Platinum Ii Complexes With Crown Thioethers And Phosphine Ligands PDF Download

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Tertiary Phosphine Complexes of Platinum(ii) and Palladium(ii).

Tertiary Phosphine Complexes of Platinum(ii) and Palladium(ii).
Author: Richard Lee Keiter
Publisher:
Total Pages: 212
Release: 1967
Genre: Palladium
ISBN:

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The results are reported of research which was undertaken (1) to determine the chemical shifts of cis and trans isomers of platinum(II) complexes in hope of gaining information about pi-bonding in the Pt-P bond, and to extend this study to palladium(II); (2) to determine trends which may exist within a series of ligands for the purpose of developing expressions that would enable calculation of chemical shifts for complexes; (3) to expand the knowledge of the chemistry of tertiary phosphine complexes of platinum(II) and palladium(II); and (4) to determine phosphorus-phosphorus coupling constants by preparing a complex of a chelating diphosphine (R2PCH2CH2PR'2) or by preparing a complex containing two different phosphines.


Platinum(II) Hydroxo, Oxo, Amido, Imido and Hydrazido Complexes

Platinum(II) Hydroxo, Oxo, Amido, Imido and Hydrazido Complexes
Author: Jian-Jun Li
Publisher:
Total Pages: 352
Release: 1996
Genre: Platinum
ISBN:

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Late transition metal oxo and imido complexes are important models for catalytic reactions involving oxygen and nitrogen transfer. The subject of this dissertation is the synthesis and reactivity study of a series of platinum(II) hydroxo, oxo, amido, imido and hydrazido complexes. The platinum(II) hydroxo complex (L$\sb2$Pt($\mu$-OH)) $\rm\sb2X\sb2$ is prepared from the reaction of L$\rm\sb2PtCl\sb2$ with two equivalents of AgX. Deprotonation of the hydroxo complex (L$\rm\sb2Pt(\mu$-OH)) $\sb2\sp{2+}$ yields corresponding oxo complexes. The site of deprotonation depends on the phosphine ligands. Pt(II) $\mu$-amido complexes are synthesized from the reaction of $\mu$-hydroxo complexes (L$\rm\sb2Pt(\mu$-OH)) $\rm\sb2(BF\sb4)\sb2$ with amines H$\sb2$NR. The result of the reaction depends on the ligand L$\sb2$ of the $\mu$-hydroxo complexes as well as on the R group of the amines. Treating (L$\rm\sb2Pt(\mu$-OH)) $\rm\sb2(BF\sb4)\sb2$ with two equivalents of H$\rm\sb2NNH\sb2$ generates an unusual hydrazido complex (L$\rm\sb2Pt(\mu$-NHNH$\rm\sb2)\rbrack\sb2(BF\sb4)\sb2$ which can be deprotonated to give ((dppm-H)Pt($\mu$-NHNH$\sb2)\rbrack\sb2$.