Some metal-ion complexes with ligands formed by reactions of amines with aliphatic carbonyl compounds. VIII. Some copper(II) β-Imino alcohol and β-Imino-olato compounds

1980 ◽  
Vol 33 (6) ◽  
pp. 1219 ◽  
Author(s):  
JWL Martin ◽  
NF Curtis
Keyword(s):  
Carbonyl Compounds ◽  
Metal Ion ◽  
Spin Coupling ◽  
Tetradentate Ligand ◽  
Coupling Constant ◽  
Spin Coupling Constant ◽  
Analogous Structure ◽  
Magnetic Susceptibility Data ◽  
Susceptibility Data ◽  
Isomeric Structure

Compounds of copper(II) with chelated β-imino alcohols are formed by reaction of 4-hydroxy-4-methylpentan-2-one, hmp, with copper(II) compounds of ethane-1,2-diamine, 2-methylpropane-1,2-diamine, meso-1,2- diphenylethane-1,2-diamine, 2-(pyridin-2-yl)ethanamine, 3-azapentane- 1,5-diamine and 4-azaheptane-1,7-diamine. A dinuclear, spin-coupled di- μ-olato bridged derivative of a β-imino alkoxide, formed by reaction of hmp with 2-(pyridin-2-yl)ethanaminecopper(II), has a spin-coupling constant J of -286 cm-1, based on magnetic susceptibility data over the 100-300 K temperature range. A related compound formed by N,N- diethylethane-1,2-diamine, which could have an analogous structure containing water, or an isomeric structure with the β-imino alcohol and with di-μ-hydroxide bridging, has a J value of about -130 cm-1, similarly determined. The preparation of a copper(11) compound with the tetradentate ligand 4,6-trimethyl-1,9-bis(pyridin-2-yl)-3,7-diazanon-3- ene, by reaction of bis[2-(pyridin-2-yl)ethanamine]copper(II) perchlorate with acetone, is reported.

Some metal-ion complexes with ligands formed by reactions of amines with aliphatic carbonyl compounds. IX. Nickel(II) compounds of some b-imino amines, a β-oximato amine and a β-hydrazino amine

1980 ◽  
Vol 33 (6) ◽  
pp. 1231 ◽  
Author(s):  
KR Morgan ◽  
NF Curtis
Keyword(s):  
Magnetic Susceptibility ◽  
Ground State ◽  
Carbonyl Compounds ◽  
Metal Ion ◽  
Spin Coupling ◽  
Singlet Ground State ◽  
Coupling Constant ◽  
Spin Coupling Constant ◽  
Complex Products ◽  
Amine Ligands

Singlet ground state compounds of nickel(II) with tetradentate β-imino amine ligands are formed by reaction of complexes of ethane-1,2- diamine, propane-1,2-diamine, 3-azapentane-1,5-diamine, 4-azaheptane- 1,7-diamine and (2-aminoethyl)piperazine with 4-amino-4-methylpentan-2- one, amp. With 3,6-diazaoctane-1,8-diamine, a compound with a pentadentate β-imino ligand is formed, water completing octahedral coordination, and with 2-aminoethanol a bis compound of a tridentate β-imino amine alcohol ligand is formed. More complex products are formed by the hydrazone and oxime of amp. The oxime compound shows appreciable antiferromagnetism, with the spin-coupling constant, J, about -70 cm-1, determined from magnetic susceptibility measurements over 100-300 K.

An estimate of the spin–spin coupling constant, 1J(1H,13C), in gaseous benzene

1996 ◽  
Vol 74 (8) ◽  
pp. 1524-1525 ◽  
Author(s):  
Ted Schaefer ◽  
Guy M. Bernard ◽  
Frank E. Hruska
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Dielectric Constant ◽  
Magnetic Resonance ◽  
Coupling Constants ◽  
Spin Coupling ◽  
Coupling Constant ◽  
Spin Coupling Constant ◽  
Spin Coupling Constants ◽  
Spin Spin Coupling ◽  
Gaseous Benzene

An excellent linear correlation (r = 0.9999) exists between the spin–spin coupling constants 1J(1H,13C), in benzene dissolved in four solvents (R. Laatikainen et al. J. Am. Chem. Soc. 117, 11006 (1995)) and Ando's solvation dielectric function, ε/(ε – 1). The solvents are cyclohexane, carbon disulfide, pyridine, and acetone. 1J(1H,13C)for gaseous benzene is predicted to be 156.99(2) Hz at 300 K. Key words: spin–spin coupling constants, 1J(1H,13C) for benzene in the vapor phase; spin–spin coupling constants, solvent dielectric constant dependence of 1J(1H,13C) in benzene; benzene, estimate of 1J(1H,13C) in the vapor; nuclear magnetic resonance, estimate of 1J(1H,13C) in gaseous benzene.

Form of the dihedral angle dependence of the spin-spin coupling constant JHNNH

1989 ◽  
Vol 25 (3) ◽  
pp. 338-341
Author(s):  
L. M. Kapkan ◽  
A. Yu. Chervinskii ◽  
T. M. Pekhtereva ◽  
Yu. I. Smirnov ◽  
A. F. Dmitruk
Keyword(s):  
Dihedral Angle ◽  
Spin Coupling ◽  
Coupling Constant ◽  
Spin Coupling Constant ◽  
Angle Dependence ◽  
Spin Spin Coupling

Temperature dependence of the carbon-13 proton spin-spin coupling constant in gaseous methane

1987 ◽  
Vol 61 (6) ◽  
pp. 1423-1430 ◽  
Author(s):  
B. Bennett ◽  
W.T. Raynes
Keyword(s):  
Temperature Dependence ◽  
Proton Spin ◽  
Spin Coupling ◽  
Coupling Constant ◽  
Spin Coupling Constant ◽  
Spin Spin Coupling

The proximate spin–spin coupling, 5J(F,CH3), as a quantitative conformational indicator in alkylfluorobenzenes and related compounds

1986 ◽  
Vol 64 (8) ◽  
pp. 1602-1606 ◽  
Author(s):  
Ted Schaefer ◽  
Rudy Sebastian ◽  
Glenn H. Penner ◽  
S. R. Salman
Keyword(s):  
Nuclear Spin ◽  
Spin Coupling ◽  
Torsional Angle ◽  
Rotational Behaviour ◽  
Coupling Constant ◽  
Spin Coupling Constant ◽  
Spin Spin Coupling ◽  
Torsional Potentials ◽  
Derivatives Of ◽  
Related Compounds

The through-space or proximate nuclear spin–spin coupling constant, 5J(F,CH3) = 5J, between methyl protons and ring fluorine nuclei in alkylfluorobenzenes is postulated as [Formula: see text] θ being the torsional angle for the [Formula: see text] bond. A and B are obtained from the known internal rotational behaviour in 2,6-difluoroethylbenzene and the corresponding cumene derivative. The parameterization is tested on the observed 5J in derivatives of 2,4,6-tri-tert-butyl- and 2,4,6-tri-isopropyl-fluorobenzene, in 2-chloro-6-fluoroisopropylbenzene, 2,6-difluoro-α-methylstyrene, and N-methyl-8-fluoroquinolinium halides. A prediction is made for 5J in 2,6-difluoro-tert-butylbenzene. It appears that the present parameterization allows the derivation of approximate torsional potentials from proximate couplings, for example in α,α-dimethyl-2,6-difluorobenzyl alcohol.

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