oaioai:acikerisim.pau.edu.tr:11499/13066

spectroscopies

Abstract

The H-1 and C-13 NMR spectra of the new calix[4]arene-based tetraketone were completely assigned by one- and two-dimensional homo- and heteronuclear experiments (H-1-H-1 COSY, H-1-C-13 HMQC, and HMBC) at 400 and 100 MHz, respectively, at 25 degrees C standard pulse sequence. I H and 13C spectra were measured at room temperature for 25,26,27,28-tetramethylcalix[4]arene tetraketone (1). C-13{H-1}, DEPT and NMR techniques were used to distinguish the methyl, methylene and methine carbon resonance signals of calix[4]arene 1. Correlation of 1D (H-1, C-13{H-1}, DEPT) and 2D (HMQC and HMBC) NMR data was used to completely assign various overlapping and broad signals of calix[4]arene 1. Heteronuclear multibond correlation (HMBC) studies were used to completely assign various carbon resonances. Our results show that the conformation of calix[4]arene 1 in the solution is very similar to the cone conformation reported in the literature. (C) 2009 Elsevier B.V. All rights reserved

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oaioai:acikerisim.pau.edu.tr:11499/13066Last time updated on 9/5/2019

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