NMR Spectral Studies of Some Six–Membered and Seven–Membered Saturated Heterocyclic Compound t[3]–Ethyl-r[2],c[7]-Diphenylhomopiperazin–5–One

V  Krishnasamy  and G  Mathubala

doi:10.17485/ijst/2014/v7sp3.15

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NMR Spectral Studies of Some Six–Membered and Seven–Membered Saturated Heterocyclic Compound t[3]–Ethyl-r[2],c[7]-Diphenylhomopiperazin–5–One

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Indian Journal of Science and Technology

DOI: 10.17485/ijst/2014/v7sp3.15

Year: 2020, Volume: 7, Issue: Supplementary 3, Pages: 69–71

Original Article

NMR Spectral Studies of Some Six–Membered and Seven–Membered Saturated Heterocyclic Compound t[3]–Ethyl-r[2],c[7]-Diphenylhomopiperazin–5–One

V. Krishnasamy* and G. Mathubala

Bharath University, Selaiyur, Chennai–600 073, India; nadippi@gmail.com, madhu2705@gmail.com

This work is licensed under a Creative Commons Attribution 4.0 International License.

Abstract

Some six and seven membered saturated hetero cyclic compounds were prepared. 1 H NMR were recorded in DMSO – d6 . The chemical shifts were compared with those in CDCl3 . The COSY, NOESY and 13C-1 H correlation spectra had been recorded to assign the signals unambiguously. The coupling constant of benzylic proton with one of the vicinal proton was found to be zero. The buffering effect of alkyl groups was also studied. The chemical shift values, area of the signals, multiplicity, COSY and NOESY spectra were used to assign the signals. Further COSY and NOESY and 13C - 1 H correlation spectra were also used. The solvent effect, concentration effect, and temperature effect were also studied using DMSO- d6 and CDCl3 . αeffect, and polar nature of the neighbouring group were also studied.

Keywords: Assignment, Correlation, Chemical shift, Isopropyl, Multiplets, NOE, Peak, Signal