Multinuclear (carbon-13, phosphorus-31, selenium-77) magnetic resonance and infrared spectroscopic studies of the interaction of W(CO)4(NO)I with potentially bidentate Group 15 and mixed Group 15/Group 16 donor ligands. Electrochemical studies on some Group 15 donor ligand derivatives

1988 ◽  
Vol 7 (8) ◽  
pp. 1774-1782 ◽  
Author(s):  
Alan M. Bond ◽  
Ray. Colton ◽  
Penny. Panagiotidou
Keyword(s):  
Magnetic Resonance ◽  
Spectroscopic Studies ◽  
Donor Ligands ◽  
Electrochemical Studies ◽  
Mixed Group ◽  
Donor Ligand ◽  
Infrared Spectroscopic ◽  
Group 15 ◽  
Group 16

Carbon-13 nuclear magnetic resonance and infrared spectroscopic studies of carbon-13 monoxide binding to rabbit hemoglobin

1973 ◽  
Vol 95 (13) ◽  
pp. 4429-4431 ◽  
Author(s):  
N. A. Matwiyoff ◽  
P. J. Vergamini ◽  
T. E. Needham ◽  
C. T. Gregg ◽  
J. A. Volpe ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Spectroscopic Studies ◽  
Infrared Spectroscopic ◽  
Nuclear Magnetic

Spectroscopic Studies of Cationic h5-Cyclopentadienyl Iron Carbonyl Derivatives

1974 ◽  
Vol 52 (5) ◽  
pp. 782-787 ◽  
Author(s):  
G. Michael Bancroft ◽  
K. David Butler ◽  
Leo E. Manzer ◽  
Alan Shaver ◽  
John E. H. Ward
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Spectroscopic Studies ◽  
Iron Carbonyl ◽  
Force Constants ◽  
Iron Compounds ◽  
Carbonyl Derivatives ◽  
Anionic Ligand ◽  
Similar Correlation ◽  
Infrared Spectroscopic

Mössbauer, 13C nuclear magnetic resonance and infrared spectroscopic studies of a series of cationic iron compounds of the type [(h5-C5H5)Fe(CO)2L]+X− (L = CO, CH3CN, C2H4, (C6H5)3P, C5H4N; X = PF6−, BF4−) are described. The Mössbauer center shifts indicate that the σ donor plus π acceptor ability (σ + π) of these ligands increases in the order CH3CN ≤ C2H4 < C5H5N < (C6H5)3P < CO < CS. The positive 57Fe quadrupole splittings strongly suggest that the sign of the quadrupole splittings for the isovalent and isoelectronic Mn and Re compounds are also positive. The correlation between carbonyl infrared force constants and 13C carbonyl shieldings is discussed in relation to a similar correlation previously reported in the literature for a series of neutral complexes (h5-C5H5)Fe(CO)2Y, where Y is an anionic ligand.

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