Substituent effects in 29Si nmr of ring-substituted phenoxy- and phenyl-silanes, enhancement by the oxygen link
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference8 articles.
1. Application of 29Si-NMR to analysis of silylated compounds. NMR spectra of (CH3)3Si-O-C derivatives
2. Zur Interpretation29Si-NMR-chemischer Verschiebungen
3. Silicon-29 nuclear magnetic resonance. Chemical shift substituent effects
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1. The effect of solvent accessible surface on Hammett-type dependencies of infinite dilution 29Si and 13C NMR shifts in ring substituted silylated phenols dissolved in chloroform and acetone;Magnetic Resonance in Chemistry;2012-02
2. Silicon-29 NMR data of C9H14OSi;Chemical Shifts and Coupling Constants for Silicon-29;2008
3. Synthesis and Spectroscopic Properties of the First Series of Heteronuclear Derivatives Containing Organosilicon/Organotin (IV) and Oxovanadium (V) Moieties;Phosphorus, Sulfur, and Silicon and the Related Elements;2006-01-01
4. Efficient O-Trimethylsilylation of Alcohols and Phenols with Trimethylsilyl Azide Catalyzed by Tetrabutylammonium Bromide under Neat Conditions;The Journal of Organic Chemistry;2001-09-11
5. SYNTHESIS AND SPECTROSCOPIC [IR, NMR (1H,13C,29Si)] CHARACTERIZATION OF METHYLSILYL N-ARYLSALICYLALDIMINATES;Phosphorus, Sulfur, and Silicon and the Related Elements;2001-08
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