphino)ethane was used to obtain the octahedral technetium complexes.
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