Carbon‐13 NMR of solid phenylazo‐2‐naphthols: Tautomerism and ( 13 C,  14 N) residual dipolar coupling | Zendy

Harris Robin K. | Zendy; Jonsen Paul | Zendy; Packer Kenneth J. | Zendy; Campbell Colin D. | Zendy

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Carbon‐13 NMR of solid phenylazo‐2‐naphthols: Tautomerism and ( 13 C, 14 N) residual dipolar coupling

Author(s) -

Harris Robin K.,

Jonsen Paul,

Packer Kenneth J.,

Campbell Colin D.

Publication year - 1986

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.1260241110

Subject(s) - tautomer , chemistry , residual dipolar coupling , residual , carbon 13 nmr , computational chemistry , coupling (piping) , dipole , magnetic dipole–dipole interaction , nuclear magnetic resonance spectroscopy , analytical chemistry (journal) , stereochemistry , organic chemistry , mechanical engineering , algorithm , computer science , engineering

The use of 13 C CP/MAS NMR is illustrated by the determination of the tautomeric structures of some phenylazo‐2‐naphthols in the solid state. The effects of ( 13 C, 14 N) residual dipolar coupling for such systems are discussed.

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