Molybdenum magnetic shielding and quadrupolar tensors for a series of molybdate salts: a solid-state 95Mo NMR study.

نویسندگان

  • Michelle A M Forgeron
  • Roderick E Wasylishen
چکیده

A series of molybdate, MoO4(2-), salts have been studied using solid-state 95Mo NMR spectroscopy at applied magnetic field strengths of 11.75, 17.63 and 21.14 T. In contrast to previous investigations, the principal components of the Mo shielding and EFG tensors have been obtained, as well as their relative orientations. At the fields employed, the anisotropic Mo shielding and quadrupolar interactions make significant contributions to the observed 95Mo central transition NMR lineshapes. Based on available structural data, the extent of distortion of the MoO4(2-) anion from T(d) symmetry is reflected in the observed 95Mo nuclear quadrupolar coupling constants for the molybdate salts with divalent cations (i.e., Ca2+, Sr2+, Cd2+, Ba2+, Pb2+), but no correlation is found for molybdate salts containing the monovalent alkali metal (Li+, K+, Rb+, Cs+) cations.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Application of multinuclear magnetic resonance and gauge-including projector-augmented-wave calculations to the study of solid group 13 chlorides.

A series of four anhydrous group 13 chloride salts has been studied by (35/37)Cl solid-state NMR spectroscopy and complementary quantum chemical calculations. Due to the large (35/37)Cl quadrupolar interactions in these salts, a high magnetic field (21.1 T) and the variable-offset QCPMG technique was used to obtain full chlorine central transition (m = -1/2 <--> 1/2) NMR spectra. Analyses of th...

متن کامل

51V solid-state magic angle spinning NMR spectroscopy and DFT studies of oxovanadium(V) complexes mimicking the active site of vanadium haloperoxidases.

A series of 11 oxovanadium(V) complexes mimicking the active site of vanadium haloperoxidases have been investigated by (51)V magic angle spinning NMR spectroscopy and density functional theory (DFT). The MAS spectra are dominated by the anisotropic quadrupolar and chemical shielding interactions; for these compounds, C(Q) ranges from 3 to 8 MHz, and delta(sigma) is in the range 340-730 ppm. Th...

متن کامل

95Mo nuclear magnetic resonance parameters of molybdenum hexacarbonyl from density functional theory: appraisal of computational and geometrical parameters.

Solid-state (95)Mo nuclear magnetic resonance (NMR) properties of molybdenum hexacarbonyl have been computed using density functional theory (DFT) based methods. Both quadrupolar coupling and chemical shift parameters were evaluated and compared with parameters of high precision determined using single-crystal (95)Mo NMR experiments. Within a molecular approach, the effects of major computation...

متن کامل

Determination of quadrupolar and chemical shielding tensors using solid-state two-dimensional NMR spectroscopy

The quadrupolar and chemical shift tensors, as well as the relative orientation of the two principle axis systems, are accurately determined using a two-dimensional nuclear magnetic resonance technique. Good agreement between experimental and simulated two-dimensional spectra is obtained for a series of rubidium and sodium compounds at multiple magnetic field strengths. Extension of this techni...

متن کامل

Quadrupolar-shielding cross-correlations in solid state nuclear magnetic resonance: Detecting antisymmetric components in chemical shift tensors

This work investigates the nature of second order effects resulting in solid state nuclear magnetic resonance ~NMR!, from cross-correlations between the quadrupolar and shielding couplings. Using an average Hamiltonian theory, it is shown that these effects can bring the nonsecular terms of the shielding interaction into the realm of conventional detection. Such terms include the antisymmetric ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Physical chemistry chemical physics : PCCP

دوره 10 4  شماره 

صفحات  -

تاریخ انتشار 2008