The possibility of contributions from contact interactions to the predominantly dipolar-induced changes in chemical shifts produced by lanthanide-shift reagents has been widely recognized. Such contributions might be expected to be especially large at the substrate atom directly coordinated to the lanthanide and, in general, be confined with saturated substrates at least to carbons and hydrogens in the immediate vicinity of the coordination site. Nonetheless, there is no firm basis for the prediction of the direction or magnitude of contact contributions to lanthanide-induced shifts on carbon or proton spectra
Bleaney’s long-standing theory of magnetic anisotropy has been employed with some success for many d...
Lanthanide ions Yb(3+) and Tb(3+), once bound to the monolayer of organic molecules coating the surf...
The ^(15)N and ^(13)C chemical shift changes have been determined for ethylenediaminetetraacetic aci...
The possibility of contributions from contact interactions to the predominantly dipolar-induced chan...
Lanthanide-induced shifts of 13C nuclear magnetic resonances are reported for several amines and n-b...
Owing to the present accuracy of the data and various other factors, it is easy to obtain agreement ...
The utility of nmr shift reagents which function predominantly by the dipolar mechanism for structur...
Paramagnetic substances can produce two principal effects on the high resolution nuclear magnetic re...
The work in this thesis describes a detailed study of the nature of the interactions occurring in so...
The paper deals with the implications of shift reagents in organic chemistry in several broad areas....
Difficulties encountered in the use of lanthanide shift reagents for study of conformational equilib...
The pattern of 13C and 1H nuclear magnetic resonance (NMR) shift changes produced by complexation of...
[[abstract]]The action of a series of lanthanide chelate complexes LnL3, where Ln=La, Pr, Nd, Sm, Eu...
The problem of using lanthanide induced shift (LIS) data to determine the structure of organic molec...
Repetitive lanthanide induced shift, LIS, experiments were performed with Eu(fod)[lowered 3] and Yb(...
Bleaney’s long-standing theory of magnetic anisotropy has been employed with some success for many d...
Lanthanide ions Yb(3+) and Tb(3+), once bound to the monolayer of organic molecules coating the surf...
The ^(15)N and ^(13)C chemical shift changes have been determined for ethylenediaminetetraacetic aci...
The possibility of contributions from contact interactions to the predominantly dipolar-induced chan...
Lanthanide-induced shifts of 13C nuclear magnetic resonances are reported for several amines and n-b...
Owing to the present accuracy of the data and various other factors, it is easy to obtain agreement ...
The utility of nmr shift reagents which function predominantly by the dipolar mechanism for structur...
Paramagnetic substances can produce two principal effects on the high resolution nuclear magnetic re...
The work in this thesis describes a detailed study of the nature of the interactions occurring in so...
The paper deals with the implications of shift reagents in organic chemistry in several broad areas....
Difficulties encountered in the use of lanthanide shift reagents for study of conformational equilib...
The pattern of 13C and 1H nuclear magnetic resonance (NMR) shift changes produced by complexation of...
[[abstract]]The action of a series of lanthanide chelate complexes LnL3, where Ln=La, Pr, Nd, Sm, Eu...
The problem of using lanthanide induced shift (LIS) data to determine the structure of organic molec...
Repetitive lanthanide induced shift, LIS, experiments were performed with Eu(fod)[lowered 3] and Yb(...
Bleaney’s long-standing theory of magnetic anisotropy has been employed with some success for many d...
Lanthanide ions Yb(3+) and Tb(3+), once bound to the monolayer of organic molecules coating the surf...
The ^(15)N and ^(13)C chemical shift changes have been determined for ethylenediaminetetraacetic aci...