scholarly journals 15N NMR Spectra of Cobalt(III) Complexes Containing15NO2−

1985 ◽  
Vol 58 (11) ◽  
pp. 3407-3408 ◽  
Author(s):  
Yoshio Odaka ◽  
Akira Yamasaki ◽  
Masatoshi Watabe
Keyword(s):  
1996 ◽  
Vol 61 (4) ◽  
pp. 589-596 ◽  
Author(s):  
Antonín Lyčka

The 1H, 13C and 15N NMR spectra have been measured of coupling products of benzenediazonium salts with nitromethane, nitroethane, 1-nitropropane, 2-nitroethanol and of their sodium salts, and the chemical shifts have been unambiguously assigned. The coupling products have been found to exist only in their hydrazone tautomeric forms. Stereospecific behaviour of the coupling constants 2J(15N,1H) and 2J(15N,13C) in the 15N isotopomers and NOESY have been used to differentiate between the E and Z geometrical isomers. The above-mentioned compounds exist as Z isomers in deuteriochloroform and predominantly (>95%) as E isomers in dimethyl sulfoxide, while the sodium salts are present only as E isomers in dimethyl sulfoxide.


2006 ◽  
Vol 44 (5) ◽  
pp. 521-523 ◽  
Author(s):  
Antonín Lyčka ◽  
Roman Doleček ◽  
Petr Šimûnek ◽  
Vladimír Macháček

1985 ◽  
Vol 63 (3) ◽  
pp. 601-604 ◽  
Author(s):  
Hans J Jakobsen ◽  
Ulla B Sørensen ◽  
Henrik Bildsøe ◽  
Ole W Sørensen

Author(s):  
Chiseko Sakuma ◽  
Mikiko Maeda ◽  
Katsumi Tabei ◽  
Akihiro Ohta ◽  
Ablikim Kerim ◽  
...  
Keyword(s):  

1987 ◽  
Vol 42 (12) ◽  
pp. 1515-1519 ◽  
Author(s):  
Carin Stader ◽  
Bernd Wrackmeyer

AbstractThe basic INEPT pulse sequence proved most useful for recording 15N NMR spectra at natural abundance of bis(amino)stannvlenes (1). -plumbylenes (2) and of imino-amino-λ2-phosphanes (3), where the nitrogen atoms carry bulky substituents like Me3Si-, t-Bu-, 2.4.4-trimethyl-2- pentyl-groups (t-Oct-groups) or are part of the 2.2.6.6-tetramethylpiperidinyl group. The sensitiv­ity of this technique is proved by the observation of 117/119Sn or 207Pb satellites owing to spin-spin coupling constants 1J(117/119Sn15N) and 1J(117/119Pb15N), respectively. NMR data of bis[bis(trimethylsilyl)methyl]tin (4) are reported in order to corroborate the arguments for the interpretation of the δ(15N) and 1J(119Sn15N) data. The 15N NMR data of the λ2-phosphanes (3) indicate a bonding situation similar to that in triazenes.


1995 ◽  
Vol 60 (6) ◽  
pp. 990-998 ◽  
Author(s):  
Josef Jirman ◽  
Alexander Popkov

1H, 13C, and 15N NMR spectra have been measured of substituted Ni(II) complexes of Schiff bases of (S)-2-(N-benzylprolyl)aminobenzophenone and glycine. The absolute configuration at C19 of the substituted glycine can be determined from 2D NOESY spectra using the NOESY interactions with the proton of the second chiral centre of the complex. It is possible to determine the rate of rotation of phenyl group of benzophenone unless its rotation is prevented by requatorialr orientation of dimethylamino group as it is the case with the Ni(II) complex of Schiff base of (S)-2-(N-benzylprolyl)aminobenzophenone and (S)-α-dimethylaminoglycine.


1993 ◽  
Vol 31 (7) ◽  
pp. 694-695 ◽  
Author(s):  
J. Hodge Markgraf ◽  
David P. Richardson ◽  
Robert C. Livingston
Keyword(s):  

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