𝔖 Bobbio Scriptorium

✦ LIBER ✦

Electronic properties of para-substituted thiophenols and disulfides from 13C NMR spectroscopy and ab initio calculations: relations to the Hammett parameters and atomic chargesElectronic supplementary information (ESI) available: all characterization data are tabulated in Table S1. A figure showing the dependence of the natural charge of the C1 atom of the disulfides on the 13C NMR chemical shift is also provided. See http://www.rsc.org/suppdata/nj/b3/b300048f/

✍ Scribed by Sengar, Raghvendra S.; Nemykin, Victor N.; Basu, Partha

Book ID: 120020575
Publisher: Royal Society of Chemistry
Year: 2003
Tongue: English
Weight: 316 KB
Volume: 27
Category: Article
ISSN: 1144-0546
DOI: 10.1039/B300048F

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,3-diazepinones, and 2,4-diazabicyclo[3.2.0]heptenesPreliminary reports on parts of this work have been published in ref 1. This paper is Diazepines, Part 3. For Part 2, see ref 2.,Electronic supplementary information (ESI) available: NMR spectra of 4a, 4c, 19v ? 20, 19a ? 25a, and 19g ? 25g (Fig. S1?S6), Arrhenius and Eyring plots for H-exchange in 4b,c (Fig. S7), views of the X-ray crystal structures of compounds 26 and 22bB (Fig. S8?S9), bond lengths and angles for compounds 4k, 22bB and 26, preparative procedures and characterization data for all compounds not described in the Experimental section, and computational data (Cartesian coordinates, absolute energies, IR, 1H and 13C NMR) for 20a?c, 21a?b, 22aA?F and 22aB dimer. See http://www.rsc.org/suppdata/ob/b3/b317099c/

✍ Reisinger, Ales; Koch, Rainer; Bernhardt, Paul V.; Wentrup, Curt 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 496 KB