Issue 33, 2012

C-HETSERF: distinction of cis/trans-isomers and measurement of long range couplings between chemically equivalent nuclei in polycyclic aromatic hydrocarbons

Abstract

The scalar couplings between chemically equivalent protons in symmetric molecules are not reflected in the NMR spectrum. The present study reports the utility of our previously reported two dimensional spin selective correlation experiment to measure the short and long range homo- and hetero-nuclear scalar couplings in such systems. In weakly coupled spin systems, the experiment also yields the relative signs of the couplings. The relative configurations of double bonded symmetrically disubstituted isomers could be determined from the measured long range vicinal proton-proton couplings (3JHH), owing to the fact that these couplings are consistently larger for trans isomers. The study also reveals that long range 2JCH cannot be utilized as an exclusive parameter for the identification of symmetrically disubstituted cis/trans isomers. The application of the methodology for the determination of couplings between the chemically equivalent protons in polycyclic aromatic hydrocarbons and in bigger molecules such as porphyrin, has also been demonstrated. The study, carried out on large number of molecules, shows the generality and wide applicability of the C-HETSERF experiment.

Graphical abstract: C-HETSERF: distinction of cis/trans-isomers and measurement of long range couplings between chemically equivalent nuclei in polycyclic aromatic hydrocarbons

Supplementary files

Article information

Article type
Paper
Submitted
22 Aug 2012
Accepted
24 Oct 2012
First published
25 Oct 2012

RSC Adv., 2012,2, 12915-12921

C-HETSERF: distinction of cis/trans-isomers and measurement of long range couplings between chemically equivalent nuclei in polycyclic aromatic hydrocarbons

S. R. Chaudhari, N. Nath and N. Suryaprakash, RSC Adv., 2012, 2, 12915 DOI: 10.1039/C2RA21898D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements