Proton And Phosphorus 31 Nmr Studies Of Tertiary Phosphine Complexes Of Palladium And Platinum 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.


Phosphorus-31 NMR Spectroscopy

Phosphorus-31 NMR Spectroscopy
Author: Olaf Kühl
Publisher: Springer Science & Business Media
Total Pages: 138
Release: 2008-08-22
Genre: Science
ISBN: 3540791183

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Nuclear Magnetic Resonance is a powerful tool, especially for the identification of 1 13 hitherto unknown organic compounds. H- and C-NMR spectroscopy is known and applied by virtually every synthetically working Organic Chemist. Con- quently, the factors governing the differences in chemical shift values, based on chemical environment, bonding, temperature, solvent, pH, etc. , are well understood, and specialty methods developed for almost every conceivable structural challenge. Proton and carbon NMR spectroscopy is part of most bachelors degree courses, with advanced methods integrated into masters degree and other graduate courses. In view of this universal knowledge about proton and carbon NMR spectr- copy within the chemical community, it is remarkable that heteronuclear NMR is still looked upon as something of a curiosity. Admittedly, most organic compounds contain only nitrogen, oxygen, and sulfur atoms, as well as the obligatory hydrogen and carbon atoms, elements that have an unfavourable isotope distribution when it comes to NMR spectroscopy. Each of these three elements has a dominant isotope: 14 16 32 16 32 N (99. 63% natural abundance), O (99. 76%), and S (95. 02%), with O, S, and 34 14 S (4. 21%) NMR silent. N has a nuclear moment I = 1 and a sizeable quadrupolar moment that makes the NMR signals usually very broad and dif cult to analyse.