Assignment of the  1 H and  13 C NMR spectra of naphtho [1′,2′:4,5]thieno[2,3‐ c ]quinoline using two‐dimensional NMR spectroscopy | Zendy

Castle Lyle W. | Zendy; Zektzer Andrew S. | Zendy; Johnston Milton D. | Zendy

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Assignment of the 1 H and 13 C NMR spectra of naphtho [1′,2′:4,5]thieno[2,3‐ c ]quinoline using two‐dimensional NMR spectroscopy

Author(s) -

Castle Lyle W.,

Zektzer Andrew S.,

Johnston Milton D.

Publication year - 1992

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.1260300815

Subject(s) - chemistry , quinoline , nuclear magnetic resonance spectroscopy , carbon 13 nmr satellite , nmr spectra database , spectral line , spectroscopy , phosphorus 31 nmr spectroscopy , transverse relaxation optimized spectroscopy , fluorine 19 nmr , carbon 13 nmr , molecule , two dimensional nuclear magnetic resonance spectroscopy , nuclear magnetic resonance crystallography , deuterium nmr , crystallography , proton nmr , nuclear magnetic resonance spectroscopy of nucleic acids , stereochemistry , organic chemistry , physics , quantum mechanics , astronomy

The 1 H NMR spectrum of naphtho [1′,2′:4,5]thieno[2,3‐ c ]quinoline is highly congested because all the protons are in an aromatic environment, and the structure of the molecule is nearly symmetric. With this in mind, the assignment of the 1 H and 13 C NMR spectra of this compound obtained using two‐dimensional NMR spectroscopy is reported.

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