Bonding in methygold(I) and trimethygold(III) compounds. Nuclear magnetic resonance, Raman, and infrared spectra and normal coordinates

1973 ◽  
Vol 12 (5) ◽  
pp. 965-978 ◽  
Author(s):  
C. Frank Shaw ◽  
R. Stuart Tobias
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Infrared Spectra ◽  
Resonance Raman ◽  
Normal Coordinates ◽  
Nuclear Magnetic

Mid-infrared spectra predict nuclear magnetic resonance spectra of soil carbon

Geoderma ◽  
2015 ◽  
Vol 247-248 ◽  
pp. 65-72 ◽  
Author(s):  
Mohsen Forouzangohar ◽  
Jeffrey A. Baldock ◽  
Ronald J. Smernik ◽  
Bruce Hawke ◽  
Lauren T. Bennett
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Soil Carbon ◽  
Infrared Spectra ◽  
Mid Infrared ◽  
Nuclear Magnetic Resonance Spectra ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

scholarly journals Synthesis of Triphenyltin (IV) and Dibutyltin (IV) Complexes of 1-Aryl-2,5-dithiohydrazodicarbonamides and Their Characterization

2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Rashmi B. Rastogi ◽  
Karuna Singh ◽  
Vinay Jaiswal
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Infrared Spectra ◽  
Mass Spectra ◽  
Molar Conductance ◽  
Fab Mass Spectra ◽  
Nuclear Magnetic

Organotin complexes of the types Ph3SnL and Bu2SnL [where Ph = phenyl and Bu = butyl; HL = 1-phenyl-2,5-dithiohydrazodicarbonamide (HPhthc), 1-benzyl-2,5-dithiohydrazodicarbonamide (Hbzthc), 1-(4-ethoxyphenyl)-2,5-dithiohydrazodicarbonamide (HEtOPhthc)] have been prepared. Molar conductance studies demonstrate the nonionic behavior of the complexes. The 1H and 13C nuclear magnetic resonance and FAB mass spectra of the complexes are consistent with the proposed stoichiometry. Infrared spectra suggest an anionic bidentate coordinating behavior of the ligands.

Perfluoroalkyl- and fluoroalkyl- complexes of rhodium(III)

1976 ◽  
Vol 54 (13) ◽  
pp. 2077-2084 ◽  
Author(s):  
Howard C. Clark ◽  
Kenneth J. Reimer
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Infrared Spectra ◽  
Oxidative Addition ◽  
Far Infrared ◽  
Addition Reactions ◽  
Nmr Data ◽  
Far Infrared Spectra ◽  
Nuclear Magnetic

A series of perfluoroalkyl (Rf—) and fluoroalkyl (RfCH2—) complexes of rhodium(III) have been prepared by oxidative addition reactions of RfI and RfCH2I (Rf = CF3, C2F5 and C3F7) with trans-RhClCO(PMe2Ph)2. The reaction of CF3I with trans-RhClCO(PMePH2)2 gave RhClI(CF3)CO(PMePh2)2 but no reaction was observed with CF3CH2I. The trans stereochemistry of addition has been assigned to all complexes by nuclear magnetic resonance measurements and the comparison of the far-infrared spectra to those of some bromo compounds: RhBrI(CF3)CO(PMe2Ph)2 and RhBrI(C3F7CH2)CO(PMe2Ph)2. Both 1H and 19F nmr data are presented and discussed.

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